Bayleigh needs her daddy

Update been hospitalized for 21 DAYS BEEN PUT ON STEROIDS TO CONTROL THE FIBROSIS NOW THAT THEY HAVE THE DOUBLE PNEUMONIA CLEARING UP. BY DOING THAT THEY HAVE TO PUT ME ON INSULIN. All funds are going to bi pap machine to get me home and stable then the rest is going to the move of which every hospital im tsken to for the transplant. I thank each and very one that is helping and hopefully i will be able to give back in return. MORE THEN ANYTHING MS. BAYLIEGH THANKS YOU!!!t

Hopefully i can get home to BAYLIEGH

I am Charles Morgensen, and I am a 100% disabled Marine.

With a four-year-old child. Her name is Bayleigh, and I'm her only parent.

About the time she was born, I was diagnosed with IPF lung disease. It's a progressive lung disease that is not curable. Only a transplant will help.

I live on oxygen 100% now at a high level rate 24/7 i can go nowhere without oxygen.

I'm only 62. The VA will pay for the transplant but will not pay for the housing where I have to be moved to or the year of staying at that place while still maintaining my home in Savannah. I'm fighting to stay alive for my little girl, so she has a parent to help her grow up and she does not get put into the system. I'm embarrassed to have to ask for help, but this disease has

drained me financially. I have always given to others, and hopefully, it will now come back in return. I humbly ask for your donation more for my child and for me, so that I can at least try and stay alive for this young lady. She needs her daddy. The smallest amount will help, or whatever you feel you are capable of giving will be much appreciated. God bless you. Have a great, wonderful day.

THIS DISEASE IS FIBROSIS OF THE LUNGS

I WAS I WAS STATIONED AT CAMP PENDLETON CALIFORNIA. AND THEY ARE UNDER THE WATER ACT BUT THE VA. FIGHTING IT

SO IM ASKING FOR HELP