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Erika Havlik - Team Reed

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Manage episode 318723794 series 3291387
Content provided by Mike Hagensick. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Mike Hagensick or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.

Erika Havlik is a mother and the founder of Team Reed. Her son, Reed, was diagnosed with an extremely rare and terminal genetic disease called Vanishing White Matter. Reed was diagnosed at the age of two after suddenly struggling to walk one day after waking up from a nap. Reed is one of less than 200 people in the world with VWM, odds of having VWM are one in 40 million. Erika and her husband's mission is to support the funding for research and development of a cure for this disease through their non-profit, Team Reed.

https://m.facebook.com/secretsoflovingrare

https://www.instagram.com/secrets_of_loving_rare/

http://www.12312design.com/index.php/product-category/team-reed/

https://www.instagram.com/TeamReedcrosby/

https://m.facebook.com/teamreedcrosby

http://www.teamreedcrosby.com/

https://www.gofundme.com/f/8rw5d7-team-reed-find-a-cure-for-vwm

--- Support this podcast: https://podcasters.spotify.com/pod/show/e3collective/support
  continue reading

20 episodes

Artwork
iconShare
 
Manage episode 318723794 series 3291387
Content provided by Mike Hagensick. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Mike Hagensick or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.

Erika Havlik is a mother and the founder of Team Reed. Her son, Reed, was diagnosed with an extremely rare and terminal genetic disease called Vanishing White Matter. Reed was diagnosed at the age of two after suddenly struggling to walk one day after waking up from a nap. Reed is one of less than 200 people in the world with VWM, odds of having VWM are one in 40 million. Erika and her husband's mission is to support the funding for research and development of a cure for this disease through their non-profit, Team Reed.

https://m.facebook.com/secretsoflovingrare

https://www.instagram.com/secrets_of_loving_rare/

http://www.12312design.com/index.php/product-category/team-reed/

https://www.instagram.com/TeamReedcrosby/

https://m.facebook.com/teamreedcrosby

http://www.teamreedcrosby.com/

https://www.gofundme.com/f/8rw5d7-team-reed-find-a-cure-for-vwm

--- Support this podcast: https://podcasters.spotify.com/pod/show/e3collective/support
  continue reading

20 episodes

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