possibly M S A
 

hello everyone
my first post so forgive me if i'm in the wrong thread ,i will get used to it !!
52 yo male thought i had pd but now think it is Multiple Systems Atrophy . I was told by letter & had to look it up on the Internet .I am aware that there is no cure or specific treatments but any advice on how to tackle the disease would be much appreciated

best wishes landlord

Hi Landlord

I split your post off that other thread so we could welcome you and try to direct you to any forums that can help in your quest for info

we have a general health forum here
http://neurotalk.psychcentral.com/forum2.html

and the PD forum is here (perhaps someone there may have helpful info for you)
http://neurotalk.psychcentral.com/forum34.html

here's the general index so you can also scroll thru to see if any of the other forums may be helpful to you
http://neurotalk.psychcentral.com/index.php

welcome to NeuroTalk
Cheri

Hi landlord and Welcome to NT. Glad you found us.

:welcome_sign:

... bump ...

Landlord,

Hello and welcome to NeuroTalk. Great to see you have come to be with us. You will find a great number of caring, supporting members here willing to help each other as they can.

Again welcome, looking forward to seeing you around.

Darlene:hug:

Hi, Landlord! :Wave-Hello: Welcome to NeuroTalk!

Hiya,
Welcome to neurotalk. If you need anything just ask
Many thanks

Dear Mr. Landlord, did you get any help?

My sister was diagnosed with Potts disease and after her tilt table test on her heart. They sent her to a Neurologist who diagnosed her with Multiple Systems Atrophy.
Were you able to find any help?

I hope things are going well for you and you have found the treatment to help control your illness.