A friend is getting ready to say goodbye to her daughter. She has Microcephaly(small head), which my daughter has. She also has Lissencephaly, smooth surface of the brain. Little Parker has been in Hospice care for a couple of weeks. Her mom, Megan, has been at her job 9mos and has no paid leave time. Megan shouldn’t have to work to make ends meet while her daughter slips away. She should be home with her.
Another good friend of mine who has lost her daughter said it’s a hell you’ve never felt before. Afraid to leave the house, to shower, to sleep, afraid you are going to miss those last final minutes.
Click on the link to read about Megan and Parker and how you can help. Please reblog.
I wasn’t going to post anything else today but I cannot in all conscience not reblog this.
I cannot imagine being in a position where I was facing losing my child and still having to worry about work and money. Please take a moment to read about this remarkable child and her family and if you can help that would be great.