Parkinsn's Email List Message

Posting to the Parkinsn List is a benefit of Subscription


[Message Prev][Message Next][Thread Prev][Thread Next][Message Index][Thread Index]

Help please!


Hello everyone,
I signed on a few weeks ago and want to express my gratitude to all of you
for your open sharing.  As I stated in my opening letter to all, I am a
friend of a person with PD (72/2).  I have been copying your letters and
sending them to him as he does not have a computer and was thrilled to know
there is this group.
I spoke with John a few days ago and he (unbenownst to me) has been having
hallucinations since uping his dose of Permax (3 caps with each meal).  He
also takes Sinemet (unknown amount) and also told me he suffers from leg
cramps off and on.  Up to this point, his major concern was the shaking of
his hands.  The doctors have tried time and time again to up his Permax, and
each time he has very bad reactions.  I felt badly, not knowing he was going
through all this (I see him infrequently as he lives a distance away) so I
did not send him pertinent letters you all had written on those subjects -
only those I knew he was going through.  I vaguely remember some mention of
the hallucinations with Permax and would very much appreciate if someone
could reply once again (my apologies) so that I can print your reply and mail
to him.  Also, I mentioned to him that I saw something about a PD specialist
in Calif. bay area (is this right).  Does anyone have any specifics, as his
dr. is not real well versed in PD.
Thank you all for your patience in this redundant request.  And thanks from
John -he expresses his gratitude for the information you provide.

Kathy    SMEHerbs@xxxxxxx


Parkinsn's List Subject Index

Parkinsn's List Thread Index

Parkinsn's Archive Treasures Doctors, students, patients and caregivers find current Parkinson's information such as the Algorithm, Caregivers Handbook, and talks by respected Movement Disorder Specialists.

Mail converted by MHonArc 2.6.10
Site Hosting donated by He.net
&
Grant from The Parkinson Alliance