If there is already a thread I guess this one will be moved or deleted.
Just wondering why steroids are not used more, made more readily available at times of needs and what everyone's story was the first time they were given Steroids.
I am assuming we were all give steroids at our first attack that landed us in the hospital. I was given steroids when I was admitted to the hospital during my 1st major attack.
Steroids was awesome! I got a little angry but the symptoms went away and I felt great.
Ever since then I have tried to get another treatment but no Dr. will help me. Anyone else run into this problem? The same thing for LDN, Cannabis and stem cell replacement.
Anyone hear anything about LDN being presented to FDA for approval as a treatment for MS?
Stories , thoughts appreciated.
Just wondering why steroids are not used more, made more readily available at times of needs and what everyone's story was the first time they were given Steroids.
I am assuming we were all give steroids at our first attack that landed us in the hospital. I was given steroids when I was admitted to the hospital during my 1st major attack.
Steroids was awesome! I got a little angry but the symptoms went away and I felt great.
Ever since then I have tried to get another treatment but no Dr. will help me. Anyone else run into this problem? The same thing for LDN, Cannabis and stem cell replacement.
Anyone hear anything about LDN being presented to FDA for approval as a treatment for MS?
Stories , thoughts appreciated.
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