what to do

[Guest guest]

>

>

> From: <tori_r_b@...>

> Subject: what to do

> Hepatitis C

> Date: Tuesday, February 9, 2010, 4:29 PM

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>  

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> I am getting scared becuase I feel bad all the time .I had a biopsy

> years ago about5 and didn't go on treatment from docs advice.Should I

> just wait it out?

>

>

> He wanted to give me interferon and ribavarin I think but the side effcts were

worse than hep c.But I wanted it gone now I can't workm or feel good very much.

>

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[Guest guest]

> > >

> > > I am getting scared becuase I feel bad all the time .I had a biopsy

> > > years ago about5 and didn't go on treatment from docs advice.Should I

> > > just wait it out?

> > >

> >

> I have no support since my fiance died from an anurysm in my bed a couple

months ago.I just am seeing dark urine,pain by my liver and light stools and so

tired.

>

>

> I got it about 12 years ago I had a routine blood test done for surgery amnd

they found my liver count sky high and then I figured out an old boyfriend was

shooting drugs all the time.I try and stay hopeful but I have a daughter and her

father died at 36 of a heartattack.She's lost 2 important men in her life I hope

I'm not next.

>

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[Guest guest]

>

> Hi Bee

>

> I have been on the complete program for a year now. For the last

> 4 months I haven't had anything solid come out of me. Explosive dia..

> every day usually just once a day as soon as I get up in the morning.

> And I have a very noisy gurgley stomach especially after I eat or when

> I start to eat. My stomach feels fine most of the time though. I have

> been very slowly but steadily losing weight and I am now about 30 lbs.

> underweight and I can't seem to stop it. I lost the first 20 lbs on

> a different diet before I started yours. The last 10 lbs. has been

> while on your diet over the past 12 months. I look completely anerexic. Please

let me know what you think I should do. Thanks for your help.

>

+++Hi ,

Have you ever had diarrhea in the past? Are you under a lot of stress other

than being unhealthy and underweight?

Are you doing everything you can to improve your digestion? You could review

that section in my candida article:

http://www.healingnaturallybybee.com/articles/intro2.php#s28

Have you done coffee enemas?

Remember I also do personal consultations:

http://www.healingnaturallybybee.com/consult.php

The best to you, Bee

All the best, Bee

[Guest guest]

Hi , this describes my family's bowel movements aswell! We have been on the

programe for 20 months and have made such progress with our other symptoms that

we are just keeping the faith and assuming its just our bodies busy detoxing! We

did suddenly stop losing weight and hair a few months back and all started to

put it back on big time! We go very steady on the carbs(hardly any) and found

stopping lemon very helpful too. Even going back to ghee instead of butter

helped. Depending on how seriously poorly some of us are, its perhaps just a

game of patience.

Besr wishes

>

> Hi Bee

>

> I have been on the complete program for a year now. For the last

> 4 months I haven't had anything solid come out of me. Explosive dia..

> every day usually just once a day as soon as I get up in the morning.

> And I have a very noisy gurgley stomach especially after I eat or when

> I start to eat. My stomach feels fine most of the time though. I have

> been very slowly but steadily losing weight and I am now about 30 lbs.

> underweight and I can't seem to stop it. I lost the first 20 lbs on

> a different diet before I started yours. The last 10 lbs. has been

> while on your diet over the past 12 months. I look completely anerexic.

> Please let me know what you think I should do. Thanks for your help.

>

>

>

[Guest guest]

We are scheduled to see Dr. G soon, but our ENT says my son needs to have his

tonsils out and tubes put back into his ears. He has had a horrible winter,

being sick with something about every other week. Seriously, he has had

vomiting, URI, ear infections, about every other week since the beginning of

November. The scheduler for surgery called and we have him scheduled for the

14th. I am concerned the anesthetic could stress him, but my other son was sick

all the time until he got his tonsils out. Has anyone here gone through this or

know what Dr. G thinks?

[Guest guest]

How old is your son? This sounds like my son, starting at 18 months until 5.

4 sets of ear tubes and adenoids removed, but removing corn from his diet

(in addition to the diet) made a HUGE difference. So did the

protocol. Now, when he gets sick (which is rarely.he's 8 now), it's more

like a typical kid and he's well again after just a few days instead of it

dragging out for months.

Kristy Nardini

Tazzini Stainless Steel Bottles

www.tazzini.com

kristy@...

