FAQ/Help |
Calendar |
Search |
Today's Posts |
![]() |
|
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) |
Reply |
|
Thread Tools | Display Modes |
|
![]() |
#1 | |||
|
||||
Member
|
Quote:
I'm sorry for what you have gone through! Like you, I too ended up with CRPS II after surgery with a similar sounding saga of the tangled bundle of nerves causing originally only my right leg to be affected. I'm sure others will chime in with more info but here is my thoughts: You mentioned above that you are taking Gabapentin but what about other medications, creams etc along with the Gaba and possibly even an increase in that? Mertazapine, Nortriptyline, Amitriptyline, Lidoderm patches, Specially formulated Compounded Cream and others. Have you discussed with your PM trying additional medications and perhaps even a low dose pain medication? In your shoes if I was managing as well as you have for the past year without pain meds but now find myself needing more to get through the day I would try a new combo of medications before going forward with the SCS to see if that gives you what you need. I personally have an SCS and although it does help, for me it just isn't enough. It would just seem a big leap to go from only gabapentin to the SCS without trying other meds first. Since you mentioned wanting to try more holistic approaches you might consider reading a book "Holistic Pain Relief" by Dr. Heather Tick. I found many useful pieces of information in this book and have since incorporated much of it into my daily coping strategies. Cheers, Tessa |
|||
![]() |
![]() |
"Thanks for this!" says: | eevo61 (08-06-2014) |
![]() |
#2 | ||
|
|||
Member
|
Iam 26 too, I got my rsd 10years ago from foot surgery and then had 2 more and it went full body. I was to the point my feet and hands were culed and my knee were frozen so couldn't walk, my bladder shut down and lost the ability to walk. I first tried the trial stimulator and with that meds and pt and ot I got walking in a month. I then got the permanent and it helped for 4 months then stopped but that was just me, I know for others it really helps all the time. I found out I had a neuroma in my nerves that was keeping them on fire which once that was removed I got walking again with meds and the ketamine.
Sam |
||
![]() |
![]() |
"Thanks for this!" says: | eevo61 (08-06-2014) |
![]() |
#3 | ||
|
|||
Grand Magnate
|
Welcome LittleKingdom.
![]()
__________________
Kitt -------------------------------------------------------------------------------------------------------- "It is what it is." |
||
![]() |
![]() |
"Thanks for this!" says: | eevo61 (08-06-2014) |
![]() |
#4 | ||
|
|||
Junior Member
|
I would recommend ketamine infusions over SCS any day. Ketamine has been a lifesaver for me.
Here's a blog entry by a PM doc in San Diego that was posted just this week cautioning against SCS! http://painsandiego.com/2014/08/06/s...verse-effects/ I have pain in my hands otherwise I'd be writing more. But I recommend staying away from SCS. Cut out gluten!!! Helped me. And remember... THERE ARE NO SILVER BULLETS. Yet. |
||
![]() |
![]() |
"Thanks for this!" says: | eevo61 (08-06-2014) |
![]() |
#5 | ||
|
|||
Junior Member
|
Also, once the SCS is in your body, it stays there. It's too risky to take them out. So, if you et one you have to be prepared to have a foreign object in your body forever.
You might try higher doses of gabapentin. Or combine it with a low dose of Lyrica in addition (what I do). |
||
![]() |
![]() |
"Thanks for this!" says: | eevo61 (08-06-2014) |
![]() |
#6 | |||
|
||||
Member
|
Welcome ,I also have scs for almost year and half now,works well but at the beginning had hard time,the setting is so important and all the medications combine. I really hope your dr finds the right combo to reduce your suffering ,we all,had travel this far and many scs didn't work as long or how we expected but trying is the way you really know.
In www.rsdsa.og you will find some extra informations ,might be helpful and also www.howtocopewithpain.org will also guide you to learn how to retrain your brain in focusing in something else beside pain. I wish you soon get some much needed relief and let us know how things are going we all,hope always the best,we are a friendly community really caring about each other's,gentle hugs from Jesika . ![]()
__________________
. |
|||
![]() |
![]() |
![]() |
#7 | |||
|
||||
Member
|
Quote:
|
|||
![]() |
![]() |
"Thanks for this!" says: | eevo61 (08-08-2014) |
![]() |
#8 | ||
|
|||
Member
|
It can be removed mine was, they wanted it out so I could have mri's a neurosurgeon took it out for me. For the surgery they used ketamine and Pain meds which helped keep me out of bad flares.
|
||
![]() |
![]() |
"Thanks for this!" says: | eevo61 (08-12-2014) |
Reply |
Thread Tools | |
Display Modes | |
|
|
![]() |
||||
Thread | Forum | |||
Contemplating Seeking Accommodations in College | General Health Conditions & Rare Disorders | |||
Battling Guilt | Survivors of Suicide | |||
Battling MS in Baghdad | Multiple Sclerosis | |||
Battling Lou Gehrig's for 14 years | ALS News & Research |