Parkinson's Disease Tulip


advertisement
Reply
 
Thread Tools Display Modes
Old 04-29-2009, 05:35 PM #1
chris101 chris101 is offline
New Member
 
Join Date: Apr 2009
Posts: 2
15 yr Member
chris101 chris101 is offline
New Member
 
Join Date: Apr 2009
Posts: 2
15 yr Member
Default physio/relative with parkinsons

Hi, I’m working towards doing a physio degree and wanted to find out a bit more about the way physio is used in Parkinson’s and about how the condition affects people. My granddad has Parkinsons and I would like to know if there is anything I can do for him, physio based or not.

Any input people have would be much appreciated.

Thanks

Chris
chris101 is offline   Reply With QuoteReply With Quote

advertisement
Old 04-29-2009, 08:50 PM #2
Chicory's Avatar
Chicory Chicory is offline
Member
 
Join Date: Oct 2006
Location: Florida
Posts: 182
15 yr Member
Chicory Chicory is offline
Member
Chicory's Avatar
 
Join Date: Oct 2006
Location: Florida
Posts: 182
15 yr Member
Default

It is very important for people with Parkinson's to get exercise and physical therapy as part of an exercise regime helps a lot. I went for physical therapy for my shoulders and I was surprised at how much it helped. Now I must keep doing the exercises every day. If do not do them, I have trouble reaching into high cupboards in my kitchen and I also have trouble driving more than a short distance because my arms hurt when I hold them up on the steering wheel.

Parkinson's makes our bodies stiff. Exercise and physical therapy can help slow the progression of the stiffness.

The book Parkinson's Disease and the Art of Moving by John Argue will help you to help your father.
__________________
Chicory
Chicory is offline   Reply With QuoteReply With Quote
Old 05-09-2009, 04:12 AM #3
chris101 chris101 is offline
New Member
 
Join Date: Apr 2009
Posts: 2
15 yr Member
chris101 chris101 is offline
New Member
 
Join Date: Apr 2009
Posts: 2
15 yr Member
Default

Quote:
Originally Posted by Chicory View Post
It is very important for people with Parkinson's to get exercise and physical therapy as part of an exercise regime helps a lot. I went for physical therapy for my shoulders and I was surprised at how much it helped. Now I must keep doing the exercises every day. If do not do them, I have trouble reaching into high cupboards in my kitchen and I also have trouble driving more than a short distance because my arms hurt when I hold them up on the steering wheel.

Parkinson's makes our bodies stiff. Exercise and physical therapy can help slow the progression of the stiffness.

The book Parkinson's Disease and the Art of Moving by John Argue will help you to help your father.
Thanks for the reply, will check out some of those books,
chris101 is offline   Reply With QuoteReply With Quote
Old 05-09-2009, 08:32 AM #4
chasmo's Avatar
chasmo chasmo is offline
Member
 
Join Date: Aug 2006
Location: Los Angeles, CA
Posts: 714
15 yr Member
chasmo chasmo is offline
Member
chasmo's Avatar
 
Join Date: Aug 2006
Location: Los Angeles, CA
Posts: 714
15 yr Member
Default thoughts

Balance ecercises are good. They are best done in a pool to cushion the inevitable falls. STretching is also advisable, that really helps, especially with dystonia.
Strength and cardiovascular training is good too. USe low weights and high reps. A recumbant exercise bike is my favorite for that. Be careful with treadmills, they tend to spit us parkies off!!

Charlie
chasmo is offline   Reply With QuoteReply With Quote
Old 05-09-2009, 01:26 PM #5
reverett123's Avatar
reverett123 reverett123 is offline
In Remembrance
 
Join Date: Aug 2006
Posts: 3,772
15 yr Member
reverett123 reverett123 is offline
In Remembrance
reverett123's Avatar
 
Join Date: Aug 2006
Posts: 3,772
15 yr Member
Default Wii? Oui!

I got a Wii game console a couple of weeks ago complete with the balance board controller and I find that I am actually using it. If you can get him to try i the might get hooked. It tracks your data, too, so that would be a big help for your project.

