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Parkinson's Disease Support Group
A community of patients, family members and friends dedicated to dealing with Parkinson's Disease, together.
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06/15/2012 03:10 PM
zandrastar
 
Posts: 15
Member

three yeasr after the day i lost my brother to comps from pd i found out i have it .Angry . dont understand why god would do this to my family . the last thing i got to say to my mom before she pasted , was i have pd . on carb/levo have been for 3 years but they no longer work and i just moved to oregan and yet to find a dr here . CANT STAND THE SHAKES ANYMORE
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06/15/2012 04:12 PM  Top
Jupiterjane
Jupiterjane
 
Posts: 509
Member

Hello Zandrastar!

It is a pleasure to meet you! I hate absolutely everything about Parkinson's! It has been nothing but a pain in my ass since I accepted that I have the damn disease! One good thing came out of all this hell and that was finding how precious every moment of living is! It's the small times, the silence of an afternoon without television, the voices of our loved ones as they tell you about their day, the smell of coffee brewing, and after you realized and accepted all those great things you were missing before, you still have this stupid, kick you when down,make you look stupid in public, fucked up disease!!

Welcome to the group!

Jupiterjane

Sometimes as writers we worry too much about creating a masterpiece when we should just be thankful the words flow at all.

06/15/2012 07:35 PM  Top
zandrastar
 
Posts: 15
Member

thanks for the welcome . and good to know that i am not alone in this stupid shit . god i wish it would go AWAY . Angry Sad

Previous discussions I participated in:
Using One Word, How Do You Feel?

06/15/2012 08:14 PM  Top
Claire138
Claire138
 
Posts: 457
Group Leader

Hi and welcome...this is a great place to share burdens and happy times, learn new things, show off our creativity and to laugh; even at ourselves. Please remember, we have Parkinson's, but don't let it have you. Strive to see and experience the positive, enjoy every good moment for the precious gift it is and know that you are not alone with this f*cked up, pain in the butt, frustrating and very unpleasant disease anymore...

...Claire

Claire aka Bonnie
Parkinson's Group Leader
Fighter

One foot in front of the other...

I am not a Dr. or medical or legal professional...any health related statements I make are my own opinions and experiences.

06/15/2012 10:30 PM  Top
mem2121

You are NOT alone. Smile

Welcome to our group.

Steve


06/16/2012 05:09 AM  Top
Priyeni
Priyeni
 
Posts: 625
Member

Welcome Zandrastar, welcome to a place you can vent yr anger. Once we do that, we can also read what others with PD are going thru & then we realise we are not alone, it helps somewhat, ofcourse it doesn't make it any easier, PD is scary but when u read about new research, medication available, how it has helped others, u'll begin to have hope.

Yr priority now is to find a doctor in Oregan. We have a wonderful member 'Origannative' maybe she can help, I will immediately write to her & draw her attention to yr post.

Meantime, I hope u receive the support / answers yr looking for with us. Atleast one thing I can assure u, u'll forge some solid friendship.

Priyeni

I'm not a doctor so I can't comment on yr meds /physical pain & symptoms but I'm a good listener & will be always there if you need to unburden /vent.

Previous discussions I participated in:
MJF Birthday
Levadopa induced Dyskinesia
John Coleman
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