Kelsea Freeman Recovery

Cystic Fibrosis and End stage liver disease sucks ... this is the reality my 17 yr old daughter, is living with.  A little background ....  

At three months old, she was diagnosed with Cystic Fibrosis (CF). The life expectancy of a child with CF was 30 years old at the time, and was recently increased to 37, due to the efforts of the Cystic Fibrosis Foundation. She was perfectly healthy (as healthy as she could be with CF) going into the 6th grade. Unfortunately, she was going to a school with some mold problems ... for more, please read here ... now to today ...  


Kelsea is a bright seventeen year old College Student who was supporting herself up until a few weeks ago. She has been inpatient at Phoenix Childrens Hospital since Halloween, has had quite a few procedures and surgeries and at this time, there is no discharge date in sight. The family is doing all we can to help and keep afloat, but it's time to reach out and ask for a little help from the community so she can eat, pay her bills, and buy her medicine.

Here is Kelsea after having an NG tube inserted as well as other procedures. I love my baby! 


If she doesn't get out soon she will lose her car and go into debt because of her apartment. We just need a little help so that she can focus on her health and not on paying her bills. 

Thank GOD for her cell phone, she can connect with friends and family, anything to make her smile! 




Here are some links that explain what Kelsea is dealing with:

Cystic Fibrosis Foundation
Aspergillus
Stomach Emptying Test
Mycobacterium Chelonae

 Thanks for your help. We truly appreciate it all! 

Regina - 
Kelsea's mom