This is what an EPF survivors "I'm alive and I can't get West Nile" happy dance looks like!! 🏇🏇🏇 I'm loving his flag but I'm not loving how he holds his tail to the side like an Arab! We're going to have to have a heart-to-heart over this 😂
Somebody doesn't think the walker goes fast enough for him! Can't complain though considering this is his first time ever on it! You got this Cass!
Cass playing with his toy! He loves him!
The 7th was a very special day for Cass. Not only did he turn 10 months old his meds were officially reduced to half of what he started. Hopefully this means we are halfway there! Although this ugly disease slowed his growth he measures 14.5 hands!
Somebody sure enjoyed his play date yesterday with his BFF! ❤🐴
Guess who has the last laugh now, Phoenix?!?! And he is pissed!! 😂 Every spring he chews up the wires on the walker. Every damn year 😠 Before that it was Chip. Well thanks to Mike Pugh I got it fixed right this year now he can't chew anything up. And what's even better he donated the money I would have paid to get this fixed to Cass's treatment fund so thank you thank you thank you Mike and Mitzi Cameron-Pugh. Me and Cass truly appreciate it however Paco and Phoenix (Cass's big bro's)not so much!! Xoxo
Feeling better and better with each passing day! ❤❤❤
Cass's reaction when presented with his new treatment plan yesterday! Happy tears! 💘💘 Keep in mind this is essential oil treatments only and nightly massages with coconut oil. He will start Phase 2 of his treatment regimen tomorrow!