Parkinson's Disease Tulip


advertisement
Reply
 
Thread Tools Display Modes
Old 09-26-2011, 01:05 PM #1
EmptyNest68's Avatar
EmptyNest68 EmptyNest68 is offline
Member
 
Join Date: Dec 2006
Location: Aridzona; dx'd 04/2003 @ 35
Posts: 130
15 yr Member
EmptyNest68 EmptyNest68 is offline
Member
EmptyNest68's Avatar
 
Join Date: Dec 2006
Location: Aridzona; dx'd 04/2003 @ 35
Posts: 130
15 yr Member
Default Had an appt w/MDS

and guess what? he says I am improved since our last visit 4 1/2 years ago, when I was ON MEDS. On the PD sclae I was a 7 and this visit I was a 5. He wasn't the doc to diagnose me, either. So I asked him if he thought it could be "something else". He was agreeable to that; it's not MS, ALS or as far as he could see any particular degnrative disease. Huh?
He wnet on to describe the channels in my brain and neurons at the mitochondiral level...kind of lost me. But in the end, wants me (if I wnat to) try magnesium & calcium at bedtime. In the shock of this, I didn't ask many questions, so have sent him an email.
He did the fingertapping, toe tapping, pushed me to check my reflexes and said it looked good. The secondary symptoms baffled him, like the voice, urinary, sense of smell, stiffness, etc....
Baffled? I am baffled, to say the least. 8 yrs I've been thinking this is PD, my health has definitely deteriorated. Not sure what to think.
EmptyNest68 is offline   Reply With QuoteReply With Quote

advertisement
Old 09-28-2011, 07:27 AM #2
marciaj marciaj is offline
Junior Member
 
Join Date: Nov 2009
Location: Texas
Posts: 65
10 yr Member
marciaj marciaj is offline
Junior Member
 
Join Date: Nov 2009
Location: Texas
Posts: 65
10 yr Member
Default

I saw a MDS who is ruling out other things it could be. I just had an MRI yesterday. He wants to rule out stroke because in 5 years the tremor hasn't crossed over. I had a blood test last week to rule out Wilson's disease. I forgot to tell him I should be checked for Lyme as we lived in New England shortly before the tremors started. I have another appointment in two weeks to discuss test results.

The neuro diagnosed me with PD in 2006 but didn't run tests to rule out other stuff. I'm glad it's being done now. Kind of confusing. I don't care what they call it as long as they do something to help symptoms if they can't cure it. But they need to know what it is to do that. So I guess I do care what they call it. Still confused after all these years.
marciaj is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
EmptyNest68 (09-28-2011)
Old 09-28-2011, 08:58 AM #3
Conductor71's Avatar
Conductor71 Conductor71 is offline
Senior Member
 
Join Date: Jul 2009
Location: Michigan
Posts: 1,474
10 yr Member
Conductor71 Conductor71 is offline
Senior Member
Conductor71's Avatar
 
Join Date: Jul 2009
Location: Michigan
Posts: 1,474
10 yr Member
Default

Thus is a great reminder to anyone who has not progressed much in the course of a year...you should begin seeking second and third opinions. Going eight years and not needing meds....and your doctor never thought not to revisit the diagnosis? Yikes.

May I ask why your docs thought PD in the first place? We should not hav the diagnosis if we only have one symptom of the three cardinal signs. For diagnostics we are too have two of three the main symptoms: Slowness, rigidity and tremor. Many conditions have secondary Parkinsonian symptoms some respond to levodopa. I am surprised doctors have not not ruled out some sort of dystonia.

For the record, I thought PD is manly an asymmetric disorder. Marcia, I presented with a right hand tremor and it is still one side going on eight years later. Difference is I added slowness and mild rigidity. If they cannot confidentially re-diagnose you then I would be packing for a regional PD and Movement Disorder clinic. Just look at Harley's post....she lost 27 years thinking she had PD so don't give in...there are ways to differentiate.

Good luck!

Laura
Conductor71 is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
EmptyNest68 (09-28-2011)
Reply


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
dr's appt today kellijo Multiple Sclerosis 19 11-22-2008 01:47 AM
Had neuro appt. lynxgal Peripheral Neuropathy 2 08-24-2008 04:55 PM
Dr's Appt kjs05 Neuromuscular 2 05-20-2007 06:58 AM
Dr. Appt. Tiger_lilly07 Epilepsy 4 04-24-2007 07:41 AM
Appt. Jebbyfur Thoracic Outlet Syndrome 2 02-24-2007 06:59 PM


All times are GMT -5. The time now is 02:59 AM.

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.