Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS)


advertisement
Reply
 
Thread Tools Display Modes
Old 04-03-2010, 10:20 PM #11
SandyS SandyS is offline
Member
 
Join Date: Jan 2009
Location: Tampa, Fl.
Posts: 409
15 yr Member
SandyS SandyS is offline
Member
 
Join Date: Jan 2009
Location: Tampa, Fl.
Posts: 409
15 yr Member
Default

Hi Wendy,

I am sorry for your pain, we also live in Florida, close to the Hyperbaric treatments. I have a 16 year old daughter with RSD. We have discussed having the treatment, but have never tried them. What part of florida are your from? We live in Tampa.
SandyS is offline   Reply With QuoteReply With Quote

advertisement
Old 04-05-2010, 10:00 AM #12
wswells wswells is offline
Junior Member
 
Join Date: Mar 2010
Posts: 94
10 yr Member
wswells wswells is offline
Junior Member
 
Join Date: Mar 2010
Posts: 94
10 yr Member
Default

Quote:
Originally Posted by SandyS View Post
Hi Wendy,

I am sorry for your pain, we also live in Florida, close to the Hyperbaric treatments. I have a 16 year old daughter with RSD. We have discussed having the treatment, but have never tried them. What part of florida are your from? We live in Tampa.
hi Sandy, I live in Palm Harbor 5 minutes from a Dr. that does the HBOT, but my current Dr.'s have never mentioned this treatment to me. A couple of people have told me I might be too advanced for this. I was diagnosed in 1986 have had surgeries,blocks,sympathectomies, been to Philly 2 times to see Dr. Schwartzman, and now all my Dr.'s tell me I am palliative care only. I am so sorry that your 16 year old daughter has this awful disease. How long has she had it? what treatments have you all tried? Having this disease is bad enough, but to have a young girl like your daughter have it, thats just not right! How on earth do you handle it, seeing your child with this stuff? I hope you are taking care of your self, as your daughter will need her mother to help her deal with this. Hope to hear from you. your new friend Wendy
wswells is offline   Reply With QuoteReply With Quote
Old 04-05-2010, 10:24 AM #13
daniella daniella is offline
Magnate
 
Join Date: May 2007
Posts: 2,998
15 yr Member
daniella daniella is offline
Magnate
 
Join Date: May 2007
Posts: 2,998
15 yr Member
Default

I think after like 10 treatments if you have not had any relief or benefit the treatment stops. I could be off on how many but it is not the full amount. There is a gentleman who bloged about his experience. The reason it caught my eye is cause he had rsd in his eyes and I may have it in mine. I think he benefited to a point but still has rsd pain. I could be off a little.
daniella is offline   Reply With QuoteReply With Quote
Old 04-07-2010, 10:17 AM #14
ALASKA MIKE ALASKA MIKE is offline
Member
 
Join Date: Apr 2009
Location: Alaska
Posts: 158
15 yr Member
ALASKA MIKE ALASKA MIKE is offline
Member
 
Join Date: Apr 2009
Location: Alaska
Posts: 158
15 yr Member
Default

I would talk to DianaA about HBOT info.....


i bought 2 books from amazon that detail how hbot works.


i looked into doing hbot but was too ill to travel but if i get better i would goto canada because its the cheapest in north america. normally you do 40 dives for a trial. 2 dives a day, 20 days in row or some places only do it monday thre friday. atm or pressure makes a big difference from what i have been told by several people. most have told me that it would be much better to goto chambers that can dive deeper like the 2.0atm or bigger. the cheaper 1.3 and 1.6atm chambers sometimes dont do a thing for crps but there is only one way to find out and that is to try it. generaly the deeper the dive the more it costs because the dive takes longer and the chamber costs way more.

the smaller chambers like the 1.3 to 1.6atm look like an enclosed tanning bed or a blown up sleeping bag with a window to see just the face.
__________________
Hoping you feel better,

ALASKA MIKE
ARACHNOIDITIS,CRPStype2/CAUSALGIA since 2004
ALASKA MIKE is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
DianaA (04-08-2010)
Old 04-27-2010, 01:06 AM #15
numb numb is offline
Member
 
Join Date: Nov 2007
Posts: 159
15 yr Member
numb numb is offline
Member
 
Join Date: Nov 2007
Posts: 159
15 yr Member
Default

Hi All,
I would like to share my HBOT experience. I had a total of 50 sessions of HBOT on two occasions (30x and 20x). My first 30x took place a few months after the onset of RSD. I had very good relief but not remission. The second 20x took place around 2 years after the onset of RSD. I had little relief. I don't know why. Perhaps the sooner the better result. In retrospect, i should not break the treatment. My insurance did not cover the cost. It was $240 per session. I had an installment plan. I paid around $3000. The clinic wrote off the balance after i applied for financial aid. Therefore, ask to see whether or not they offer financial assistance.
Take care,
numb is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
wswells (04-27-2010)
Old 04-27-2010, 08:23 AM #16
mjl1261 mjl1261 is offline
Junior Member
 
Join Date: Nov 2009
Posts: 33
10 yr Member
mjl1261 mjl1261 is offline
Junior Member
 
Join Date: Nov 2009
Posts: 33
10 yr Member
Default

Quote:
Originally Posted by daniella View Post
I think after like 10 treatments if you have not had any relief or benefit the treatment stops. I could be off on how many but it is not the full amount. There is a gentleman who bloged about his experience. The reason it caught my eye is cause he had rsd in his eyes and I may have it in mine. I think he benefited to a point but still has rsd pain. I could be off a little.
Here is the blog of the guy who wrote about his experience. He is full body and got good relief. Don't know what the long-term results have been.

http://painisafourletterword.blogspo...&max-results=7
mjl1261 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
Anybody have any info on Vic H Grammie 2 3 Multiple Sclerosis 2 06-30-2009 11:54 AM
Looking for info KLS2007 Thoracic Outlet Syndrome 2 06-29-2009 12:36 PM
for pcs info vini Traumatic Brain Injury and Post Concussion Syndrome 0 02-28-2009 03:12 PM
looking for info jaybee New Member Introductions 5 02-06-2008 07:44 AM
More INFO smallboysomuch2deal Colloid Cyst 0 07-17-2007 10:22 AM


All times are GMT -5. The time now is 12:53 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.