Chronically Jenni
Spreading Awareness & Helping Others with EDS & POTS
Dysautonomia Awareness Month & Recent Vlogs
Dysautonomia Awareness Month may be over but Dysautonomia is something people have to live with every day of the year. I made a video last month with 4 other lovely ladies who were all brave enough to share their story about Living with POTS. Here’s the video to give you an insight into what it’s like to live with dysautonomia.
[youtube https://www.youtube.com/watch?v=mEdNKuozG0o]
I also haven’t kept you up to date with my vlogs since leaving uni so here you can find all the videos from the last month or so. It includes my vlog of the HMSA & EDS UK conference and what I learned from it and a video calling out for Questions for those who have been asking me to do a University with Chronic Illness video.
- Adventures with EDS : Uni Prep, Moving in & Mini Room Tour
- Adventures with EDS : First Week of Uni
- EDS UK & HMSA Conference – Top 5 things I learned #livewellbendy17
- Adventures with EDS : Post conference slump, Radio demo fail & the big gig
- Adventures with EDS : DSA assessment, panic button accident & Back on the radio
- I have an invisible illness – #invisibledisabilitiesweek
- Adventures with EDS : 5am fire alarm, Radio Reunion & POTS flare
- Ask Me Questions! – University with Chronic Illness Q&A
- Adventures with EDS : Migraines, Stanmore appointment & Doing things differently
- Adventures with EDS : Halloween, shorts festival & Movember
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