top of page

The only financial resource for pediatric lymphedema…

Updated: Nov 1, 2022

Guys, our CLT told us about this foundation and you must check it out. Even if you don’t have this disease its a great place to donate to! They don’t just help children with lymphedema finically they also put on a summer camp here in the USA for children and their parents! It is called CAMP WATCH ME. It’s where kids can be surrounded by other kids who have the same thing they have. It’s not just a “fun camp” it is also a place where they bring in Drs, CLTs, and resources to further educate the kids and parents.

I plan on signing Jo up for this! I know this would do her little 6 year old mind a world of good to see others just like her, doing things just like her! My goal would be for one day to help raise money for this AMAZING organization/foundation! I just LOVE this.

Short blog .. but such a BIG resource to share. So, what are you waiting for? Click the link and check out BryalnsFeat!

6 views0 comments

Recent Posts

See All

Brandy’s Story

When Brandy first received her lymphedema diagnosis, she was in excruciating pain and desperate for help. She turned to an online lymphedema support group, hoping for some guidance. She posted her sto

Our Experience with the Fast 'n Go Wraps

Fast 'n Go Wraps from Rivera Hybrid Solution As a mom caring for Jo, who has lymphedema, finding effective and convenient treatment options is always a top priority. Back in April, we started using a


Rated 0 out of 5 stars.
No ratings yet

Add a rating
bottom of page