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 01-15-2010, 05:21 PM #11
momzpeachy momzpeachy is offline
Member
 
Join Date: Feb 2007
Location: NE PA
Posts: 150
15 yr Member
momzpeachy momzpeachy is offline
Member
 
Join Date: Feb 2007
Location: NE PA
Posts: 150
15 yr Member
Default

Thank you so much for all of your replies and prayers. I finally got on the computer today and feel like typing. I've had a rough week and havent felt like doing anything. Talking to anyone has been difficult. I had a breakdown the other day and just shut down. Wednesday was awful. I spent pretty much the entire day crying. My Doctor's office called me (not the Doc of course) and she told me "no more ketamine". I can no longer have the ketamine boosters and I was removed from the inpatient list. I was really upset because I was just weeks away from doing the 5 day inpatient. I was hoping that would work. I did have a reaction to the ketamine. I am feeling better now and I can swallow once again. It did feel like an allergic type reaction. It also seemed like the RSD got worse which she said can happen. It was an adverse reaction and it just doesn't seem to work for me. Nothing does! I'm allergic to EVERYTHING and that's not a joke...I mean everything! I can't take most meds out there and when I did the allergy testing it showed that I am allergic to everything. They couldn't believe it. Morpheine is the only thing I can take and I was on it for almost 3 years and found that it can progress the RSD. I was taken off of it.

Currently I'm taking 2400 mg neurontin daily, 60mg cymbalta, and something for headaches that I can't remember the name off hand. Not much really. That's it. I'm in lots of pain and feel like crap. Today was a little better. The weather got a bit warmer so it helped. I'm just really really having a tough time. My face is so swollen and red. Actually my whole upper body is. Now my skin has also changed alot and is so shiny and pulling tight. It looks horrible. My skin always feels sweaty and gross. I wouldn't wish this on anyone.

Can anyone help me with what can I do to feel better? Any techniques. I want to stretch but it's hard. I so badly want to exercise but can't. 5 minutes of exercise puts me into a bad flare. I have gained so much weight. I'm flat out miserable and now I don't know where to go with this. I don't want to live the rest of my life this way but I don't have a choice. Some days I do wish I'd go to bed and not wake up or when I do wake up..all this would just be GONE! wishful thinking.

Take care everyone..I will hopefully keep posting..I need to vent and all of your support will help...thank you

I will try and respond to those who pm'd. I can only sit here for little bits at a time. If you want to talk by phone..please send a phone number. I can call you. Thanks again!
momzpeachy is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
bobber (01-16-2010), loretta (01-17-2010), SandyS (01-17-2010)

advertisement
Old 01-15-2010, 06:39 PM #12
SandyRI SandyRI is offline
Senior Member
 
Join Date: Dec 2008
Location: Rhode Island
Posts: 1,056
15 yr Member
SandyRI SandyRI is offline
Senior Member
 
Join Date: Dec 2008
Location: Rhode Island
Posts: 1,056
15 yr Member
Default

Dear Momz,

I'm sorry about your allergies. How relaxing in a warm water bath with epsom salts? Mindfulness Stress Reduction techniques have helped me a lot as well, just learning to relax and ease the muscle tension in my body. FMichael has posted a lot on the subject.

Also - Loretta is waiting to try HBOT, which has helped a number of people with RSD and maybe could be an option for you.

Never, never give up. Spring and warmer weather are around the corner. Please hang in there and know that we all have you in our prayers.

XOXOX Sandy
SandyRI is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
bobber (01-16-2010), loretta (01-17-2010), SandyS (01-17-2010)
Old 01-16-2010, 01:33 AM #13
loretta loretta is offline
Senior Member
 
Join Date: Feb 2007
Posts: 1,090
15 yr Member
loretta loretta is offline
Senior Member
 
