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I WILL PUT IT IN CAPS FOR YOU. I HAVE BEEN ON LDN FOR 21

DAYS AND JUST ORDERED MY FIRST REFILL. I DID NOT EXPERIENCE ANY UNUSUAL SIDE

EFFECTS OTHER THAN HAVING TO TAKE A NAP DURING THE DAY. I AM A 70 YEAR OLD

MALE SO NAPS ARE PROBABLY NORMAL ANYWAY ALTHOUGH I AM STILL WORKING A FULL DAY

AS AN ADMINISTRATOR.

KEEP SMILING AND I WISH YOU THE BEST.

BOB LAKE

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  • 2 weeks later...

> Would anyone please send me and email to teesixx@l... and

> tell my how the LDN has improved you lifestyle and how you got the

> medicine.

> My wife is the one with ms and she is anxious to hear from

someone

> who is taking the LDN

> My wife is 60 years old and is in a wheelchair most of the time

> and sometimes trys to walk with her walker. Some day she does

pretty

> good with it and we were hoping the LDN might be able to make this

> better.

> Any response from anyone will be greatly appreciated.

>

> thank you very much ann and Terry

Hi ann & Terry,

I was diagnosed with MS and Transverse Myelitis in November of 2004

and

I am only 38 years old. I was on Betaseron to begin with but stopped

it

because I got a really bad infection in my right upper thigh from the

injection and it took 3 months and surgery to get over that.I just

got

my LDN but have to wait till I get the Vicodin out of my system to

start taking it and I can't wait.

I am so sorry to hear about your wife and my thoughts and prayers are

with you both.

Here is a few links you can check out on LDN and the injections:

http://www.thecompounder.com/diseaseawaste.html

www.crystalangel.org (This is my Website I made for MS & Transverse

Myelitis and I have a page on LDN so please check it out).

I feel that with all the research I have done and people I have

talked

to thats taking LDN that its the most promising thing out there for

us

with MS at this time.

Thanks,

Crystal

P.S. I tried your email but it came back to me.

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