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 09-22-2006, 06:58 AM #1
Cake Cake is offline
Member
 
Join Date: Sep 2006
Location: Australia
Posts: 148
15 yr Member
Cake Cake is offline
Member
 
Join Date: Sep 2006
Location: Australia
Posts: 148
15 yr Member
Default Trying Lyrica and a Magnesium Infusion

This is our next plan of attack for me

I started the Lyrica last night, at 75mg then going up over the next few days till I get to about 225mg daily. I haven't had any bad side effects yet, just a migraine that's been going on all day, but I can put up with that

I'm also waiting for a magnesium infusion, hopefully that'll be soon (Dr put me down as Priority One, to get it done asap as my RSD is so out of control at the moment- with it spreading to my foot and up to hip, and also symptoms coming back in my arm that I haven't had for over 2 years). It works the same way as a ketamine infusion, but is only a day procedure, so I'm only in hospital for one day. Its another one of those things that helps some people, but not others (as with all RSD meds ) but I'll give it a shot.

I'm very lucky to have a great RSD doctor who never questions what I say about my symptoms etc, and can get me access to the latest and most successful medications and treatments, I know a good RSD Dr is hard to find so I'm hanging on to this one! As much as I hate the cold weather here in Melbourne and would LOVE to move north, we're staying here so we can be near my RSD dr, as that's so important.

Anyway, I'll let you know how I get on....

x Kate
__________________
RSD in right arm for 13 years, right leg for 8 years, left arm since May 2013, with full body symptoms and CNS.
Cake is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Sandel (05-30-2010)
Old 09-22-2006, 10:18 AM #2
ATallOne's Avatar
ATallOne ATallOne is offline
Member
 
Join Date: Aug 2006
Posts: 202
15 yr Member
ATallOne ATallOne is offline
Member
ATallOne's Avatar
 
Join Date: Aug 2006
Posts: 202
15 yr Member
Default Good Luck Kate

Keeping my fingers crossed for you Kate. I would love to go to Florida for the winters but I can't handle moving around alot anymore. I'm stuck in the mud. Sounds like you struck gold with your doc. Thats rare. Keep em. Good RSD docs are few and far between. Glad your here. Chin Up!!

Mark
ATallOne is offline   Reply With QuoteReply With Quote
Old 09-23-2006, 08:43 PM #3
Cake Cake is offline
Member
 
Join Date: Sep 2006
Location: Australia
Posts: 148
15 yr Member
Cake Cake is offline
Member
 
Join Date: Sep 2006
Location: Australia
Posts: 148
15 yr Member
Default

lol, I gotta say, I love your pic Mark!

x Kate
__________________
RSD in right arm for 13 years, right leg for 8 years, left arm since May 2013, with full body symptoms and CNS.
Cake is offline   Reply With QuoteReply With Quote
Old 10-20-2006, 01:03 PM #4
rsdpainradar rsdpainradar is offline
Junior Member
 
Join Date: Oct 2006
Posts: 17
15 yr Member
rsdpainradar rsdpainradar is offline
Junior Member
 
Join Date: Oct 2006
Posts: 17
15 yr Member
Default pamidradate infusions?

Hi Cake,
Just wondering if this is the same thing as the pamidradate infusion? I had this in July and it was a great relief. Let me know if it is.
rsdradarpain
rsdpainradar is offline   Reply With QuoteReply With Quote
Old 10-20-2006, 02:52 PM #5
emilys gramma's Avatar
emilys gramma emilys gramma is offline
Member
 
Join Date: Sep 2006
Location: michigan/ florida
Posts: 231
15 yr Member
emilys gramma emilys gramma is offline
Member
emilys gramma's Avatar
 
Join Date: Sep 2006
Location: michigan/ florida
Posts: 231
15 yr Member
Default

hi kate.................the doctor just gave frank lyrica and so far he said he just feels his pain in a more precise way.?// meaning he can feel it as it runs all the way down his arm... from his shoulder to his fingers.................hopefully this will help him tho. he started with 75 mg and then in five days will go to 150 mg
good luck with the magnesium infusion
__________________

.
claudia
.
emilys gramma is offline   Reply With QuoteReply With Quote
Old 10-20-2006, 03:00 PM #6
HopeLivesHere HopeLivesHere is offline
Member
 
