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OUR STORY THIS CHRISTMAS

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Hi,

THROUGHOUT THIS TIME AND UP TO NOW, GOD HAS BEEN

SO FAITHFUL TO US. HE IS BEAUTIFUL AND AWESOME. WE ARE SO

THANKFUL FOR THE PRIVILEGE OF "CARRYING" US AND MOLDING US.

HE WHO DWELLS IN THE SHELTER OF THE MOST HIGH WILL REST

IN THE SHADOW OF THE ALMIGHTY. - PSALM 91:1

A day after Christmas, we share our story to our love ones, to our families

and friends. After many years since 2008, we hide our predicament to them.

The reaon we hide it because the father of Abe had hypertension and wedon't want him to worry. And also his Dad and Mom will surely go to Manaog, a placein the Philippines where they say they see the image of the Virgin .Peope go there for petition to the Virgin . We don't want it to happen because itwill steal the glory of the Lord Jesus in their mind. They will say, Abe is healed bec.of this. His Mom had a heart problem and died without knowing the condition of Abe.

I know my Mom will always call me everyday crying. We don't like it either,

will put our spirit down. And also during that time, our life is just normal, we could care,

give, work, serve without our family and others worrying about us. This e-mail is

the one I sent to them, I just cut the portion that I asked forgiveness for not telling

our family and close friends for a long time. May the Lord bless you... I know my e-mail is long. Jan. 2008, Abe, my husband was diagnosed with colorectal CA. Jan. 24, 2008 they startchemotherapy and radiation. Chemo , he had a pump in a bag and will still go towork. This was during winter time in Iowa. The chemo will flow 48 hours and by thethird day , a nurse will come to the house and remove it every 2 weeks. Aside from that,

he needed to go to hospital for IV chemo once every 2 weeks and radiation Monday

to Friday for 28 sessions and go back to work after that. He will still work more

hours the following day to make up the hours lost during chemo and radiation and had on-call

at night. He cannot hide this bag from co-workers even working in lab. gown.

Chemo and radiation was done by April. May 17, 2008, we attended my nephew's

wedding (my eldest brother's son) with . In all these things,

God is very faithful. We even danced for 5 hours continuously. At this time,

Abe had a port for chemo in his chest. God is carrying us. It's a privelege that Lord Jesusis carrying us throughout. He never leave us nor forsake us. God gave us a comforting

peace and no one knew our predicament.

June, 2008, the surgeons did a resection of the colorectal mass (cancer)

and had ileostomy. So, Abe need to have colostomy bag/pouch for his # 2 for 6 months.

After surgery, they did chmotherapy for 6 months. Still the same, he was still working.

By January, 2009, they reversed the ileostomy and now he could use his bottom again.

He went to the Philippines to attend the funeral of Abe's Mom. The plan was to tell

them now the past health history of Abe but since they still in mourn, Abe was not

able to say it and it means we cannot say it to everyone. We wanted to tell the Dad in person

so that he could see that Abe is well.

Before we leave Iowa, they saw a new mass in the lung and we came to California,

it was confirmed through biopsy that the colorectal cancer metastasize or meaning

same cells went to the left lung. Abe did chemo for 6 months again, this time

the chemo was more aggressive. Chemo started Monday with an IV chemo in cancer

center that lasted about 4 hours, then will go home with a chemo pump in a bag that will flow

for 48 hours. Then Wednesday, he would go back to the center for them to remove

the chemo pump. After 6 months of chemo, had another set of chemotherapy, higher dose and much

more aggresive. During that time, he had 2 works, Antelope Valley Hosp. and Palmalde Regional

Hospital where he was confined. Then he lost the job in Antelope Valley and just concentrate

on Palmdale Regional Hospital. He was still working and only absent himself every chemo time and a day.

Then, he had rest for 1 1/2 months from chemo and had upper lobe lobectomy of the

left lung. Left lung has 2 lobes and they got the upper lobe. Right lung has 3 lobes.

The lobectomy was done Dec 8, 2011 (Thursday). This is for CURE, unlike other

Stage 4 that do treatments only for control. We went home Dec. 11 (Sunday)

and by Wednesday, Dec. 14, he had a stroke. Dec. 16, Friday, he had right decompression

of the brain. Today, Christmas time, a chest tube was placed because of pneumo-

thorax (the left lung that had operation was collapsed due to air outside of the left lung, in the

pleural space. The chest tube was needed to get rid of the air and made the left lung to function well

again and they do successive x-rays to compare things). Before the chest tube was

placed, we had a good talk to surrender ourselves to God and testify about his grace

and mercy to us. And Abe said YES. Praise the Lord. We are just waiting for rehab but since we are

still in the hospital, the doctor ordered chest x-ray and was found to have pneumothorax. It's

a blessing in disguise since we were still in the hospital and no difficulty of

breathing yet. If we already go to the rehab, for sure at some point we will go back

to emergency room because of this. GOD IS GOOD.

The situation made us closer to Him and to each other. I will usually go to him Wednesday

and eat lunch at the car, parked in the hospital and will enjoy each other. We chose Wednesday

bec. this day is longer than the other days, the family attends Midweek Service at Highland's

Church. Even we were married 12 years next June of 2012, I still consider him my boyfriend and

I'm his girlfriend. I cannot explain, in the midst of everything, we are so happy and content.

God's way is so different, work helped him a lot than not doing anything Thank you Lord.

Thank you very much for reading our story. We lived a "normal" life withot our family and

other close friends knowing it. We had the privilege of giving and caring without them worrying

about us. Some people asked for help without hesitation. Aside from this, we also had therapies

for AJ , our younger daughter who was diagnosed with autism secondary to metals from vaccination.

She was found to have different kinds of metals in her body that needed to be chelated and the

same sypmptoms with autism. We tried a lot of alternative medicine and up to now

we are still believing that she will be healed in the name of Jesus. She is so normal

and so intelligent. At 1 and 1/2 years old, she knew all the sounds of the letters.

At 2 years old, she was almost reading then also at this time after 18 months

vaccination, she started to regress and was unable to speak. Now, she could

speak per word but then we are still not losing hope for her. It's very hard

because I saw her potentials. But since insurance won't shoulder alternative medicine,

we needed to pay out of our pocket. We are still doing alternative medicine. The

doctor is healing first her gut due to a lot of food insensitivities/ GIT inflammation

damaged by the metals. Then the doctor will do chelation to get rid of metals.

Please pray also for AJ. She is already 6 years old, attending special education,

first grade and doing therapies, 3 1/2 hours of therapies everyday in our house,

total of 20 hours per week in our house. I joined a yahoo group, the same condition

of AJ, and some kids were recovered from this condition. The parents who recovered

their kids are helping those who wanted to recover other kids thru discussion

via e-mails. There's no particular treatment. Each child was affected by

metals differently. Companies uses metals to preserve the vaccines. The statistic

of autism before is 1 in 10,000 around, 1980's ..now it's 1 in 100 , increased

statistic not only in US but other countries.

During those time, and up to now, It is the Lord Jesus carrying us.

This is God's battle, not ours and we won already through CHRIST. I hope

our family won't feel betrayed, we experienced the care of our Lord Jesus in

a very special way.

THANK YOU ALL FOR YOUR PRAYERS. GOD IS IN CONTROL.

I LOVE YOU, LORD. PLEASE PRAY FOR FASTER AND COMPLETE RECOVERY.

BY JESUS' STRIPES, ABE AND AJ WERE HEALED.

Victory in Christ,

Mhel

PS. I JUST FELT THAT ABE'S DAD NEED TO KNOW THIS FIRST.

I CALLED HIM AND HE KNEW ALREADY AND RECEIVED THE NEWS

WELL. IT'S A BLESSING THAT WE WERE IN THE UNITED STATES OR

ELSE WE DON'T KNOW HOW TO GET RESOURCES FOR THE TREATMENT.

I TOLD HIM THAT THE REASON WE DID NOT TELL HIM IS FOR HIM NOT TO WORRY AND ALSO

WE DON'T WANT THEM TO GO TO MANAOG AND PETITION

IT THERE BECAUSE THE VIRGIIN MARY IS ONLY HUMAN AND JESUS

IS THE LORD BUT MARY WOULD BE HAPPY IF HE WILL RECEIVE JESUS

IN HIS HEART. THANK YOU HOLY SPIRIT FOR ANNOINTING THIS E-MAIL.

WE LOVE YOU DADDY VERY MUCH.

FOR THOSE WHO WANTED TO EXPERIENCE THE LOVE, CARE , SUPPORT,

COMFORTING AND SAVING PEACE OF GOD: JUST RECEIVE THE GIFT

AND SAY THIS PRAYER AND MEAN IT FROM YOUR HEART:

LORD JESUS, COME TO MY HEART. I BELIEVE THAT YOU DIED IN THE

CROSS FOR MY SINS. BE MY SAVIOR AND TAKE CONTROL OF MY LIFE.

THANK YOU LORD.

JUST BY PRAYING THIS SIMPLE PRAYER, YOU BECOME A CHILD OF

GOD. EXPECT CHANGES IN YOUR LIFE AND YOU WILL BE ASSURED

OF ETERNAL LIFE IN HEAVEN. YOU WILL HAVE A DESIRE TO READ

THE BIBLE, THE WORD OF GOD. YOU WON'T REGRET.

MERRY CHRISTMAS AND HAVE A BLESSED NEW YEAR !!!

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oh Mhel....what can i say except that I feel you a kindred spirit and love you with all my heart even thou i never met you....may Gods angels continue to lift you up and give you strength...

To: mb12valtrex Sent: Thursday, December 29, 2011 4:59 AMSubject: OUR STORY THIS CHRISTMAS

Hi,

THROUGHOUT THIS TIME AND UP TO NOW, GOD HAS BEEN

SO FAITHFUL TO US. HE IS BEAUTIFUL AND AWESOME. WE ARE SO

THANKFUL FOR THE PRIVILEGE OF "CARRYING" US AND MOLDING US.

HE WHO DWELLS IN THE SHELTER OF THE MOST HIGH WILL REST

IN THE SHADOW OF THE ALMIGHTY. - PSALM 91:1

A day after Christmas, we share our story to our love ones, to our families

and friends. After many years since 2008, we hide our predicament to them.

The reaon we hide it because the father of Abe had hypertension and wedon't want him to worry. And also his Dad and Mom will surely go to Manaog, a placein the Philippines where they say they see the image of the Virgin .Peope go there for petition to the Virgin . We don't want it to happen because itwill steal the glory of the Lord Jesus in their mind. They will say, Abe is healed bec.of this. His Mom had a heart problem and died without knowing the condition of Abe.

I know my Mom will always call me everyday crying. We don't like it either,

will put our spirit down. And also during that time, our life is just normal, we could care,

give, work, serve without our family and others worrying about us. This e-mail is

the one I sent to them, I just cut the portion that I asked forgiveness for not telling

our family and close friends for a long time. May the Lord bless you... I know my e-mail is long. Jan. 2008, Abe, my husband was diagnosed with colorectal CA. Jan. 24, 2008 they startchemotherapy and radiation. Chemo , he had a pump in a bag and will still go towork. This was during winter time in Iowa. The chemo will flow 48 hours and by thethird day , a nurse will come to the house and remove it every 2 weeks. Aside from that,

he needed to go to hospital for IV chemo once every 2 weeks and radiation Monday

to Friday for 28 sessions and go back to work after that. He will still work more

hours the following day to make up the hours lost during chemo and radiation and had on-call

at night. He cannot hide this bag from co-workers even working in lab. gown.

Chemo and radiation was done by April. May 17, 2008, we attended my nephew's

wedding (my eldest brother's son) with . In all these things,

God is very faithful. We even danced for 5 hours continuously. At this time,

Abe had a port for chemo in his chest. God is carrying us. It's a privelege that Lord Jesusis carrying us throughout. He never leave us nor forsake us. God gave us a comforting

peace and no one knew our predicament.

June, 2008, the surgeons did a resection of the colorectal mass (cancer)

and had ileostomy. So, Abe need to have colostomy bag/pouch for his # 2 for 6 months.

After surgery, they did chmotherapy for 6 months. Still the same, he was still working.

By January, 2009, they reversed the ileostomy and now he could use his bottom again.

He went to the Philippines to attend the funeral of Abe's Mom. The plan was to tell

them now the past health history of Abe but since they still in mourn, Abe was not

able to say it and it means we cannot say it to everyone. We wanted to tell the Dad in person

so that he could see that Abe is well.

Before we leave Iowa, they saw a new mass in the lung and we came to California,

it was confirmed through biopsy that the colorectal cancer metastasize or meaning

same cells went to the left lung. Abe did chemo for 6 months again, this time

the chemo was more aggressive. Chemo started Monday with an IV chemo in cancer

center that lasted about 4 hours, then will go home with a chemo pump in a bag that will flow

for 48 hours. Then Wednesday, he would go back to the center for them to remove

the chemo pump. After 6 months of chemo, had another set of chemotherapy, higher dose and much

more aggresive. During that time, he had 2 works, Antelope Valley Hosp. and Palmalde Regional

Hospital where he was confined. Then he lost the job in Antelope Valley and just concentrate

on Palmdale Regional Hospital. He was still working and only absent himself every chemo time and a day.

Then, he had rest for 1 1/2 months from chemo and had upper lobe lobectomy of the

left lung. Left lung has 2 lobes and they got the upper lobe. Right lung has 3 lobes.

