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New site and why I am doing this

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I am so excited to have launched this website, zacsattack.com and am grateful you are reading this.​​

The collage of photos are some baby photos my parents put together to give a visual to some of what I went through at a young age. The photos are hard for me look at for sure, but it makes me appreciate where I am now and how far I have come. I still struggle almost daily, mostly with tongue swelling and pain. But with the support of my family and my amazing doctor, Dr. Joseph Edmonds in the Texas Medical Center, I manage the pain and do everything I can to keep a smile on my face and stay positive.

Part of why I am doing all this is to share and hopefully touch others who are struggling. And then there's the whole raise money and awareness thing! I sure would love to see some progress on a cure for lymphatic malformation in my lifetime!

For now, you can donate here, directly to the Lymphatic Education & Research Network (LE&RN). Soon, I will have my own donation capabilities, for which I will give to LE&RN and put together events to raise even more money!

 
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©2019 by Zac's Attack for a Cure - Supporting the Lymphatic Education & Research Network https://lymphaticnetwork.org/