Dakota talks about VACTERL Association and waiting 16 years for a transplant
カートのアイテムが多すぎます
カートに追加できませんでした。
ウィッシュリストに追加できませんでした。
ほしい物リストの削除に失敗しました。
ポッドキャストのフォローに失敗しました
ポッドキャストのフォロー解除に失敗しました
Dakota talks about VACTERL Association and waiting 16 years for a transplant
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Dakota Watson is 20 years and diagnosed with VACTERL Association at birth. He has spent his whole life living with this syndrome and the medical complications that come with it. At 16 years old he received his first transplant.
The information in this episode is from the perspective of the interviewee and their own understanding of their disease and the medical terms that come with managing that disease. Please discuss any treatments, conditions with your own medical team.
This podcast is produced by NW Kidney Kids, a 501(c)3 serving children with CKD since 2006. To get more information about programs please visit www.nwkidneykids.org. Also, find us on social @nwkidneykids
The podcast Host is Jill Brown, we can connect at jill@nwkidneykids.org, LinkedIn, or Twitter.
More Information on VATERS Syndrome (AKA VACTERL Association): https://rarediseases.org/rare-diseases/vacterl-association/