Share in "Kimber Parr's Journey"

My name is Mary and I am Kimber's Nana.  I have started this fund on behalf of my son Corey and his wife Charlene.  In January while having a routine checkup and sonogram of their new baby, they found out that their baby girl was going to be born with a bilateral cleft lip and palate.  This is the kind of news every new parent dreads hearing, that something is wrong with their child. 
Kimber was born April 4 (4 weeks early). She was born with the worse case of bilateral cleft and palate that you can have.  This type of disability has no quick fix.  She is looking at many surgeries and devices from now until maybe even the age of 21.  She will see not one doctor, but a team of doctors through these years.  Much of this is not covered by insurance.  They were not prepared for the bills that will be coming in, just as no average family living from paycheck to paycheck would be.  They also have 3 other children to take care of during Kimber's journey.  They have applied to some agencies for help, but have not heard from them yet.  They are very hard working people and do not want to ask for help, so I'm asking for them, if anyone can find it in your heart to help even emotionally, it would be greatly appreciated, and thank you in advance!!