Also, you might want to look into Electric Muscle Stimulators since as a Physio you will be using them. See the thread about spinal stimulation.
__________________
Born in 1953, 1st symptoms and misdiagnosed as essential tremor in 1992. Dx with PD in 2000.
Currently (2011) taking 200/50 Sinemet CR 8 times a day + 10/100 Sinemet 3 times a day. Functional 90% of waking day but fragile. Failure at exercise but still trying. Constantly experimenting. Beta blocker and ACE inhibitor at present. Currently (01/2013) taking ldopa/carbadopa 200/50 CR six times a day + 10/100 form 3 times daily. Functional 90% of day. Update 04/2013: L/C 200/50 8x; Beta Blocker; ACE Inhib; Ginger; Turmeric; Creatine; Magnesium; Potassium. Doing well.
reverett123 is offline   Reply With QuoteReply With Quote
Old 05-09-2009, 10:20 PM #6
caya caya is offline
Junior Member
 
Join Date: Jan 2007
Posts: 39
15 yr Member
caya caya is offline
Junior Member
 
Join Date: Jan 2007
Posts: 39
15 yr Member
Default

Chasmo:

Please forgive me if I appear a little stupid around the edged but what does it mean where you say "be careful of treadmills, as they tend to spit off us parkies"? What does spitting have to do with a treadmill? Again, I apologize but I think I just do not fully understand the language like I should.I use a treadmill almost daily and your warning concerns me greatly. I just do not know what exactly it is I am concerned about. Can you explain this to me. Thank you for your patience and understnding.


caya
caya is offline   Reply With QuoteReply With Quote
Old 05-10-2009, 08:19 AM #7
chasmo's Avatar
chasmo chasmo is offline
Member
 
Join Date: Aug 2006
Location: Los Angeles, CA
Posts: 714
15 yr Member
chasmo chasmo is offline
Member
chasmo's Avatar
 
Join Date: Aug 2006
Location: Los Angeles, CA
Posts: 714
15 yr Member
Default

Caya;
Sorry 'bout that!!

What I meant was many of us have difficulty walking and it is hard for us to keep up with a treadmill. This is NOT to say that many of us cannot use one, just be careful when you start using one.

Hope this explains things!

Charlie
chasmo is offline   Reply With QuoteReply With Quote
Old 05-10-2009, 09:32 AM #8
Curious Curious is offline
Yappiest Elder Member
 
Join Date: Aug 2006
Location: Texas
Posts: 13,418
15 yr Member
Curious Curious is offline
Yappiest Elder Member
 
Join Date: Aug 2006
Location: Texas
Posts: 13,418
15 yr Member
Default

Quote:
Originally Posted by caya View Post
Chasmo:

Please forgive me if I appear a little stupid around the edged but what does it mean where you say "be careful of treadmills, as they tend to spit off us parkies"? What does spitting have to do with a treadmill? Again, I apologize but I think I just do not fully understand the language like I should.I use a treadmill almost daily and your warning concerns me greatly. I just do not know what exactly it is I am concerned about. Can you explain this to me. Thank you for your patience and understnding.


caya
Hi Caya,

My husband and I own a gym. He has clients who have PD, as does my father.

Since a treadmill has a belt that keeps you walking, if you shuffle or have any problem picking your feet up with every step, the belt can catch the bottom of your foot...and spit..throw you off the back.

If you are using a treadmill at a gym, let the staff know you have PD, so they can keep an eye out for any potential accidents.

Using an eliptical, stepper or bike are great alternatives. Not that people with PD can't or shouldn't use a treadmill, just use caution.

Really...everyone should. We had a member the other day who decided to take his sweatshirt off right in the middle of jogging on the treadmill. Yep..he got spit off. Didn't get hurt thank goodness.

Chris, how old is your dad? Stabilty exercises and building a good core really help. Doing exercises that are more in an occupational manner too.

One of my husbands clients hadn't been able to climb stair in years. Doing step up exercises fixed that. Christmas before last during a party, his wife found him upstairs showing guests the house. He had never been upstairs in that house.
__________________

.
Curious is offline   Reply With QuoteReply With Quote
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
Fundraising for ALS is a family affair, 12th relative known to die from BobbyB ALS News & Research 0 03-25-2008 08:30 AM
Why would a Physio ask this...? ali12 Reflex Sympathetic Dystrophy (RSD and CRPS) 17 12-06-2007 08:11 AM
ms or parkinsons bamyx4jc Multiple Sclerosis 3 11-12-2006 10:22 AM


All times are GMT -5. The time now is 07:37 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.