Support Jasmin Fighting Chiari

My name is Jasmin Lawrence, and I have Arnold Chiari and Hydrocephalus, which is a rare genetic disease, and another rare disorder. I’ve just went under for my 5th brain surgery, and I’m going to have many more. My husband has had to take un paid time off work, to be with me and the kids. We have a three year old who is completely deaf, and 8 month old twins. We are needing help to be able to stay cought up on bills, which are quickly falling behind, and gas and food for transportation, to and from Lexington at the University of Kentucky. We also have to afford diapers, wipes, for three kids, and extra baby food that WIC doesn’t provide. And im not able to try to earn money,because I am not able to do anything. I’m not even able to help take care of the kids because I’m not allowed to lift and can sit up for long periods of time. Normally I would never want to ask for help, but right now, we need it. Anything helps, and anything over what we need will be donated to an Arnold Chiari research center. Thank you ❤️