ahri11
Peer Supporter
Overall, half way through and doing well...my journal is filling up and my punching bag has been getting regular beatings!
Jan, if you are reading this, thank you for recommending on another thread, Nicole's recent video on nerve pain. It was a perfect introduction to her work and she's yet another fantastic resource of support and guidance. What is it about TMS folk?! you are ALL such wonderful humans!
The reason I am writing today...I am deep down in the emotional muck and it's fertile soil for sure!
Today I am exhausted. The intense nerve pain at my solar plexus, just under my ribs(anyone else?!), comes mostly at night (pretty steadily for the last 8 years), when I lay down, and it's tending to stay all night long lately. I have a growing list of evidence for it being TMS but without the ability to actually get a diagnosis to have nerve damage/pinching?? ruled out it is feeling like a battle of wills with my rascally brain. These long nights are wearing me down. Somatic tracking, journalling etc; my tools box is growing...I am just not sure how to move beyond not having a structural cause ruled out; I do have significant congenital thoracic spinal abnormalities and my brain uses that to the max...especially at 4am!
I keep reading and hearing "in order to be diagnosed with TMS, physical causes of the pain must be ruled out." But from who, where?! Doctors have been zero help. Specialists(good luck getting into one before next year!) could easily point to structural causes. And of course they would!
I imagine there are many many here that go without that "ruling out" simply because of the lack of doctors who understand? Does anyone have experience/insight to share about how they found their way through the weeds of not actually having a TMS diagnosis? I could just use a little help atm...feeling rather alone and overwhelmed with both the intensified emotions and pain in the long dark nights. Thanks
Jan, if you are reading this, thank you for recommending on another thread, Nicole's recent video on nerve pain. It was a perfect introduction to her work and she's yet another fantastic resource of support and guidance. What is it about TMS folk?! you are ALL such wonderful humans!
The reason I am writing today...I am deep down in the emotional muck and it's fertile soil for sure!
Today I am exhausted. The intense nerve pain at my solar plexus, just under my ribs(anyone else?!), comes mostly at night (pretty steadily for the last 8 years), when I lay down, and it's tending to stay all night long lately. I have a growing list of evidence for it being TMS but without the ability to actually get a diagnosis to have nerve damage/pinching?? ruled out it is feeling like a battle of wills with my rascally brain. These long nights are wearing me down. Somatic tracking, journalling etc; my tools box is growing...I am just not sure how to move beyond not having a structural cause ruled out; I do have significant congenital thoracic spinal abnormalities and my brain uses that to the max...especially at 4am!
I keep reading and hearing "in order to be diagnosed with TMS, physical causes of the pain must be ruled out." But from who, where?! Doctors have been zero help. Specialists(good luck getting into one before next year!) could easily point to structural causes. And of course they would!
I imagine there are many many here that go without that "ruling out" simply because of the lack of doctors who understand? Does anyone have experience/insight to share about how they found their way through the weeds of not actually having a TMS diagnosis? I could just use a little help atm...feeling rather alone and overwhelmed with both the intensified emotions and pain in the long dark nights. Thanks