The lobectomy was done Dec 8, 2011 (Thursday). This is for CURE, unlike other

Stage 4 that do treatments only for control. We went home Dec. 11 (Sunday)

and by Wednesday, Dec. 14, he had a stroke. Dec. 16, Friday, he had right decompression

of the brain. Today, Christmas time, a chest tube was placed because of pneumo-

thorax (the left lung that had operation was collapsed due to air outside of the left lung, in the

pleural space. The chest tube was needed to get rid of the air and made the left lung to function well

again and they do successive x-rays to compare things). Before the chest tube was

placed, we had a good talk to surrender ourselves to God and testify about his grace

and mercy to us. And Abe said YES. Praise the Lord. We are just waiting for rehab but since we are

still in the hospital, the doctor ordered chest x-ray and was found to have pneumothorax. It's

a blessing in disguise since we were still in the hospital and no difficulty of

breathing yet. If we already go to the rehab, for sure at some point we will go back

to emergency room because of this. GOD IS GOOD.

The situation made us closer to Him and to each other. I will usually go to him Wednesday

and eat lunch at the car, parked in the hospital and will enjoy each other. We chose Wednesday

bec. this day is longer than the other days, the family attends Midweek Service at Highland's

Church. Even we were married 12 years next June of 2012, I still consider him my boyfriend and

I'm his girlfriend. I cannot explain, in the midst of everything, we are so happy and content.

God's way is so different, work helped him a lot than not doing anything Thank you Lord.

Thank you very much for reading our story. We lived a "normal" life withot our family and

other close friends knowing it. We had the privilege of giving and caring without them worrying

about us. Some people asked for help without hesitation. Aside from this, we also had therapies

for AJ , our younger daughter who was diagnosed with autism secondary to metals from vaccination.

She was found to have different kinds of metals in her body that needed to be chelated and the

same sypmptoms with autism. We tried a lot of alternative medicine and up to now

we are still believing that she will be healed in the name of Jesus. She is so normal

and so intelligent. At 1 and 1/2 years old, she knew all the sounds of the letters.

At 2 years old, she was almost reading then also at this time after 18 months

vaccination, she started to regress and was unable to speak. Now, she could

speak per word but then we are still not losing hope for her. It's very hard

because I saw her potentials. But since insurance won't shoulder alternative medicine,

we needed to pay out of our pocket. We are still doing alternative medicine. The

doctor is healing first her gut due to a lot of food insensitivities/ GIT inflammation

damaged by the metals. Then the doctor will do chelation to get rid of metals.

Please pray also for AJ. She is already 6 years old, attending special education,

first grade and doing therapies, 3 1/2 hours of therapies everyday in our house,

total of 20 hours per week in our house. I joined a yahoo group, the same condition

of AJ, and some kids were recovered from this condition. The parents who recovered

their kids are helping those who wanted to recover other kids thru discussion

via e-mails. There's no particular treatment. Each child was affected by

metals differently. Companies uses metals to preserve the vaccines. The statistic

of autism before is 1 in 10,000 around, 1980's ..now it's 1 in 100 , increased

statistic not only in US but other countries.

During those time, and up to now, It is the Lord Jesus carrying us.

This is God's battle, not ours and we won already through CHRIST. I hope

our family won't feel betrayed, we experienced the care of our Lord Jesus in

a very special way.

THANK YOU ALL FOR YOUR PRAYERS. GOD IS IN CONTROL.

I LOVE YOU, LORD. PLEASE PRAY FOR FASTER AND COMPLETE RECOVERY.

BY JESUS' STRIPES, ABE AND AJ WERE HEALED.

Victory in Christ,

Mhel

PS. I JUST FELT THAT ABE'S DAD NEED TO KNOW THIS FIRST.

I CALLED HIM AND HE KNEW ALREADY AND RECEIVED THE NEWS

WELL. IT'S A BLESSING THAT WE WERE IN THE UNITED STATES OR

ELSE WE DON'T KNOW HOW TO GET RESOURCES FOR THE TREATMENT.

I TOLD HIM THAT THE REASON WE DID NOT TELL HIM IS FOR HIM NOT TO WORRY AND ALSO

WE DON'T WANT THEM TO GO TO MANAOG AND PETITION

IT THERE BECAUSE THE VIRGIIN MARY IS ONLY HUMAN AND JESUS

IS THE LORD BUT MARY WOULD BE HAPPY IF HE WILL RECEIVE JESUS

IN HIS HEART. THANK YOU HOLY SPIRIT FOR ANNOINTING THIS E-MAIL.

WE LOVE YOU DADDY VERY MUCH.

FOR THOSE WHO WANTED TO EXPERIENCE THE LOVE, CARE , SUPPORT,

COMFORTING AND SAVING PEACE OF GOD: JUST RECEIVE THE GIFT

AND SAY THIS PRAYER AND MEAN IT FROM YOUR HEART:

LORD JESUS, COME TO MY HEART. I BELIEVE THAT YOU DIED IN THE

CROSS FOR MY SINS. BE MY SAVIOR AND TAKE CONTROL OF MY LIFE.

THANK YOU LORD.

JUST BY PRAYING THIS SIMPLE PRAYER, YOU BECOME A CHILD OF

GOD. EXPECT CHANGES IN YOUR LIFE AND YOU WILL BE ASSURED

OF ETERNAL LIFE IN HEAVEN. YOU WILL HAVE A DESIRE TO READ

THE BIBLE, THE WORD OF GOD. YOU WON'T REGRET.

MERRY CHRISTMAS AND HAVE A BLESSED NEW YEAR !!!

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Share on other sites

Thank you for sharing your story, Mhel. I will keep you and your family close to my heart and in my prayers. Faith will carry you through and provide a beautiful testimony to those around you. May the Lord continue to give you strength. Much love to you and yours! -Tammy To: "mb12valtrex " <mb12valtrex > Sent: Thursday, December 29, 2011 11:02 AM Subject: Re: OUR STORY THIS CHRISTMAS

oh Mhel....what can i say except that I feel you a kindred spirit and love you with all my heart even thou i never met you....may Gods angels continue to lift you up and give you strength...

To: mb12valtrex Sent: Thursday, December 29, 2011 4:59 AMSubject: OUR STORY THIS CHRISTMAS

Hi,

THROUGHOUT THIS TIME AND UP TO NOW, GOD HAS BEEN

SO FAITHFUL TO US. HE IS BEAUTIFUL AND AWESOME. WE ARE SO

THANKFUL FOR THE PRIVILEGE OF "CARRYING" US AND MOLDING US.

HE WHO DWELLS IN THE SHELTER OF THE MOST HIGH WILL REST

IN THE SHADOW OF THE ALMIGHTY. - PSALM 91:1

A day after Christmas, we share our story to our love ones, to our families

and friends. After many years since 2008, we hide our predicament to them.

The reaon we hide it because the father of Abe had hypertension and wedon't want him to worry. And also his Dad and Mom will surely go to Manaog, a placein the Philippines where they say they see the image of the Virgin .Peope go there for petition to the Virgin . We don't want it to happen because itwill steal the glory of the Lord Jesus in their mind. They will say, Abe is healed bec.of this. His Mom had a heart problem and died without knowing the condition of Abe.

I know my Mom will always call me everyday crying. We don't like it either,

will put our spirit down. And also during that time, our life is just normal, we could care,

give, work, serve without our family and others worrying about us. This e-mail is

the one I sent to them, I just cut the portion that I asked forgiveness for not telling

our family and close friends for a long time. May the Lord bless you... I know my e-mail is long. Jan. 2008, Abe, my husband was diagnosed with colorectal CA. Jan. 24, 2008 they startchemotherapy and radiation. Chemo , he had a pump in a bag and will still go towork. This was during winter time in Iowa. The chemo will flow 48 hours and by thethird day , a nurse will come to the house and remove it every 2 weeks. Aside from that,

he needed to go to hospital for IV chemo once every 2 weeks and radiation Monday

to Friday for 28 sessions and go back to work after that. He will still work more

hours the following day to make up the hours lost during chemo and radiation and had on-call

at night. He cannot hide this bag from co-workers even working in lab. gown.

Chemo and radiation was done by April. May 17, 2008, we attended my nephew's

wedding (my eldest brother's son) with . In all these things,

God is very faithful. We even danced for 5 hours continuously. At this time,

Abe had a port for chemo in his chest. God is carrying us. It's a privelege that Lord Jesusis carrying us throughout. He never leave us nor forsake us. God gave us a comforting

peace and no one knew our predicament.

June, 2008, the surgeons did a resection of the colorectal mass (cancer)

and had ileostomy. So, Abe need to have colostomy bag/pouch for his # 2 for 6 months.

After surgery, they did chmotherapy for 6 months. Still the same, he was still working.

By January, 2009, they reversed the ileostomy and now he could use his bottom again.

He went to the Philippines to attend the funeral of Abe's Mom. The plan was to tell

them now the past health history of Abe but since they still in mourn, Abe was not

able to say it and it means we cannot say it to everyone. We wanted to tell the Dad in person

so that he could see that Abe is well.

Before we leave Iowa, they saw a new mass in the lung and we came to California,

it was confirmed through biopsy that the colorectal cancer metastasize or meaning

same cells went to the left lung. Abe did chemo for 6 months again, this time

the chemo was more aggressive. Chemo started Monday with an IV chemo in cancer

center that lasted about 4 hours, then will go home with a chemo pump in a bag that will flow

for 48 hours. Then Wednesday, he would go back to the center for them to remove

the chemo pump. After 6 months of chemo, had another set of chemotherapy, higher dose and much

more aggresive. During that time, he had 2 works, Antelope Valley Hosp. and Palmalde Regional

Hospital where he was confined. Then he lost the job in Antelope Valley and just concentrate

on Palmdale Regional Hospital. He was still working and only absent himself every chemo time and a day.

Then, he had rest for 1 1/2 months from chemo and had upper lobe lobectomy of the

left lung. Left lung has 2 lobes and they got the upper lobe. Right lung has 3 lobes.

The lobectomy was done Dec 8, 2011 (Thursday). This is for CURE, unlike other

Stage 4 that do treatments only for control. We went home Dec. 11 (Sunday)

and by Wednesday, Dec. 14, he had a stroke. Dec. 16, Friday, he had right decompression

of the brain. Today, Christmas time, a chest tube was placed because of pneumo-

thorax (the left lung that had operation was collapsed due to air outside of the left lung, in the

pleural space. The chest tube was needed to get rid of the air and made the left lung to function well

again and they do successive x-rays to compare things). Before the chest tube was

placed, we had a good talk to surrender ourselves to God and testify about his grace

and mercy to us. And Abe said YES. Praise the Lord. We are just waiting for rehab but since we are

still in the hospital, the doctor ordered chest x-ray and was found to have pneumothorax. It's

a blessing in disguise since we were still in the hospital and no difficulty of

breathing yet. If we already go to the rehab, for sure at some point we will go back

to emergency room because of this. GOD IS GOOD.

The situation made us closer to Him and to each other. I will usually go to him Wednesday

and eat lunch at the car, parked in the hospital and will enjoy each other. We chose Wednesday

bec. this day is longer than the other days, the family attends Midweek Service at Highland's

Church. Even we were married 12 years next June of 2012, I still consider him my boyfriend and

I'm his girlfriend. I cannot explain, in the midst of everything, we are so happy and content.

God's way is so different, work helped him a lot than not doing anything Thank you Lord.

Thank you very much for reading our story. We lived a "normal" life withot our family and

other close friends knowing it. We had the privilege of giving and caring without them worrying

about us. Some people asked for help without hesitation. Aside from this, we also had therapies

for AJ , our younger daughter who was diagnosed with autism secondary to metals from vaccination.

She was found to have different kinds of metals in her body that needed to be chelated and the

same sypmptoms with autism. We tried a lot of alternative medicine and up to now

we are still believing that she will be healed in the name of Jesus. She is so normal

and so intelligent. At 1 and 1/2 years old, she knew all the sounds of the letters.

At 2 years old, she was almost reading then also at this time after 18 months

vaccination, she started to regress and was unable to speak. Now, she could

speak per word but then we are still not losing hope for her. It's very hard

because I saw her potentials. But since insurance won't shoulder alternative medicine,

we needed to pay out of our pocket. We are still doing alternative medicine. The

doctor is healing first her gut due to a lot of food insensitivities/ GIT inflammation

damaged by the metals. Then the doctor will do chelation to get rid of metals.

Please pray also for AJ. She is already 6 years old, attending special education,

first grade and doing therapies, 3 1/2 hours of therapies everyday in our house,

total of 20 hours per week in our house. I joined a yahoo group, the same condition

of AJ, and some kids were recovered from this condition. The parents who recovered

their kids are helping those who wanted to recover other kids thru discussion

via e-mails. There's no particular treatment. Each child was affected by

metals differently. Companies uses metals to preserve the vaccines. The statistic

of autism before is 1 in 10,000 around, 1980's ..now it's 1 in 100 , increased

statistic not only in US but other countries.

During those time, and up to now, It is the Lord Jesus carrying us.

This is God's battle, not ours and we won already through CHRIST. I hope

our family won't feel betrayed, we experienced the care of our Lord Jesus in

a very special way.

THANK YOU ALL FOR YOUR PRAYERS. GOD IS IN CONTROL.

I LOVE YOU, LORD. PLEASE PRAY FOR FASTER AND COMPLETE RECOVERY.

BY JESUS' STRIPES, ABE AND AJ WERE HEALED.

Victory in Christ,

Mhel

PS. I JUST FELT THAT ABE'S DAD NEED TO KNOW THIS FIRST.

I CALLED HIM AND HE KNEW ALREADY AND RECEIVED THE NEWS

WELL. IT'S A BLESSING THAT WE WERE IN THE UNITED STATES OR

ELSE WE DON'T KNOW HOW TO GET RESOURCES FOR THE TREATMENT.

