Hi.. I just got Dx with PPMS....

New Topic Post Reply Printable Version
[ << Previous Thread | Next Thread >> ]

Regular Member

Date Joined Feb 2008
Total Posts : 29
   Posted 9/6/2009 4:21 PM (GMT -6)   
Hi there, I really don't have a question right now, but wanted to say hi and let you know that I just got Dx with PPMS.  I was undx for approx 4 years.  I notice that there isn't that much info or people online with PPMS.  I wonder if its my age..in my 50s.
well, I'll talk again..

Veteran Member

Date Joined Jun 2005
Total Posts : 1852
   Posted 9/7/2009 11:05 AM (GMT -6)   
Hi Quack,
    It's nice to meet you.   PPMS is an unusual form of MS only affecting about 10% of MS patients.   It typically does not follow the noticable attacks of other types, but instead slowly (usually so slow you dont notice) getting worse over time.  My husband also has this type and went for more than a decade before he was diagnosed. 
     Not so much info out there on it unfortunately, probably due to the few that have it and limited amount of research that's been done on this particular form.  I'd be more than happy to share what info I have though, been researching a long time =)
Take care,

Regular Member

Date Joined Feb 2008
Total Posts : 29
   Posted 9/9/2009 11:17 AM (GMT -6)   

Hi there, thanks for the information.... the more info I can get the better I feel about this condition.  I appreciate any information available from you. 


I don't know much about stem cell and will look at this website..

thanks again

be well

Quack  tongue

Regular Member

Date Joined Aug 2008
Total Posts : 271
   Posted 9/18/2009 11:54 PM (GMT -6)   
I think drs have just "discovered" PPMS as a diagnosis though I admit am rather cynical about drs generally but mine just suggested that I might have PPMS. Eventhough I had a very strong attack at 15 and minor ones every 10 years after that. All the symptoms that reappeared after 45 when I was diagnosed with SPMS are the same as I experienced at 15.

I won't let anyone put me in a box that I am not happy with.
Have had relapsing/remitting MS since 10 yrs old. Secondary/progressive since 1995. Baclofen pump since 2008.

"The past is history, the future is a mystery, the present is a gift."

New Topic Post Reply Printable Version
Forum Information
Currently it is Sunday, September 23, 2018 3:12 AM (GMT -6)
There are a total of 3,005,804 posts in 329,264 threads.
View Active Threads

Who's Online
This forum has 161804 registered members. Please welcome our newest member, FADE IN:.
235 Guest(s), 1 Registered Member(s) are currently online.  Details