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PPers on LDN

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hi Group-

Hi Martha-

I'm trying to remember how the succession goes.

I think I may be...

I've had MS for 26 years- too.

and on LDN for 1 week now- 3mg. Although I di8d try 4.5 for 3 nights.

Until I talked to Wayne Loveland and Dr. 's office. I'll continue

at 3 for one more week- then they will up it to 4.5 and make the

filler CC.

yea!

Now here's the nifty thing-

today for the fist time, I felt something change. It wasn't much and

it didn't last long but it was incredible. For the past year I've had

to use my can every time I leave the house (in the house I'm a wall

walker).

I was walking out in the (unlevel) parking lot and realized... I

didn't need my cane. I picked it up and held it in the middle like a

toy stick and walked to the house without one stumble or loss of

balance. I remember!!! I remember what it felt like to need a cane. I

mean at all! It's been years since I walked without fear of stumbling

or falling over. I was so excited I came in and sat down right away

and just soaked it up. Then called my friend who drove with me to Dr.

's office a week ago monday.

What an incredible feeling!

God bless me!

God bless us all.

I'm grateful just for the very clear reminder of being whole.

I hope it does it again someday soon.

ok- I'm done floating.

I'll land now-

thank you all for being here!

alex

> Hi--I'd like to hear from primary progressive MSers who've been on LDN

> more than three months. Any symptomatic improvement? Any progression?

> Thanks--Martha

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OH ALEX...WOW...I AM SO HAPPY FOR YOU...AND I AM REALLY GLAD I

STEERED YOU TO DR. SCOTT AND WAYNE.....WONDERFUL NEWS...KEEP IT UP

FOR ALL OF US.

LOVE, SALLY

> > Hi--I'd like to hear from primary progressive MSers who've been

on LDN

> > more than three months. Any symptomatic improvement? Any

progression?

> > Thanks--Martha

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