I TOLD HIM THAT THE REASON WE DID NOT TELL HIM IS FOR HIM NOT TO WORRY AND ALSO

WE DON'T WANT THEM TO GO TO MANAOG AND PETITION

IT THERE BECAUSE THE VIRGIIN MARY IS ONLY HUMAN AND JESUS

IS THE LORD BUT MARY WOULD BE HAPPY IF HE WILL RECEIVE JESUS

IN HIS HEART. THANK YOU HOLY SPIRIT FOR ANNOINTING THIS E-MAIL.

WE LOVE YOU DADDY VERY MUCH.

FOR THOSE WHO WANTED TO EXPERIENCE THE LOVE, CARE , SUPPORT,

COMFORTING AND SAVING PEACE OF GOD: JUST RECEIVE THE GIFT

AND SAY THIS PRAYER AND MEAN IT FROM YOUR HEART:

LORD JESUS, COME TO MY HEART. I BELIEVE THAT YOU DIED IN THE

CROSS FOR MY SINS. BE MY SAVIOR AND TAKE CONTROL OF MY LIFE.

THANK YOU LORD.

JUST BY PRAYING THIS SIMPLE PRAYER, YOU BECOME A CHILD OF

GOD. EXPECT CHANGES IN YOUR LIFE AND YOU WILL BE ASSURED

OF ETERNAL LIFE IN HEAVEN. YOU WILL HAVE A DESIRE TO READ

THE BIBLE, THE WORD OF GOD. YOU WON'T REGRET.

MERRY CHRISTMAS AND HAVE A BLESSED NEW YEAR !!!

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Share on other sites

Dear Channa and Tammy,

Thank you very much. Your response means a lot. God is faithful. He

uses people like you to encourage us. May God bless you beyond your

imagination. I'm so happy that I'm part of this group. Your post/support really

help a lot of Moms and Dads.

Hugs and kisses,

Mhel

To: mb12valtrex From: t.lynn28@...Date: Thu, 29 Dec 2011 08:34:36 -0800Subject: Re: OUR STORY THIS CHRISTMAS

Thank you for sharing your story, Mhel. I will keep you and your family close to my heart and in my prayers. Faith will carry you through and provide a beautiful testimony to those around you. May the Lord continue to give you strength.

Much love to you and yours!

-Tammy

To: "mb12valtrex " <mb12valtrex > Sent: Thursday, December 29, 2011 11:02 AMSubject: Re: OUR STORY THIS CHRISTMAS

oh Mhel....what can i say except that I feel you a kindred spirit and love you with all my heart even thou i never met you....may Gods angels continue to lift you up and give you strength...

To: mb12valtrex Sent: Thursday, December 29, 2011 4:59 AMSubject: OUR STORY THIS CHRISTMAS

Hi,

THROUGHOUT THIS TIME AND UP TO NOW, GOD HAS BEEN

SO FAITHFUL TO US. HE IS BEAUTIFUL AND AWESOME. WE ARE SO

THANKFUL FOR THE PRIVILEGE OF "CARRYING" US AND MOLDING US.

HE WHO DWELLS IN THE SHELTER OF THE MOST HIGH WILL REST

IN THE SHADOW OF THE ALMIGHTY. - PSALM 91:1

A day after Christmas, we share our story to our love ones, to our families

and friends. After many years since 2008, we hide our predicament to them.

The reaon we hide it because the father of Abe had hypertension and wedon't want him to worry. And also his Dad and Mom will surely go to Manaog, a placein the Philippines where they say they see the image of the Virgin .Peope go there for petition to the Virgin . We don't want it to happen because itwill steal the glory of the Lord Jesus in their mind. They will say, Abe is healed bec.of this. His Mom had a heart problem and died without knowing the condition of Abe.

I know my Mom will always call me everyday crying. We don't like it either,

will put our spirit down. And also during that time, our life is just normal, we could care,

give, work, serve without our family and others worrying about us. This e-mail is

the one I sent to them, I just cut the portion that I asked forgiveness for not telling

our family and close friends for a long time. May the Lord bless you... I know my e-mail is long. Jan. 2008, Abe, my husband was diagnosed with colorectal CA. Jan. 24, 2008 they startchemotherapy and radiation. Chemo , he had a pump in a bag and will still go towork. This was during winter time in Iowa. The chemo will flow 48 hours and by thethird day , a nurse will come to the house and remove it every 2 weeks. Aside from that,

he needed to go to hospital for IV chemo once every 2 weeks and radiation Monday

to Friday for 28 sessions and go back to work after that. He will still work more

hours the following day to make up the hours lost during chemo and radiation and had on-call

at night. He cannot hide this bag from co-workers even working in lab. gown.

Chemo and radiation was done by April. May 17, 2008, we attended my nephew's

wedding (my eldest brother's son) with . In all these things,

God is very faithful. We even danced for 5 hours continuously. At this time,

Abe had a port for chemo in his chest. God is carrying us. It's a privelege that Lord Jesusis carrying us throughout. He never leave us nor forsake us. God gave us a comforting

peace and no one knew our predicament.

June, 2008, the surgeons did a resection of the colorectal mass (cancer)

and had ileostomy. So, Abe need to have colostomy bag/pouch for his # 2 for 6 months.

After surgery, they did chmotherapy for 6 months. Still the same, he was still working.

By January, 2009, they reversed the ileostomy and now he could use his bottom again.

He went to the Philippines to attend the funeral of Abe's Mom. The plan was to tell

them now the past health history of Abe but since they still in mourn, Abe was not

able to say it and it means we cannot say it to everyone. We wanted to tell the Dad in person

so that he could see that Abe is well.

Before we leave Iowa, they saw a new mass in the lung and we came to California,

it was confirmed through biopsy that the colorectal cancer metastasize or meaning

same cells went to the left lung. Abe did chemo for 6 months again, this time

the chemo was more aggressive. Chemo started Monday with an IV chemo in cancer

center that lasted about 4 hours, then will go home with a chemo pump in a bag that will flow

for 48 hours. Then Wednesday, he would go back to the center for them to remove

the chemo pump. After 6 months of chemo, had another set of chemotherapy, higher dose and much

more aggresive. During that time, he had 2 works, Antelope Valley Hosp. and Palmalde Regional

Hospital where he was confined. Then he lost the job in Antelope Valley and just concentrate

on Palmdale Regional Hospital. He was still working and only absent himself every chemo time and a day.

Then, he had rest for 1 1/2 months from chemo and had upper lobe lobectomy of the

left lung. Left lung has 2 lobes and they got the upper lobe. Right lung has 3 lobes.

The lobectomy was done Dec 8, 2011 (Thursday). This is for CURE, unlike other

Stage 4 that do treatments only for control. We went home Dec. 11 (Sunday)

and by Wednesday, Dec. 14, he had a stroke. Dec. 16, Friday, he had right decompression

of the brain. Today, Christmas time, a chest tube was placed because of pneumo-

thorax (the left lung that had operation was collapsed due to air outside of the left lung, in the

pleural space. The chest tube was needed to get rid of the air and made the left lung to function well

again and they do successive x-rays to compare things). Before the chest tube was

placed, we had a good talk to surrender ourselves to God and testify about his grace

and mercy to us. And Abe said YES. Praise the Lord. We are just waiting for rehab but since we are

still in the hospital, the doctor ordered chest x-ray and was found to have pneumothorax. It's

a blessing in disguise since we were still in the hospital and no difficulty of

breathing yet. If we already go to the rehab, for sure at some point we will go back

to emergency room because of this. GOD IS GOOD.

The situation made us closer to Him and to each other. I will usually go to him Wednesday

and eat lunch at the car, parked in the hospital and will enjoy each other. We chose Wednesday

bec. this day is longer than the other days, the family attends Midweek Service at Highland's

Church. Even we were married 12 years next June of 2012, I still consider him my boyfriend and

I'm his girlfriend. I cannot explain, in the midst of everything, we are so happy and content.

God's way is so different, work helped him a lot than not doing anything Thank you Lord.

Thank you very much for reading our story. We lived a "normal" life withot our family and

other close friends knowing it. We had the privilege of giving and caring without them worrying

about us. Some people asked for help without hesitation. Aside from this, we also had therapies

for AJ , our younger daughter who was diagnosed with autism secondary to metals from vaccination.

She was found to have different kinds of metals in her body that needed to be chelated and the

same sypmptoms with autism. We tried a lot of alternative medicine and up to now

we are still believing that she will be healed in the name of Jesus. She is so normal

and so intelligent. At 1 and 1/2 years old, she knew all the sounds of the letters.

At 2 years old, she was almost reading then also at this time after 18 months

vaccination, she started to regress and was unable to speak. Now, she could

speak per word but then we are still not losing hope for her. It's very hard

because I saw her potentials. But since insurance won't shoulder alternative medicine,

we needed to pay out of our pocket. We are still doing alternative medicine. The

doctor is healing first her gut due to a lot of food insensitivities/ GIT inflammation

damaged by the metals. Then the doctor will do chelation to get rid of metals.

Please pray also for AJ. She is already 6 years old, attending special education,

first grade and doing therapies, 3 1/2 hours of therapies everyday in our house,

total of 20 hours per week in our house. I joined a yahoo group, the same condition

of AJ, and some kids were recovered from this condition. The parents who recovered

their kids are helping those who wanted to recover other kids thru discussion

via e-mails. There's no particular treatment. Each child was affected by

metals differently. Companies uses metals to preserve the vaccines. The statistic

of autism before is 1 in 10,000 around, 1980's ..now it's 1 in 100 , increased

statistic not only in US but other countries.

During those time, and up to now, It is the Lord Jesus carrying us.

This is God's battle, not ours and we won already through CHRIST. I hope

our family won't feel betrayed, we experienced the care of our Lord Jesus in

a very special way.

THANK YOU ALL FOR YOUR PRAYERS. GOD IS IN CONTROL.

I LOVE YOU, LORD. PLEASE PRAY FOR FASTER AND COMPLETE RECOVERY.

BY JESUS' STRIPES, ABE AND AJ WERE HEALED.

Victory in Christ,

Mhel

PS. I JUST FELT THAT ABE'S DAD NEED TO KNOW THIS FIRST.

I CALLED HIM AND HE KNEW ALREADY AND RECEIVED THE NEWS

WELL. IT'S A BLESSING THAT WE WERE IN THE UNITED STATES OR

ELSE WE DON'T KNOW HOW TO GET RESOURCES FOR THE TREATMENT.

I TOLD HIM THAT THE REASON WE DID NOT TELL HIM IS FOR HIM NOT TO WORRY AND ALSO

WE DON'T WANT THEM TO GO TO MANAOG AND PETITION

IT THERE BECAUSE THE VIRGIIN MARY IS ONLY HUMAN AND JESUS

IS THE LORD BUT MARY WOULD BE HAPPY IF HE WILL RECEIVE JESUS

IN HIS HEART. THANK YOU HOLY SPIRIT FOR ANNOINTING THIS E-MAIL.

WE LOVE YOU DADDY VERY MUCH.

FOR THOSE WHO WANTED TO EXPERIENCE THE LOVE, CARE , SUPPORT,

COMFORTING AND SAVING PEACE OF GOD: JUST RECEIVE THE GIFT

AND SAY THIS PRAYER AND MEAN IT FROM YOUR HEART:

LORD JESUS, COME TO MY HEART. I BELIEVE THAT YOU DIED IN THE

CROSS FOR MY SINS. BE MY SAVIOR AND TAKE CONTROL OF MY LIFE.

THANK YOU LORD.

JUST BY PRAYING THIS SIMPLE PRAYER, YOU BECOME A CHILD OF

GOD. EXPECT CHANGES IN YOUR LIFE AND YOU WILL BE ASSURED

OF ETERNAL LIFE IN HEAVEN. YOU WILL HAVE A DESIRE TO READ

THE BIBLE, THE WORD OF GOD. YOU WON'T REGRET.

MERRY CHRISTMAS AND HAVE A BLESSED NEW YEAR !!!

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Share on other sites

You already r a very strong person but I will pray for u and ur family to have

even more strength to go thru all the struggles. Not many people have the

strength and faith that u have. U r not alone as all your friends here will pray

for u and would love to assist u in your daughter's recovery.

is

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

> Hi,

>

> THROUGHOUT THIS TIME AND UP TO NOW, GOD HAS BEEN

> SO FAITHFUL TO US. HE IS BEAUTIFUL AND AWESOME. WE ARE SO

> THANKFUL FOR THE PRIVILEGE OF " CARRYING " US AND MOLDING US.

>

> HE WHO DWELLS IN THE SHELTER OF THE MOST HIGH WILL REST

> IN THE SHADOW OF THE ALMIGHTY. - PSALM 91:1

>

> A day after Christmas, we share our story to our love ones, to our families

> and friends. After many years since 2008, we hide our predicament to them.

> The reaon we hide it because the father of Abe had hypertension and we

> don't want him to worry. And also his Dad and Mom will surely go to Manaog, a

place

> in the Philippines where they say they see the image of the Virgin .

> Peope go there for petition to the Virgin . We don't want it to happen

because it

> will steal the glory of the Lord Jesus in their mind. They will say, Abe is

healed bec.

> of this. His Mom had a heart problem and died without knowing the condition of

Abe.

> I know my Mom will always call me everyday crying. We don't like it either,

> will put our spirit down. And also during that time, our life is just normal,

we could care,

> give, work, serve without our family and others worrying about us. This e-mail

is

> the one I sent to them, I just cut the portion that I asked forgiveness for

not telling

> our family and close friends for a long time. May the Lord bless you... I know

my e-mail is long.

