This is a video of my Tedx Talk speech about the story of my disability with Ehlers-Danlos Syndrome. At the live York University event where I originalyl gave the Tedx Talk I met two film directors who wanted to make a documentary about my story which has now been released! You can watch for free here:    • Bend or Break | EDS Documentary (AWAR...  
If you want to connect with me or join any of my numerous invisible/chronic illness advocacy projects, here are a bunch of helpful links!

If you want to connect with me or join any of my numerous invisible/chronic illness/EDS advocacy projects, here are a bunch of helpful links!
1. The Bend or Break medical blog group where people can read my memoir that the documentary was based on (film covers events up to 2018, recent blog posts continue the story):   / 16329.  .
2. Direct link to my blog/memoir for if you don't have Facebook: https://breakorbend.blogspot.com/
3. My Bend or Break EDS/medical Instagram page:   / _bend_or_br.  .
4.My personal Instagram page for non-EDS-related fun:   / mitchmartow  
5. My game streaming twitch channel catered to those with chronic illness, but all are welcome to hang out and have fun:   / druidzebra  
6. My discord server for gamers with chronic illness/zebras (we play all kinds of games together!)   / discord  
7. My Facebook group for those who want to be notified when I goes live on twitch:   / 44602.  .
8. My YouTube Account:
https://www.youtube.com/watch?v=OMCPf...
9. EDS Canada page: You do not need to be Canadian to follow   / edscanada  
10. EDS Canada support group where I am a moderator; you need to be a Canadian with EDS to join   / 11573.  .
11: An International Support Group for men with EDS where I am an admin:
  / 1439334896366752  

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