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Today in 18 day, my son awakes up early in the morning again!!(he has been

sleeping until 10 or 11 o'clock) he was happy, with energy, good awareness,

smiling, stammering (he is 9 but he can’t talk), of course I felt really happy.

He was great until he made his second meal (we are trying he eats 5 times a day)

at 12 o’clock and after he went to the bathroom to make poop, he made it a lot

and really “watery”, two days ago his poop had a good consistence. This

situation is diarrhea? He just made it once a day. After he finish to make poop

all the energy disappear like a magic act. Only after the second meal he was

recovering the energy again.

During the 18 SCD days, he had has days with a normal poop, and days like

today. He is eating the same foods. I can’t understand what is going on. Thanks

for your help.

Mother of a Brain injury Boy.

__________________________________________________

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,

I'm glad you saw a ray of hope today... I'm sure he will have many more good

days to come.

Since he has been on SCD for less than three weeks, I'm sure you will still see

some " ups and downs " . With this diet, it is uncommon to see a steady, even

course of improvement. It is much more common to see some good days, followed by

bad.

You must remember that if there was an imbalance in the gut, with bad gut

pathogens growing out of control, they need to die and be eliminated from the

body. This will not all happen at once, in the first week of the diet. It will

likely take time, and occur in " waves " .

Think of a trying to climb a very steep mountain. Would you expect to go

STRAIGHT up... from the bottom, directly to the top, without slipping back?

No... you would probably go one way, then turn and criss-cross, carefully

winding your way back and forth. At times, on that winding mountain path, you

may slip back.... until you are used to the effort of climbing. Now and then,

you would need to stop and rest. SLOWLY, you will eventually reach the top,

despite some missed steps.

It's the same with SCD. You are working with a living body... and this is a very

organic process. You may feel distressed to see him with diarrhea again... but

it is one way his body is trying to eliminate toxins. This is hard work for your

sweet boy. But, I am sure there will be many more happy, smiling days to come.

Are you making sure to peel and cook all fruits and vegetables well? Making

everything as easy to digest as possible?

My daughter is also 9 yrs old... (with cerebral palsy, epilepsy, does not have

speech, etc.) .

my best to you,

Patti, mom to Katera

doubt

Today in 18 day, my son awakes up early in the morning again!!(he has been

sleeping until 10 or 11 o'clock) he was happy, with energy, good awareness,

smiling, stammering (he is 9 but he can't talk), of course I felt really happy.

He was great until he made his second meal (we are trying he eats 5 times a day)

at 12 o'clock and after he went to the bathroom to make poop, he made it a lot

and really " watery " , two days ago his poop had a good consistence. This

situation is diarrhea? He just made it once a day. After he finish to make poop

all the energy disappear like a magic act. Only after the second meal he was

recovering the energy again.

During the 18 SCD days, he had has days with a normal poop, and days like

today. He is eating the same foods. I can't understand what is going on. Thanks

for your help.

Mother of a Brain injury Boy.

__________________________________________________

Correo Yahoo!

Espacio para todos tus mensajes, antivirus y antispam ¡gratis!

Regístrate ya - http://correo.yahoo.com.mx/

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Share on other sites

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Patti:

I really appreciate your help with all my doubts.

Thank you very much.

Patti escribió:

,

I'm glad you saw a ray of hope today... I'm sure he will have many more good

days to come.

Since he has been on SCD for less than three weeks, I'm sure you will still see

some " ups and downs " . With this diet, it is uncommon to see a steady, even

course of improvement. It is much more common to see some good days, followed by

bad.

You must remember that if there was an imbalance in the gut, with bad gut

pathogens growing out of control, they need to die and be eliminated from the

body. This will not all happen at once, in the first week of the diet. It will

likely take time, and occur in " waves " .

Think of a trying to climb a very steep mountain. Would you expect to go

STRAIGHT up... from the bottom, directly to the top, without slipping back?

No... you would probably go one way, then turn and criss-cross, carefully

winding your way back and forth. At times, on that winding mountain path, you

may slip back.... until you are used to the effort of climbing. Now and then,

you would need to stop and rest. SLOWLY, you will eventually reach the top,

despite some missed steps.

It's the same with SCD. You are working with a living body... and this is a very

organic process. You may feel distressed to see him with diarrhea again... but

it is one way his body is trying to eliminate toxins. This is hard work for your

sweet boy. But, I am sure there will be many more happy, smiling days to come.

Are you making sure to peel and cook all fruits and vegetables well? Making

everything as easy to digest as possible?