<http://www.facebook.com/tazzinicompany> Find us on Facebook!

<http://www.twitter.com/tazzini> Follow us on Twitter!

From: [mailto: ] On Behalf Of

lappe1191@...

Sent: Saturday, March 05, 2011 8:33 PM

Subject: what to do

We are scheduled to see Dr. G soon, but our ENT says my son needs to have

his tonsils out and tubes put back into his ears. He has had a horrible

winter, being sick with something about every other week. Seriously, he has

had vomiting, URI, ear infections, about every other week since the

beginning of November. The scheduler for surgery called and we have him

scheduled for the 14th. I am concerned the anesthetic could stress him, but

my other son was sick all the time until he got his tonsils out. Has anyone

here gone through this or know what Dr. G thinks?

[Guest guest]

Yes. Don't know who you saw but try Childrens mercy in kc mo. They are Mehta

trained if you end up going that route. Low muscle tone is neurologically

related but I don't think it is neccesarily related to scoliosis. My son has low

tone also. What early interventions does your state have? We have early steps.

It sounds like your child could qualify. Look into it.

Tame

I'm from ks originally:)

Sent from my iPhone

On Nov 11, 2011, at 8:21 AM, " " <alicia.marie@...> wrote:

Hello! First of all I am so happy that I found a group of parents who can relate

to what my youngest son, Ayden, and our family is going through. Ayden just

turned 1 last week. He is a strong boy, who loves to be silly, and has infantile

scoliosis. He has a 21 degree dextroconvex curve between the T5 and L4. After a

2 month wait we finally saw an Ortho last week, only for the doctor to take 5

minutes asking us family history questions, and then tell us to wait 4-5 month

to see if it gets worse. Ayden, although he is a year old, cannot sit

unassisted, crawl, or even use his arms to reach for toys or hold his bottles

(he was deamed to have low muscle tone- but we have no confirmation on whether

this is scoliosis related). I am sooooo frustrated. I have a 1 year old, who we

have been told by his developmental pediatrician, functions like a 3-4 month

old. Immediately after the appnt with the Ortho I called both his PCP and

Developmental specialist to ask if

they could refer us to another Ortho for a second opinion. They both told us to

just wait it out, like the Ortho had also told us to do. I refuse to sit here

and let my son get further behing in life. Is there anyone else in the Kansas

City area that can offer advise or a great Ortho for us to get a second opinion?

Or has anyone else had a problem with all doctors telling them to wait it out?

------------------------------------

[Guest guest]

Thank you for the replies and suggestions! We saw an ortho at Children's Mercy

General (I hesitate to say names because I do not have a good thing to say about

him). All of my son's doctors are Children's Mercy related... which is why I

hesitate to get a second opinion at Children's Mercy. I have heard a couple

people mention KU Med Center as a place nearby to try also. We are also working

with an early intervention program through the state and have an occupational

therapist and physical therapist visit the house once a week. He is also severly

near sighted with an astigmatism and has worn glasses for about 4 months now. We

have had so appointments and doctors visit I just feel so overwhelmed.

Genetics clinic is next week, and we are still waiting until late Dec before he

can get an MRI. I have been very unimpressed with Children's Mercy (thoughh up

until now they have always been THE best- we have 2 older children and we would

never dream of taking them anywhere else). Part of me wants to keep trying to

get help and answers and the other part wants to take a deep breath and see

what happens over the next 4 months. Do I keep pressing to find a second

opinion, or wait like the Ortho told us????

>

> Hello! First of all I am so happy that I found a group of parents who can

relate to what my youngest son, Ayden, and our family is going through. Ayden

just turned 1 last week. He is a strong boy, who loves to be silly, and has

infantile scoliosis. He has a 21 degree dextroconvex curve between the T5 and

L4. After a 2 month wait we finally saw an Ortho last week, only for the doctor

to take 5 minutes asking us family history questions, and then tell us to wait

4-5 month to see if it gets worse. Ayden, although he is a year old, cannot sit

unassisted, crawl, or even use his arms to reach for toys or hold his bottles

(he was deamed to have low muscle tone- but we have no confirmation on whether

this is scoliosis related). I am sooooo frustrated. I have a 1 year old, who we

have been told by his developmental pediatrician, functions like a 3-4 month

old. Immediately after the appnt with the Ortho I called both his PCP and

Developmental specialist to ask if

> they could refer us to another Ortho for a second opinion. They both told us

to just wait it out, like the Ortho had also told us to do. I refuse to sit here

and let my son get further behing in life. Is there anyone else in the Kansas

City area that can offer advise or a great Ortho for us to get a second opinion?

