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KatelynElizabeth

About this Forum

5 posts in this topic

Hello, Everyone.

 

I am a Therapeutic Recreation student and am currently writing a paper on Parkinson's disease. Part of this paper focuses on the supports that exist for those who struggle with this disease. A friend, who's husband has Parkinson's, directed me here--she and her husband think highly of this forum. And I am wondering if you would mind sharing your opinion with me too...

 

What makes this a good forum?

What are some of the benefits of being a member?

Are there any drawbacks?

What other support resources can you recommend?

 

Thank you very much, in advance. Having "real life" evidence will add great value to my paper.

 

Best wishes,

Kate

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a place to learn

learn about drugs and PD in general... the bad, the ugly and the good

no

PD chatroom/ and having a great / wonderful wife.

Edited by Luthersfaith
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This is a good forum because people with Pd are welcomed; they can find answers to their questions, they can often find others who are experiencing similar symptoms, people can problem solve and share how to deal with specific aspects of the disease and how it is effecting them. Some very informed people offer their expertise. Plus it is a place to share the emotionsl ups and downs as we each figure out how to accept/grieve lost healthy expectations we once had. The forum is a place to debate (sometimes), argue (sometines), discuss, support, offer compassion and understanding. The face of Pd becomes personal here.

We are also Lucky to have the Ask the Dr. ,Ask the Pharmacist, Ask the Nutrionist, forums ETC. This has been a fantastic support for myself and many others.

 

Drawbacks? Hm...rarely getting to meet the other members in person. Occasionally it happens but not often enough

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The greatest benefit of this forum is simply being able to talk with other people who understand what I am going through. A person can study a subject for their entire life but never truly understand it until they personally experience it. It has been amazing to me to discover how many symptoms that we all share in common, yet are often discounted as not being related to PD or seemingly unrecognized by medical science. In some strange way it's comforting to know that there are other people out there who are experiencing the same thing and who simply understand - even when those closest to you don't.

 

There aren't any drawbacks that I can think of, and I really don't utilize any other "support" services other than this forum.

 

Kevin

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What other support resources can you recommend? Parkinson's Fourm on PatientslikeMe.

 

What are some of the benefits of being a member? Resources supplied by NPF.

 

Ken

Edited by kmcclung
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