> Jan. 2008, Abe, my husband was diagnosed with colorectal CA.

Jan. 24, 2008 they start

> chemotherapy and radiation. Chemo , he had a pump in a bag and will still go

to

> work. This was during winter time in Iowa. The chemo will flow 48 hours and by

the

> third day , a nurse will come to the house and remove it every 2 weeks. Aside

from that,

> he needed to go to hospital for IV chemo once every 2 weeks and radiation

Monday

> to Friday for 28 sessions and go back to work after that. He will still work

more

> hours the following day to make up the hours lost during chemo and radiation

and had on-call

> at night. He cannot hide this bag from co-workers even working in lab. gown.

> Chemo and radiation was done by April. May 17, 2008, we attended my nephew's

> wedding (my eldest brother's son) with . In all these things,

> God is very faithful. We even danced for 5 hours continuously. At this time,

> Abe had a port for chemo in his chest. God is carrying us. It's a privelege

that Lord Jesus

> is carrying us throughout. He never leave us nor forsake us. God gave us a

comforting

> peace and no one knew our predicament.

>

> June, 2008, the surgeons did a resection of the colorectal

mass (cancer)

> and had ileostomy. So, Abe need to have colostomy bag/pouch for his # 2 for 6

months.

> After surgery, they did chmotherapy for 6 months. Still the same, he was still

working.

> By January, 2009, they reversed the ileostomy and now he could use his bottom

again.

> He went to the Philippines to attend the funeral of Abe's Mom. The plan was to

tell

> them now the past health history of Abe but since they still in mourn, Abe was

not

> able to say it and it means we cannot say it to everyone. We wanted to tell

the Dad in person

> so that he could see that Abe is well.

> Before we leave Iowa, they saw a new mass in the lung and we

came to California,

> it was confirmed through biopsy that the colorectal cancer metastasize or

meaning

> same cells went to the left lung. Abe did chemo for 6 months again, this time

> the chemo was more aggressive. Chemo started Monday with an IV chemo in cancer

> center that lasted about 4 hours, then will go home with a chemo pump in a bag

that will flow

> for 48 hours. Then Wednesday, he would go back to the center for them to

remove

> the chemo pump. After 6 months of chemo, had another set of chemotherapy,

higher dose and much

> more aggresive. During that time, he had 2 works, Antelope Valley Hosp. and

Palmalde Regional

> Hospital where he was confined. Then he lost the job in Antelope Valley and

just concentrate

> on Palmdale Regional Hospital. He was still working and only absent himself

every chemo time and a day.

> Then, he had rest for 1 1/2 months from chemo and had upper lobe lobectomy of

the

> left lung. Left lung has 2 lobes and they got the upper lobe. Right lung has

3 lobes.

> The lobectomy was done Dec 8, 2011 (Thursday). This is for CURE, unlike other

> Stage 4 that do treatments only for control. We went home Dec. 11 (Sunday)

> and by Wednesday, Dec. 14, he had a stroke. Dec. 16, Friday, he had right

decompression

> of the brain. Today, Christmas time, a chest tube was placed because of

pneumo-

> thorax (the left lung that had operation was collapsed due to air outside of

the left lung, in the

> pleural space. The chest tube was needed to get rid of the air and made the

left lung to function well

> again and they do successive x-rays to compare things). Before the chest tube

was

> placed, we had a good talk to surrender ourselves to God and testify about

his grace

> and mercy to us. And Abe said YES. Praise the Lord. We are just waiting for

rehab but since we are

> still in the hospital, the doctor ordered chest x-ray and was found to have

pneumothorax. It's

> a blessing in disguise since we were still in the hospital and no difficulty

of

> breathing yet. If we already go to the rehab, for sure at some point we will

go back

> to emergency room because of this. GOD IS GOOD.

>

> The situation made us closer to Him and to each other. I will usually go to

him Wednesday

> and eat lunch at the car, parked in the hospital and will enjoy each other. We

chose Wednesday

> bec. this day is longer than the other days, the family attends Midweek

Service at Highland's

> Church. Even we were married 12 years next June of 2012, I still consider him

my boyfriend and

> I'm his girlfriend. I cannot explain, in the midst of everything, we are so

happy and content.

> God's way is so different, work helped him a lot than not doing anything

Thank you Lord.

>

>

> Thank you very much for reading our story. We lived a " normal " life withot

our family and

> other close friends knowing it. We had the privilege of giving and caring

without them worrying

> about us. Some people asked for help without hesitation. Aside from this, we

also had therapies

> for AJ , our younger daughter who was diagnosed with autism secondary to

metals from vaccination.

> She was found to have different kinds of metals in her body that needed to be

chelated and the

> same sypmptoms with autism. We tried a lot of alternative medicine and up to

now

> we are still believing that she will be healed in the name of Jesus. She is so

normal

> and so intelligent. At 1 and 1/2 years old, she knew all the sounds of the

letters.

> At 2 years old, she was almost reading then also at this time after 18 months

> vaccination, she started to regress and was unable to speak. Now, she could

> speak per word but then we are still not losing hope for her. It's very hard

> because I saw her potentials. But since insurance won't shoulder alternative

medicine,

> we needed to pay out of our pocket. We are still doing alternative medicine.

The

> doctor is healing first her gut due to a lot of food insensitivities/ GIT

inflammation

> damaged by the metals. Then the doctor will do chelation to get rid of metals.

> Please pray also for AJ. She is already 6 years old, attending special

education,

> first grade and doing therapies, 3 1/2 hours of therapies everyday in our

house,

> total of 20 hours per week in our house. I joined a yahoo group, the same

condition

> of AJ, and some kids were recovered from this condition. The parents who

recovered

> their kids are helping those who wanted to recover other kids thru discussion

> via e-mails. There's no particular treatment. Each child was affected by

> metals differently. Companies uses metals to preserve the vaccines. The

statistic

> of autism before is 1 in 10,000 around, 1980's ..now it's 1 in 100 , increased

> statistic not only in US but other countries.

>

>

> During those time, and up to now, It is the Lord Jesus carrying us.

> This is God's battle, not ours and we won already through CHRIST. I hope

> our family won't feel betrayed, we experienced the care of our Lord Jesus in

> a very special way.

>

> THANK YOU ALL FOR YOUR PRAYERS. GOD IS IN CONTROL.

> I LOVE YOU, LORD. PLEASE PRAY FOR FASTER AND COMPLETE RECOVERY.

> BY JESUS' STRIPES, ABE AND AJ WERE HEALED.

>

> Victory

in Christ,

>

Mhel

>

>

> PS. I JUST FELT THAT ABE'S DAD NEED TO KNOW THIS FIRST.

> I CALLED HIM AND HE KNEW ALREADY AND RECEIVED THE NEWS

> WELL. IT'S A BLESSING THAT WE WERE IN THE UNITED STATES OR

> ELSE WE DON'T KNOW HOW TO GET RESOURCES FOR THE TREATMENT.

> I TOLD HIM THAT THE REASON WE DID NOT TELL HIM IS FOR HIM NOT TO WORRY AND

ALSO

> WE DON'T WANT THEM TO GO TO MANAOG AND PETITION

> IT THERE BECAUSE THE VIRGIIN MARY IS ONLY HUMAN AND JESUS

> IS THE LORD BUT MARY WOULD BE HAPPY IF HE WILL RECEIVE JESUS

> IN HIS HEART. THANK YOU HOLY SPIRIT FOR ANNOINTING THIS E-MAIL.

> WE LOVE YOU DADDY VERY MUCH.

>

> FOR THOSE WHO WANTED TO EXPERIENCE THE LOVE, CARE , SUPPORT,

> COMFORTING AND SAVING PEACE OF GOD: JUST RECEIVE THE GIFT

> AND SAY THIS PRAYER AND MEAN IT FROM YOUR HEART:

>

> LORD JESUS, COME TO MY HEART. I BELIEVE THAT YOU DIED IN THE

> CROSS FOR MY SINS. BE MY SAVIOR AND TAKE CONTROL OF MY LIFE.

> THANK YOU LORD.

>

> JUST BY PRAYING THIS SIMPLE PRAYER, YOU BECOME A CHILD OF

> GOD. EXPECT CHANGES IN YOUR LIFE AND YOU WILL BE ASSURED

> OF ETERNAL LIFE IN HEAVEN. YOU WILL HAVE A DESIRE TO READ

> THE BIBLE, THE WORD OF GOD. YOU WON'T REGRET.

>

> MERRY CHRISTMAS AND HAVE A BLESSED NEW YEAR !!!

>

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Share on other sites

Hi iis,

Thank you very much. My strength comes from your prayers.

God bless us all. I'm so encouraged that now, more people are

praying for us. I know in my heart, you'll respond. You are

very compassionate person. Keep it up.

Sincerely,

Mhel

To: mb12valtrex From: alexis_d3378@...Date: Thu, 29 Dec 2011 22:58:37 +0000Subject: Re: OUR STORY THIS CHRISTMAS

