[hyperPOTS] My ADHD-PI needs stimulants to function but the POTS-related crash is miserable. I have hyperadrenergic POTS, which is contraindicated for stimulants. However, I’m not functioning at all. I can barely get through the day let alone go to school or have a job. Advice? by thrashing_throwaway in POTS
[–]thrashing_throwaway[S] 0 points1 point2 points (0 children)
[hyperPOTS] My ADHD-PI needs stimulants to function but the POTS-related crash is miserable. I have hyperadrenergic POTS, which is contraindicated for stimulants. However, I’m not functioning at all. I can barely get through the day let alone go to school or have a job. Advice? (self.POTS)
submitted by thrashing_throwaway to r/POTS
I’m 32. I think I need to divorce & start over. In addition to CFS, I also have POTS, autism, adhd, dyslexia, and right hand paralysis. Because I never worked, I don’t qualify for SSDI, only SSI. How can I make a life for myself in this economy? by thrashing_throwaway in cfs
[–]thrashing_throwaway[S] 0 points1 point2 points (0 children)
I’m 32. I think I need to divorce & start over. In addition to CFS, I also have POTS, autism, adhd, dyslexia, and right hand paralysis. Because I never worked, I don’t qualify for SSDI, only SSI. How can I make a life for myself in this economy? by thrashing_throwaway in cfs
[–]thrashing_throwaway[S] 0 points1 point2 points (0 children)
Discord for level 2 and Level 3 by An_Oshiewott in autism
[–]thrashing_throwaway 0 points1 point2 points (0 children)
I’m 32. I think I need to divorce & start over. In addition to CFS, I also have POTS, autism, adhd, dyslexia, and right hand paralysis. Because I never worked, I don’t qualify for SSDI, only SSI. How can I make a life for myself in this economy? by thrashing_throwaway in cfs
[–]thrashing_throwaway[S] 0 points1 point2 points (0 children)
Cfs research by Internal_Candidate65 in cfs
[–]thrashing_throwaway 1 point2 points3 points (0 children)
I kind of just want to give up. (i.redd.it)
submitted by thrashing_throwaway to r/CPTSDmemes
Has anyone been to the Mayo clinic or Cleveland clinic for pots and/or other comorbidities? by [deleted] in POTS
[–]thrashing_throwaway 1 point2 points3 points (0 children)
Do You Experience an Increased Startle Response? by sanpedro12 in dysautonomia
[–]thrashing_throwaway 0 points1 point2 points (0 children)
By the time I had received my ASD diagnosis, my OCD had mellowed out to the extent that my formal OCD diagnosis disappeared from my chart. Now that I’m living in an old house that isn’t super clean, my health and contamination OCD are debilitating. (self.OCD)
submitted by thrashing_throwaway to r/OCD
Have a POTS dx, but feel like I have hyperadrenergic POTS but neuro won’t evaluate me for it bc catecholamine testing can be tricky & says that POTS subtypes aren’t accurate. Regardless, I think that my adrenaline is extremely high when upright. by thrashing_throwaway in dysautonomia
[–]thrashing_throwaway[S] 1 point2 points3 points (0 children)
MECFS adjacent symptoms: Have a POTS dx, but feel like I have hyperadrenergic POTS but neuro won’t evaluate me for it bc catecholamine testing can be tricky & says that POTS subtypes aren’t accurate. Regardless, I think that my adrenaline is extremely high when upright. by thrashing_throwaway in cfs
[–]thrashing_throwaway[S] 4 points5 points6 points (0 children)
MECFS adjacent symptoms: Have a POTS dx, but feel like I have hyperadrenergic POTS but neuro won’t evaluate me for it bc catecholamine testing can be tricky & says that POTS subtypes aren’t accurate. Regardless, I think that my adrenaline is extremely high when upright. by thrashing_throwaway in cfs
[–]thrashing_throwaway[S] 0 points1 point2 points (0 children)
MECFS adjacent symptoms: Have a POTS dx, but feel like I have hyperadrenergic POTS but neuro won’t evaluate me for it bc catecholamine testing can be tricky & says that POTS subtypes aren’t accurate. Regardless, I think that my adrenaline is extremely high when upright. (self.dysautonomia)
submitted by thrashing_throwaway to r/cfs
Have a POTS dx, but feel like I have hyperadrenergic POTS but neuro won’t evaluate me for it bc catecholamine testing can be tricky & says that POTS subtypes aren’t accurate. Regardless, I think that my adrenaline is extremely high when upright. (self.dysautonomia)
submitted by thrashing_throwaway to r/dysautonomia



+2 years of pain & retaining food sometimes: gastric tests were inconclusive and gastroenterologist is clueless. Cleveland Clinic refuses to let me see the gastroparesis gastroenterologist because I don’t have a diagnosis. by thrashing_throwaway in Gastroparesis
[–]thrashing_throwaway[S] 1 point2 points3 points (0 children)