Join Date: Feb 2007
Posts: 1,090
15 yr Member
Default

Quote:
Originally Posted by momzpeachy View Post
Thank you so much for all of your replies and prayers. I finally got on the computer today and feel like typing. I've had a rough week and havent felt like doing anything. Talking to anyone has been difficult. I had a breakdown the other day and just shut down. Wednesday was awful. I spent pretty much the entire day crying. My Doctor's office called me (not the Doc of course) and she told me "no more ketamine". I can no longer have the ketamine boosters and I was removed from the inpatient list. I was really upset because I was just weeks away from doing the 5 day inpatient. I was hoping that would work. I did have a reaction to the ketamine. I am feeling better now and I can swallow once again. It did feel like an allergic type reaction. It also seemed like the RSD got worse which she said can happen. It was an adverse reaction and it just doesn't seem to work for me. Nothing does! I'm allergic to EVERYTHING and that's not a joke...I mean everything! I can't take most meds out there and when I did the allergy testing it showed that I am allergic to everything. They couldn't believe it. Morpheine is the only thing I can take and I was on it for almost 3 years and found that it can progress the RSD. I was taken off of it.

Currently I'm taking 2400 mg neurontin daily, 60mg cymbalta, and something for headaches that I can't remember the name off hand. Not much really. That's it. I'm in lots of pain and feel like crap. Today was a little better. The weather got a bit warmer so it helped. I'm just really really having a tough time. My face is so swollen and red. Actually my whole upper body is. Now my skin has also changed alot and is so shiny and pulling tight. It looks horrible. My skin always feels sweaty and gross. I wouldn't wish this on anyone.

Can anyone help me with what can I do to feel better? Any techniques. I want to stretch but it's hard. I so badly want to exercise but can't. 5 minutes of exercise puts me into a bad flare. I have gained so much weight. I'm flat out miserable and now I don't know where to go with this. I don't want to live the rest of my life this way but I don't have a choice. Some days I do wish I'd go to bed and not wake up or when I do wake up..all this would just be GONE! wishful thinking.

Take care everyone..I will hopefully keep posting..I need to vent and all of your support will help...thank you

I will try and respond to those who pm'd. I can only sit here for little bits at a time. If you want to talk by phone..please send a phone number. I can call you. Thanks again!
Hi Momzpeachy, My heart goes out to you. I know how it feels to be full body or generalized. I hate the sweating entire body-the redness, and skin blemishes or break outs. I have a room in our house, where I hide out, and pretty much like to be alone. I've had RSD 15 years ago-diagnosed 11 years ago. My husband is very supportive, although not at the beginning when none of us knew what was going on. It was 4 years before a diagnosis. Our daughter is 30-married 9 years. They moved to Chicago from Arizona 2 years ago and have been back for a year. They are staying with us for a few more months. He flys for one of the airlines and our daughter has worked for the same court reporting firm for 10 years. I'm grateful for everyones support, now that we all know what is going on.
Have you checked out HBOT? I'm going to try it, as soon as I save the $$.
I had very good success with physical therapy and massage therapy. Got full range of both shoulders back. It was very painful, but I'm so glad I stayed with it. Also, one of the biggest helps for me was swimming, and water exercises in the pool-86 degrees. It was kept my toes from curling up. There are gym clubs and Y that have pools for very little $$.
I hate the weight gain too. I had always been thin and very athletic. My daughter and I played tennis-5 days a week, water skiied, snow skiied, horse back riding. aerobics, dance classes. 10 K runs. I had a wonderful psychiatrist that helped me thru the losses.Also miss traveling a lot. But, I think it's like the earthquake, some lose their legs, but are happy to be alive and find other things to be grateful for. That helps in healing. I have several 'tools' that help during 'low' times. I Cry, too, but some of my tools are
music, scented candles, meditation, visualization, journaling,j comedy, sports games, sending cards to friends, keeping in touch with you dear friends, reading, e-mailing, stetching, massage, light exercising, do my nails, I'm on a high antioxidant diet, healthy chocolate. The cocoa bean is the #1 highest antioxidant in the world-the one I eat has a patented cold pressed method formula, thus not loosing nutritional value thru the cooking process like other chocolates. It also has the #2 highest antioxidant Acai Berry from the Amazon Forest. I know I won't be at peace with myself, till I loose that weight I gained from Neurotin and Lyrica. I really feel, I'll be able to cut down at least one of my high blood pressure meds, with weight loss.
So I'm working on healthy eating, exercise, and running a small business from my bed, healthy chocolate.
I wrote you last week by private message. I gave you a website with a lot of good information. Please don't loose hope, I know it's awful to deal with, but we aren't alone.
Last week, when I saw my RSD Dr., he told me about a RSD patient. There was a car accident here in Phoenix. Two cars collided on the freeway and hit a metal fence. One of the poles became a air missle and went thru the windshield of this ladies car. It took off her little finger and part of her arm and impaled her shoulder to the back of the seat. She had 18 surgeries. Her neurologist asked my neurologist if he would take her has his patient and do the HBOT series on her. She had frozen shoulder and couldn't raise her shoulder. After 9 treatments she was waiving to the TV crew. The tv crew came out and interviewed her and my Dr. I went thru 100 pt treatments to be able to get full use of my shoulder when it became frozen after breast surgery. plus 100 massagae therapy treatments.
The VA Hospital in Florida just put in 16 brand new HBOT for treatment of the wounded etc.
Take care of yourself, loretta with soft hugs
loretta is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
bobber (01-16-2010), SandyS (01-17-2010)
Old 01-16-2010, 09:12 AM #14
keep smilin keep smilin is offline
Member
 