You already r a very strong person but I will pray for u and ur family to have even more strength to go thru all the struggles. Not many people have the strength and faith that u have. U r not alone as all your friends here will pray for u and would love to assist u in your daughter's recovery.is>> > > > > > > > > > > > > > > > > > > Hi, > > THROUGHOUT THIS TIME AND UP TO NOW, GOD HAS BEEN> SO FAITHFUL TO US. HE IS BEAUTIFUL AND AWESOME. WE ARE SO> THANKFUL FOR THE PRIVILEGE OF "CARRYING" US AND MOLDING US.> > HE WHO DWELLS IN THE SHELTER OF THE MOST HIGH WILL REST> IN THE SHADOW OF THE ALMIGHTY. - PSALM 91:1> > A day after Christmas, we share our story to our love ones, to our families > and friends. After many years since 2008, we hide our predicament to them.> The reaon we hide it because the father of Abe had hypertension and we> don't want him to worry. And also his Dad and Mom will surely go to Manaog, a place> in the Philippines where they say they see the image of the Virgin .> Peope go there for petition to the Virgin . We don't want it to happen because it> will steal the glory of the Lord Jesus in their mind. They will say, Abe is healed bec.> of this. His Mom had a heart problem and died without knowing the condition of Abe.> I know my Mom will always call me everyday crying. We don't like it either, > will put our spirit down. And also during that time, our life is just normal, we could care, > give, work, serve without our family and others worrying about us. This e-mail is> the one I sent to them, I just cut the portion that I asked forgiveness for not telling> our family and close friends for a long time. May the Lord bless you... I know my e-mail is long.> Jan. 2008, Abe, my husband was diagnosed with colorectal CA. Jan. 24, 2008 they start> chemotherapy and radiation. Chemo , he had a pump in a bag and will still go to> work. This was during winter time in Iowa. The chemo will flow 48 hours and by the> third day , a nurse will come to the house and remove it every 2 weeks. Aside from that, > he needed to go to hospital for IV chemo once every 2 weeks and radiation Monday> to Friday for 28 sessions and go back to work after that. He will still work more> hours the following day to make up the hours lost during chemo and radiation and had on-call> at night. He cannot hide this bag from co-workers even working in lab. gown.> Chemo and radiation was done by April. May 17, 2008, we attended my nephew's> wedding (my eldest brother's son) with . In all these things,> God is very faithful. We even danced for 5 hours continuously. At this time,> Abe had a port for chemo in his chest. God is carrying us. It's a privelege that Lord Jesus> is carrying us throughout. He never leave us nor forsake us. God gave us a comforting> peace and no one knew our predicament.> > June, 2008, the surgeons did a resection of the colorectal mass (cancer)> and had ileostomy. So, Abe need to have colostomy bag/pouch for his # 2 for 6 months. > After surgery, they did chmotherapy for 6 months. Still the same, he was still working.> By January, 2009, they reversed the ileostomy and now he could use his bottom again.> He went to the Philippines to attend the funeral of Abe's Mom. The plan was to tell> them now the past health history of Abe but since they still in mourn, Abe was not> able to say it and it means we cannot say it to everyone. We wanted to tell the Dad in person > so that he could see that Abe is well. > Before we leave Iowa, they saw a new mass in the lung and we came to California,> it was confirmed through biopsy that the colorectal cancer metastasize or meaning> same cells went to the left lung. Abe did chemo for 6 months again, this time> the chemo was more aggressive. Chemo started Monday with an IV chemo in cancer> center that lasted about 4 hours, then will go home with a chemo pump in a bag that will flow> for 48 hours. Then Wednesday, he would go back to the center for them to remove> the chemo pump. After 6 months of chemo, had another set of chemotherapy, higher dose and much> more aggresive. During that time, he had 2 works, Antelope Valley Hosp. and Palmalde Regional> Hospital where he was confined. Then he lost the job in Antelope Valley and just concentrate> on Palmdale Regional Hospital. He was still working and only absent himself every chemo time and a day.> Then, he had rest for 1 1/2 months from chemo and had upper lobe lobectomy of the> left lung. Left lung has 2 lobes and they got the upper lobe. Right lung has 3 lobes.> The lobectomy was done Dec 8, 2011 (Thursday). This is for CURE, unlike other> Stage 4 that do treatments only for control. We went home Dec. 11 (Sunday)> and by Wednesday, Dec. 14, he had a stroke. Dec. 16, Friday, he had right decompression> of the brain. Today, Christmas time, a chest tube was placed because of pneumo-> thorax (the left lung that had operation was collapsed due to air outside of the left lung, in the> pleural space. The chest tube was needed to get rid of the air and made the left lung to function well> again and they do successive x-rays to compare things). Before the chest tube was> placed, we had a good talk to surrender ourselves to God and testify about his grace> and mercy to us. And Abe said YES. Praise the Lord. We are just waiting for rehab but since we are > still in the hospital, the doctor ordered chest x-ray and was found to have pneumothorax. It's > a blessing in disguise since we were still in the hospital and no difficulty of> breathing yet. If we already go to the rehab, for sure at some point we will go back> to emergency room because of this. GOD IS GOOD.> > The situation made us closer to Him and to each other. I will usually go to him Wednesday > and eat lunch at the car, parked in the hospital and will enjoy each other. We chose Wednesday > bec. this day is longer than the other days, the family attends Midweek Service at Highland's > Church. Even we were married 12 years next June of 2012, I still consider him my boyfriend and > I'm his girlfriend. I cannot explain, in the midst of everything, we are so happy and content. > God's way is so different, work helped him a lot than not doing anything Thank you Lord.> > > Thank you very much for reading our story. We lived a "normal" life withot our family and > other close friends knowing it. We had the privilege of giving and caring without them worrying > about us. Some people asked for help without hesitation. Aside from this, we also had therapies> for AJ , our younger daughter who was diagnosed with autism secondary to metals from vaccination. > She was found to have different kinds of metals in her body that needed to be chelated and the> same sypmptoms with autism. We tried a lot of alternative medicine and up to now> we are still believing that she will be healed in the name of Jesus. She is so normal> and so intelligent. At 1 and 1/2 years old, she knew all the sounds of the letters.> At 2 years old, she was almost reading then also at this time after 18 months> vaccination, she started to regress and was unable to speak. Now, she could> speak per word but then we are still not losing hope for her. It's very hard> because I saw her potentials. But since insurance won't shoulder alternative medicine,> we needed to pay out of our pocket. We are still doing alternative medicine. The> doctor is healing first her gut due to a lot of food insensitivities/ GIT inflammation> damaged by the metals. Then the doctor will do chelation to get rid of metals.> Please pray also for AJ. She is already 6 years old, attending special education,> first grade and doing therapies, 3 1/2 hours of therapies everyday in our house,> total of 20 hours per week in our house. I joined a yahoo group, the same condition> of AJ, and some kids were recovered from this condition. The parents who recovered> their kids are helping those who wanted to recover other kids thru discussion> via e-mails. There's no particular treatment. Each child was affected by> metals differently. Companies uses metals to preserve the vaccines. The statistic> of autism before is 1 in 10,000 around, 1980's ..now it's 1 in 100 , increased> statistic not only in US but other countries. > > > During those time, and up to now, It is the Lord Jesus carrying us. > This is God's battle, not ours and we won already through CHRIST. I hope> our family won't feel betrayed, we experienced the care of our Lord Jesus in> a very special way. > > THANK YOU ALL FOR YOUR PRAYERS. GOD IS IN CONTROL.> I LOVE YOU, LORD. PLEASE PRAY FOR FASTER AND COMPLETE RECOVERY.> BY JESUS' STRIPES, ABE AND AJ WERE HEALED. > > Victory in Christ,> Mhel> > > PS. I JUST FELT THAT ABE'S DAD NEED TO KNOW THIS FIRST.> I CALLED HIM AND HE KNEW ALREADY AND RECEIVED THE NEWS> WELL. IT'S A BLESSING THAT WE WERE IN THE UNITED STATES OR > ELSE WE DON'T KNOW HOW TO GET RESOURCES FOR THE TREATMENT. > I TOLD HIM THAT THE REASON WE DID NOT TELL HIM IS FOR HIM NOT TO WORRY AND ALSO> WE DON'T WANT THEM TO GO TO MANAOG AND PETITION> IT THERE BECAUSE THE VIRGIIN MARY IS ONLY HUMAN AND JESUS > IS THE LORD BUT MARY WOULD BE HAPPY IF HE WILL RECEIVE JESUS > IN HIS HEART. THANK YOU HOLY SPIRIT FOR ANNOINTING THIS E-MAIL.> WE LOVE YOU DADDY VERY MUCH.> > FOR THOSE WHO WANTED TO EXPERIENCE THE LOVE, CARE , SUPPORT,> COMFORTING AND SAVING PEACE OF GOD: JUST RECEIVE THE GIFT> AND SAY THIS PRAYER AND MEAN IT FROM YOUR HEART:> > LORD JESUS, COME TO MY HEART. I BELIEVE THAT YOU DIED IN THE> CROSS FOR MY SINS. BE MY SAVIOR AND TAKE CONTROL OF MY LIFE.> THANK YOU LORD.> > JUST BY PRAYING THIS SIMPLE PRAYER, YOU BECOME A CHILD OF> GOD. EXPECT CHANGES IN YOUR LIFE AND YOU WILL BE ASSURED> OF ETERNAL LIFE IN HEAVEN. YOU WILL HAVE A DESIRE TO READ> THE BIBLE, THE WORD OF GOD. YOU WON'T REGRET. > > MERRY CHRISTMAS AND HAVE A BLESSED NEW YEAR !!!>

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Dear Mhel,May God's blessing be upon you and your family. It is really hard to get by with all these difficulties, but without families help even harder. Your faith will carry you all, and make you come out of this as a winner. My prayers are with you and your family every day.

Take careTunde

 

 

 Hi,

 

         THROUGHOUT THIS TIME AND UP TO NOW, GOD HAS BEEN

SO FAITHFUL TO US. HE IS BEAUTIFUL AND AWESOME. WE ARE SO

THANKFUL FOR THE PRIVILEGE OF " CARRYING " US AND MOLDING US.

 

HE WHO DWELLS IN THE SHELTER OF THE MOST HIGH WILL REST

IN THE SHADOW OF THE ALMIGHTY.  - PSALM 91:1

 

 A day after Christmas, we share our story to our love ones, to our families

and friends.  After many years since 2008, we hide our predicament to them.

The reaon we hide it because the father of Abe had hypertension and wedon't want him to worry. And also his Dad and Mom will surely go to Manaog, a placein the Philippines where they say they see the image of the Virgin .

Peope go there for petition to the Virgin . We don't want it to happen because itwill steal the glory of the Lord Jesus in their mind. They will say, Abe is healed bec.of this. His Mom had a heart problem and died without knowing the condition of Abe.

 I know my Mom will  always call me everyday crying. We don't like it either,

will put our spirit down. And also during that time, our life is just normal, we could care,

give, work, serve without our family and others worrying about us. This e-mail is

the one I sent to them, I just cut the portion that I asked forgiveness for not telling

our family and close friends for a long time. May the Lord bless you... I know my e-mail is long.               Jan. 2008, Abe, my husband was diagnosed with colorectal CA. Jan. 24, 2008 they start

chemotherapy and radiation. Chemo , he had a pump in a bag and will still go towork. This was during winter time in Iowa. The chemo will flow 48 hours and by thethird day , a nurse will come to the house and remove it every 2 weeks. Aside from that,

he needed to go to hospital for IV chemo once every 2 weeks and radiation Monday

to Friday for 28 sessions and go back to work after that.  He will still work more

hours the following day to make up the hours lost during chemo and radiation and had on-call

at night. He cannot hide this bag from co-workers even working in lab. gown.

Chemo and radiation was done by April. May 17, 2008, we attended my  nephew's

wedding (my eldest brother's son) with . In all these things,

God is very faithful. We even danced for 5 hours continuously. At this time,

Abe had a port for chemo in his chest. God is carrying us. It's a privelege that Lord Jesusis carrying us throughout. He never leave us nor forsake us. God gave us a comforting

peace and no one knew our predicament.

                June, 2008, the surgeons did a resection of the colorectal mass (cancer)

and had ileostomy. So, Abe need to have colostomy bag/pouch for his # 2 for 6 months.

After surgery, they did chmotherapy for 6 months. Still the same, he was still working.

By January, 2009, they reversed the ileostomy and now he could use his bottom again.

He went to the Philippines to attend the funeral of Abe's Mom. The plan was to tell

them now the past health history of Abe but since they still in mourn, Abe was not

able to say it and it means we cannot say it to everyone. We wanted to tell the Dad in person

so that he could see that Abe is well.

                 Before we leave Iowa, they saw a new mass in the lung and we came to California,

it was confirmed through biopsy that the colorectal cancer metastasize or meaning

same cells went to the left lung. Abe did chemo for 6 months again, this time

the chemo was more aggressive. Chemo started Monday with an IV chemo in cancer

center that lasted about 4 hours, then will go home with a chemo pump in a bag that will flow

for 48 hours. Then Wednesday, he would go back to the center for them to remove

the chemo pump. After 6 months of chemo, had another set of chemotherapy, higher dose and much

more aggresive. During that time, he had 2 works, Antelope Valley Hosp. and Palmalde Regional

Hospital where he was confined. Then he lost the job in Antelope Valley and just concentrate

on Palmdale Regional Hospital. He was still working and only absent himself every chemo time and a day.

Then, he had rest for 1 1/2 months from chemo and had upper lobe lobectomy of the

left lung. Left lung has 2  lobes and they got the upper lobe. Right lung has 3 lobes.

The lobectomy was done Dec 8, 2011 (Thursday). This is for CURE, unlike other

Stage 4 that do treatments only for control. We went home Dec. 11 (Sunday)

and by Wednesday, Dec. 14, he had a stroke. Dec. 16, Friday, he had right decompression

of the brain. Today, Christmas time, a chest tube was placed because of pneumo-

thorax (the left lung that had operation was collapsed due to air outside of the left lung, in the

pleural space. The chest tube was needed to get rid of the air and made the left lung to function well

again and they do successive x-rays to compare things). Before the chest tube was

placed, we  had a good talk to surrender ourselves to God and testify about his grace

and mercy to us.  And Abe said YES. Praise the Lord. We are just waiting for rehab but since we are

still in the hospital, the doctor ordered chest x-ray and was found to have pneumothorax. It's

a blessing in disguise since we were still in the hospital and no difficulty of

breathing yet. If we already go to the rehab, for sure at some point we will go back

to emergency room because of this. GOD IS GOOD.

 

The situation made us closer to Him and to each other. I will usually go to him Wednesday

and eat lunch at the car, parked in the hospital and will enjoy each other. We chose Wednesday

 bec. this day is longer than the other days, the family  attends Midweek Service at Highland's

Church. Even we were married 12 years next June of 2012, I still consider him my boyfriend and

I'm his girlfriend. I cannot explain, in the midst of everything, we are so happy and content.

God's way is so different, work helped him a lot than not doing anything  Thank you Lord.

 

           

 Thank you very much for reading our story. We lived a " normal " life withot our family and

other close friends knowing it. We had the privilege of giving and caring without them worrying

about us. Some people asked for help without hesitation. Aside from this, we also had therapies

 for AJ , our younger daughter who was diagnosed with autism secondary to metals from vaccination.

She was found to have different kinds of metals in her body that needed to be chelated and the

same sypmptoms with autism. We tried a lot of alternative medicine and up to now

we are still believing that she will be healed in the name of Jesus. She is so normal

and so intelligent. At  1 and 1/2 years old, she knew all the sounds of the letters.

At 2 years old, she was almost reading then also at this time after 18 months

vaccination, she started to regress and was unable to speak. Now, she could

speak per word but then we are still not losing hope for her. It's very hard

because I saw her potentials. But since insurance won't shoulder alternative medicine,

we needed to pay out of our pocket. We are still doing alternative medicine. The

doctor is healing first her gut due to a lot of food insensitivities/ GIT inflammation

damaged by the metals. Then the doctor will do chelation to get rid of metals.

Please pray also for AJ. She is already 6 years old, attending special education,

first grade and doing therapies, 3 1/2 hours of therapies everyday in our house,

total of 20 hours per week in our house. I joined a yahoo group, the same condition

of AJ, and some kids were recovered from this condition. The parents who recovered

their kids are helping those who wanted to recover other kids thru discussion

via e-mails. There's no particular treatment. Each child was affected by

metals differently. Companies uses metals to preserve the vaccines. The statistic

of autism before is 1 in 10,000 around, 1980's ..now it's 1 in 100 , increased

statistic not only in US but other countries.

 

 

During those time, and up to now, It is the Lord Jesus carrying us.

This is God's battle, not ours and we won already through CHRIST. I hope

our family won't feel betrayed, we experienced the care of our Lord Jesus in

a very special way.

                    

THANK YOU ALL FOR YOUR PRAYERS. GOD IS IN CONTROL.

I LOVE YOU, LORD. PLEASE PRAY FOR FASTER AND COMPLETE RECOVERY.

BY JESUS' STRIPES, ABE AND AJ  WERE HEALED.

 

                                                                       Victory in Christ,

                                                                            Mhel

 

 

 PS. I JUST FELT THAT ABE'S DAD NEED TO KNOW THIS FIRST.

I CALLED HIM AND HE KNEW ALREADY AND RECEIVED THE NEWS

WELL.  IT'S A BLESSING THAT WE WERE IN THE UNITED STATES  OR

ELSE WE DON'T KNOW HOW TO GET RESOURCES FOR THE TREATMENT.

I TOLD HIM THAT THE REASON WE DID NOT TELL HIM IS FOR HIM NOT TO WORRY AND ALSO

WE DON'T WANT THEM TO GO TO MANAOG AND PETITION

IT THERE  BECAUSE THE VIRGIIN MARY IS ONLY HUMAN AND JESUS

IS THE LORD BUT MARY WOULD BE HAPPY IF HE WILL RECEIVE JESUS

IN HIS HEART.  THANK YOU HOLY SPIRIT FOR ANNOINTING THIS E-MAIL.

WE LOVE YOU DADDY VERY MUCH.

