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

 
 
Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 07-06-2012, 10:58 PM #23
OzKira OzKira is offline
Junior Member
 
Join Date: Dec 2010
Location: Melbourne Australia
Posts: 83
10 yr Member
OzKira OzKira is offline
Junior Member
 
Join Date: Dec 2010
Location: Melbourne Australia
Posts: 83
10 yr Member
Frown

Quote:
Originally Posted by Jo*mar View Post
I think I'm skeptical of anyone saying 100% success rate..
Unless they are mega picky about the pts they choose to do surgery on...

How long post op are pts being tracked...?? 2 months, 6 months, years?
I totally agree with you there Jo.


I have just come back from my family doctor who has already had correspondence from the vascular surgeon. I have an extra rib which is what not I was expecting. When I saw the surgeon on first consultation the other week he was concentrating on a particular area which now I believe to be where the extra rib is. My radial pulse is very weak when arms are beside me. This is something I was certain was happening but now I have it confirmed. I still have to have a MRI with contrast to check if there are fibrous bands and it's this that will determine how the surgeon approaches the surgery. He has said I have not only venus TOS but also arterial and neuro TOS. On a good note my blood clotting medication has been changed to Pradaxa which I have been waiting years to have. This drug will make it easier post surgery to make sure I don't clot but will also be a lifelong drug because I have suffered 2 clots in my lungs as a result of my TOS.

The MRI is posing difficult to obtain fully covered in my local hospital in Australia. I know when I have had the previous blood clots that the MRI department did not want to do the tests the doctor had ordered. As my surgeon is a consultant at the hospital he should be able pressure them to do the test or refer me to another MRI company who run out of one of the other hospitals. At the end of the day with my local hospital it's about cost cutting and not that they don't do the test. They tried to tell me they don't do the test but i have had similar there before but it was radioactive iodine and this time it's not radioactive.

I will post any updates as they happen to save me typing lol
__________________
[SIGPIC][SIGPIC]

Last edited by OzKira; 07-06-2012 at 11:37 PM.
OzKira is offline   Reply With QuoteReply With Quote
 


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
My journey to SCS twinmom SCS & Pain Pumps 28 05-14-2011 07:02 PM
My journey with RSD Cindioh1 New Member Introductions 4 09-22-2010 12:28 AM
My Journey! ConnieS Myasthenia Gravis 32 07-10-2009 09:47 AM
Update on diagnostic journey Megan Peripheral Neuropathy 6 08-16-2008 09:13 AM
Mom's Journey BJ Coping with Grief & Loss 5 05-13-2007 09:53 AM


All times are GMT -5. The time now is 11:54 PM.


Powered by vBulletin • Copyright ©2000 - 2025, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise (Lite) - vBulletin Mods & Addons Copyright © 2025 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.