First of all God bless u all by taking the time to read my post and I truly thank u all!
Nikki is my sister who was born with cerebral palsy the most beautiful smiling non stop talking (lol) angel you will ever meet... In no matter what situations she is or how much pain she got, she will always put a smile on your face and be an example to each and everyone of us- by what she's been through all her life- too never give up! Our little fighter she is...She's the strongest person I knw for all she been through. Im really grateful to God that he gave her to us and will never be able, dnt even want to imagine a life without her. She's our pillar of strength!!
But since last year February she started complaining about severe pain in her lower back was in and out of hospital for about 11 times , doctors could not find fault and then send her home with Morphine, tranquilizers, sleeping tablet, taking away the little bubbly girl we use to know. Day in day out she would tell us that she cant take it anymore the pain is just to much ,tears streaming dwn her face the most heartbreaking thing to see and hear not knowing how to help her... Until we found this beautiful doctor who works with "these type of people" as the others would say. Long story short doctor found the fault... All her ligaments shortened over time and was pulling her whole body into a really painful little angel, so she had to go through a 13hour op to rectify all that and also get plates and screws in her right leg and left arm. The op went well but she had an I.V line in her chest which started leaking into her lungs by the time the doctors realised that she was barely breathing on half a lung , we were chased out of I.c.u as they just shouted for help and started working on her all u could see is all kinds of machines being rushed into her room in that moment they had to push needles live into her little body and drain 2.4L of fluid from her lungs it was the scariest day, from there they took her to critical care were we where only allowed to see her twice a day. It was the most saddest thing to see her hooked up on so many machines ,pipes,fluid still being drained from her lungs, she not opening her eyes broke me inside. But with lots of prayer and by the good Grace of God she proved again the little fighter that she is.
My dream for her is to realize her dream by being able to get her that wheelchair ,the one without a doubt she so badly deserves and ask about when she sees one on the TV. Her "car" as she would say... She took so good care of the one she got now always make sure it charged on time and she won't sleep if her "car" as she would call it is not "parked" in her room. It was a second hand one a good Samaritan sponsored her with about nine years ago, but now after the op its really uncomfortable for her to sit in it that's when she'll be asking us to squeeze a pillow in here and there just to make it lil bit more comfortable for her and lately its been giving us some battery problems as well, so we have to charge it twice a day then its still not lasting. Really can't afford for it to break down she will be absolutely devastated like the time we had to take it in to put some new tipping wheels at the back she was crying the whole day for her car to just come back.
I'm sorry this is such a long post people I can go on and on.
I humbly ask each and everyone of you'll anything will help pls and greatly appreciated, just to help me realize this dream of my little sister it will mean the world to her. Even Jst by sharing the post please.
I can't say thank you enough for taking the time reading through my post its like 3:00am right now I still can't sleep... Just had to think of a way too help my lil sis.
Thanks again to each and everyone of you'll.