 

FOR THOSE WHO WANTED TO EXPERIENCE THE LOVE, CARE , SUPPORT,

COMFORTING AND SAVING PEACE OF GOD: JUST RECEIVE THE GIFT

AND SAY THIS PRAYER AND  MEAN IT FROM YOUR HEART:

 

LORD JESUS, COME TO MY HEART. I BELIEVE THAT YOU DIED IN THE

CROSS FOR MY SINS. BE MY SAVIOR AND TAKE CONTROL OF MY LIFE.

THANK YOU LORD.

 

JUST BY PRAYING THIS SIMPLE PRAYER, YOU BECOME A CHILD OF

GOD. EXPECT CHANGES IN YOUR LIFE AND YOU WILL BE ASSURED

OF ETERNAL LIFE IN HEAVEN. YOU WILL HAVE A DESIRE TO READ

THE BIBLE, THE WORD OF GOD. YOU WON'T REGRET.

 

MERRY CHRISTMAS AND HAVE A BLESSED NEW YEAR !!!

   

-- " Our lives begin to end the day we become silent about things that matter. " MLK

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Dear Mhel,

I have also just lifted you up in prayer. Your post brought tears knowing how

much you are going through. As I've walked through so many valley's in my life I

lean on His word. One of my favorite verses in deep times of unknown, I've

learned to deeply depend on it is Proverbs 3:5-8

vs5 " Trust in the Lord with all your heart, and lean not on your own

understanding. In ALL your ways acknowledge Him, and HE will make your paths

straight. "

vs8 " It will be healing to your body, and refreshment to your bones. "

So many times I did not know what to do but kneel...I'm kneeling for you

now...may the Lord give you strength, wisdom, knowledge in what to do & most of

all healing for your precious family.

I have decided to copy the below post I did on another list recently for a

friend that is going through a similar situation. Use it prayerfully to see if

it fits in the path God has for your family...it has been used in people I've

spoken w/in conjunction with your current path. Our prayers are with you in all

your ways.

Blessings,

Rita

------------part of a Post from another list:

ok...for you my dear friend I'll carefully talk, not naming anything specific in

this post. I'm purposefully avoiding many autoimmune issues that I've learned

about in researching this to protect the product.....I've got to start w/the

disclaimer....it is not FDA approved for this & the manufacturer can not say

that it does.....

It has turned around many severe autoimmune issues including many, many cases of

this...several that I have personally spoken with....1 that was given 2 months

to live several years ago :o)

I know of 1 case of mouth...he swished his first dose around in his mouth,

gargled it then had to spit it out (expelling all the initial toxins/pathogens

from the initial gargles). Immediately after that he took it normally...he was

worked up quickly to the full adult dose of a sick person (16 drops 3x

day)...yes, it was effective. I've know of some with other types including 1

severe brain that was on 30 drops 3x a day, she's in canada w/the group homes

they put you in there..she's the only one that was not sick as a dog yellow

through her docs smt (standard western treatment)..she'd just smile as the doc

continued to comment about her good labs....

I've personally been through A LOT with this. My mom passed away 22+ years ago

from it....I was by her side through a 3 year swt battle. My husband's parents

both passed away from a swt battle (3 of our parents never met our

children...both our moms before 50...we're now older than they were).

My sister-in-law passed away 2 years ago at 51 years old, also of it...she

fought her battle mainly naturally as she knew that the swt was so toxic it was

not for her...as she was only given a 50/50 chance at her stage with the stw

when diagnosed. She did many natural things including diet (for several months

it was pure juicing only allowed, some herbs, hydrocolon therapy, oxygen therapy

& even one of those natural recovery retreat places). She did have several

surgeries including loosing a breast & many lymph nodes & reconstructive. We

supported her emotionally in all that she did. Of note, as we worked through

this with her she told us her first memory as a child was her mom doing enemas

as she was always so constipated going only 1-2 times a week from as long as she

could remember...we talked about how no one ever talked about it...or really

tried to help fix it, but we fully believe the toxin load over the years

shortened her life.

Knowing what I now know after both the swt & natural there is 3 things I'd

personally do if I found out I personally had this.... & frankly, with my family

load it is one of the big reasons my husband & I faithfully take the Immusist,

we want to be around longer than our parents were for our children.

If I were told I had it, I'd immediately ramp up to a high dose of Immusist. In

addition to doing what we all do w/keeping the toxins down like diet &

supporting the body w/good vits/good fats, etc I'd have at the top of my list of

important fighting things being:

1) Immusist ( http://immusist.com/ )

2) Kangen water only (no other types of drinks) including a whole house KDF

filter for showers/baths.

These 2 things hydrate & oxygenate & the Kangen alkalinizes...like many other

organisms/illnesses, cancer does not like oxygen rich, alkaline environment.

3) After what I've heard about Payne's new Solamar:

http://lwtinternational.com/programs/

I'd recognise the life & death situation at hand, cash out everything I had & do

his Solamar including the Solamar intensive which I understand he follows the

organism & organ support through the systems programs (I'd do this over the rife

that my friend has used recovering her breast).

btw....please, if a doc does not get this stuff...don't start bragging w/the doc

or hard core swt believers when the labs turn around, it stirs way to much

up....it's not the 1st to smile, say how amazing prayer is & go on their way

when the doc asks what they did. Also, please pray for him...I'd personally lay

hands & pray over him & the bottle before dosing as well for an extra blessing

over the situation. "

>

> > **

> >

> >

> >

> >

> > Hi,

> >

> > THROUGHOUT THIS TIME AND UP TO NOW, GOD HAS BEEN

> > SO FAITHFUL TO US. HE IS BEAUTIFUL AND AWESOME. WE ARE SO

> > THANKFUL FOR THE PRIVILEGE OF " CARRYING " US AND MOLDING US.

> >

> > HE WHO DWELLS IN THE SHELTER OF THE MOST HIGH WILL REST

> > IN THE SHADOW OF THE ALMIGHTY. - PSALM 91:1

> >

> > A day after Christmas, we share our story to our love ones, to our

> > families

> > and friends. After many years since 2008, we hide our predicament to them.

> > The reaon we hide it because the father of Abe had hypertension and we

> > don't want him to worry. And also his Dad and Mom will surely go to

> > Manaog, a place

> > in the Philippines where they say they see the image of the Virgin .

> > Peope go there for petition to the Virgin . We don't want it to happen

> > because it

> > will steal the glory of the Lord Jesus in their mind. They will say, Abe

> > is healed bec.

> > of this. His Mom had a heart problem and died without knowing the

> > condition of Abe.

> > I know my Mom will always call me everyday crying. We don't like it

> > either,

> > will put our spirit down. And also during that time, our life is just

> > normal, we could care,

> > give, work, serve without our family and others worrying about us. This

> > e-mail is

> > the one I sent to them, I just cut the portion that I asked forgiveness

> > for not telling

> > our family and close friends for a long time. May the Lord bless you... I

> > know my e-mail is long.

> > Jan. 2008, Abe, my husband was diagnosed with colorectal

> > CA. Jan. 24, 2008 they start

> > chemotherapy and radiation. Chemo , he had a pump in a bag and will still

> > go to

> > work. This was during winter time in Iowa. The chemo will flow 48 hours

> > and by the

> > third day , a nurse will come to the house and remove it every 2

> > weeks. Aside from that,

> > he needed to go to hospital for IV chemo once every 2 weeks and radiation

> > Monday

> > to Friday for 28 sessions and go back to work after that. He will still

> > work more

> > hours the following day to make up the hours lost during chemo and

> > radiation and had on-call

> > at night. He cannot hide this bag from co-workers even working in lab.

> > gown.

> > Chemo and radiation was done by April. May 17, 2008, we attended my

> > nephew's

> > wedding (my eldest brother's son) with . In all these things,

> > God is very faithful. We even danced for 5 hours continuously. At this

> > time,

> > Abe had a port for chemo in his chest. God is carrying us. It's a

> > privelege that Lord Jesus

> > is carrying us throughout. He never leave us nor forsake us. God gave us a

> > comforting

> > peace and no one knew our predicament.

> > June, 2008, the surgeons did a resection of the colorectal

> > mass (cancer)

> > and had ileostomy. So, Abe need to have colostomy bag/pouch for his # 2

> > for 6 months.

> > After surgery, they did chmotherapy for 6 months. Still the same, he was

> > still working.

> > By January, 2009, they reversed the ileostomy and now he could use his

> > bottom again.

> > He went to the Philippines to attend the funeral of Abe's Mom. The plan

> > was to tell

> > them now the past health history of Abe but since they still in mourn, Abe

> > was not

> > able to say it and it means we cannot say it to everyone. We wanted to

> > tell the Dad in person

> > so that he could see that Abe is well.

> > Before we leave Iowa, they saw a new mass in the lung and

> > we came to California,

> > it was confirmed through biopsy that the colorectal cancer metastasize or

> > meaning

> > same cells went to the left lung. Abe did chemo for 6 months again, this

> > time

> > the chemo was more aggressive. Chemo started Monday with an IV chemo in

> > cancer

> > center that lasted about 4 hours, then will go home with a chemo pump in a

> > bag that will flow

> > for 48 hours. Then Wednesday, he would go back to the center for them to

> > remove

> > the chemo pump. After 6 months of chemo, had another set of chemotherapy,

> > higher dose and much

> > more aggresive. During that time, he had 2 works, Antelope Valley Hosp.

> > and Palmalde Regional

> > Hospital where he was confined. Then he lost the job in Antelope Valley

> > and just concentrate

> > on Palmdale Regional Hospital. He was still working and only absent

> > himself every chemo time and a day.

> > Then, he had rest for 1 1/2 months from chemo and had upper lobe lobectomy

> > of the

> > left lung. Left lung has 2 lobes and they got the upper lobe. Right lung

> > has 3 lobes.

> > The lobectomy was done Dec 8, 2011 (Thursday). This is for CURE, unlike

> > other

> > Stage 4 that do treatments only for control. We went home Dec. 11 (Sunday)

> > and by Wednesday, Dec. 14, he had a stroke. Dec. 16, Friday, he had right

> > decompression

> > of the brain. Today, Christmas time, a chest tube was placed because of

> > pneumo-

> > thorax (the left lung that had operation was collapsed due to air outside

> > of the left lung, in the

> > pleural space. The chest tube was needed to get rid of the air and made

> > the left lung to function well

> > again and they do successive x-rays to compare things). Before the chest

> > tube was

> > placed, we had a good talk to surrender ourselves to God and testify

> > about his grace

> > and mercy to us. And Abe said YES. Praise the Lord. We are just waiting

> > for rehab but since we are

> > still in the hospital, the doctor ordered chest x-ray and was found to

> > have pneumothorax. It's

> > a blessing in disguise since we were still in the hospital and no

> > difficulty of

> > breathing yet. If we already go to the rehab, for sure at some point we

> > will go back

> > to emergency room because of this. GOD IS GOOD.

> >

> > The situation made us closer to Him and to each other. I will usually go

> > to him Wednesday

> > and eat lunch at the car, parked in the hospital and will enjoy each

> > other. We chose Wednesday

> > bec. this day is longer than the other days, the family attends Midweek

> > Service at Highland's

> > Church. Even we were married 12 years next June of 2012, I still consider

> > him my boyfriend and

> > I'm his girlfriend. I cannot explain, in the midst of everything, we are

> > so happy and content.

> > God's way is so different, work helped him a lot than not doing

> > anything Thank you Lord.

> >

> >

> > Thank you very much for reading our story. We lived a " normal " life

> > withot our family and

> > other close friends knowing it. We had the privilege of giving and caring

> > without them worrying

> > about us. Some people asked for help without hesitation. Aside from this,

> > we also had therapies

> > for AJ , our younger daughter who was diagnosed with autism secondary to

> > metals from vaccination.

> > She was found to have different kinds of metals in her body that needed to

> > be chelated and the

> > same sypmptoms with autism. We tried a lot of alternative medicine and up

> > to now

> > we are still believing that she will be healed in the name of Jesus. She

> > is so normal

> > and so intelligent. At 1 and 1/2 years old, she knew all the sounds of

> > the letters.

> > At 2 years old, she was almost reading then also at this time after 18

> > months

> > vaccination, she started to regress and was unable to speak. Now, she could

> > speak per word but then we are still not losing hope for her. It's very

> > hard

> > because I saw her potentials. But since insurance won't shoulder

> > alternative medicine,

> > we needed to pay out of our pocket. We are still doing alternative

> > medicine. The

> > doctor is healing first her gut due to a lot of food insensitivities/ GIT

> > inflammation

> > damaged by the metals. Then the doctor will do chelation to get rid of

> > metals.

> > Please pray also for AJ. She is already 6 years old, attending special

> > education,

> > first grade and doing therapies, 3 1/2 hours of therapies everyday in our

> > house,

> > total of 20 hours per week in our house. I joined a yahoo group, the same

> > condition

> > of AJ, and some kids were recovered from this condition. The parents who

> > recovered

> > their kids are helping those who wanted to recover other kids thru

> > discussion

> > via e-mails. There's no particular treatment. Each child was affected by

> > metals differently. Companies uses metals to preserve the vaccines. The

> > statistic

> > of autism before is 1 in 10,000 around, 1980's ..now it's 1 in 100 ,

> > increased

> > statistic not only in US but other countries.

> >

> >

> > During those time, and up to now, It is the Lord Jesus carrying us.

> > This is God's battle, not ours and we won already through CHRIST. I hope

> > our family won't feel betrayed, we experienced the care of our Lord Jesus

> > in

> > a very special way.

