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Clinical Use of Anabolics and Hormones
Clinical Use of Anabolics and Hormones
Nerve Degenerative Disease, wasting and testosterone
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<blockquote data-quote="masfield" data-source="post: 46250" data-attributes="member: 13737"><p>Ero: Maybe it shouldnt have an impact on my legs but it definitely did. And it was almost immediate. I could feel the numbness descending like a thick fog. I'm sure it has everything to do with the nature of my hated CIDP disease. I'll try an injection in my shoulder and see what happens.</p><p> My T dose was 100 mg once a week. And, like I said, I only did it three times before stopping.</p><p> I'm really hoping that T or something else can help me out with my failing, sagging muscles. Three years ago, my neurologist gave me 4 to 6 years before I'd be in a wheelchair. I hate doctors who give terrible predictions like that, but it has stuck with me ever since. And if he's right, gulp. I haven't given up the fight, however. At the same time, my disease is rare enough that no one really studies it and there are no acknowledged experts on it. So, everything is a crap shoot.</p><p> I've tried the standard treatments, with no success. Last one up is prednisone, which the doc is against, because of the complications.</p><p> So, I've been trying to find new treatments on my own ...</p><p></p><p>R-R: Great suggestions. I think nandrolone has been useful with MS. My thing is roughly in the MS family, so maybe it'd be helpful to me, too. I'll continue to research your other suggestions. </p><p></p><p> I did write Defy's office, to see if they had any experience with CIDP but haven't heard back from them. Hopefully, they have and hopefully I will.</p></blockquote><p></p>
[QUOTE="masfield, post: 46250, member: 13737"] Ero: Maybe it shouldnt have an impact on my legs but it definitely did. And it was almost immediate. I could feel the numbness descending like a thick fog. I'm sure it has everything to do with the nature of my hated CIDP disease. I'll try an injection in my shoulder and see what happens. My T dose was 100 mg once a week. And, like I said, I only did it three times before stopping. I'm really hoping that T or something else can help me out with my failing, sagging muscles. Three years ago, my neurologist gave me 4 to 6 years before I'd be in a wheelchair. I hate doctors who give terrible predictions like that, but it has stuck with me ever since. And if he's right, gulp. I haven't given up the fight, however. At the same time, my disease is rare enough that no one really studies it and there are no acknowledged experts on it. So, everything is a crap shoot. I've tried the standard treatments, with no success. Last one up is prednisone, which the doc is against, because of the complications. So, I've been trying to find new treatments on my own ... R-R: Great suggestions. I think nandrolone has been useful with MS. My thing is roughly in the MS family, so maybe it'd be helpful to me, too. I'll continue to research your other suggestions. I did write Defy's office, to see if they had any experience with CIDP but haven't heard back from them. Hopefully, they have and hopefully I will. [/QUOTE]
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Clinical Use of Anabolics and Hormones
Clinical Use of Anabolics and Hormones
Nerve Degenerative Disease, wasting and testosterone
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