Getting The Right Pompe Disease Treatment
June 3, 2014
Positively impacting the lives of people with Pompe
Have you heard of Pompe disease? Most people haven’t. Pompe disease is a rare genetic neuromuscular disorder caused by an excessive buildup and storage of glycogen in the muscle cells, resulting in degenerative muscle weakness. The muscle weakness can affect many different parts of the body and cause a variety of health problems.
Common symptoms of Late Onset Pompe Disease include:
o Difficulty walking
o Trouble breathing at night while laying down
o Falling asleep during the day
o Headache during the day
o Progressive muscle weakness
o Pompe disease is often misdiagnosed because many of its symptoms are shared with other more common diseases.
It’s a devastating medical mystery: random symptoms that present in many common diseases; low awareness and misconceptions among physicians; rare incidence and lack of awareness about the disease’s existence. Chances are you’ve never heard of Pompe disease – a degenerative, genetic neuromuscular disease. But thanks to specialists like Dr. Barry Byrne, medical geneticist and Genzyme, leader in discovering and delivering transformative therapies for patients with rare genetic conditions, awareness of Pompe symptoms and disease management is growing. By increasing awareness, physicians can achieve earlier diagnoses and patients can be armed with disease information, allowing them to more successfully self-advocate and manage Pompe disease treatment plan.
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