hI.....
I am from the porthuron mich area and I do not know anyone who
has this disease...I feel alone and scared...My family lives in Wis
and I have been here for about six years...I would greatly appreciat
it if anyone would please contact me to share..I was diganosed with
this a few months ago, but have been suffering for years...I have has
all toghther 3 back surgeries which all included going in to the
nerve sak...where tumor was mixed in with the nerves...I have had 4
myograms...and the first 2 where oilbased...
This last surgery was all i could take....and 6 months later I was
diganosed with arach...and live on morphone pills that dont even help.
please someone contact me back,
Trish