Join Date: Sep 2006
Posts: 292
15 yr Member
HopeLivesHere HopeLivesHere is offline
Member
 
Join Date: Sep 2006
Posts: 292
15 yr Member
Default

Good luck Kate.
I hope this will be a great success for you. Thanks for letting us now.
All the best, Hope
HopeLivesHere is offline   Reply With QuoteReply With Quote
Old 05-24-2010, 08:34 PM #7
beck437 beck437 is offline
New Member
 
Join Date: Apr 2009
Posts: 4
15 yr Member
beck437 beck437 is offline
New Member
 
Join Date: Apr 2009
Posts: 4
15 yr Member
Default

Quote:
Originally Posted by rsdpainradar View Post
Hi Cake,
Just wondering if this is the same thing as the pamidradate infusion? I had this in July and it was a great relief. Let me know if it is.
rsdradarpain
I just came across your post. It was encouraging to see that you were helped by the pamidronate. I've tried many treatments that haven't helped, but I never heard of this. Could you tell me more about it? Has it continued to help you? Thanks!
beck437 is offline   Reply With QuoteReply With Quote
Old 05-24-2010, 11:41 PM #8
fmichael's Avatar
fmichael fmichael is offline
Senior Member
 
Join Date: Sep 2006
Location: California
Posts: 1,239
15 yr Member
fmichael fmichael is offline
Senior Member
fmichael's Avatar
 
Join Date: Sep 2006
Location: California
Posts: 1,239
15 yr Member
Blank

Quote:
Originally Posted by beck437 View Post
I just came across your post. It was encouraging to see that you were helped by the pamidronate. I've tried many treatments that haven't helped, but I never heard of this. Could you tell me more about it? Has it continued to help you? Thanks!
Please see my post #7 today in the Rsd/crps can't cope thread http://neurotalk.psychcentral.com/thread122821.html discussing the use of Zometa, a drug closely related to pamidromate in the biphosphonate family, along with some other newer therapies.
fmichael is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
sukadog (05-25-2010)
Old 05-29-2010, 07:36 PM #9
RNcrps2 RNcrps2 is offline
Member
 
Join Date: Nov 2009
Posts: 180
10 yr Member
RNcrps2 RNcrps2 is offline
Member
 
Join Date: Nov 2009
Posts: 180
10 yr Member
Default

Good luck Cake. Lyrica has really helped me and I've read a few articles on Mg infusions that sound promising. Hope you get relief. momof4
RNcrps2 is offline   Reply With QuoteReply With Quote
Old 05-30-2010, 04:35 AM #10
Sandel's Avatar
Sandel Sandel is offline
Member
 
Join Date: Oct 2006
Location: Western Canada
Posts: 844
15 yr Member
Sandel Sandel is offline
Member
Sandel's Avatar
 
Join Date: Oct 2006
Location: Western Canada
Posts: 844
15 yr Member
Blush

Quote:
Originally Posted by Cake View Post
This is our next plan of attack for me

I started the Lyrica last night, at 75mg then going up over the next few days till I get to about 225mg daily. I haven't had any bad side effects yet, just a migraine that's been going on all day, but I can put up with that

I'm also waiting for a magnesium infusion, hopefully that'll be soon (Dr put me down as Priority One, to get it done asap as my RSD is so out of control at the moment- with it spreading to my foot and up to hip, and also symptoms coming back in my arm that I haven't had for over 2 years). It works the same way as a ketamine infusion, but is only a day procedure, so I'm only in hospital for one day. Its another one of those things that helps some people, but not others (as with all RSD meds ) but I'll give it a shot.

I'm very lucky to have a great RSD doctor who never questions what I say about my symptoms etc, and can get me access to the latest and most successful medications and treatments, I know a good RSD Dr is hard to find so I'm hanging on to this one! As much as I hate the cold weather here in Melbourne and would LOVE to move north, we're staying here so we can be near my RSD dr, as that's so important.

Anyway, I'll let you know how I get on....

x Kate
Hi Kate,
I had some good results with lyrica till a realy bad side effect made me stop taking it, catastrophic thoughts, suicidal thoughts.. just out of the blue, nasty stuff not like me at all.. and not all about me either it just wasn't nice. Aparently some people have killed themselves on these drugs.. so just be aware ok.

Healing ((hugs))
~Sandra
Sandel 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



All times are GMT -5. The time now is 04:52 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.