Help for Mallory Constancio

On Tuesday, June 20th, my daughter, Mallory, woke up with double vision, numbness in her hands and feet, dizziness, and had difficulty walking. The symptoms continued to worsen throughout the week, I took her to many doctor appointments and the emergency room several times in order to figure out what was happening to her. On Friday, June 23rd, it was determined to be Guillain-Barré syndrome (GBS), more specifically Miller Fisher syndrome, a variant of GBS. Miller Fisher syndrome is an auto-immune disease that attacks her nerves and muscles causing extreme weakness and paralysis. For the time being she can’t walk or take care of herself; further, she will need months of physical therapy both in a rehab facility as well as home therapy in order to get her back to her normal self. The rehabilitation center she is currently at is 2.5 hours away from home and she’ll need to be there for at least a couple of weeks. I have to take time off of work until Mallory can take care of herself again. Despite the great support system, emotional support can only go so far. The expenses of this medical emergency are building up and I am worried about making ends meet. Most of you that know my family and I know our story and all the things we have overcome, this is just another setback to that story. The last thing that my family and I want to worry about at this time is money, rather we want to help Mallory recover. Any and all help is appreciated!