Living with a rare condition
For most people, a health app is for counting calories. For someone living with McArdle disease, the first ten minutes of a brisk walk can mean the difference between a muscle contracture — and an ordinary day.
This type V glycogen storage disease prevents muscle from using its glycogen during exercise. It upends how you eat before, during and after exertion — and no mainstream app took that into account. Starting too hard, too fast is the classic trap: pain, contracture, and in severe cases rhabdomyolysis, the muscle breakdown that can land you in the emergency department.
MyFit.care was born of this observation, told in detail on our about page: start with the most demanding case, solve it properly, and only then generalise. The “second wind” protocol, managing the pre-exercise carbohydrate load, tracking rhabdomyolysis episodes: these features do not exist out of marketing opportunism, but because patients needed them — a need documented in the publications of associations such as AFG France, AGSD UK and IamGSD.
The most tangible proof of this mission fits on a piece of paper: the McArdle emergency card, a free printable document listing the contraindicated drugs and the anaesthesia protocol to hand to clinicians. Because in hospital, facing a team that has never heard of the disease, a folded sheet in a wallet can change the course of your care.
I want to track my health every day
Nutrition, sport, sleep, hydration, goals. Sync your watch and stay on track, simply — ad-free, with a serious CIQUAL/ANSES nutrition database.
Get started for free →I live with a condition
Specialised tracking, AI insights, symptom journal and export for your doctor. Reinforced support, informed by protocols published by patient associations.
See the conditions covered →