Cindi's ALS Fund

It's very hard to write this post about the love of my life for over 30 years but it's something I must do. In March 2017 after nearly two years of doctors my wife Cindi Morgano was diagnosed with ALS. This had to be the worse day of our life together. There is no cure for ALS at this time.  I can not express to you how awful it is to see the love of your life waste away. Cindi can no longer speak, unable to be mobile without a wheelchair or a walker.  We are currently waiting for a communication alternate speaking device (est cost 8-10k) and this is just the beginning, we have no idea what the amount will come to, and at this point are in dire need now.  We are waiting to start getting infusion medication from Japan that has a huge co-pay. She has to gain 10 lbs first. The amount of medical needs for supplies, nutrition, and equipment is endless. Cindy has a  feeding tube put in as her ability to swallow is no longer possible.  We do the best we can. We have been urged to set up a Go Fund me page as the cost are going to be staggering. Anything you can do would be greatly appreciated. Imagine watching your loved one have to go through this every day. The need is urgent!  Anyone's help is greatly appreciated.

Thank you,
Cindi and Charlie