EHLERS DANLOS CHALLENGE *EDS Awareness Month 2018*

I am late posting as EDS awareness month was May, haha, but better late than never!

Ehlers Danlos Syndrome Q&A 👇
   • Ehlers Danlos Syndrome Q&A  

Channels I tagged!

Emma Grace👇
   / @emmagrace  

Chronically Jaquie👇
   / @chronicallyjaquie  

Fran Gray👇
   / @frangray2446  

Christina Dohery👇    / @christinadoherty3212  

Ehlers Danlos Challenge Questions! I encourage you to make a video answering them for yourself! The more people raising awareness the better 😊

1. What type of EDS do you have?
2 .When were you diagnosed?
3. Comorbidities?
4. How hypermobile are you?
5. Are you stretchy?
6. Mobility Aids?
7. Pain Management?
8. Surgeries?
9. Hospital stays?
10. What is your "normal"?
11. What is your flare like?
12. What specialists or types of doctors do you see?
13. Funniest EDS story?
14. Worst doctor experience?
15. Best doctor experience
16 .What is your support system like?
17. Do you think EDS is "expensive"?
18. Do you consider yourself disabled?
19. Have you experienced ableism?
20. Worst part of EDS?
21. One thing EDS has taken from you?
22. One thing EDS has given you?
23. Something you wish everyone understood?
24. If you could rid yourself of one EDS symptom, what would it be?
25. One person you're grateful for?
26. Scariest part of your future with EDS?
27. What are your health goals?
28. Have you ever met someone in person with EDS?
29. If there was a cure for EDS, Would you take it?
30. How do you make your invisible illness visible?
31. What does awareness mean to you?

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