Byrds Fore A Cure-Cast
About This Show
Byrds Fore A Cure-Cast is dedicated to sharing the latest on SMA research as well as other topics of interest to our muscular dystrophy family and the special needs community. I am a parent of three children, two of whom have type 2 spinal muscular atrophy.
Most Recent Episode
Episode 6: Flu Season + Holiday Gift Ideas
4 days ago
Welcome back, and happy #GivingTuesday! Don't worry, I'm not asking you to give money. I have a tip or two for getting through cold and flu season, as well as some holiday gift suggestions for kiddos with neuromuscular disease or other special needs. SMA makes one's muscles weak, which can pose a challenge at the holidays when trying to come up with toy ideas for the kids (until you just give up and hand them an iPad), so I have a list of around a dozen options you may not have considered. If you have things to add to this list, email me: firstname.lastname@example.org Follow us on Facebook, Twitter, Instagram, and now on LinkedIn, too!