This Is MS Multiple Sclerosis Community: Knowledge & Support

While 1000s of people with MS have been taking LDN for years with good results,
there continues to be a reluctance by many neurologists to prescribe it for
their patients because LDN has not been approved by the FDA for multiple
sclerosis.

To be approved, a clinical trial needs to be conducted yielding positive
results. No private drug company is willing to invest millions in a LDN
clinical trial due to the fact LDN is a generic drug and they can't make any
money off it.

One organization that could fund a clinical trial is the National Institutes of
Health.

We The People is a new initiative by the White House that aims to respond to any
issue petitioned by at least 5,000 people. In short, if we get 5,000 signatures
in 30 days, they say someone in the Obama Administration will pay attention.

While LDN is being successfully used for other autoimmune conditions as well as
cancer, this petition focuses on MS because Michelle Obama's father had MS and,
well, it's my petition and I have MS.

Here is the petition link:

http://wh.gov/gZa

Please Note: You must have a US email address to sign.

If you agree, please sign and send it along to friends and family. We have 30
days.

Thank You

Malcolm West
Co-Founder - LDNaware.org

Hi,
I went to sign the petition. I set up an account, email, password but when I click on sign the petition it won't do anything. What do you think I am doing wrong?

Thanks

I am not american enough.
My e-mail is fine but I am from Slovakia, Europe.
Erika

_________________
Aug. 7, 09 Doppler Ultras. in Poland, left Jugul. valve problem, RRMS since 1996, now SPMS,
- Nov.3,09: one stent in the left jug. vein in Katowice, Poland, LDN, never on DMDs
- Jan. 19, 11: control venography in Katowice - negative but I feel worse