Muscular Dystrophy and AAS?

[lanky]

good post,, i understand and have been in your situation many times, heart breaking most assured connsidering the amount of time he was under your care. In progressive diseases like this that effect mobility, quality of life becomes nonmedically speaking "crap". some cope beter than others. because you work in a nursing home/long term care facility the two main problems are pain and mobility issues. . I to believe there should be the use of anabolics more frequently in long term care. It takes a special type of person to work in long term care..i did it for a short(few months) peroid but became very frustrated with the whole immobility/constant pain issues. again great post prizz

 

[Prizz]

Well thanks for the kind words Lanky.... I actually don't work in a long term facility anymore, I work in a hospital.... The hospital I work in used to contract with some long term facilities, so I would work in different ones here and there.... I'm kinda glad that is over, as I like the hussle and bussle of the hospital setting..... Again, I'm glad you see my side of the situation...

P Rizz

 

[lanky]

just curious to what your level of training is?

 

[y1der]

Anyone know if AAS/GH can help people with MD? I have a close friend (female) who has MD, and I've been curious about assistance with the disease using AAS and/or GH. Anyone know if this is a method of dealing with the disease?

Hey..i know this is an old post..BUT i have MD type Lgmd2i and currently I am in a trial we expect to take about 2 years...first 12 weeks have shown promising results using AAS Test and OX and a couple others...at the age of 56 i have nothing to loose and everything to gain by this trial..I think the mainstream medical field is definitely missing it here! The first Cycle has shown enough promise..im really excited for round 2..ive had the best summer i have had in years! My strength has increased as has my energy..my appetite and my mobility have improved.I was going down hill...and have actually regained somee ground here!...while it may not be a "Genetic Cure" i do feel at this point it will be a valid treatment that will put this disease in the background enough to where i can live with a decent quality of life with the years i have left.....Im onboard to fight this crappy disease...with all i have in me! I will NEVER give up!