I'm new to having a name(PPMS) to my issues.
I've never really heard to much about it before I learned I have it.
Wow the reading we've been doing is crazy which is why I sought out real people.
I believe I'll begin Ocervus in April, even I don't back out. I don't usually care about side effects, but I've had Shingles twice already, 3 family members with breast cancer. So yeah I'm leery.
But we've read about Stem Cells. Does anyone know what the talk is about. Are they have any help for us?
I've never really heard to much about it before I learned I have it.
Wow the reading we've been doing is crazy which is why I sought out real people.
I believe I'll begin Ocervus in April, even I don't back out. I don't usually care about side effects, but I've had Shingles twice already, 3 family members with breast cancer. So yeah I'm leery.
But we've read about Stem Cells. Does anyone know what the talk is about. Are they have any help for us?
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