Camp Watchme is the first summer camp for children with lymphedema in the United States. Betty Westbrook, Certified Lymphedema Therapist and Host of Lymphedema Podcast, had the idea to create Camp Watchme, a safe and nurturing environment for children fighting lymphedema. She then joined forces with two lymphedema non-profits, Brylan’s Feat Foundation and Ninjas Fighting Lymphedema to make her idea come to reality. Camp Watchme is free to children ranging in ages 3-18. During camp (July 18-21), 5 children were able to meet others just like them for the first time.
Each child was given the special opportunity to have a traditional summer camp experience without having to worry about explaining their differences. Camp Watchme is unique in that it also offers a parent retreat. One parent/caregiver is encouraged to join their child at camp to participate in educational sessions ranging from MLD basics to nutrition for lymphedema. In addition to gaining knowledge about their child’s disease, the parents also built strong connections with others parents through daily support group sessions.
Camp Watchme was just a thought less than 3 months ago and its success is due to the support of the lymphedema community and those who believed in this cause.
For more camp information as well as our special episode featuring interviews from campers subscribe to Lymphedema Podcast. You can visit these websites for updates and announcements for next summer's dates.
The National Lymphedema Network is pleased to join this effort and we look forward to
Camp Watchme 2020.
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