As some of you may know, from previous articles, Lisa was in People Magazine last year spreading awareness for this HORRIBLE syndrome, SMAS. (Feel free to GOOGLE Lisa Brown SMAS, you will see all the articles about her) She was also later diagnosed with Gastroparesis. She spent a lot of time trying to help others, which i know she has. She dedicated so much time trying to cheer up anyone who was down. She would handmake personal cards for people who were/are sick, down about something, or just needed a little brightness in their day. She still continues to do this, however it is extremely hard for her to make time because she is so sick and weak.
This October she entered into hospice care because she was declining so quickly. They have been trying to help keep her symptoms under control and trying their best to keep her pain free. Her overall health has and is declining rapidly now. I, her husband, am taking off of work on FMLA, and not getting paid, to spend the rest of the time she has with her.
I am starting this fund to help pay for anything that she may want to keep her happy and comfortable in the last days she will be with us. It will also help cover the cost of her Memorial and for taking off work with no pay. We appreciate any help you may be able to give. I hope that her story has touch your life as i know it has for many people.
Thank you much,