Me and Mr Parkinson
 

Hello, I'm spanish man of 57 years and since a LITTLE TIME (a lot of time) I'm living with this new "friend", who never loose me and who takes my right hand and shakes it constantly, like with the leg.
At first I was thinking it was a mistake, but the crude reality shows me there was not a mistake it was my fake of life. IT was a hard time to live with this sensation of no future, and I was very lucky to have a wife like mine who was at total time courageous my and don't leave fell down.
Now, i live with Mr Parkinson and I know he wants to defeat me but I don't want to put my cheek, I'm gonna fight against him with all my forces and with a little help of other persons like you, the members of this community, because I think if we share our experiences, problems and success we can afford this disease more effectively.
I decide not take levodopa because it's a future problem and I think it's earlier to take it.
Next post i'm gonna explain you my automedication. Today i typed a lot and actually it's hard and difficult to me.
Ah! excuse me my poor english level but I promise you to study it and improve it with the time.

lLittlejoe

Welcome littlejoe, I hope that you find help and support here on the boards. I hope that maybe I can help you if need be. Everyone here is extremely supportive and understanding and some may even know what you're going through and can give you amazing tips to help you cope!

I myself am a new member of the boards, but even after one day I already feel comfortable talking about what's going on in my life. I hope you too feel comfortable.


We are here for you!:grouphug:

Welcome to NeuroTalk littlejoe.

I'm sorry to hear about the Parkinson's Disease, but we have a great forum for people who also have PD. Hopefully you'll meet some wonderful people there, and get lots of advice and support.

Click onto this link and it will take you straight there. http://neurotalk.psychcentral.com/forum34.html

Joe welcome to th NT boards, you will find many helpful, kind individuals here.I admire the stance you have taken against Mr Parkinson. If I may ask, stopping this med because you think its too early??? Is there any chance this med can help slow the progress and if so, wouldn't the sooner you take this med, the less Mr Parkinson can take?. I am not familiar with this medicine, so please excuse my ignorance of the MED. Again welcome Joe, and i do admire your determination

Hi and welcome to NeuroTalk! You've come to the right place for support and encouragement.

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

Your English is fine! Do not be disturbed, some of us have spoken it all our lives and still make errors! :)

Hello and welcome to Neurotalk - you will meet many great and supportive people here!!
I am so sorry to hear that you suffer from Parkinson's Disease :hug:
If you ever need anything please don't hesitate to ask - I am more than happy to help you in any way I possibly can!
I also want to say "Congratulations on your English, it was really good!"
Love and best wishes
Alison

Hi, Littlejoe!
 

I'm very pleased to meet you. I think it's very courageous of you to take the attitude you have toward your illness. Always fight back and never give it a moment to breathe if that's possible. I hope that we can help you with your fight, too. I'm always here to help in any way I can. Good luck to you, Littlejoe, and all my best wishes! :)

Welcome to NeuroTalk, Little Joe! You know what? Your English is a heckuva lot better than my Spanish! Muy bueno and good for you!

Sorry about you and your constant (and uninvited) companion, Mr. P. Glad you have a good wife by your side.

I look forward to getting to know you better. :hug:

Hello little joe and another welcome to NeuroTalk here. Glad you found us. Oh, and don't you fret about your English; we seem to all understand each other just fine.

http://dl3.glitter-graphics.net/pub/...alm620kgf6.gif