MDJunction - People Helping People
 

Why wear a ribbon?

 
"I have just been diagnosed with Sjogrens Syndrome" (Mcbluemun)

MDJunction to me

2steveb" In life we all have trials and tribulations to endure weather it be physical, mental or social. For me personally when i encountered MDJunction i was astounded. Since i joined MDJunction to me it has been a god send and a life saver. I have met and been able to converse freely with so many people in the same situation as myself, (that alone is a big help, to know your not alone) to be able to discuss and get good advice from a braud section of people. One of lifes hardest things is to discuss personal issues with friends/family and yet the mdj family is non judgmental and you will be made totally welcome to talk through any issue thats on your mind. There are forums for every known issue to mankind, to me MDJ.com has become my family extension, id be lost without these good people and the extremely good guide lines that group leaders help us all with to keep threads topical and friendly." (2steveb)

more testimonials
Reflex Sympathetic Dystrophy Support Group
A community of patients, family members and friends dedicated to dealing with Reflex Sympathetic Dystrophy, together.
Join This Group
Group Home   Forums   Articles   Members (899)   Diaries   Videos   Leaders   Guidelines
RSD Group RSS Feed
RSD ForumsGeneral & Supportsevere pain/burning ,sleeplessness
02/24/2010 03:28 AM
Barb117
Barb117
 
Posts: 12
Member

Hi everyone;

I am new here,though I've had RSD for 20 some yrs.I want to ask if anyone has tried Hyperbaric oxygen therapy for relief of their RSD pain.

I have had a morphine pump and a scs in the past,but I built up a tolerance to morphine 3 years ago,and the scs actually started causing me additional pain so i have had them both removed.There is nothing that is helping with my pain-I don't sleep hardly at all anymore,maybe 1 or 2 hours,usually I don't even get that much.Is HBOT covered now for RSD? Iappreciate any help that anyone can give me. Smile

Reply

02/24/2010 05:35 AM  Top
darlaa
darlaa
 
Posts: 172
Member

Welcome to the group! I tried HBOT once, unfortunately it's not covered by most insurances. It also takes many treatments, or so they say, to tell a difference. It caused issues with my ears so I didnt go back. I saw your other post about ketamine; I would recommend trying it. It is just about the only thing that helps me. If you have any specific questions, let me know. Every doctor does the procedure differently. I have found my form to be quite helpful with almost immediate results (within a few days). The only thing is, your body doesnt respond to it as well with each treatment. My doctor does a 5 day inpatient continuous infusion. feel free to PM if you want to know more.

Previous discussions I participated in:
The new kid
Sauna?
Snapping!

02/24/2010 06:11 AM  Top
Barb117
Barb117
 
Posts: 12
Member

Hi Darla;

Thanks for your info,I do have more questions on the ketamine treatment that your doctor does.I live in Michigan and am wondering how to find a doctor who does this treatment here-I did call my pain management center a few minutes ago to see if they have heard of the treatment.

Thanks,

Barb


Previous discussions I participated in:
friendship
Ketamine Therapy

02/24/2010 12:19 PM  Top
darlaa
darlaa
 
Posts: 172
Member

I would look up a list of facilities and call them one by one to see...My doctor is in Ohio if all else fails. Some states (like SC) don't do ketamine treatments for some reason, so you may have to travel, but i can promise you it will be worth it. (it was for me!) I drove 10 hours there and back to my past two infusions. You would just need to bring someone with you.

Previous discussions I participated in:
The new kid
Sauna?
Snapping!

02/24/2010 06:21 PM  Top
revvanbus
revvanbus
 
Posts: 1985
VIP Member

I will agree - look for a good PMD or Neurologist who has experience using low-dose outpatient ketamine or as I understand it the in-patient lower-dose ketamine given over a few days. I have no experience with the latter but have heard some good results from that. Me, I go with the outpatient: I don't do well in hospitals and avoid them at all costs.(~:

Rev. Maryanne

PS If you want to arrange it with my PMD I can offer a good, comfortable guest bed and some good food for the night before as my PMD likes to do the treatment in the early morning. You have to stay until noon so you are awake and ready for a meal. (you have to skip breakfast.)

Rev.
RSD: THE GREAT DECIEVER. IT FOOLS US INTO SEEING OUR PAIN AS INJURY, BELIEVING OUR MOVEMENT WILL BREAK A BONE INSTEAD OF HELPING OUR OSTEOPOROSIS. THE DISEASE FEELS LIKE IT RESIDES IN OUR HANDS/ARMS, FEET/LEGS WHEN IT LIVES IN THE DORSAL HORN Of THE SPINAL CORD AND THE BRAIN PAIN RECEPTOR CELLS. MOVE, REST, MOVE, REST, MOVE.
Reply

Share this discussion with your friends:
Members who viewed this page also read:

RSDRSD ForumsGeneral & Supportsevere pain/burning ,sleeplessness

Disclaimer: The information provided in MDJunction is not a replacement for medical diagnosis, treatment, or professional medical advice.
In case of EMERGENCY call 911 or 1.800.273.TALK (8255) to the National Suicide Prevention Lifeline. Read more.
Contact Us | Bookmark Us | FAQ | Awareness Ribbons
About Us | Terms & Conditions | Privacy | Spread the Word | MDJ Advocates | Advertise
Copyright (c) 2006-2013 MDJunction.com All Rights Reserved