POTS is more than just fainting from standing up. Not to mention, some people with POTS faint and some people with POTS don’t faint. #PotSyndrome #PotsSymptoms #Dysautonomia
In honor of Ehlers Danlos Syndrome and Hypermobility Spectrum Disorder, here are a few signs that you may have hypermobile Ehlers Danlos Syndrome or Hypermobility Spectrum Disorder. #Hypermobile #HypermobileEhlersDanlosSyndrome #HypermobilitySpectrumDisorder
Replying to @Jes Land it’s incredibly painful. It doesn’t look like much, but it feels like all my bones are being broken. #Dystonia #Hypermobile #HypermobileEhlersDanlosSyndrome
Replying to @StabbyRoomba I hope this helps! You might want to google more images. #PiezogenicPapules #HypermobileEhlersDanlosSyndrome #ConnectiveTissueDisorder
I wish google would have told me that. If you experience a thunderclap headache, get seen right away, or at least within 72 hours. The spinal tap was ultimately my choice, btw. Don’t worry, no one is going to force a spinal tap on you. #ThunderClapHeadache #SubarachnoidHemorrhage #SpinalTap
Replying to @kariemartinez535 here are a few vocal cord issues that hypermobile people tend to deal with. #VocalCordDysfunction #Hypermobile #EhlersDanlosSyndrome
If you have arachnodactyly, I recommend checking in with a geneticist and a cardiologist. #Arachnodactyly #PositiveThumbSign #ConnectiveTissueDisorder #greenscreen
Just to be clear, NOTHING I said is true about Hypermobile Ehlers Danlos Syndrome. 👏 #HypermobileEhlersDanlosSyndrome #MedicalGaslighting #ConnectiveTissueDisorder
Who wants to see more things and places that people with POTS should avoid or at least proceed with caution? There are many more things. 😭 #PotSyndrome #PotsTriggers #Dysautonomia