Limb-Girdle Muscular Dystrophies
Limb-girdle muscular dystrophy (LGMD) is a diverse group of disorders with many subtypes categorized by disease gene and inheritance. LGMD usually manifests in the proximal muscles around the hips and shoulders. (The proximal muscles are those closest to the center of the body; distal muscles are farther away from the center — for example, in the hands and feet).
The shoulder girdle is the bony structure that surrounds the shoulder area, and the pelvic girdle is the bony structure surrounding the hips. Collectively, these are called the limb girdles, and it is the observed weakness and atrophy (wasting) of the muscles connected to the limb girdles that has given this group of disorders its name.
Together, the group of disorders that constitute LGMD is the fourth most common genetic cause of muscle weakness with an estimated prevalence in about 2 in every 100,000 individuals
Post-COVID conditions are a wide range of new, returning, or ongoing health problems that people experience after first being infected with the virus that causes COVID-19. Most people with COVID-19 get better within a few days to a few weeks after infection, so at least four weeks after infection is the start of when post-COVID conditions could first be identified. Anyone who was infected can experience post-COVID conditions. Most people with post-COVID conditions experienced symptoms days after their SARS CoV-2 infection when they knew they had COVID-19, but some people with post-COVID conditions did not notice when they first had an infection.
There is no test to diagnose post-COVID conditions, and people may have a wide variety of symptoms that could come from other health problems. This can make it difficult for healthcare providers to recognize post-COVID conditions. Your healthcare provider considers a diagnosis of post-COVID conditions based on your health history, including if you had a diagnosis of COVID-19 either by a positive test or by symptoms or exposure, as well as doing a health examination.
The people driving Percheron.
What else we're working on.
“Any progress in helping improve or maintain quality of life is vitally important and would be a game changer for all of us. It would improve self-esteem, independence, and mental outlook/emotional well-being for the patient and the caregiver.”
Regina - Mother of Jordan
“The most important things for Austin to maintain are the ability to self-feed, ability to use a keyboard, ability to lift a cell phone, ability to brush teeth, ability to adjust (put on, remove) headphones (gaming is a big deal in the Duchenne community).”
Trina - Mother of Austin
“I would ask companies considering developing a therapy for non-ambulatory patients to please do so. It could make a huge difference in the quality of life of the non-ambulatory person and their caregivers/families. ”