Dr. Lynn is not on the board, she is an advisor to the board. There are not
many doctors willing to just sit down, learn about TM, and write an article.
Yes, Dr. Lynn was asked to write the article. She was a willing participant.
It was a great article from both the doctors.
One of the goals of the TMA is to create a doctor/neuro directory by state.
The membership to the TMA has grown from less than 200 to over 700 in a few
short months. At the last meeting held by the officers we talked about having
a few contacts from each state(people who have TM). These contacts would have
that states information on doctors, medical services, etc. for any member in
their state.
I've had TM for 19 years and live in a big city, I've never seen a doctor who
has had any other TM patient before. I would love to see a doctor with TM
experience.
Another goal of the TMA is research. It takes a great deal of funds and a
willing group of researchers to pull it off. Any government funds granted
require detailed and specific plans on how the $$ is used. I hope we can get
to this soon.
You ideas are good. We do need to take to take the time to have the
appropriate spokesperson and plan of attack on fund raising and research.
Thanks,
Paula