Parkinson's Disease Tulip


advertisement
Reply
 
Thread Tools Display Modes
Old 02-08-2012, 07:31 AM #11
lindylanka lindylanka is offline
Senior Member
 
Join Date: Sep 2006
Posts: 1,271
15 yr Member
lindylanka lindylanka is offline
Senior Member
 
Join Date: Sep 2006
Posts: 1,271
15 yr Member
Default

I use a trekking pole, just the one, and only sometimes. If my hands are not feeling that coordinated I don't use it because picking it up/dropping it can put me at more risk of falling. It has the advantage of a more natural hand position for me, not sure if everyone would feel the same, I just don't get on with the horizontal hand position on a cane. I had a special rubber tip added to mine at the shop, and the assistant showed me how to adjust it to an optimal height for my needs.....
lindylanka is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
mrsD (02-08-2012)

advertisement
Old 02-08-2012, 09:29 AM #12
mrsD's Avatar
mrsD mrsD is offline
Wisest Elder Ever
 
Join Date: Aug 2006
Location: Great Lakes
Posts: 33,508
15 yr Member
mrsD mrsD is offline
Wisest Elder Ever
mrsD's Avatar
 
Join Date: Aug 2006
Location: Great Lakes
Posts: 33,508
15 yr Member
Lightbulb

I don't have PD or MS, but I do have peripheral neuropathy.

I used to use a cane quite a bit, but it was hard on my hand.

I use a hiking pole, light weight and the grip is vertical rather than horizontal, like a crutch or cane. Much much better for me.
I use it on stairs all the time, and for longer walks. When I have a bad time like last week, I use it in the house.

I bought it for $15 at Dunham's..and have purchased new rubber tips made for Leki poles on it now. The Leki tip has lasted me 2 yrs now
on concrete...very good quality. Hiking poles can be really expensive... but mine has served me well, and stabilized me from any falls due to poor balance. I also find people don't stare at you so much when you use a pole. I used to get long stares with my canes!
__________________
All truths are easy to understand once they are discovered; the point is to discover them.-- Galileo Galilei

************************************

.
Weezie looking at petunias 8.25.2017


****************************
These forums are for mutual support and information sharing only. The forums are 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.
mrsD is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
lindylanka (02-08-2012)
Old 02-08-2012, 12:51 PM #13
Peony Peony is offline
Member
 
Join Date: Jul 2009
Location: Northern California
Posts: 134
10 yr Member
Peony Peony is offline
Member
 
Join Date: Jul 2009
Location: Northern California
Posts: 134
10 yr Member
Default

I agree, the poles look cooler than canes or walkers, and also appear to have many benefits if sized & used correctly. Lots of people without mobility issues use them for exercise. The speaker who addressed our local PD support group was Jayah Paley, a very experienced Bay Area Nordic Walking instructor who has 2 websites. This one includes a lot of good info on how to get the right pole: http://polesformobility.com/pole-buyers-guide.htm . She is herself a breast cancer survivor who used trekking poles to help recover from lymphedema,

I've learned a lot of useful things from people who share info on this forum, so I really value that function. However, lest anyone is suspicious of "new" members pushing cures or products (which has been controversial lately on this forum), let me just say: I offer this info strictly in the spirit of possibly helping someone. It certainly looked very promising to me, but make up your own mind after reading her website info. I do know she is who she says she is. She certainly isn't promoting a "cure," and I'm not a new forum member (joined 2009), and I do have Parkinson's (diagnosed 2007). For me, gait & balance are not my major problems (tremor is), so I haven't bought a pole yet, but definitely intend to as soon as symptoms & budget dictate! Good luck!
Peony 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
Photos from our dive trip TXBatman The Stumble Inn 11 10-05-2011 05:23 PM
Dry nose and congestion kidgie Trigeminal Neuralgia 2 09-17-2011 09:02 PM
Water out the nose? moonbug Dentistry & Dental Issues 1 04-14-2009 09:42 PM
My Nose.... Alffe Survivors of Suicide 7 12-06-2007 03:04 PM
Stuffy Nose geraldo Parkinson's Disease 0 10-17-2006 05:55 PM


All times are GMT -5. The time now is 03:28 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.