Or has anyone else had a problem with all doctors telling them to wait it out?

>

>

>

> ------------------------------------

>

>

[Guest guest]

I think because we are so new to this I feel like I dont even know where to

begin. We have seen a cardiologist, ortho, developmental specialist and have

Genetics clinic on Monday... so far every doctor has said " I need to wait for

MRI results " ... all these doctors are a part of the same medical hospital-all

appnts were set up by our PCP at the same time, so my frustration is do we have

to wait 4 month for an MRI, but all of the doctors appointments were schelduled

before an MRI was ever done...

> >

> > Hello! First of all I am so happy that I found a group of parents who can

relate to what my youngest son, Ayden, and our family is going through. Ayden

just turned 1 last week. He is a strong boy, who loves to be silly, and has

infantile scoliosis. He has a 21 degree dextroconvex curve between the T5 and

L4. After a 2 month wait we finally saw an Ortho last week, only for the doctor

to take 5 minutes asking us family history questions, and then tell us to wait

4-5 month to see if it gets worse. Ayden, although he is a year old, cannot sit

unassisted, crawl, or even use his arms to reach for toys or hold his bottles

(he was deamed to have low muscle tone- but we have no confirmation on whether

this is scoliosis related). I am sooooo frustrated. I have a 1 year old, who we

have been told by his developmental pediatrician, functions like a 3-4 month

old. Immediately after the appnt with the Ortho I called both his PCP and

Developmental specialist to ask if

> > they could refer us to another Ortho for a second opinion. They both told

us to just wait it out, like the Ortho had also told us to do. I refuse to sit

here and let my son get further behing in life. Is there anyone else in the

Kansas City area that can offer advise or a great Ortho for us to get a second

opinion? Or has anyone else had a problem with all doctors telling them to wait

it out?

> >

> >

> >

> > ------------------------------------

> >

> >

[Guest guest]

Maybe think about a second opinion. I think TX ish Rite and ST Louis are

the closest facilities in driving distance. My Mil just retired from KU Med.

Don't think you would go there....... Not sure they have services. I will ask

her. There was another parent on this site not happy w Childrens Mercy. Maybe

they will see your post n have a suggestion. Would the branch in mo have

different physicians? Or is that the one you are at.

Sent from my iPhone

On Nov 11, 2011, at 10:59 AM, " " <alicia.marie@...> wrote:

Thank you for the replies and suggestions! We saw an ortho at Children's Mercy

General (I hesitate to say names because I do not have a good thing to say about

him). All of my son's doctors are Children's Mercy related... which is why I

hesitate to get a second opinion at Children's Mercy. I have heard a couple

people mention KU Med Center as a place nearby to try also. We are also working

with an early intervention program through the state and have an occupational

therapist and physical therapist visit the house once a week. He is also severly

near sighted with an astigmatism and has worn glasses for about 4 months now. We

have had so appointments and doctors visit I just feel so overwhelmed.

Genetics clinic is next week, and we are still waiting until late Dec before he

can get an MRI. I have been very unimpressed with Children's Mercy (thoughh up

until now they have always been THE best- we have 2 older children and we would

never dream of taking

them anywhere else). Part of me wants to keep trying to get help and answers

and the other part wants to take a deep breath and see what happens over the

next 4 months. Do I keep pressing to find a second opinion, or wait like the

Ortho told us????

Hello! First of all I am so happy that I found a group of parents who can relate

to what my youngest son, Ayden, and our family is going through. Ayden just

turned 1 last week. He is a strong boy, who loves to be silly, and has infantile

scoliosis. He has a 21 degree dextroconvex curve between the T5 and L4. After a

2 month wait we finally saw an Ortho last week, only for the doctor to take 5

minutes asking us family history questions, and then tell us to wait 4-5 month

to see if it gets worse. Ayden, although he is a year old, cannot sit

unassisted, crawl, or even use his arms to reach for toys or hold his bottles

(he was deamed to have low muscle tone- but we have no confirmation on whether

this is scoliosis related). I am sooooo frustrated. I have a 1 year old, who we

have been told by his developmental pediatrician, functions like a 3-4 month

old. Immediately after the appnt with the Ortho I called both his PCP and

Developmental specialist to ask if

they could refer us to another Ortho for a second opinion. They both told us to

just wait it out, like the Ortho had also told us to do. I refuse to sit here

and let my son get further behing in life. Is there anyone else in the Kansas

City area that can offer advise or a great Ortho for us to get a second opinion?

