One of my closest friends’ son, Walker, has a very rare disease called Achalasia. He had surgery last May and things were going great until two weeks ago when symptoms started coming back with choking and vomiting. The day the article was released (below) he had an Upper GI and got the results his esophagus was indeed closing again. They fortunately got an opening at Mayo Clinic this Tuesday and they are meeting with the top specialist for his disease - a huge blessing. But as you can imagine with medical bills piling up and trips to the Mayo Clinic (flights, car rental, hotel, etc), expenses are piling up. If you know the Freese family and would like to help out in any way, this would be one less thing they would need to worry about as they wait to find out what will happen with Walker. Please also continue to pray for Walker. He is such a strong kid. If anyone can beat this, he can. 
*Updated the amount due to increasing expenses for the Freese family.  

https://healthbeat.spectrumhealth.org/one-in-a-million-achalasia-digestive-disorder-eager-for-food/