My daughter is also 9 yrs old... (with cerebral palsy, epilepsy, does not have

speech, etc.) .

my best to you,

Patti, mom to Katera

doubt

Today in 18 day, my son awakes up early in the morning again!!(he has been

sleeping until 10 or 11 o'clock) he was happy, with energy, good awareness,

smiling, stammering (he is 9 but he can't talk), of course I felt really happy.

He was great until he made his second meal (we are trying he eats 5 times a day)

at 12 o'clock and after he went to the bathroom to make poop, he made it a lot

and really " watery " , two days ago his poop had a good consistence. This

situation is diarrhea? He just made it once a day. After he finish to make poop

all the energy disappear like a magic act. Only after the second meal he was

recovering the energy again.

During the 18 SCD days, he had has days with a normal poop, and days like today.

He is eating the same foods. I can't understand what is going on. Thanks for

your help.

Mother of a Brain injury Boy.

__________________________________________________

Correo Yahoo!

Espacio para todos tus mensajes, antivirus y antispam ¡gratis!

Regístrate ya - http://correo.yahoo.com.mx/

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Share on other sites

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Patti said to Katera: " Think of a trying to climb a very steep mountain. Would

you expect to go STRAIGHT up... from the bottom, directly to the top, without

slipping back? No... you would probably go one way, then turn and criss-cross,

carefully winding your way back and forth. At times, on that winding mountain

path, you may slip back.... until you are used to the effort of climbing. Now

and then, you would need to stop and rest. SLOWLY, you will eventually reach the

top, despite some missed steps. It's the same with SCD. "

Dear Katera, I understand your frustrations. This first year(s) of healing is

going to be a challenge for all of us new here.

I am glad that we are not alone. It is so nice to have those with more time, to

help us keep our hope when we have doubt and feel overwhelmed by his roller

coaster ride...or as Patti eloquently compared to a steep mountain climb.

What keeps us going is the beautiful view when so " high " in these " mysterious

mountains " ....when our daughter started to talk, our first hug from her, her

first ability to have imagination, to play and smile for the first time. The

beautiful scenery at such heights is the delight...the " breathlessness and

exhaustion " ...well " rest " when you can....just keep eating SCD and enjoy the

ride! This is what I do to keep me going: I Take advantage of those " hours "

that will some day turn to days.....and enjoy the " scenery " when I can.

Journaling helps me much. I Mark good hours or days with smile faces....so on

the bad days, or when we have regressions and set backs, I can flip back and

easily spot them and read them.

Or I do searches for SCD testimonials...this keeps us going to...sometimes the

" good scenery scenes " of others keep one going when they are having doubt...I

know that they have helped us during " regressions " or " slow progress " times.

God Bless you Antoinette and (celiac) parents to -5 (celiac/adhd)

Kiki-2 (celiac/autism) and Bubbles -1 (Hyperekplexia/and more) SCD 2/06

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Repost because Patti brought to my attention that I addressed it to

the worng person...sorry.

>

Patti said to : " Think of a trying to climb a very steep

mountain. Would you expect to go STRAIGHT up... from the bottom,

directly to the top, without slipping back? No... you would probably

go one way, then turn and criss-cross, carefully winding your way

back and forth. At times, on that winding mountain path, you may

slip back.... until you are used to the effort of climbing. Now and

then, you would need to stop and rest. SLOWLY, you will eventually

reach the top, despite some missed steps. It's the same with SCD. "

>

> Dear , I understand your frustrations. This first year(s)

of healing is going to be a challenge for all of us new here.

>

> I am glad that we are not alone. It is so nice to have those with

more time, to help us keep our hope when we have doubt and feel

overwhelmed by his roller coaster ride...or as Patti eloquently

compared to a steep mountain climb.

>

> What keeps us going is the beautiful view when so " high " in

these " mysterious mountains " ....when our daughter started to talk,

our first hug from her, her first ability to have imagination, to

play and smile for the first time. The beautiful scenery at such

heights is the delight...the " breathlessness and

exhaustion " ...well " rest " when you can....just keep eating SCD and

enjoy the ride! This is what I do to keep me going: I Take

advantage of those " hours " that will some day turn to days.....and

enjoy the " scenery " when I can. Journaling helps me much. I Mark

good hours or days with smile faces....so on the bad days, or when

we have regressions and set backs, I can flip back and easily spot

them and read them.

> Or I do searches for SCD testimonials...this keeps us going

to...sometimes the " good scenery scenes " of others keep one going

when they are having doubt...I know that they have helped us

during " regressions " or " slow progress " times.

>

> God Bless you Antoinette and (celiac) parents to -5

(celiac/adhd) Kiki-2 (celiac/autism) and Bubbles -1

(Hyperekplexia/and more) SCD 2/06

>

>

>

>

>

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