Dorado
Beloved Grand Eagle
I’ll give you both a personal example. I have hypermobile Ehlers-Danlos, a structural disorder I've had since birth. The majority of my pain and other symptoms stem from autonomic dysfunction (often said to be the mechanism behind TMS). You know what hypermobile Ehlers-Danlos is notorious for?
Causing severe autonomic dysfunction, including postural orthostatic tachycardia syndrome (POTS), orthostatic intolerance, Raynaud’s, etc. Some Ehlers-Danlos patients are completely bedridden and disabled.
I could just as easily blame my sympathetic overactivity on my Ehlers-Danlos. And lots of other symptoms I’ve dealt with since childhood. The symptoms are absolutely endless: https://www.google.com/amp/s/www.pinterest.com/amp/pin/561331541026445694/?source=images (Ehlers-Danlos Syndrome)
In fact, some doctors and fellow patients have told me just as much. I know how it feels to stand up and have my heart rate increase so much, I start blacking out. I’m all too familiar with adrenaline surges that wake me up throughout the night. I could go on and on and on, literally.
But saying Ehlers-Danlos is 100% responsible wouldn’t explain why my pain went from me not being able to type on a computer or pet my cat without excruciating pain (I’m the one who was applying for assisted suicide because I was so miserable), to me rarely having any pain at all. Or why my heart rate has significantly gone down, whether I’m resting or walking. Or why my autonomic nervous system went from not being able to tolerate certain chemicals at all, to me (responsibly!) enjoying both again. The truth is that stress is behind the severity and majority of my symptoms. To hell with Ehlers-Danlos. Sure, my jaw loves to pop out when I chew or sneeze or yawn. But I am back in charge.
Your attitude is everything. We just had a discussion about Parkinson’s patients being able to increase their dopamine with a placebo or stop hand tremors through meditation.
If we can do it, so can you. And again, all of these posts are TMSing.
Causing severe autonomic dysfunction, including postural orthostatic tachycardia syndrome (POTS), orthostatic intolerance, Raynaud’s, etc. Some Ehlers-Danlos patients are completely bedridden and disabled.
I could just as easily blame my sympathetic overactivity on my Ehlers-Danlos. And lots of other symptoms I’ve dealt with since childhood. The symptoms are absolutely endless: https://www.google.com/amp/s/www.pinterest.com/amp/pin/561331541026445694/?source=images (Ehlers-Danlos Syndrome)
In fact, some doctors and fellow patients have told me just as much. I know how it feels to stand up and have my heart rate increase so much, I start blacking out. I’m all too familiar with adrenaline surges that wake me up throughout the night. I could go on and on and on, literally.
But saying Ehlers-Danlos is 100% responsible wouldn’t explain why my pain went from me not being able to type on a computer or pet my cat without excruciating pain (I’m the one who was applying for assisted suicide because I was so miserable), to me rarely having any pain at all. Or why my heart rate has significantly gone down, whether I’m resting or walking. Or why my autonomic nervous system went from not being able to tolerate certain chemicals at all, to me (responsibly!) enjoying both again. The truth is that stress is behind the severity and majority of my symptoms. To hell with Ehlers-Danlos. Sure, my jaw loves to pop out when I chew or sneeze or yawn. But I am back in charge.
Your attitude is everything. We just had a discussion about Parkinson’s patients being able to increase their dopamine with a placebo or stop hand tremors through meditation.
If we can do it, so can you. And again, all of these posts are TMSing.
Last edited by a moderator: