Diagnosed with thoracic myelopathy, no relief in sight
I am going on 20 months with thoracic myelopathy (diagnosed at the Mayo Clinic) with no relief in sight.
Extreme numbness from toes-feet-legs, knees, thighs, hips, pelvis, buttocks, lower back is 24/7. There is no pain with this condition, only the constant numbness/tingling/lower extremities stiffness with spasms-twitching in my right leg while sitting for long periods of time.
I have been a life-long runner, but that had to stop when this condition reared its ugly head. Inflammation is visible in ankles and knees, accounting for the stiffness and reduced mobility when walking and exercising and standing or sitting for long periods of time.
My balance continues to be off, with a sometimes unsteady gait. These symptoms continue to get worse. Mayo Clinic cannot find the source of the spinal lesion nor can they - up to this point- find a solution to the problem, or even a way to minimize or slow the progression of the disease.
Six month regimen of Intraveneous and oral prednisone plus a few other meds did nothing to abate the symptoms. The side effects of these meds were terrible and not worth the risk to continue.
I have had dozens of blood workups and tests, two spinal taps, an artery angiogram, and scans and imaging that are now into the double digit count. I have been med-free since February, but my symptoms have slowly progressed.
I turned 70 in February, and I thought it might be time to change directions with a different approach. Dr. Flanagan (Mayo neurology) and I agreed to forego more testing for the time being and try a more homeopathic agenda, which I have done since February: CBD oil/CBD inflammation cream, myofascial release, water aerobics, chair yoga, mindfulness/meditation, turmeric/anti-inflammatory supplements, compression stockings, hot/cold packs.
Unfortunately, these yielded no positive results.
Throughout all of this, I have been faithful to my daily exercise routine of 20 minute stretching/strengthening lower extremities and 30-40 minute aerobic exercise (treadmill, bike, walking, hiking w/trekking poles). I have to push myself more now than ever before, and I feel extremely tired and weak after these sessions rather than invigorated or attaining that feeling of well being ("runners high").
I feel I am now at a crossroads. I am scheduled for another round of tests next week followed by a visit with Dr. Flanagan with the hope of coming up with yet another health care plan for this diagnosis.
Honestly, this scenerio is getting more difficult to endure without some hope that Mayo will "help me find the answers." Any feedback would be greatly appreciated. Thanks for listening.
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Sounds like another unintentional "anti-feminist" & "agism" treatment to me.
I have two friends in their 80s. They have been diagnosed with breast cancer. I took my self off for a mamogram after hearing about them. I discovered that the rate of cancer goes up as you age. Yet they tell you to stop having mamograms after a "certain age." Why? Is it because they think you are going to die anyway?
Going through cancer treatments is not funny. Living with cancer when you could have done something about it is even worse.
Im 70 and getting biopsies for calcifications new after three years??
Vic
My mammogram in December ‘24 showed calcifications, but I’ve received nothing from my GYN about it. And not sure she shared this and my bone density scans, I better drop off the reports to my primary doctor. I’m being tested for cervical and lower left lumbar pain, it seems like I’m on an endless hamster wheel trying to find the reasons behind my pain and neuropathy. I’m 73, feels like my age is used as the reason for it.