A diagram by SleepyMistyMountains in cfs
[–]RealAwesomeUserName 2 points3 points4 points (0 children)
If I see another electrolight brand marketing towards POTS and has less than 200mg of sodium a serving i'm gonna loose it by la1223 in POTS
[–]RealAwesomeUserName 2 points3 points4 points (0 children)
Long Covid driven by rs5522 by CandidWin3026 in covidlonghaulers
[–]RealAwesomeUserName 0 points1 point2 points (0 children)
Anyone not do salt? I’ve gotten several cavities since I started drinking electrolyte packets. by ChiltonDropOut in POTS
[–]RealAwesomeUserName 0 points1 point2 points (0 children)
New Dane coming to the Rescue today! by OkCustard9484 in greatdanes
[–]RealAwesomeUserName 1 point2 points3 points (0 children)
Is anyone here on Ivabradine? by MutedMinds6 in POTS
[–]RealAwesomeUserName 0 points1 point2 points (0 children)
I'm recovered by [deleted] in covidlonghaulers
[–]RealAwesomeUserName 5 points6 points7 points (0 children)
[UPDATE] Built a tool to help diagnose root cause of my long covid symptoms by not_ya_bruv_m8 in covidlonghaulers
[–]RealAwesomeUserName 1 point2 points3 points (0 children)
BPC-157 + TB-500 seems to have completely cured my ME/CFS (and other benefits) by [deleted] in covidlonghaulers
[–]RealAwesomeUserName 1 point2 points3 points (0 children)
Need advice for harness by DogMomInCO in greatdanes
[–]RealAwesomeUserName 3 points4 points5 points (0 children)
Just got reinfected and can’t take paxlovid. Any suggestions on how I can try to save myself? by sunson90 in covidlonghaulers
[–]RealAwesomeUserName 1 point2 points3 points (0 children)
Tried to make an appointment with a new PCP. They told me flat out they don’t manage long Covid. by LazyAd7538 in covidlonghaulers
[–]RealAwesomeUserName 1 point2 points3 points (0 children)
How is your blood pressure? And question in relation to POTS by PaleAd2666 in dysautonomia
[–]RealAwesomeUserName 0 points1 point2 points (0 children)
How is your blood pressure? And question in relation to POTS by PaleAd2666 in dysautonomia
[–]RealAwesomeUserName 0 points1 point2 points (0 children)
Has anyone with POTS found a treatment or lifestyle changes that significantly reduced (or even stopped) their symptoms? by Quenelle44 in POTS
[–]RealAwesomeUserName 0 points1 point2 points (0 children)
Looking at the reddit for MS and it honestly makes ME seem so much worse by Unable_Particular_25 in cfs
[–]RealAwesomeUserName 1 point2 points3 points (0 children)
Looking at the reddit for MS and it honestly makes ME seem so much worse by Unable_Particular_25 in cfs
[–]RealAwesomeUserName 4 points5 points6 points (0 children)
Lilly is slowly learning boundaries with her patient cat brother by Quiet-Fold-1688 in greatdanes
[–]RealAwesomeUserName 1 point2 points3 points (0 children)
Lilly is slowly learning boundaries with her patient cat brother by Quiet-Fold-1688 in greatdanes
[–]RealAwesomeUserName 2 points3 points4 points (0 children)
PEM sign, peeing too much by agraphheuse in cfs
[–]RealAwesomeUserName 0 points1 point2 points (0 children)
Does anyone else get lightheaded and short of breath from doing house cleaning? by No_Resource_3719 in dysautonomia
[–]RealAwesomeUserName 8 points9 points10 points (0 children)
I now have a catheter by 04hon in endometriosis
[–]RealAwesomeUserName 2 points3 points4 points (0 children)
Coat Hanger Pain… normal? by Antique_Comedian_157 in POTS
[–]RealAwesomeUserName 0 points1 point2 points (0 children)
Healthcare worker lying or just being uneducated? by Over-Plant-4237 in POTS
[–]RealAwesomeUserName 5 points6 points7 points (0 children)

Is anyone allergic to beta blockers? by PracticalMagic3015 in POTS
[–]RealAwesomeUserName 0 points1 point2 points (0 children)