Neuropathy Advocate and Patient Update

Hi everyone, I got to thanking about my life changes since I was dx. I now love helping others with there neuropathy. I belong to The Neuropathy Association. I went to Las Vegas to support my friend Michelle from the Alliance for Plasma Therapy. It was a great successful fund raiser. Last June I was able to go to Sacramento for a Neuropathy Action Day and it to was a huge success. Now this coming Dec 3- 5. I will be able to go to Washington D.C. for a Neuropathy Summit where Doctors and Patients alike to meet together and co-mingle and share
each other's thought and opinions.

In 2008 I started up a neuropathy support group in Murrietta, Calif. and then another in Palm Springs, Calif. Where we enjoy over 60 members. I feel its time to start another group and I've decided on the Loma Linda Univ. Medical school and hospital area. We will be able to use a room at the univ. My neurologist works out of the university medical center and that was a big plus.

Thank you,
David Hines
Patient and Advocate

Neuropathy Action Day Eugene and I

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Neuropahty updates and corn flakes

Hi everyone, Here I go again letting to much time go by between post. So much going on. I"ve been to Sacramento for a Neuropathy Action day. I returned home from Las Vegas and didn't put one dime in a slot machine but there for a great cause, a fund raiser for a documentary called "Dying to help". Google it. I'm going to get the ball rolling with the non-profit and I"m going to do my damnest to get to Washington D.C. first weekend in December for a neuropathy summit. Keep me in your prayers. I'm eating sugar frosted corn flakes as I type