My POTS story // How I was diagnosed & underlying conditions

Before being diagnosed with POTS (Postural Orthostatic Tachycardia Syndrome) in 2016, I was an avid rock climber. It only took about 3 months to be diagnosed, but for many it takes MUCH longer. Living with chronic illness required many life changes for me and continues to be a challenge every day. I want to do everything I can to help others that are suffering.

POTS is a form of dysautonomia that leaves about 25% of patients so debilitated that they are unable to work or go to school. Though it isn't rare, many doctors are unaware of the condition. I made this video for Dysautonomia Awareness Month (which is October, sorry for posting late) in hopes of spreading awareness.

Some other chronic illnesses I have are: Ehlers-Danlos Syndrome (hEDS), Idiopathic Intracranial Hypertension (IIH), Chiari Malformation, Craniocervical Instability, Celiac Disease, TMJD , Chronic Mono, and UARS.

If you feel may have an underlying condition, please advocate for yourself by doing your own research & finding the right doctors. It's been over 2 years since diagnosis for me, and I am still being evaluated for comorbid conditions.

Don't give up hope!

My blog → https://gonetopots.com
My instagram → https://www.instagram.com/gonnetopots/
My facebook page → https://www.facebook.com/gonetopots.rachael
My twitter → https://twitter.com/gone_to_pots

#PosturalOrthostaticTachycardiaSyndrome #POTS #ChronicIllness

Видео My POTS story // How I was diagnosed & underlying conditions канала Rachael Elizabeth