Or has anyone else had a problem with all doctors telling them to wait it out?

------------------------------------

[Guest guest]

Call and try to reschedule the MRI to bump the time frame up. Just play dumb and

call and say you cannot come that day bc something came up and if possible you

would like to reschedule at an earlier date. It's called the appointment game:)

Im a pro at it. If that's not possible see if there is a waiting list for

cancelations.

Sent from my iPhone

On Nov 11, 2011, at 11:15 AM, " " <alicia.marie@...> wrote:

I think because we are so new to this I feel like I dont even know where to

begin. We have seen a cardiologist, ortho, developmental specialist and have

Genetics clinic on Monday... so far every doctor has said " I need to wait for

MRI results " ... all these doctors are a part of the same medical hospital-all

appnts were set up by our PCP at the same time, so my frustration is do we have

to wait 4 month for an MRI, but all of the doctors appointments were schelduled

before an MRI was ever done...

Hello! First of all I am so happy that I found a group of parents who can relate

to what my youngest son, Ayden, and our family is going through. Ayden just

turned 1 last week. He is a strong boy, who loves to be silly, and has infantile

scoliosis. He has a 21 degree dextroconvex curve between the T5 and L4. After a

2 month wait we finally saw an Ortho last week, only for the doctor to take 5

minutes asking us family history questions, and then tell us to wait 4-5 month

to see if it gets worse. Ayden, although he is a year old, cannot sit

unassisted, crawl, or even use his arms to reach for toys or hold his bottles

(he was deamed to have low muscle tone- but we have no confirmation on whether

this is scoliosis related). I am sooooo frustrated. I have a 1 year old, who we

have been told by his developmental pediatrician, functions like a 3-4 month

old. Immediately after the appnt with the Ortho I called both his PCP and

Developmental specialist to ask if

they could refer us to another Ortho for a second opinion. They both told us to

just wait it out, like the Ortho had also told us to do. I refuse to sit here

and let my son get further behing in life. Is there anyone else in the Kansas

City area that can offer advise or a great Ortho for us to get a second opinion?

Or has anyone else had a problem with all doctors telling them to wait it out?

------------------------------------

[Guest guest]

Any way to press them for a sooner MRI?

HRH

> I think because we are so new to this I feel like I dont even know where

> to begin. We have seen a cardiologist, ortho, developmental specialist and

> have Genetics clinic on Monday... so far every doctor has said " I need to

> wait for MRI results " ... all these doctors are a part of the same medical

> hospital-all appnts were set up by our PCP at the same time, so my

> frustration is do we have to wait 4 month for an MRI, but all of the

> doctors appointments were schelduled before an MRI was ever done...

>

>

>> >

>> > Hello! First of all I am so happy that I found a group of parents who

>> can relate to what my youngest son, Ayden, and our family is going

>> through. Ayden just turned 1 last week. He is a strong boy, who loves

>> to be silly, and has infantile scoliosis. He has a 21 degree

>> dextroconvex curve between the T5 and L4. After a 2 month wait we

>> finally saw an Ortho last week, only for the doctor to take 5 minutes

>> asking us family history questions, and then tell us to wait 4-5 month

>> to see if it gets worse. Ayden, although he is a year old, cannot sit

>> unassisted, crawl, or even use his arms to reach for toys or hold his

>> bottles (he was deamed to have low muscle tone- but we have no

>> confirmation on whether this is scoliosis related). I am sooooo

>> frustrated. I have a 1 year old, who we have been told by his

>> developmental pediatrician, functions like a 3-4 month old.

>> Immediately after the appnt with the Ortho I called both his PCP and

>> Developmental specialist to ask if

>> > they could refer us to another Ortho for a second opinion. They both

>> told us to just wait it out, like the Ortho had also told us to do. I

>> refuse to sit here and let my son get further behing in life. Is

>> there anyone else in the Kansas City area that can offer advise or a

>> great Ortho for us to get a second opinion? Or has anyone else had a

>> problem with all doctors telling them to wait it out?

>> >

>> >

>> >

>> > ------------------------------------

>> >

>> >