Comments on: pain medication used by persons suffering from reflex sympathetic dystrophy

By: Oxymoumma

Oxymoumma — Wed, 08 Feb 2012 06:34:01 +0000

adobe fangsong std r

аудиокнигу код да винчи

бланк справки 027 у

sony ericsson w880i прошивку

хайнлайн тоннель в небе

игры для 5800 торрент

алмазная колесница том 2

paul oakenfold виктор цой

пикник фотошоп на русском

смысловые галлюцинации большие планы

патч v29 для кс

By: angela

angela — Fri, 03 Jun 2011 05:19:58 +0000

my name is angela, I live in oklahoma city. I’m 33yrs. I just found out I have rsd, 3 months ago.
I have looked all the over the internet for a rsd doctor in oklahoma city that could help me, and i can’t find one. If theres anyone out there that could help me, i would be so grateful. Im in terrible pain.Also, if there is anyone that could help teach me more on this diease. please reply. I’m very scared. thanks, angela

By: angela

angela — Fri, 03 Jun 2011 05:19:55 +0000

By: Amanda

Amanda — Sat, 01 Jan 2011 23:37:56 +0000

Hi, well I was just diagnosed qith RSD from my doctor, I broke my foot six months ago, finally had surgery a month ago and now I;m in more pain than I was before. My foot is reddish blue looking, It’s swollen to no belief, Icannot move my big toe at all and when you touch it it hurts like no end. I hane statred to develop blotches on my skin. My foot sweats and i have a lot of muscle tremors that actually affect my whole leg. It hurts to even put a sock on. I;m 24 years old and this is the worst news that I have recieved. I have seen what RSD can do to people and I dont want to end up like them. Right now Im taking lyrica and a NSAID, and Norco 10mg, waiting to see the pain management and nero doctor. I just got diagnosed but I think this has been going on awhile. I’m 24 been out of work since June and all I want to do is go back to work. I have a 1 year old son that my husband has taken off work for my surgery to take care of him for me. I have been misserable and seem to get no relief yet. Im afraid to get hooked on pain meds so very afraid of going to the pain doctor but I need some type of relief. Any type of information someone can give me is great. I read the study and it was very informing.

By: Sheri

Sheri — Tue, 20 Jul 2010 03:30:05 +0000

I have had RSD for 4yrs. I am having a really hard time right now. I had foot surgery on my RSD limb, which caused a flair, then ended up with 2 large blood clots in my lungs. I currently am not on any meds for my RSD because nothing was working. The last thing I did was ketamine infusions and only one worked. I am in physio now and she wants my doc to send me back to the pain clinic because I am suffering to much. It has taken over my whole body now. I don’t know what to do. The meds only made be gain weight and everything else only works for a small amount of time and then stops working. Any suggestions would be great!

By: isabella mori

isabella mori — Fri, 04 Jun 2010 03:00:42 +0000

hi steve, actually, all you need to do is read the article. if you still have questions after this, let me know. please also keep in mind that this study is now quite a few years old.

By: steve wilson

steve wilson — Thu, 03 Jun 2010 12:28:56 +0000

yes i have r sd i have had it a little over 2yrs now and i need to know this i have been on so many pain meds to help me with this and i would like to know as far as the pain meds what did most people have the best luck with i hope you can send me the info on this and any other info or sites or groups i could go to the meds i take now are hydro 10/325 for break thru methadone 10 mg i take 10 of those a day lexapro for sleep and it does no good before i gut hurt i was on zanex and i have ask my doc to put me back on that but he says you cant take zanex with methadone but i cant find any where it says that i aslo have talk to the drug store and ask them about it and they also say they have never heard you could not take it so any info you could help me with would be great

thank. you
steve

By: Linda

Linda — Fri, 07 May 2010 21:50:04 +0000

I’ve had RSD for 12 yrs. Have had the injections into the joint, stellate blocks, Physical therapy,
Spinal cord stimulator. The doctor that put in the stimulator told me that RSD doesn’t spread UP from the hand to the area of the shoulder and neck, although that was my complaint when
I initially saw him. Now that we have found that
the stimulator isn’t going to work in the fingertips as hoped, I’m became more and more depressed. For the last 2 years I seldom got out out of bed, brushed my teeth, showered, let alone, got out out of the house, OBVIOUSLY.
I could not sleep, when I did, I had terrible nightmares. Considering suicide was the last straw. I knew that it was now or never. I had to change Dr’s because I had to go on Medicaid disability until my Social Security goes through.
My previous doctor was very supportive and understood that I wasn’t looking for strong narcotics. This new one has farmed me out to a physiatrist and a pain management doctor for medication. The pain management doctor that I was referred to initially 3 mo ago has never called me, and her office won’t contact them. She referred me to another doctor, who was very
nice, but doesn’t prescribe medication, but would revise the stimulator surgery and do it they way I thought it should be in the first place, with 2 leads and not in the thin area of my shoulder where I was already having pain. My newer family doctor did eventually give me 2 prescriptions, 1 for a muscle relaxor and migraine medication called to the pharmacy to the tune of about $550.00—how do you think Medicaid would like that when generic would be just as good? She finally gave in and let me pick up a script as long as I has photo ID enough for 2 weeks, knowing that I still did not have a pain management physician. I finally asked–am I suppose to find one myself that will prescribe medications? Yes, because this doctor is not going to give you narcotics!
P.S. I had my records from my previous doctor
with me on my very 1st visit which consisted of a letter to the Medicaid disability department,
the form he completed for them, his office notes, and his medication list for me. Two (2)
staff members refused to take them, stating, give to the back office. I even told the doctor. No response. I called today to change doctors and the ISMA and Family and Social Services has a letter going to them. She thought it was all about being a drug seeker. NO! It was about someone who is in pain, has been in pain and suffering from depression because of it. She should be ashamed and embarassed to treat anyone this way.

By: pool table dimensions

pool table dimensions — Fri, 15 Jan 2010 05:33:11 +0000

The prognosis for CRPS varies from person to person. Spontaneous remission from symptoms occurs in certain individuals. Others can have unremitting pain and crippling, irreversible changes in spite of treatment.

By: isabella mori

isabella mori — Thu, 03 Sep 2009 05:20:40 +0000

hi natalia – have you been to this site? http://www.rsdalert.co.uk/help-groups/help-groups.htm