Parkinson's Disease Tulip


advertisement
 
 
Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 10-27-2015, 05:16 AM #2
Niggs Niggs is offline
Member
 
Join Date: Jul 2015
Location: Guiseley,West Yorkshire,England
Posts: 165
8 yr Member
Niggs Niggs is offline
Member
 
Join Date: Jul 2015
Location: Guiseley,West Yorkshire,England
Posts: 165
8 yr Member
Default

Quote:
Originally Posted by Grace1 View Post
My dad (69) was diagnosed with early stages Parkinsons, yesterday.
He's had a tremor in his jaw and a few other issues for around 18 months, but as he also has fibromyalgia and was taking lyrica, we put his symptoms down to lyrica (side effects; slurred speech, slowness of movement, poor balance etc).

Anyway, several people have told me it's possible to live a good life with the meds out there and to be really positive. That's our best line of attack, and also making sure we don't surround ourselves with negative people. Nothing worse than other people who drag you down with their nonsense. Can anyone offer any advice? Cheery thoughts? Best things to do next?
Hi Grace,

So sorry to read about your dad. But you've come to the right place. There is a lot to learn about living in the land of Parkinsonia and it would be easiest to ask the very knowledgeable and kind people on this forum as questions arise.

In general you will find people vary both in symptoms and drug response. The same is true regarding the rate of progression. There are people who have had PD for 30y so try,once the shock/reality has passed/sunk in to be positive.
Once the correct drug dose is found your dad will most likely feel better than he has for years. Given his age, the treatments available and the supporting therapies (exercise,physio etc) I don't think the future is as bleak as it first appears.
The best advice I was given was by my Gp (md) who said "its important to manage your own meds" Basically only the Parki person can decide whether a particular drug regime is for them.

Im in my 50's,diagnosed 2009,just in the process of adjusting my meds,helping my daughter with her university application,planning a party and looking forward to Christmas. Still enjoying life and treating this pathetic little disease with the contempt it deserves.

Keep in touch

Nigel
Niggs is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
eds195 (10-27-2015), johnt (10-27-2015)
 


Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off


Similar Threads
Thread Thread Starter Forum Replies Last Post
My yesterday Always_Believe Reflex Sympathetic Dystrophy (RSD and CRPS) 5 07-10-2015 11:02 PM
Saw my dr. yesterday fionab SCS & Pain Pumps 1 10-01-2010 01:38 PM
So, Yesterday . . . Nervous PN Tips, Resources, Supplements & Other Treatments 1 08-13-2010 05:06 PM
HELP! Scared...Surgery today diagnosed yesterday rhibbing New Member Introductions 15 09-25-2009 02:38 PM
diagnosed yesterday sinic New Member Introductions 7 06-21-2009 10:44 PM


All times are GMT -5. The time now is 06:40 PM.

Powered by vBulletin • Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise v2.7.1 (Lite) - vBulletin Mods & Addons Copyright © 2024 DragonByte Technologies Ltd.
 

NeuroTalk Forums

Helping support those with neurological and related conditions.

 

The material on this site is for informational purposes only,
and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider.


Always consult your doctor before trying anything you read here.