LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » physical therapy

 - UBBFriend: Email this page to someone!    
Author Topic: physical therapy
Theresa
LymeNet Contributor
Member # 421

Icon 1 posted      Profile for Theresa     Send New Private Message       Edit/Delete Post   Reply With Quote 
Does anyone with neuropathy on ivig go for physical therapy or participate in any structured exercises. I can't seem to exert myself without getting worse. How can I keep from losing muscle. Theresa
Posts: 479 | From nj | Registered: Nov 2000  |  IP: Logged | Report this post to a Moderator
Notti
LymeNet Contributor
Member # 43843

Icon 1 posted      Profile for Notti     Send New Private Message       Edit/Delete Post   Reply With Quote 
These two links/documents have been very helpful to me. I pick the exercises that I can do and omit the ones that cause pain or discomfort. You can try to work around your limitations that way and still keep your strength and flexibility.

I have worked with physical therapists before, but they always pushed me over my limits, which did not only cause physical problems but also a lot of frustration. Somehow they don't understand that too much too soon causes a relapse.

As soon as my doctor gave me permission to start physical therapy after approximately half a year on IVIG and antibiotics, I decided not to search for an official therapist, but to do it myself. I started with very simple light exercises and now I can do exercises that I could have never even dreamed of. You do need discipline, motivation and patience, but it is very rewarding!

http://www.nationalmssociety.org/NationalMSSociety/media/MSNationalFiles/Brochures/Brochure-Stretching-for-People-with-MS-An-Illustrated-Manual.pdf

http://www.cancersupportivecare.com/exercises.html

I hope this is helpful.

Best wishes,

Notti

Posts: 109 | From The Netherlands | Registered: May 2014  |  IP: Logged | Report this post to a Moderator
droid1226
Frequent Contributor (1K+ posts)
Member # 34930

Icon 1 posted      Profile for droid1226     Send New Private Message       Edit/Delete Post   Reply With Quote 
I lost a large part of my right leg. My PT didn't understand lyme. So if you are going to PT, make sure they understand where you are on your baseline. I had a walker & a cain & my guy insisted I get on the treadmill.

It really is necessary though. Just make sure you do it correctly. If you have some discipline you could do basic Youtube videos. I started with very very mild yoga & moved up from there.

--------------------
http://www.youtube.com/user/droid1226/videos?view=0&flow=grid

Posts: 1181 | From ohio | Registered: Nov 2011  |  IP: Logged | Report this post to a Moderator
LisaK
Frequent Contributor (1K+ posts)
Member # 41384

Icon 1 posted      Profile for LisaK     Send New Private Message       Edit/Delete Post   Reply With Quote 
droid, I have just begun thinking about going to a PT. how do they know where you are on you baseline??

Theresa, good luck with this. I hope you get results.

--------------------
Be thankful in all things- even difficult times and sickness and trials - because there is something GOOD to be seen

Posts: 3558 | From Eastern USA | Registered: Jul 2013  |  IP: Logged | Report this post to a Moderator
Tincup
Honored Contributor (10K+ posts)
Member # 5829

Icon 1 posted      Profile for Tincup         Edit/Delete Post   Reply With Quote 
Excellent advise Notti & Droid.

Dr. B found the therapist often overworked the patients so he addressed it in his guidelines.

Click on link below, scroll to the bottom and find "Dr. Jo... Bur... Advanced Topics in Lyme Disease" Full Guidelines

https://sites.google.com/site/getitrighttreatthebite/ticks/treat-the-bite

A snip from them says, concerning exercise...

"This program may begin with classical physical therapy if necessary. The physical therapy should involve massage, heat, ultrasound and simple range of motion exercises to relieve discomfort and promote better sleep and flexibility.

Ice (vasoconstriction) and electrical stimulation (muscle spasm and trauma) should not be used!

The program must evolve into a graded, ultimately strenuous exercise program that consists of a specific regimen of non-aerobic conditioning- see below.

Have the patient complete a gentle hour of prescribed exercise, then go home, have a hot bath or shower, than try to take a nap. Initially, patients will need this sleep, but as they recover, the exercise will energize them and then a nap will no longer be needed.

NOTE: a cardiac stress test may be necessary prior to exercising to ensure safety."

He goes on to give specific instructions worth the read.

I suggest this because as Notti and Droid said, the therapists can easily over do it. I use to call mine "Darth Vadar". She thought I was kidding, but I wasn't. And I went for five years straight 2-3 times each week, then 2-3 years I stopped, then another couple of years.

Then I found a chiropractor. In my opinion, much better, much faster, a lot cheaper and very effective.

Hope this helps.

--------------------
www.TreatTheBite.com
www.DrJonesKids.org
www.MarylandLyme.org
www.LymeDoc.org

Posts: 20353 | From The Moon | Registered: Jun 2004  |  IP: Logged | Report this post to a Moderator
Maia_Azure
LymeNet Contributor
Member # 44330

Icon 1 posted      Profile for Maia_Azure     Send New Private Message       Edit/Delete Post   Reply With Quote 
I did PT for awhile, was told my only option was surgery, this was before my lyme diagnosis.

I don't have the money to continue PT, so I am trying to do yoga now and gentle stretching of my problem areas.

It seems like the PT would be helpful regaining, but I am afraid to do it too soon and waste my time!

--------------------
Sick since 2000
Bulls eye 2005
Dx Babesia, Lyme 2014

Posts: 247 | From New Hampshire | Registered: Aug 2014  |  IP: Logged | Report this post to a Moderator
Keebler
Honored Contributor (25K+ posts)
Member # 12673

Icon 1 posted      Profile for Keebler     Send New Private Message       Edit/Delete Post   Reply With Quote 
-
very helpful for many:

QI GONG (Chi Gong) ]a sort of Tai Chi with less moving of the head from side to side]
-

Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.