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LDN Advocates |
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Meet the advocates who are making a difference! Low Dose Naltrexone faces an uphill battle when it comes to research, because it is an inexpensive generic drug. That's why patients have taken it upon themselves to raise awareness and funds. And it is working!
Meet Vicki Finlayson on the Capitol steps May 19th 2pm Send Governor Schwarzenegger an email and tell him to meet with Vicki! Vicki Finlayson, a patient with multiple sclerosis (MS), used to have trouble walking from her living room to her kitchen. Now, with the help of one generic medication prescribed off-label, she is walking 53 miles from her home in Auburn California to Sacramento. Vicki is raising funds for research into the drug protocol that brought her MS into remission, low dose naltrexone (LDN). Besides its benefits in MS, LDN has been shown to improve many different autoimmune, oncological, and neurodegenerative conditions. Vicki's conviction is as a strong as her stride. "I've been calling and writing Governor Schwarzenegger office. To make sure he hears me, I'm marching up the Capital steps! This medication deserves immediate research funding, it can help more than MS, it stabilizes the immune system, so it helps all manner of diseases, like cancer, Parkinson's, Lupus - many autoimmune disorders." Join Vicki in her fight. For more information, see www.LDNers.org Vicki's fundraiser in 2006 was responsible for raising
the majority of the funds for the first human trial of LDN
for MS at UCSF. Her current efforts are directed towards the
LDN research at Penn State, where
Dr. Ian Zagon has made key discoveries about LDN's
effects on the immune system.
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For Vicki's contact info, please send an email.
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