mobility

I wrote a column this spring about my 5-year-old son, Cayden, needing to see an orthopedic specialist again. Well, we finally had that appointment late last month, with a doctor he hadn’t seen before. It didn’t go as well as I’d hoped. When Cayden’s metabolic specialist sent the…

Last week, we had our first pool day of the summer. I got pool passes for myself and my 5-year-old son, Cayden, who really enjoyed it last year. In fact, he’s been consistently asking to go again. But here in Pennsylvania, summer is the only time it’s warm enough to…

Motor problems in people with Pompe disease may be explained by damage to muscle spindles, which are sensory receptors that detect muscle movement and help regulate muscle tone and maintain posture, a mouse study suggested. Muscle spindle structure and function were “severely compromised” in Pompe mice, resulting in a…

I have this recurring dream where I’m driving a sublime green 2015 Dodge Challenger down the Pacific Coast Highway toward the beach. I call it my “I have no muscle” muscle car. It’s trimmed out in light blue with “Pompe Champ” and “Smashing Pompe” printed on the sides and hood.

Typically, when we think of playgrounds, we envision children running around, having the time of their lives. But this isn’t always the case. For my 5-year-old son, Cayden, it’s a bit hard to enjoy the playground. Cayden is in a wheelchair, so sometimes he has trouble accessing playground equipment.

“Every Move Counts” is a message that’s stuck with me in recent days, helping me build a healthier view of my exercise goals and limitations. That was a theme of International Pompe Day on April 15, reaffirming that no matter how big or small, every move does…

“Every Move Counts” on this year’s International Pompe Day, which is held every year to raise awareness and increase understanding of Pompe disease. This year’s Pompe Day will be celebrated April 15. According to the International Pompe Association (IPA), this year’s observance will focus on the importance of…

Back in the summer of 2018, when I started experiencing some serious symptoms, I wondered if I had ALS or another similar disorder. I noticed I wasn’t able to stand up from a seated position. If I was sitting on the couch, I’d have to extend my arms…

This past week, my best friend, Joe, and his son Dane came from Montana to visit me in California. I decided to take Monday off from work to meet up with them so I could watch Dane, an adventurous young man, as he went rock climbing. In fact, he’s been…

Awhile back, I donated my 4-year-old son Cayden’s used adaptive equipment. He’d outgrown his old stander, so we no longer had any use for it. While I was sad to see these things go — because it’s a reminder that he is getting older and bigger — I was…