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This section is a place to share stories about Living with RSD
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My RSD in remission
by: dantesnana
on Wed, Sep 19 2007
I had RSD. It started in 1993 after a flu shot. Instead of being localized in one area, it started in my feet and spread over my entire body. Every nerve burned and stung, hummed and vibrated. I developed brain fog, fasciculations, waves of feeling desperately ill, sensations of weakness, ear buzzing, jolts of pain like lightening bolts, etc. I was miserable. I could hardly function. I lived like this for a long time, with no diagnosis, no treatment, no hope of recovery.
Without going into detail, I will just say that I was blessed to find a doctor who successfully treats RSD with a machine he designed. And he put my RSD into remission. His treatment uses electrodes to provide electro-magentic stimulation to the sympathetic nervous system. This doctor is ahead of his time. Since I live in his home town, I have spent lots of time at his clinic. I have known him since 2001 and have seen patients streaming through his clinic, getting better, most becoming pain free. The majority of his patients come to him after years of failed therapies, but he still is able to help them when other doctors have made them worse, not better.
These patients come in wheel chairs, on morphine pumps, with failed nerve blocks,
some so mutilated from previous failed therapies that I don’t know how they have managed to stay alive through it all. He still helps them.
His goal is to make his patients pain free. Most of them achieve that status eventually. It takes time.
There is hope. There is remission. I have experienced it myself. I have witnessed it in many, many patients of this doctor, who is a pioneer. He himself had RSD and treated himself with his machine. He has lived pain free ever since.
I don’t know if this forum allows me to give you contact information for this doctor, so I will not do so at this time.
I just wanted everyone to know that a pioneering doctor has developed a treatment that works, so hope abounds.
Comment on this
Comments
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Wed, Nov 07 2007
Could you please email me the doctor's name? I have had RSD for 18 years and would like some relief.
[moderator note: e-mail address has been removed...Read
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Sat, Sep 22 2007
i think i went to the same doctor as you... iss he located in TExas? i use his machine the Rhodestim. please write to me. i dont know any other people...Read
September 2007
- 2 years with RSD - by Lori - (Tue, Sep 25 2007)
Its been 2 years since I was diagnosed with RSD and the only thing that has changed is the size of my leg. I broke my ankle and within weeks the leg swelled to twice its size, the coloring changed and it burned like someone set me on fire. I have a hard time wearing shoes, walking distances and steps.
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- Left Hospital with RSD - by Lori - (Tue, Sep 25 2007)
I went into the local hospital for a kidney infection and 8 days later I went home with RSD. The nurse had placed the IV incorrectly and I had a reaction to an antibiotic that caused clotting in my right arm, then RSD set in. It has now been 2.5 yrs and it has only temporarily improved with nerve blocks and vicodin.
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- rsd and spinal cord stimulator - by ML - (Mon, Sep 24 2007)
I would like to know if anyone has used a spinal cord stimulator and if it helped. I have had RSD for four years - it is now whole body RSD and the doctors now want to implant the stimulator after numerous failed blocks and too many drugs and too much pain.
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- Life with RSD - by claudna - (Fri, Sep 21 2007)
i was diagnose in 2000, and nerve bblocks surgery to relief stress on the nerves and every tape of pills their is. I was hit on my left hand by a burglar bar at work from a student.
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- I’m 15 yrs old and have RSD - by Amber - (Thu, Sep 20 2007)
My name is Amber. I am 15 years old and have RSD. I first got RSD when i was 2 years old. But I was finally diagnosed when i was 12. I have had a lot of compications with RSD. But any doctors I have gone to have been unable to treat me.
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- The doctors act like it magically disappeared! - by BB - (Wed, Sep 19 2007)
Seven years ago I had an achillies tendon repair and suffered horribly afterward. I developed RSD in that foot/leg and it spread to the other leg/foot also.
