Thoracic Outlet Syndrome Thoracic Outlet Syndrome/Brachial Plexopathy. In Memory Of DeAnne Marie.


advertisement
Reply
 
Thread Tools Display Modes
Old 10-12-2013, 02:42 PM #1
Coop42's Avatar
Coop42 Coop42 is offline
Member
 
Join Date: Feb 2007
Location: Petaluma Ca
Posts: 571
15 yr Member
Coop42 Coop42 is offline
Member
Coop42's Avatar
 
Join Date: Feb 2007
Location: Petaluma Ca
Posts: 571
15 yr Member
Default Amount of Therapy Needed Following Surgery, 3 1/2 Years so far, for me

Hey everyone, I've had TOS for about 33 years total now. I had surgery on one side 22 years ago and it made me worse, been on disability ever since. I also had 2 lower back surgeries, years ago, that left me with chronic lower back and leg pain. The physical therapists I saw back then were no help to me. They had no clue what to do with me. It was all the wrong stuff.

In last 3 1/2 years I've improved a lot, mainly by doing joint mobility exercises. The one's taught by Scott Sonnon and Steve Maxwell. I've also been doing a lot of self-myofascial release, and vacuum cupping. Those three things have helped me tremendously. I wish I had known about them years ago.

I've come to the conclusion, that having the right type of therapy following surgery is critical, and it may take years. I think it all depends on how long you've had TOS before you were diagnosed. It was 11 or 12 years in my case.

I also think, that the longer you've had TOS, the more of your body it starts to affect. It really helped me out a lot learning about fascia, and how it covers your entire body. Once I it started to understand that, and take a full-body approach to my movement, I started to make good progress.

Like I said, I've been working on this for 3 1/2 years, so far, but I feel like I can improve a lot more if I keep at it. I started making videos of some of the things I've been doing and posting them on my Youtube channel. I had a few people asking me some questions about the things I do, and I figured it would be easier to make videos, than to try and explain things here. Hopefully, they will be helpful to someone out there.

The link is below.
__________________
Obsessed with reclaiming mobility, and functional, pain-free movement. Check out my YouTube channels

.

My Easy Cooking Channel
.

Last edited by Coop42; 10-12-2013 at 03:04 PM.
Coop42 is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
cyclist (10-12-2013), Jomar (10-12-2013), tosmother (10-14-2013)

advertisement
Old 10-13-2013, 08:47 PM #2
semmons semmons is offline
Junior Member
 
Join Date: Oct 2013
Posts: 9
10 yr Member
semmons semmons is offline
Junior Member
 
Join Date: Oct 2013
Posts: 9
10 yr Member
Default

I had TOS undiagnosed for 4 years. I recently came into contact with a doctor who diagnosed me and sent me to a physical therapist. I was introduced to the Edgelow Protocol, it relieved some of the pain and I am able to be without my medication. I met Peter Edgelow in Hayward, CA. I called therapy offices locally and found another therapist who knows of this program and they tuned it to what i needed and i did see improvements. It is always worth a shot, the most important thing is posture, it is hard to break habits but it does make a difference. Good luck.
semmons is offline   Reply With QuoteReply With Quote
Old 10-14-2013, 02:27 PM #3
Coop42's Avatar
Coop42 Coop42 is offline
Member
 
Join Date: Feb 2007
Location: Petaluma Ca
Posts: 571
15 yr Member
Coop42 Coop42 is offline
Member
Coop42's Avatar
 
Join Date: Feb 2007
Location: Petaluma Ca
Posts: 571
15 yr Member
Default

Quote:
Originally Posted by semmons View Post
I had TOS undiagnosed for 4 years. I recently came into contact with a doctor who diagnosed me and sent me to a physical therapist. I was introduced to the Edgelow Protocol, it relieved some of the pain and I am able to be without my medication. I met Peter Edgelow in Hayward, CA. I called therapy offices locally and found another therapist who knows of this program and they tuned it to what i needed and i did see improvements. It is always worth a shot, the most important thing is posture, it is hard to break habits but it does make a difference. Good luck.
I've done some of the Edgelow protocol, and it really didn't work well for me, but that's great that it's helped you. I know a few other people have had good luck with that. I agree with you that posture is very important, but lasting improvements have taken a long time, for me. Slow and steady wins the race here.
__________________
Obsessed with reclaiming mobility, and functional, pain-free movement. Check out my YouTube channels

.

My Easy Cooking Channel
.
Coop42 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
mri results-surgery needed vbagley11 Spinal Disorders & Back Pain 3 02-09-2012 06:57 PM
Therapy Dog Needed in MA for Epilepsy Girl Red Rover New Member Introductions 6 06-03-2011 11:35 PM
New learning stratigies needed after surgery?? Tattoo2 Epilepsy 9 08-18-2009 03:46 PM


All times are GMT -5. The time now is 10:48 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.