Thousands of Multiple Sclerosis patients are getting worse each day, when currently used medications are not working for them or their body refuses to accept the medication.
Another Option is needed and this Option Should be Lemtrada
The FDA on December 30, 2013 Denies the use of Lemtrada for MS Patients. THIS was A sad day for people with more active Multiple Sclerosis.
Lemtrada has been approved worldwide, but not good enough for us it seems, in the USA.
We are more than 400,000 strong (living with MS) in the USA
WE NEED YOUR VOTE to give another OPTION to those that Can benefit from this medication; hoping to keep them from severe disability.
NEW CONTACT INFORMATION — (SEE BELOW)
YES, WE NEED YOUR VOTE.
Also we need you to write directly. WE NEED YOU TO send emails. –
We need this request to go Viral —
• Let us FLOOD the OFFICE of this FDA committee with emails, WITH the information shown above.
• Please copy and paste what is typed and attach your name to that email and then send to:
submit all Petitions to the new contact information showing below:
Janet Woodcock, MD
Director, Center for Drug Evaluation and Research
Food and Drug Administration
10903 New Hampshire Ave
Silver Spring, MD 20993
Update
I (Stuart) for one, have nothing present to gain from Lemtrada being approved.
Not
financially and not by use of the medication.
financially and not by use of the medication.
I
just believe in Choice and options for those affected by MS.
just believe in Choice and options for those affected by MS.
This is why I
created my
petition.
created my
petition.
PLEASE click the above link to sign our petition
And
Please copy the letter shown above and send along with your message to:
janet.woodcock@fda.hhs.gov
VOTE FOR CHOICE of Medications
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