![]() Of course it was too late to fix the femur head to the socket as the bones were matured. Then my mother realized that something is wrong and she started to take me to several hospitals, where she learnt my condition. I had painkillers almost everyday at such a young age. ![]() From the age of 5-8, I was mostly ignored in the pretext of making excuses to not to do my homework. I started complaining of pain after a whole day out in school and on playground when it was time to do homework (to sit down). They took me to a child doctor (pediatrician) and he overlooked and sent them back home stating that children are playful, they do it. My parents also noticed my limp when I just started learning to walk. Whose story is so similar to mine and it encouraged me to share through this platform. I happened to stumble upon the story of "Jenni" on this platform. and knowing the fact that there is no cure except hip-replacement which in itself not recommended to an active adult in her twenties or thirties or even forties. Being a science student I was challenged by a person to discover the knowledge about my condition and to find a cure but without a warning sign that it can lead me in depression and anxiety to know of possible future of acquiring early arthritis etc. Since the age of 22 I started to look upon my condition and study through online sources, I even read research papers. ![]() ![]() ![]() Its been a roller coaster ride from visiting doctors to fighting with anxiety, gut issues and multiple depressions, self-doubts and concurring every episode. I have been living with a painful and fatigued body since I have got senses of myself and my surroundings. I have a congenital hip Dysplasia in my left leg. JAn invisible disability Hello this is Aabha. ![]()
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