Central Sensitization - please share your stories
Hello everyone
I would like to better understand this diagnosis from personal experiences and compare what I feel to others accounts. I have not been diagnosed with central sensitization however, it seems to line up. Thank you very much and I look forward to reading your stories.
Rachel
Interested in more discussions like this? Go to the Chronic Pain Support Group.
Hi Roger, You'll notice that I moved your message to this discussion where members are talking about Central Sensitization Syndrome.
To learn more about the use of mindful meditation techniques at Mayo's Pain Rehab Program, I'd like to also invite @rwinney @iriahmak @goldleaf @healingone @menville @kelseylmontague and @legalese1972 into the discussion. While you wait to hear more, you can read more about their experiences in this discussion:
- Has anyone been diagnosed with Central Sensitization? https://connect.mayoclinic.org/discussion/has-anyone-been-diagnosed-with-central-sensitization-if-so-id-like-to/
Thanks Colleen, for initiating the meditation discussion as it relates to Mayo's PRP.
@skier That would be a big YES! PRC teaches a multitude of coping mechanisms from learning how to properly breathe and relax through bio feedback sessions, imagery, daily morning stretches, therapeutic physical therapy and cardio sessions on a recumbent bike to promote safe physical activity and produce endorphins naturally to the brain. Occupational therapy sessions teach you how to work smarter, not harder with your body. Nutrition is covered as to understand the foods that help, not provoke CSS. Last but not least, Cognitive Behavioral Therapy. I can not say enough about these daily sessions. They were most helpful to explore self care, acceptance, anger, depression, dependency, anxiety, stress management/reducers, difficult day planning, scheduling, problem solving, habits and behaviors. And of course the scientific and medical teachings of central sensitization and chronic pain, by Dr. Sletten, was invaluable.
Thanks Rachel for your detailed comments about the program, very informative. I'm trying to get accepted for the PRP.
Does one have to be diagnosed as having CSS before being admitted into the program?
thanks again.
Roger (@skier)
@skier Yes, you do need to be diagnosed in order to be accepted. Mayo will require your medical records for review first. The next step is being interviewed. My interviews were via Zoom with Mayo's medical Dr and Dr. Sletten.
Rachel, thanks for the immediate rely. My primary physician is in the process of submitting my referral. I'm assuming sending my medical records is part of the first step. I'll be attending the Rochester Mayo, if accepted.
thanks,
@skier
Hello @dk007 and @cldmeyers how have you each been doing? It's been a while since we've spoke.
@dk21 How have you been working on accepting your diagnosis of Fibromyalgia and chronic fatigue syndrome? What are you doing to calm your body and your mind?
@cldmeyers Are you still able to walk every other day? What new techniques are you using to deal with your chronic pain syndrome?
I graduated Mayo Pain Rehab Center (PRC) last year and have come to accept my central sensitization chronic pain.. I mourned the loss of my A life (ready and able to do anything), said good riddance to my B life (non-accepting, searching, unstable), and welcomed my C Life (stable, moderate, flexible).
I look forward to hearing from you and hope you are living your best possible C Life.
These researchers are phenomenal. Rachel Zoffness is a pain educator whose book, The Chronic Pain Workbook, was just released and is excellent. A good portion can be read online. Unfortunately, so many doctors take this information and think it means the pain is in their patients' heads. I found it on my own and started doing "movement snacks" and worked my way up to full exercise and activity. My pain was chronic migraine and thoracic back pain. Neurogists had told me once chronis, it's permanent.
I've had fibromyalgia symptoms since childhood, and I'm now 74. Throughout my life I've researched everything on the topic (even before the internet!). I participated in Kaiser's pain management program 12 years ago, and I'm grateful for all the tools it gave me which I continue to use to this day. There is no panacea, but there is life with chronic pain. My challenges are myofascial pain syndrome (thoracic) as well as occiptal neuralgia and depression. In addition to all the conventional medical treatments, I use alternative treatments such as massage, chiropractic,etc. Most recently I've added a spiritual component to my life. It has all come together for me to a place where I can live my life in peace and acceptance - and even share what I've learned with others; i.e., my recent publication called More Than Tender Points: A Fibromyalgia Memoir (available on Amazon). There is life after diagnosis. It may not be the exact life we would have chosen, but we can learn to make that life the best it can be.
I was diagnosed with Central Sensitization a month or so ago by pain medicine. Went to my rheumatologist yesterday and he does not agree thinks the pain is from my connective tissue disease, ehlers danlos syndrome, prior joint replacements and severe Raynauds. Not sure what to do…keep my next appointment with pain medicine?