Hello, my name is Juliana and I'm rare In October 2020, the first signs appeared, but I had no idea what was coming. It could be anything, including parsonage turner syndrome and herpes zoster. It wasn't... Só em março de 2022 conseguimos o diagnóstico: Doença do Neuro Motor. Mas não é da comum não! É flail arms, afinal eu sou muito diferenciada. Everything was going well until I caught covid. Yea I went to hell but back A little more damaged but standing Since then, my routine has consisted of complete treatment based on diet, respiratory physical therapy, audiology, medical follow-up, medications and supplements, along with a lot of love and support from family and friends. Hence the weakness and loss of muscle mass, It's degenerative there is no cure. I plea everyone to support me for my frequent treatments to enjoy the precious time with my families ? on earth.