> >

> > THANK YOU ALL FOR YOUR PRAYERS. GOD IS IN CONTROL.

> > I LOVE YOU, LORD. PLEASE PRAY FOR FASTER AND COMPLETE RECOVERY.

> > BY JESUS' STRIPES, ABE AND AJ WERE HEALED.

> >

> >

Victory

> > in Christ,

> >

> > Mhel

> >

> >

> > PS. I JUST FELT THAT ABE'S DAD NEED TO KNOW THIS FIRST.

> > I CALLED HIM AND HE KNEW ALREADY AND RECEIVED THE NEWS

> > WELL. IT'S A BLESSING THAT WE WERE IN THE UNITED STATES OR

> > ELSE WE DON'T KNOW HOW TO GET RESOURCES FOR THE TREATMENT.

> > I TOLD HIM THAT THE REASON WE DID NOT TELL HIM IS FOR HIM NOT TO WORRY AND

> > ALSO

> > WE DON'T WANT THEM TO GO TO MANAOG AND PETITION

> > IT THERE BECAUSE THE VIRGIIN MARY IS ONLY HUMAN AND JESUS

> > IS THE LORD BUT MARY WOULD BE HAPPY IF HE WILL RECEIVE JESUS

> > IN HIS HEART. THANK YOU HOLY SPIRIT FOR ANNOINTING THIS E-MAIL.

> > WE LOVE YOU DADDY VERY MUCH.

> >

> > FOR THOSE WHO WANTED TO EXPERIENCE THE LOVE, CARE , SUPPORT,

> > COMFORTING AND SAVING PEACE OF GOD: JUST RECEIVE THE GIFT

> > AND SAY THIS PRAYER AND MEAN IT FROM YOUR HEART:

> >

> > LORD JESUS, COME TO MY HEART. I BELIEVE THAT YOU DIED IN THE

> > CROSS FOR MY SINS. BE MY SAVIOR AND TAKE CONTROL OF MY LIFE.

> > THANK YOU LORD.

> >

> > JUST BY PRAYING THIS SIMPLE PRAYER, YOU BECOME A CHILD OF

> > GOD. EXPECT CHANGES IN YOUR LIFE AND YOU WILL BE ASSURED

> > OF ETERNAL LIFE IN HEAVEN. YOU WILL HAVE A DESIRE TO READ

> > THE BIBLE, THE WORD OF GOD. YOU WON'T REGRET.

> >

> > MERRY CHRISTMAS AND HAVE A BLESSED NEW YEAR !!!

> >

> >

> >

> >

> >

> >

>

>

>

> --

> * " Our lives begin to end the day we become silent about things that

> matter. " MLK*

>

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Dear Tunde,

Thank you very much for the encouragement.

We are victorious in Christ. Thank you also

for praying for us . This one keep us strengthened.

May the Lord bless you and your family beyond

your imagination.

Take care, too,

Mhel

To: mb12valtrex From: tbrazlik@...Date: Fri, 30 Dec 2011 08:51:10 +0300Subject: Re: OUR STORY THIS CHRISTMAS

Dear Mhel,May God's blessing be upon you and your family. It is really hard to get by with all these difficulties, but without families help even harder. Your faith will carry you all, and make you come out of this as a winner. My prayers are with you and your family every day.Take careTunde

Hi,

THROUGHOUT THIS TIME AND UP TO NOW, GOD HAS BEEN

SO FAITHFUL TO US. HE IS BEAUTIFUL AND AWESOME. WE ARE SO

THANKFUL FOR THE PRIVILEGE OF "CARRYING" US AND MOLDING US.

HE WHO DWELLS IN THE SHELTER OF THE MOST HIGH WILL REST

IN THE SHADOW OF THE ALMIGHTY. - PSALM 91:1

A day after Christmas, we share our story to our love ones, to our families

and friends. After many years since 2008, we hide our predicament to them.

The reaon we hide it because the father of Abe had hypertension and wedon't want him to worry. And also his Dad and Mom will surely go to Manaog, a placein the Philippines where they say they see the image of the Virgin .Peope go there for petition to the Virgin . We don't want it to happen because itwill steal the glory of the Lord Jesus in their mind. They will say, Abe is healed bec.of this. His Mom had a heart problem and died without knowing the condition of Abe.

I know my Mom will always call me everyday crying. We don't like it either,

will put our spirit down. And also during that time, our life is just normal, we could care,

give, work, serve without our family and others worrying about us. This e-mail is

the one I sent to them, I just cut the portion that I asked forgiveness for not telling

our family and close friends for a long time. May the Lord bless you... I know my e-mail is long. Jan. 2008, Abe, my husband was diagnosed with colorectal CA. Jan. 24, 2008 they startchemotherapy and radiation. Chemo , he had a pump in a bag and will still go towork. This was during winter time in Iowa. The chemo will flow 48 hours and by thethird day , a nurse will come to the house and remove it every 2 weeks. Aside from that,

he needed to go to hospital for IV chemo once every 2 weeks and radiation Monday

to Friday for 28 sessions and go back to work after that. He will still work more

hours the following day to make up the hours lost during chemo and radiation and had on-call

at night. He cannot hide this bag from co-workers even working in lab. gown.

Chemo and radiation was done by April. May 17, 2008, we attended my nephew's

wedding (my eldest brother's son) with . In all these things,

God is very faithful. We even danced for 5 hours continuously. At this time,

Abe had a port for chemo in his chest. God is carrying us. It's a privelege that Lord Jesusis carrying us throughout. He never leave us nor forsake us. God gave us a comforting

peace and no one knew our predicament.

June, 2008, the surgeons did a resection of the colorectal mass (cancer)

and had ileostomy. So, Abe need to have colostomy bag/pouch for his # 2 for 6 months.

After surgery, they did chmotherapy for 6 months. Still the same, he was still working.

By January, 2009, they reversed the ileostomy and now he could use his bottom again.

He went to the Philippines to attend the funeral of Abe's Mom. The plan was to tell

them now the past health history of Abe but since they still in mourn, Abe was not

able to say it and it means we cannot say it to everyone. We wanted to tell the Dad in person

so that he could see that Abe is well.

Before we leave Iowa, they saw a new mass in the lung and we came to California,

it was confirmed through biopsy that the colorectal cancer metastasize or meaning

same cells went to the left lung. Abe did chemo for 6 months again, this time

the chemo was more aggressive. Chemo started Monday with an IV chemo in cancer

center that lasted about 4 hours, then will go home with a chemo pump in a bag that will flow

for 48 hours. Then Wednesday, he would go back to the center for them to remove

the chemo pump. After 6 months of chemo, had another set of chemotherapy, higher dose and much

more aggresive. During that time, he had 2 works, Antelope Valley Hosp. and Palmalde Regional

Hospital where he was confined. Then he lost the job in Antelope Valley and just concentrate

on Palmdale Regional Hospital. He was still working and only absent himself every chemo time and a day.

Then, he had rest for 1 1/2 months from chemo and had upper lobe lobectomy of the

left lung. Left lung has 2 lobes and they got the upper lobe. Right lung has 3 lobes.

The lobectomy was done Dec 8, 2011 (Thursday). This is for CURE, unlike other

Stage 4 that do treatments only for control. We went home Dec. 11 (Sunday)

and by Wednesday, Dec. 14, he had a stroke. Dec. 16, Friday, he had right decompression

of the brain. Today, Christmas time, a chest tube was placed because of pneumo-

thorax (the left lung that had operation was collapsed due to air outside of the left lung, in the

pleural space. The chest tube was needed to get rid of the air and made the left lung to function well

again and they do successive x-rays to compare things). Before the chest tube was

placed, we had a good talk to surrender ourselves to God and testify about his grace

and mercy to us. And Abe said YES. Praise the Lord. We are just waiting for rehab but since we are

still in the hospital, the doctor ordered chest x-ray and was found to have pneumothorax. It's

a blessing in disguise since we were still in the hospital and no difficulty of

breathing yet. If we already go to the rehab, for sure at some point we will go back

to emergency room because of this. GOD IS GOOD.

The situation made us closer to Him and to each other. I will usually go to him Wednesday

and eat lunch at the car, parked in the hospital and will enjoy each other. We chose Wednesday

bec. this day is longer than the other days, the family attends Midweek Service at Highland's

Church. Even we were married 12 years next June of 2012, I still consider him my boyfriend and

I'm his girlfriend. I cannot explain, in the midst of everything, we are so happy and content.

God's way is so different, work helped him a lot than not doing anything Thank you Lord.

Thank you very much for reading our story. We lived a "normal" life withot our family and

other close friends knowing it. We had the privilege of giving and caring without them worrying

about us. Some people asked for help without hesitation. Aside from this, we also had therapies

for AJ , our younger daughter who was diagnosed with autism secondary to metals from vaccination.

She was found to have different kinds of metals in her body that needed to be chelated and the

same sypmptoms with autism. We tried a lot of alternative medicine and up to now

we are still believing that she will be healed in the name of Jesus. She is so normal

and so intelligent. At 1 and 1/2 years old, she knew all the sounds of the letters.

At 2 years old, she was almost reading then also at this time after 18 months

vaccination, she started to regress and was unable to speak. Now, she could

speak per word but then we are still not losing hope for her. It's very hard

because I saw her potentials. But since insurance won't shoulder alternative medicine,

we needed to pay out of our pocket. We are still doing alternative medicine. The

doctor is healing first her gut due to a lot of food insensitivities/ GIT inflammation

damaged by the metals. Then the doctor will do chelation to get rid of metals.

Please pray also for AJ. She is already 6 years old, attending special education,

first grade and doing therapies, 3 1/2 hours of therapies everyday in our house,

total of 20 hours per week in our house. I joined a yahoo group, the same condition

of AJ, and some kids were recovered from this condition. The parents who recovered

their kids are helping those who wanted to recover other kids thru discussion

via e-mails. There's no particular treatment. Each child was affected by

metals differently. Companies uses metals to preserve the vaccines. The statistic

of autism before is 1 in 10,000 around, 1980's ..now it's 1 in 100 , increased

statistic not only in US but other countries.

During those time, and up to now, It is the Lord Jesus carrying us.

This is God's battle, not ours and we won already through CHRIST. I hope

our family won't feel betrayed, we experienced the care of our Lord Jesus in

a very special way.

THANK YOU ALL FOR YOUR PRAYERS. GOD IS IN CONTROL.

I LOVE YOU, LORD. PLEASE PRAY FOR FASTER AND COMPLETE RECOVERY.

BY JESUS' STRIPES, ABE AND AJ WERE HEALED.

Victory in Christ,

Mhel

PS. I JUST FELT THAT ABE'S DAD NEED TO KNOW THIS FIRST.

I CALLED HIM AND HE KNEW ALREADY AND RECEIVED THE NEWS

WELL. IT'S A BLESSING THAT WE WERE IN THE UNITED STATES OR

ELSE WE DON'T KNOW HOW TO GET RESOURCES FOR THE TREATMENT.

I TOLD HIM THAT THE REASON WE DID NOT TELL HIM IS FOR HIM NOT TO WORRY AND ALSO

WE DON'T WANT THEM TO GO TO MANAOG AND PETITION

IT THERE BECAUSE THE VIRGIIN MARY IS ONLY HUMAN AND JESUS

IS THE LORD BUT MARY WOULD BE HAPPY IF HE WILL RECEIVE JESUS

IN HIS HEART. THANK YOU HOLY SPIRIT FOR ANNOINTING THIS E-MAIL.

WE LOVE YOU DADDY VERY MUCH.

FOR THOSE WHO WANTED TO EXPERIENCE THE LOVE, CARE , SUPPORT,

COMFORTING AND SAVING PEACE OF GOD: JUST RECEIVE THE GIFT

AND SAY THIS PRAYER AND MEAN IT FROM YOUR HEART:

LORD JESUS, COME TO MY HEART. I BELIEVE THAT YOU DIED IN THE

CROSS FOR MY SINS. BE MY SAVIOR AND TAKE CONTROL OF MY LIFE.

THANK YOU LORD.

JUST BY PRAYING THIS SIMPLE PRAYER, YOU BECOME A CHILD OF

GOD. EXPECT CHANGES IN YOUR LIFE AND YOU WILL BE ASSURED

OF ETERNAL LIFE IN HEAVEN. YOU WILL HAVE A DESIRE TO READ

THE BIBLE, THE WORD OF GOD. YOU WON'T REGRET.

MERRY CHRISTMAS AND HAVE A BLESSED NEW YEAR !!!

-- "Our lives begin to end the day we become silent about things that matter." MLK

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Dear Rita,

Thank you for taking time to read my long post. I really appeciate your

prayers and support. I'll keep also the part of a post from another list that

might help in our situation.Thank you for declaring blessings to our family

and for the encouragement. God bless you and your family.

