Re: Vit C update

[Guest guest]

, you are so funny, we think so much alike, i would

feel the same way. But you are not crazy and you wont jinx

yourself. I am so happy for you. Whatever it is its

working,just keep doing it.I know you posted what and how

much you are taking and I thought I saved it but i cant

find it. can you post it again. i too am taking vitamin c

but i dont know if I feel any different yet . but as we all

know cmt is so different in all of us. Another thing that i

am doing is seeing a personal trainer in New York City. He

has alot of experience with cmt population, i got his name

from the hereditary neuropathy web site.I saw him for the

first time yesterday and he has high hopes for me so we will

see.(See now I am afraid to be too positive in fear of

jinxing myself)COOCOO LOL. thanks Pam O

[Guest guest]

,

What form of Vit C are you taking, and how much a day?

[Guest guest]

Yep that is just how I feel! Today (Sunday) is even better. I walked across

the street and back with worrying about balancing.

I am taking 10,000 mils a day . I just started taking 2 of the time release

and 1 regular Vit C 3 times a day. I was taking the regular release pills 3

times a day. But the time release stays in your body for 8 hours.

[Guest guest]

thanks for the info jenny. I am so happy for you.

[Guest guest]

,

I can't tell you how happy I am for your kids!! I'm so happy for you too,

but I know that as a mother you must be radiating for your kids. I already made

the decision to have my own (the man said that is what the wants too) when

the time comes so I'm with you on that. I just know how we all want the best

for our kids and to see a child smile is the best feeling.

YEA to you and yours!!!!!!!!