The story of Markéta
My name is Markéta Kamešová and i have son Jaroslav, from his birth he had many illnesses, many of them went away some parcially some for good, but one stayed i would say ugliest one or at least most life changing and not in good way. It is very strong Narcolepsy and Cataplexy, this illnesses cause you to fall asleep uncontrollably even when you are walking, eating, also when you laught you loose control of you muscells, you can fall on the ground and you get really quckly tired thefore you need to rest a lot (sleep). First weak symptoms started showing them self when my son was in kindergarten at that time i didn’t pay it to much attetion at the time i just thought that my son is more sleepy or cumbersome. When my son was in 1.st grade its symptoms got really strong and it was obvious that wasn’t normal, he was sleeping all time, not cable of doing anything like going for walk or to play with other children. So started long process of searching for help. We found it 5 years later in doctor Nevšímalová, it took a lot of work, stress sometimes even tears. Doctor Nevšímalová helped us a lot since, she gave my son medication that mitigate some symptoms of Narcolepsy and Cataplexy. I must therfore thank her here for her help. Im also sharing info about Narcolepsy and Cataplexy on social medias, i want to say that everybody should at least share or promote their rare illness…
Greetings from Czech Republic EU…