Following the nice tip i was given here , here is the transcript of my email to the FDA (just 1 email for now, but i got many email addresses, so let’s say i will “be a regular” on this subject):

__________________________________________________________

On Apr 11, 2009, at 5:00 PM, Pedro B. wrote:

To whom it may concern: (should be you, but i wonder)

I am diagnosed with Multiple Sclerosis.

It has come to my attention that my own stem cells are considered by you as drugs.

Dear sirs, let’s be real, i am not a walking, living, breathing drug fountain. I am, however, a drug RECIPIENT of all the medicine needed to delay the advance of my disease.

Every single MS sufferer (and everyone else, i’m sure) should be happy with the opportunity of having access to safe stem cell therapy using each one’s own adult stem cells.

I urge you to see the dramatic implications of considering a possible way to find a cure as “a drug”.

The ASCTA and their efforts to establish safe practice guidelines on stem cell research provide the MS sufferers with hope. We don’t get many “doses” of hope lately. What we get is needles, injections, and medicine that only delays the condition.

PLEASE do NOT reject our hopes of a cure with your obscure deals with moneymaking-only-concerned pharmaceuticals.

This matter concerns everyone. I mean everyone as in, worldwide, and not only the ones who have this condition, but -everyone-.

Every single human being.

Regards,

your local MS sufferer,

PmB