Re: MRI recommendations

[Guest guest]

Hello Group;

To all that offered me suggestions on how to prepare

for my MRI I say thanks. I had the test yesterday, and

used a facecloth to cover my eyes what a huge

difference that made for me. So whoever suggested I do

that, I send you a world of thanks, as did the

ativan. I am thankful that I had the support of

everyone who posts here. Not sure what the results are

on the test, but I see the Neurologist at the end of

the month and I will be curious to see if there are

any new lesions or discoveries that will be made. I am

now on the LDN 9 weeks. and have noticed a huge

change. I walk better, the tightness in my legs has

lessened, and although some of the symptoms do still

remain, ie: numbness in my torso,feet, and hands,

along with spasticity in my legs, I feel the LDN is

doing it's job of halting the progression of my MS.For

me that is a miracle in itself. I do have more days

lately where I am fatigued. But I am sure that will

settle down in time. I am presently on 4.5 and have

only been on that dose for 5 days. I slowly progressed

to that dose from 1.5mg. I will post again after I see

my Neurologist and I hear what the results were of my

MRI.

Thanks again to all of you. Keep well everyone.

All the best,

________________________________________________________________________________\

____

Never miss a thing. Make your home page.

http://www./r/hs

[Guest guest]

Hi ,

I am so glad your experience of MRI changed,

and also that you have found that LDN has given

a huge change, nothing is better than that. Using

LDN is not expensive at all, and should give only

minimal side-effects initially (the first 14 days app.)

Often we find that LDN help us from the very first

days starting to take it, this happened also to me,

and I have Crohns Disease.

So far, so good,

hope you will as a lot of us

find to get a new life Ingrid

[low dose naltrexone] Re: MRI recommendationsHello Group;To all that offered me suggestions on how to preparefor my MRI I say thanks. I had the test yesterday, andused a facecloth to cover my eyes what a hugedifference that made for me. So whoever suggested I dothat, I send you a world of thanks, as did theativan. I am thankful that I had the support ofeveryone who posts here. Not sure what the results areon the test, but I see the Neurologist at the end ofthe month and I will be curious to see if there areany new lesions or discoveries that will be made. I amnow on the LDN 9 weeks. and have noticed a hugechange. I walk better, the

tightness in my legs haslessened, and although some of the symptoms do stillremain, ie: numbness in my torso,feet, and hands,along with spasticity in my legs, I feel the LDN isdoing it's job of halting the progression of my MS.Forme that is a miracle in itself. I do have more dayslately where I am fatigued. But I am sure that willsettle down in time. I am presently on 4.5 and haveonly been on that dose for 5 days. I slowly progressedto that dose from 1.5mg. I will post again after I seemy Neurologist and I hear what the results were of myMRI. Thanks again to all of you. Keep well everyone.All the best, ____________________________________________________________________________________Never miss a thing. Make your home page. http://www./r/hs! Groups

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