Draw My EDS #ThisIsMyEDS [CC]
As part of #ThisIsMyEDS and sharing our diverse experiences with Ehlers-Danlos Syndrome I wanted to try and give you a tour of how it currently affects my body a la "Draw My Life" with "Draw My EDS". There are just a couple more days to get your #EDSAwareness shirt! http://bonfire.com/ehlers-danlos-zebr... Correction: I said "heel spurs" when I meant "Piezogenic papules", they are occasional painful bumps that appear on my heels BTS: Was dealing with a lot of lower back pain at the time of shooting this video, it has me very stiff, making it very difficult for me to move. I wasn't as careful or patient while drawing this because I was rushing to lay back down. You can find Part 1 of #ThisIsMyEDS here: • What EDS is like on MY Body #ThisIsMyEDS T... You can find the questions for the tag here: https://docs.google.com/document/d/1c... SUPPORT THIS CREATOR If you enjoy my videos, please consider supporting this channel! Patreon: / annieelainey PayPal: http://paypal.me/annieelainey Amazon Wish List: http://a.co/gyCgqsf CONTRIBUTE CAPTIONS/SUBTITLES FOR THIS VIDEO -Click on the gear in the lower-right corner of the video -Click "Subtitles/CC" -Click "Add subtitles/CC -You can contribute Closed Captions in English or subtitles in ANY other language LIST OF VIDEOS YET TO BE CAPTIONED https://www.youtube.com/timedtext_cs_... FIND ME ON THE INTERNET / ann.e.segarra / annieelainey / annieelainey / annieelainey / annieelainey Periscope: AnnieElainey IN THIS VIDEO Mic used: http://amzn.to/2ahAuT5 Camera used: http://amzn.to/2a5jPCq My Associate Store: http://astore.amazon.com/annielai-20 CHANNEL DESCRIPTION Annie Segarra (Annie Elainey) creates mainly first-person videos on introspective topics, social topics, sharing her experiences and thoughts on disability, body image, LGBT topics, gender equality, etc, as well as creative content; a variety of music/artistic media and short films. Annie identifies as a queer Latinx disabled woman and uses she and they pronouns.

Why EDS is more than "just loose joints" | (MIS)Treated
![What EDS is like on MY Body #ThisIsMyEDS Tag [CC]](https://i.ytimg.com/vi/qMk-JpMauPw/hqdefault.jpg?sqp=-oaymwEjCNACELwBSFryq4qpAxUIARUAAAAAGAElAADIQj0AgKJDeAE=&rs=AOn4CLB-8vXeDoSSBKnbvItdx4H5Or9sBA)
What EDS is like on MY Body #ThisIsMyEDS Tag [CC]
![The Importance of Visibility for Invisible Disabilities [CC]](https://i.ytimg.com/vi/3uQ2aXKgDVw/hqdefault.jpg?sqp=-oaymwEjCNACELwBSFryq4qpAxUIARUAAAAAGAElAADIQj0AgKJDeAE=&rs=AOn4CLD1zXVWH0hCShZHFiarsTsOCbJW0A)
The Importance of Visibility for Invisible Disabilities [CC]
![Disability Misconceptions Tag (EDS) [CC]](https://i.ytimg.com/vi/sBSzm9RbXAY/hqdefault.jpg?sqp=-oaymwEjCNACELwBSFryq4qpAxUIARUAAAAAGAElAADIQj0AgKJDeAE=&rs=AOn4CLDSWO1ai7gT9QfooRc6pwtNYrfQbg)
Disability Misconceptions Tag (EDS) [CC]

Alan Pocinki - Evaluation and Management of Fatigue in Patients with EDS

you should keep a commonplace book (& how)

EDS & HSD Tips | Managing & Preventing Dislocations & Subluxations

Hypermobility, POTS + ADHD, Autism, ND Connection with Leading Expert Dr Jessica Eccles

Living with EDS: Spinal Instability

Why The Ocean's Deadliest Predator Refuses To Kill Us
![Ehlers-Danlos Syndrome: My Diagnosis Journey [CC]](https://i.ytimg.com/vi/ot1HFF7QWbQ/hqdefault.jpg?sqp=-oaymwEjCNACELwBSFryq4qpAxUIARUAAAAAGAElAADIQj0AgKJDeAE=&rs=AOn4CLC6l-cTeSJh0lmZz1ns-Bv2nIAF-A)
Ehlers-Danlos Syndrome: My Diagnosis Journey [CC]

Why We Use Power Wheelchairs w/ ALS and EDS #AmbulatoryWheelchairUsersExist

Kristin Means - Life With EDS

Living with Complex PTSD (And Constant Dissociation)

Do NOT Trust Your Friends on Discord.

Vlogging with EDS: What is Wrong With My Brain? | Week 84

Paldeep Atwal - Discovery of AEBP1-related EDS

Living with Chronic Pain and Ehlers-Danlos Syndrome

What is EDS? (Ehlers-Danlos Syndrome|Hypermobility) & How to Control Pain

