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Has anyone got any information about LDN and MRI results showing

disease progression? Have not started taking LDN but am gathering

information. Would appreciate any input.

Carolyne

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I for one am not putting much stock in MRI at this point and probably will

not have another done. The last neuro that I saw says that he does not even

go by them but rather by symptoms because the MRI's seem to vary anyway. He

has seen where some spots on one will mysteriously be gone by the next time

one is done. Good luck to you Carolyne. This whole thing is such a leap of

faith isn't it? Not sure why I just embraced it right from the beginning but

I did and am happy that I did. Joyce.

From: " carolyne_reed " <carolyne_reed@...>

low dose naltrexone

Subject: [low dose naltrexone] MRI

Date: Tue, 01 Jul 2003 15:18:09 -0000

Has anyone got any information about LDN and MRI results showing

disease progression? Have not started taking LDN but am gathering

information. Would appreciate any input.

Carolyne

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I will be getting a MRI in November at which time it will have been one year since my last MRI and six months on LDN. Which means if it shows I am better, wonderful but if I it shows progression so what. There was progression in the first six months after my last MRI. Unknown what is going on since LDN but I feel like I am improving.

----- Original Message -----

From: carolyne_reed

low dose naltrexone

Sent: Tuesday, July 01, 2003 11:18 AM

Subject: [low dose naltrexone] MRI

Has anyone got any information about LDN and MRI results showing disease progression? Have not started taking LDN but am gathering information. Would appreciate any input.Carolyne

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My daughter, (GA) started LDN in May, 2000. She had an MRI

at that time. In August, 2002 she had another MRI that showed all

the lesions on her spine (substantial amount)were gone. The lesions

on her brain were still there but inactive. She feels that since

the spinal lesions healed, it's possible to get the ones on the

brain too. Her neuro will do another MRI in 2004 and we'll see how

things are going.

> Has anyone got any information about LDN and MRI results showing

> disease progression? Have not started taking LDN but am gathering

> information. Would appreciate any input.

> Carolyne

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  • 5 months later...

Hi Ilene, glad it is working for you. From what Dr. Bihari told me, I would probably regain what I had lost the prior 3 months. It seems he was right, I did regain my bladder and my left hand is much stronger. My walking has improved but I still need my cane.My legs were the first to feel the MS 8 yrs ago, so I guess they may never correct. It was only this past year and a half I need the cane. I am sorry I did not start the LDN before I had reached this point, but who knew? No one can really answer what will happen, but we are all hoping for a miracle. Hold onto that thought, who knows? Kiki

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