Mayo Clinic Connect
Has anyone been diagnosed with Central Sensitization? If so I’d like to discuss.
Liked by Leonard Holloway
@keri and @tiredofpain have spoken about being diagnosed with Central Sensitization a while back. Hopefully they’ll join this discussion to share with you @leh09.
I have not been officially diagnosed with “central sensitization” but I
know I have it. I have fibromyalgia and with FM, something happens in the
central nervous system so that a person with this condition feels a lot of
pain from a stimuli wherast a “normal” person will feel little or not pain.
We are cursed!!
Liked by Colleen Young, Connect Director, lolomarie, peggyj4411
I’m also assuming that central sensitization is FM, very nasty to us as you noted. As many ” treatments” as symptoms LOL. A sense of humor is not enough for this level of pain, though, and sometimes you really don’t know how you will make it through the day. There are a lot us dealing with this.
Liked by peggyj4411
Is it definitive that Central Sensitization is indeed Fibromyalgia?
@want2bme, I moved your message to this discussion where you’ll meet @capefibro, @lolomarie and @leh09 who are talking about Central Sensitization and Fibromyalgia.
See the last paragraph of “What is Central Sensitization?” in this article http://www.instituteforchronicpain.org/understanding-chronic-pain/what-is-chronic-pain/central-sensitization
“Central sensitization has long been recognized as a possible consequence of stroke and spinal cord injury. However, it has become increasingly clear that it plays a role in many different chronic pain disorders. It can occur with chronic low back pain, chronic neck pain , whiplash injuries, chronic tension headaches, migraine headaches, rheumatoid arthritis, osteoarthritis of the knee, endometriosis, injuries sustained in a motor vehicle accident, and after surgeries. Fibromyalgia, irritable bowel syndrome, and chronic fatigue syndrome, all seem to have the common denominator of central sensitization as well.”
Liked by lolomarie, peggyj4411, aharvey523
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As Colleen’s article noted, there are a number of disorders which have central sensitization as a hallmark symptom, with FM being one. I like the article suggesting that “mild aerobic exercise” lowers central sensitization pain. There is no “mild” aerobic exercise, it’s either aerobic ( very difficult, especially for us) or not aerobic. My pain management specialist, who recently fired me and said, essentially, suck up the day-to-day pain and do aerobic exercise for an hour each day, was clueless. I sent her a nasty letter and copied it to the chief medical officer at the hospital. It’s very unfortunate that my FM pain got much worse the last three years as the “opioid crisis” caused doctors to throw people in real pain under the bus. This is a difficult time to have chronic pain in America.
Liked by peggyj4411, jmd86
I was diagnosed with it in 2012 by the May Clinic in Jacksonville.
JadiAnn, welcome to Connect.
Can you tell us a bit more about yourself? What led to your diagnosis? How are you coping today?
Yes, I was diagnosed about 6 years ago.
I went through Mayo’s Pain Rehab Clinic and was a little better for a short time. It was there that I learned of Central Sensitization. I’ve had progressive symptoms over the past 5 years. It’s reached a point where the fatigue is so profound that I have trouble getting up the energy to do much of anything. And the pain…..some days I can control the pain…..most days I cannot. I take pain medication but am developing a tolerance. How do you cope?
The one thing I remember Dr Malovat saying to me, was “don’t give in to the pain, and do something for your self and your family every day.” It can be as simple as showering and putting on make up, or making my husbands lunch for work ( no matter how small). I know the pain and fatigue is so bad still some days, that I wish it would just kill me, but then I remember that there are easier days of pain if I can just get through this one day. I did develope a dependency for the meds. I came off ALL of them and went to all non narcotic meds and feel SO MUCH better. I take Tramadol for pain, with Lyrica, and an anti depressant, and Trazadone for sleep. I really do feel better than I did when I was first diagnosed.
Well, I sure can understand what you both are talking about pain as my fibro just gets worse despite acupuncture, Tramadol, etc. I like the idea of doing something for yourself or your family every day. A personal trainer friends says start the day with a win. The pain is pretty awful, though, and unless you have, you don’t really understand it or the psychological effects to.
Liked by jmd86
Yes, I was diagnosed with Central Sensitization this month at Mayo. Last year diagnosed with Burning Mouth syndrome and candida of the mouth and esophagus. It’s miserable and I fight taking gabapentin and search for any answers as to what makes with better, foods that could make it works, anything natural I can do to keep from taking gabapentin due to the side effects involved. Any suggestions?
Have you found anything that helps?
Once again, asking if anyone has been diagnosed with burning mouth syndrome or central sensitization? Looking for any natural alternatives that have helped.
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