Join Date: Aug 2009
Posts: 851
10 yr Member
keep smilin keep smilin is offline
Member
 
Join Date: Aug 2009
Posts: 851
10 yr Member
Red face

Quote:
Originally Posted by loretta View Post
Hi Momzpeachy, My heart goes out to you. I know how it feels to be full body or generalized. I hate the sweating entire body-the redness, and skin blemishes or break outs. I have a room in our house, where I hide out, and pretty much like to be alone. I've had RSD 15 years ago-diagnosed 11 years ago. My husband is very supportive, although not at the beginning when none of us knew what was going on. It was 4 years before a diagnosis. Our daughter is 30-married 9 years. They moved to Chicago from Arizona 2 years ago and have been back for a year. They are staying with us for a few more months. He flys for one of the airlines and our daughter has worked for the same court reporting firm for 10 years. I'm grateful for everyones support, now that we all know what is going on.
Have you checked out HBOT? I'm going to try it, as soon as I save the $$.
I had very good success with physical therapy and massage therapy. Got full range of both shoulders back. It was very painful, but I'm so glad I stayed with it. Also, one of the biggest helps for me was swimming, and water exercises in the pool-86 degrees. It was kept my toes from curling up. There are gym clubs and Y that have pools for very little $$.
I hate the weight gain too. I had always been thin and very athletic. My daughter and I played tennis-5 days a week, water skiied, snow skiied, horse back riding. aerobics, dance classes. 10 K runs. I had a wonderful psychiatrist that helped me thru the losses.Also miss traveling a lot. But, I think it's like the earthquake, some lose their legs, but are happy to be alive and find other things to be grateful for. That helps in healing. I have several 'tools' that help during 'low' times. I Cry, too, but some of my tools are
music, scented candles, meditation, visualization, journaling,j comedy, sports games, sending cards to friends, keeping in touch with you dear friends, reading, e-mailing, stetching, massage, light exercising, do my nails, I'm on a high antioxidant diet, healthy chocolate. The cocoa bean is the #1 highest antioxidant in the world-the one I eat has a patented cold pressed method formula, thus not loosing nutritional value thru the cooking process like other chocolates. It also has the #2 highest antioxidant Acai Berry from the Amazon Forest. I know I won't be at peace with myself, till I loose that weight I gained from Neurotin and Lyrica. I really feel, I'll be able to cut down at least one of my high blood pressure meds, with weight loss.
So I'm working on healthy eating, exercise, and running a small business from my bed, healthy chocolate.
I wrote you last week by private message. I gave you a website with a lot of good information. Please don't loose hope, I know it's awful to deal with, but we aren't alone.
Last week, when I saw my RSD Dr., he told me about a RSD patient. There was a car accident here in Phoenix. Two cars collided on the freeway and hit a metal fence. One of the poles became a air missle and went thru the windshield of this ladies car. It took off her little finger and part of her arm and impaled her shoulder to the back of the seat. She had 18 surgeries. Her neurologist asked my neurologist if he would take her has his patient and do the HBOT series on her. She had frozen shoulder and couldn't raise her shoulder. After 9 treatments she was waiving to the TV crew. The tv crew came out and interviewed her and my Dr. I went thru 100 pt treatments to be able to get full use of my shoulder when it became frozen after breast surgery. plus 100 massagae therapy treatments.
The VA Hospital in Florida just put in 16 brand new HBOT for treatment of the wounded etc.
Take care of yourself, loretta with soft hugs

So nice to hear from you all!!!!

