LDN and Spinal Cord Lesions

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Sally,

I tried the 3mg dose and it did absolutely nothing. I wonder if it is due the lesions which have accumulated in the spinal cord and atrophy of the cord. MS will celebrate ten years in this body in October. I lost the ability to walk for any distance in May and am going Monday for an ultrasound to see if I can tolerate Novantrone. The neurologist says it is my last hope. Anybody have any suggestions?

Thanks,

Beth

>From: "Sally"

>low dose naltrexone >Subject: [low dose naltrexone] Re: Great experience with LDN >Date: Sat, 28 Jun 2003 18:26:03 -0000 > >WELCOME GIRLFRIEND! >SO GLAD YOU SHARED YOUR SUCCESS STORY WITH THE OTHERS! >I WILL DEFFINATELY BE TRYING TO FOLLOW IN YOUR FOOTSTEPS (LITERALLY) >LOL >YOUR PAL, SAL > > > > > Hi Everyone > > I am so glad to see so many people that have discovered LDN, It is >a > > god sent for all of us with MS. I have been on 4.5mg since dec of > > last year and everyday there is improvement. All numbness is gone, > > my balance is so much improved and lately I can even walk normally > > for the first time in years. I used to have constant movement in >my > > head and I called them shock waves that would go through my head > > when i bent my head down and that is all gone to what a relief >that > > was my head is clear now. I didn't experience any stiffness at >all > > but we are individul so our experiences are different. I have had >MS > > now for 34 yrs maybe that is why the 4.5mg worked for me with all > > the damage I have on my brain I have lesions in both hemispheres, > > and the cerubellm. thought I would tell my story so everybody >could > > benefit from my experience. > > > > Love and Peace to all in the group > > Kathy > Protect your PC - Click here for McAfee.com VirusScan Online