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- My RSD in remission - by dantesnana - (Wed, Sep 19 2007)
I had RSD. It started in 1993 after a flu shot. Instead of being localized in one area, it started in my feet and spread over my entire body. Every nerve burned and stung, hummed and vibrated.
[more..]
- My experience with RSD - by Jenna - (Fri, Sep 14 2007)
I was 9 years old when I was getting ready for a basketball game and I was coming down the stairs and tripped and fell. I had a weird pain in my right ancle and it hurt to move it. I was taken by my mother to the hospital to get some x-rays to make sure that I didn’t break anything… nothing came back on the x-ray and they simply told me that I spraned it and it would be fine in a couple of days armed with a pair of crutches I left.
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- My Story, My Journey with RSD - by Debbie - (Fri, Sep 14 2007)
I could have never imagined that a fall I took on a stairwell so many years ago that finally led to surgery for my shoulder to help 1) with the instability n the shoulder to help stop the ongoing pain I was having would turn into a lifelong journey of dealing with pain.
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- The pain is MOVING - by Kelly - (Thu, Sep 13 2007)
I hurt my left elbow at work in 1997. After my second surgery in 1999 my O.T. questioned my doctor if I had R.S.D. it hurt his feelings and he did nothing for MONTHS. I lost my marriage, my child is pulling away from me.
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- where do i try now? - by Linda - (Wed, Sep 12 2007)
In Oct 2006 I had knee surgery..the knee felt great for a few weeks after the surgery. Then the pain started again, couldn’t go up any stairs without practically screaming. They drained fluid off the knee did xrays and said everything was good. Several weeks later my right hand swelled up and was so painfull i knew something wasn’t right.
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- RSD Has Changed My Life - by DonnaM - (Wed, Sep 12 2007)
I fell and broke my pinkie finger on my dominant hand in early May 2006.
I can’t remember feeling pain that intensely before in my life.
My experience at the emergency room hurt almost as bad as my hand did. I was treated like I was some sort of “cry baby”, or “whiner”.
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- My Story - by Michael - (Tue, Sep 11 2007)
I contracted RSD in June 1989 after left knee arthroscopic surgery. The severe burning pain that I awoke with after the surgery was unbearable. After many months, appointments, tests, and procedures, I was diagnosed. I presently am on my third implanted morphine pump, and take a large amount of oral medications.
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- Yet to be undiagnosed RSD - by Diane - (Tue, Sep 11 2007)
In 2004,I has an accident involving my right arm, for several months I had every symptom from the pain, bluish olor, hot/cold feeling to my right hand.
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- Living with it - by Colleen - (Fri, Sep 07 2007)
I fell and broke my right wrist.I was diagnosed shortly after the cast came off. I have a lot of faith in Dr S. in Phila. He wanted me to go to Germany to be put into a coma for a week.
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- I have RSD & Need advice! - by Michele - (Thu, Sep 06 2007)
In 2005, I fell in a restaurant on wet cobblestone flooring, breaking both sides of my ankle. I was a temp & had no insurance at the time, and ER would not do surgery! They wrapped me up and sent me home.
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- HOPE FOR RSD SUFFERERS - by LT - (Wed, Sep 05 2007)
I too have had RSD since I was 24. I still have it today and I am 28 but I barely notice it. I can walk, not limp and I am not bed ridden anymore. After being mis diagnosed I learned I had to be my own doctor, and demand the BEST care.
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- Torturous nightmare - by BJ - (Mon, Sep 03 2007)
My RSD started after i fractured my left ankle Feb 1996, nerve blocks ,sympathectomies and suppressive, sedative debilitating drugs and nothing works, 1999 started work in wheelchair, 2005 pain increases, 2007 to dangerous to drive anymore,
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- The Pain is Real - by EW - (Mon, Sep 03 2007)
I suffered a major trauma to my left foot in December 2006. I had an x-ray and and I&D immediately after the injury. The pain was unbearable for 6 weeks afterwards. MRI’s and Ultrasounds were inconclusive.
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