Momzpeachy... I worry about you and that you are so sad..as we can all relate and we sink to the bottom at times... Thats when all of our friends here jump on and pull you back to the top..cuz you need support and you need us..we are here fro you and know that we share you desperate sad feelings.....

I see myself in the future going thru the same reaction with the Ketamine as yourself...possibly, as I can not take anything due allergic/ bad tummy reactions..to everything... I mean everything..I am cold turkey RSD.. no drugs for help for my pain.. not even a patch as I can tak it off my skin due to the sensitivity of my skin....so I will take heed when my time comes..I am due to go to Dr. S in March...see we learn a bunch from each other here...

I agree about the relaxation techniques as I 've tryed it all..even acupuncture.. no luck there either but I do like my music and quiet..oh sure i have days I would like to cry.. (get this) I am not a cryer...I think I have only cryed, really cryed once since diagnosised 2+ yrs. ago... just can't do it! I am newly out of work (1+ months) due to my inability to physically do it anymore... I fought a galant fight to stay I will tell you....25 yrs. there but now .... my days are quiet... I slowly monuver thru my days here at home now..having my music in the background, light chores and talk with my friends here...still adjusting to my new routine...

Loretta, I am excited to see what your outcome from the HBOT treatment will be... My Dr. had encouraged me to do it also..but that very day at my apt. she placed a call to the hosp. where it is performed, she was told I am not a candidate due to the stage of my illness..too advanced.. so we have not explored that thought since..

To everyone here...we all need lifts and encouragement and advice from day to day..I know you have all made me feel better and educated and encouraged me...Time to lift momzpeachy and Kate up and many others as we can not let our RSD get the best of us..it would be easy to let it control us...but we are in control and it needs to stay that way...

Much love to all...

KS
keep smilin is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
loretta (01-17-2010), SandyS (01-17-2010)
Old 01-17-2010, 02:20 PM #15
kathy d kathy d is offline
Member
 
Join Date: Nov 2006
Posts: 327
15 yr Member
kathy d kathy d is offline
Member
 
Join Date: Nov 2006
Posts: 327
15 yr Member
Default

Dear Momzpeachy,
Wow, what is going on with your body? It is insane that you are having all these problems and Dr. S office isn't helping you in any way? I am a patient of Dr. S too and it sounds real odd that they even let you go home in the condition you were in. I think you need to call HIM and no one else about this and see what he says and then call your family doc for some relief. RSD is bad in itself but to have all the other problems you are having is too much for one person to handle.

I see you are in NE PA...so am I. I am in Levittown which is about 13 miles NE of Phully. Just curious. It is nice to know we are all so far away from each other but are really brothers and sisters in RSD. I hope you are feeling better. I just thought of maybe you could take Benadryl since you are having an allergic reaction to it all. Maybe it would calm things down a bit. Just a suggestion. I have the children's liquid so I can control it more. Maybe you could give yourself just a small bit and see how you react to it. Maybe it will make you sleep which would be a Godsend right now. I pray you will be better soon.
Best of luck,
kathy d
kathy d is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
loretta (01-17-2010), SandyS (01-17-2010)
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
Horrible night. :-( Hope15 Peripheral Neuropathy 21 05-18-2009 11:28 AM
does anyone have horrible nightmares angelrsd Reflex Sympathetic Dystrophy (RSD and CRPS) 20 02-17-2009 02:00 AM
horrible times mommy Depression 35 08-13-2007 11:29 PM
Feeling so horrible-Help! debbiehub Reflex Sympathetic Dystrophy (RSD and CRPS) 12 04-24-2007 06:10 PM
Horrible Nightmares Melanie C New Member Introductions 3 03-21-2007 01:18 PM


All times are GMT -5. The time now is 08:10 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.