Hugs and kisses,

Mhel

To: mb12valtrex From: rchildbalance@...Date: Fri, 30 Dec 2011 07:47:38 +0000Subject: Re: OUR STORY THIS CHRISTMAS

Dear Mhel,I have also just lifted you up in prayer. Your post brought tears knowing how much you are going through. As I've walked through so many valley's in my life I lean on His word. One of my favorite verses in deep times of unknown, I've learned to deeply depend on it is Proverbs 3:5-8vs5 "Trust in the Lord with all your heart, and lean not on your own understanding. In ALL your ways acknowledge Him, and HE will make your paths straight."vs8 "It will be healing to your body, and refreshment to your bones."So many times I did not know what to do but kneel...I'm kneeling for you now...may the Lord give you strength, wisdom, knowledge in what to do & most of all healing for your precious family.I have decided to copy the below post I did on another list recently for a friend that is going through a similar situation. Use it prayerfully to see if it fits in the path God has for your family...it has been used in people I've spoken w/in conjunction with your current path. Our prayers are with you in all your ways.Blessings,Rita------------part of a Post from another list:ok...for you my dear friend I'll carefully talk, not naming anything specific in this post. I'm purposefully avoiding many autoimmune issues that I've learned about in researching this to protect the product.....I've got to start w/the disclaimer....it is not FDA approved for this & the manufacturer can not say that it does.....It has turned around many severe autoimmune issues including many, many cases of this...several that I have personally spoken with....1 that was given 2 months to live several years ago :o)I know of 1 case of mouth...he swished his first dose around in his mouth, gargled it then had to spit it out (expelling all the initial toxins/pathogens from the initial gargles). Immediately after that he took it normally...he was worked up quickly to the full adult dose of a sick person (16 drops 3x day)...yes, it was effective. I've know of some with other types including 1 severe brain that was on 30 drops 3x a day, she's in canada w/the group homes they put you in there..she's the only one that was not sick as a dog yellow through her docs smt (standard western treatment)..she'd just smile as the doc continued to comment about her good labs....I've personally been through A LOT with this. My mom passed away 22+ years ago from it....I was by her side through a 3 year swt battle. My husband's parents both passed away from a swt battle (3 of our parents never met our children...both our moms before 50...we're now older than they were).My sister-in-law passed away 2 years ago at 51 years old, also of it...she fought her battle mainly naturally as she knew that the swt was so toxic it was not for her...as she was only given a 50/50 chance at her stage with the stw when diagnosed. She did many natural things including diet (for several months it was pure juicing only allowed, some herbs, hydrocolon therapy, oxygen therapy & even one of those natural recovery retreat places). She did have several surgeries including loosing a breast & many lymph nodes & reconstructive. We supported her emotionally in all that she did. Of note, as we worked through this with her she told us her first memory as a child was her mom doing enemas as she was always so constipated going only 1-2 times a week from as long as she could remember...we talked about how no one ever talked about it...or really tried to help fix it, but we fully believe the toxin load over the years shortened her life.Knowing what I now know after both the swt & natural there is 3 things I'd personally do if I found out I personally had this.... & frankly, with my family load it is one of the big reasons my husband & I faithfully take the Immusist, we want to be around longer than our parents were for our children.If I were told I had it, I'd immediately ramp up to a high dose of Immusist. In addition to doing what we all do w/keeping the toxins down like diet & supporting the body w/good vits/good fats, etc I'd have at the top of my list of important fighting things being:1) Immusist ( http://immusist.com/ )2) Kangen water only (no other types of drinks) including a whole house KDF filter for showers/baths.These 2 things hydrate & oxygenate & the Kangen alkalinizes...like many other organisms/illnesses, cancer does not like oxygen rich, alkaline environment.3) After what I've heard about Payne's new Solamar:http://lwtinternational.com/programs/I'd recognise the life & death situation at hand, cash out everything I had & do his Solamar including the Solamar intensive which I understand he follows the organism & organ support through the systems programs (I'd do this over the rife that my friend has used recovering her breast).btw....please, if a doc does not get this stuff...don't start bragging w/the doc or hard core swt believers when the labs turn around, it stirs way to much up....it's not the 1st to smile, say how amazing prayer is & go on their way when the doc asks what they did. Also, please pray for him...I'd personally lay hands & pray over him & the bottle before dosing as well for an extra blessing over the situation."> > > **> >> >> >> >> > Hi,> >> > THROUGHOUT THIS TIME AND UP TO NOW, GOD HAS BEEN> > SO FAITHFUL TO US. HE IS BEAUTIFUL AND AWESOME. WE ARE SO> > THANKFUL FOR THE PRIVILEGE OF "CARRYING" US AND MOLDING US.> >> > HE WHO DWELLS IN THE SHELTER OF THE MOST HIGH WILL REST> > IN THE SHADOW OF THE ALMIGHTY. - PSALM 91:1> >> > A day after Christmas, we share our story to our love ones, to our> > families> > and friends. After many years since 2008, we hide our predicament to them.> > The reaon we hide it because the father of Abe had hypertension and we> > don't want him to worry. And also his Dad and Mom will surely go to> > Manaog, a place> > in the Philippines where they say they see the image of the Virgin .> > Peope go there for petition to the Virgin . We don't want it to happen> > because it> > will steal the glory of the Lord Jesus in their mind. They will say, Abe> > is healed bec.> > of this. His Mom had a heart problem and died without knowing the> > condition of Abe.> > I know my Mom will always call me everyday crying. We don't like it> > either,> > will put our spirit down. And also during that time, our life is just> > normal, we could care,> > give, work, serve without our family and others worrying about us. This> > e-mail is> > the one I sent to them, I just cut the portion that I asked forgiveness> > for not telling> > our family and close friends for a long time. May the Lord bless you... I> > know my e-mail is long.> > Jan. 2008, Abe, my husband was diagnosed with colorectal> > CA. Jan. 24, 2008 they start> > chemotherapy and radiation. Chemo , he had a pump in a bag and will still> > go to> > work. This was during winter time in Iowa. The chemo will flow 48 hours> > and by the> > third day , a nurse will come to the house and remove it every 2> > weeks. Aside from that,> > he needed to go to hospital for IV chemo once every 2 weeks and radiation> > Monday> > to Friday for 28 sessions and go back to work after that. He will still> > work more> > hours the following day to make up the hours lost during chemo and> > radiation and had on-call> > at night. He cannot hide this bag from co-workers even working in lab.> > gown.> > Chemo and radiation was done by April. May 17, 2008, we attended my> > nephew's> > wedding (my eldest brother's son) with . In all these things,> > God is very faithful. We even danced for 5 hours continuously. At this> > time,> > Abe had a port for chemo in his chest. God is carrying us. It's a> > privelege that Lord Jesus> > is carrying us throughout. He never leave us nor forsake us. God gave us a> > comforting> > peace and no one knew our predicament.> > June, 2008, the surgeons did a resection of the colorectal> > mass (cancer)> > and had ileostomy. So, Abe need to have colostomy bag/pouch for his # 2> > for 6 months.> > After surgery, they did chmotherapy for 6 months. Still the same, he was> > still working.> > By January, 2009, they reversed the ileostomy and now he could use his> > bottom again.> > He went to the Philippines to attend the funeral of Abe's Mom. The plan> > was to tell> > them now the past health history of Abe but since they still in mourn, Abe> > was not> > able to say it and it means we cannot say it to everyone. We wanted to> > tell the Dad in person> > so that he could see that Abe is well.> > Before we leave Iowa, they saw a new mass in the lung and> > we came to California,> > it was confirmed through biopsy that the colorectal cancer metastasize or> > meaning> > same cells went to the left lung. Abe did chemo for 6 months again, this> > time> > the chemo was more aggressive. Chemo started Monday with an IV chemo in> > cancer> > center that lasted about 4 hours, then will go home with a chemo pump in a> > bag that will flow> > for 48 hours. Then Wednesday, he would go back to the center for them to> > remove> > the chemo pump. After 6 months of chemo, had another set of chemotherapy,> > higher dose and much> > more aggresive. During that time, he had 2 works, Antelope Valley Hosp.> > and Palmalde Regional> > Hospital where he was confined. Then he lost the job in Antelope Valley> > and just concentrate> > on Palmdale Regional Hospital. He was still working and only absent> > himself every chemo time and a day.> > Then, he had rest for 1 1/2 months from chemo and had upper lobe lobectomy> > of the> > left lung. Left lung has 2 lobes and they got the upper lobe. Right lung> > has 3 lobes.> > The lobectomy was done Dec 8, 2011 (Thursday). This is for CURE, unlike> > other> > Stage 4 that do treatments only for control. We went home Dec. 11 (Sunday)> > and by Wednesday, Dec. 14, he had a stroke. Dec. 16, Friday, he had right> > decompression> > of the brain. Today, Christmas time, a chest tube was placed because of> > pneumo-> > thorax (the left lung that had operation was collapsed due to air outside> > of the left lung, in the> > pleural space. The chest tube was needed to get rid of the air and made> > the left lung to function well> > again and they do successive x-rays to compare things). Before the chest> > tube was> > placed, we had a good talk to surrender ourselves to God and testify> > about his grace> > and mercy to us. And Abe said YES. Praise the Lord. We are just waiting> > for rehab but since we are> > still in the hospital, the doctor ordered chest x-ray and was found to> > have pneumothorax. It's> > a blessing in disguise since we were still in the hospital and no> > difficulty of> > breathing yet. If we already go to the rehab, for sure at some point we> > will go back> > to emergency room because of this. GOD IS GOOD.> >> > The situation made us closer to Him and to each other. I will usually go> > to him Wednesday> > and eat lunch at the car, parked in the hospital and will enjoy each> > other. We chose Wednesday> > bec. this day is longer than the other days, the family attends Midweek> > Service at Highland's> > Church. Even we were married 12 years next June of 2012, I still consider> > him my boyfriend and> > I'm his girlfriend. I cannot explain, in the midst of everything, we are> > so happy and content.> > God's way is so different, work helped him a lot than not doing> > anything Thank you Lord.> >> >> > Thank you very much for reading our story. We lived a "normal" life> > withot our family and> > other close friends knowing it. We had the privilege of giving and caring> > without them worrying> > about us. Some people asked for help without hesitation. Aside from this,> > we also had therapies> > for AJ , our younger daughter who was diagnosed with autism secondary to> > metals from vaccination.> > She was found to have different kinds of metals in her body that needed to> > be chelated and the> > same sypmptoms with autism. We tried a lot of alternative medicine and up> > to now> > we are still believing that she will be healed in the name of Jesus. She> > is so normal> > and so intelligent. At 1 and 1/2 years old, she knew all the sounds of> > the letters.> > At 2 years old, she was almost reading then also at this time after 18> > months> > vaccination, she started to regress and was unable to speak. Now, she could> > speak per word but then we are still not losing hope for her. It's very> > hard> > because I saw her potentials. But since insurance won't shoulder> > alternative medicine,> > we needed to pay out of our pocket. We are still doing alternative> > medicine. The> > doctor is healing first her gut due to a lot of food insensitivities/ GIT> > inflammation> > damaged by the metals. Then the doctor will do chelation to get rid of> > metals.> > Please pray also for AJ. She is already 6 years old, attending special> > education,> > first grade and doing therapies, 3 1/2 hours of therapies everyday in our> > house,> > total of 20 hours per week in our house. I joined a yahoo group, the same> > condition> > of AJ, and some kids were recovered from this condition. The parents who> > recovered> > their kids are helping those who wanted to recover other kids thru> > discussion> > via e-mails. There's no particular treatment. Each child was affected by> > metals differently. Companies uses metals to preserve the vaccines. The> > statistic> > of autism before is 1 in 10,000 around, 1980's ..now it's 1 in 100 ,> > increased> > statistic not only in US but other countries.> >> >> > During those time, and up to now, It is the Lord Jesus carrying us.> > This is God's battle, not ours and we won already through CHRIST. I hope> > our family won't feel betrayed, we experienced the care of our Lord Jesus> > in> > a very special way.> >> > THANK YOU ALL FOR YOUR PRAYERS. GOD IS IN CONTROL.> > I LOVE YOU, LORD. PLEASE PRAY FOR FASTER AND COMPLETE RECOVERY.> > BY JESUS' STRIPES, ABE AND AJ WERE HEALED.> >> > Victory> > in Christ,> >> > Mhel> >> >> > PS. I JUST FELT THAT ABE'S DAD NEED TO KNOW THIS FIRST.> > I CALLED HIM AND HE KNEW ALREADY AND RECEIVED THE NEWS> > WELL. IT'S A BLESSING THAT WE WERE IN THE UNITED STATES OR> > ELSE WE DON'T KNOW HOW TO GET RESOURCES FOR THE TREATMENT.> > I TOLD HIM THAT THE REASON WE DID NOT TELL HIM IS FOR HIM NOT TO WORRY AND> > ALSO> > WE DON'T WANT THEM TO GO TO MANAOG AND PETITION> > IT THERE BECAUSE THE VIRGIIN MARY IS ONLY HUMAN AND JESUS> > IS THE LORD BUT MARY WOULD BE HAPPY IF HE WILL RECEIVE JESUS> > IN HIS HEART. THANK YOU HOLY SPIRIT FOR ANNOINTING THIS E-MAIL.> > WE LOVE YOU DADDY VERY MUCH.> >> > FOR THOSE WHO WANTED TO EXPERIENCE THE LOVE, CARE , SUPPORT,> > COMFORTING AND SAVING PEACE OF GOD: JUST RECEIVE THE GIFT> > AND SAY THIS PRAYER AND MEAN IT FROM YOUR HEART:> >> > LORD JESUS, COME TO MY HEART. I BELIEVE THAT YOU DIED IN THE> > CROSS FOR MY SINS. BE MY SAVIOR AND TAKE CONTROL OF MY LIFE.> > THANK YOU LORD.> >> > JUST BY PRAYING THIS SIMPLE PRAYER, YOU BECOME A CHILD OF> > GOD. EXPECT CHANGES IN YOUR LIFE AND YOU WILL BE ASSURED> > OF ETERNAL LIFE IN HEAVEN. YOU WILL HAVE A DESIRE TO READ> > THE BIBLE, THE WORD OF GOD. YOU WON'T REGRET.> >> > MERRY CHRISTMAS AND HAVE A BLESSED NEW YEAR !!!> >> >> >> >> > > >> > > > -- > *"Our lives begin to end the day we become silent about things that> matter." MLK*>

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