Byrds For A Cure

The Byrd twins have made it BIG. They have their own logo, blog, website, Facebook fan page, and Twitter account. They also have their own tax id, but it's not presently 501(c)(3), so I won't bother elaborating on that yet.

For those of you new to my blog, Spinal Muscular Atrophy is a degenerative and terminal neuromuscular disease. There is no treatment or cure for SMA. My twins (Kyle & Lauren) have SMA type 2 and are two and a half years old. Their big sister, Jenna, is 6 years old and is SMA-free.

Our good friend, Guy Saenger, designed the website for us. He's brilliant, not to mention funny and clever and Good People and also another parent of twins. His company is Avacata and based in Fort Worth, TX, and I heart him. And his wife, Heather. xoxo to you two!

If you're reading this and have the inclination to do so, please consider clicking over to byrdsforacure.org and signing the guestbook!