HUNTERS FPIES THERAPY + EXPENSES
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https://m.facebook.com/Hunters-Journey-435058996908005/
Hi everyone! Thanks for taking a look at this. This account is to help the Davidson family. Their youngest, Hunter, has been diagnosed with FPIES. It is “Food Protein-Induced Enterocolitis Syndrome (FPIES) is a type of food allergy affecting the gastrointestinal (GI) tract. Classic symptoms of FPIES include profound vomiting, diarrhea, and dehydration. These symptoms can lead to severe lethargy, change in body temperature and blood pressure.” Hunter just turned two and gets his main source of nutrients from formula (which is also very expensive, as it has to be a certain type of formula) He has very few known “safe foods” that he is just now able to put in his mouth and occasionally known to swallow them. Currently they are headed to Colorado to visit a team of doctors who specialize in FPIES, and syndromes like it (which as you can imagine is also very expensive) Katie, Hunter’s mom, quit her job to be able to focus more on Hunter and all the therapy and doctors appointments he needs. She’s also able to practice sensory skills with him at home too. She is selling all kinds of old toys, and things she doesn’t use to help raise money. She has a MASSIVE prayer team behind her, backing her up through Christ— and He has been delivering! I am setting this account up in case anyone out there is willing to help their situation, no matter how small. She may kill me for this because she is not one to ask for money, and rarely do I see her even ask for help- so I decided to do this FOR them. Love you guys!
https://m.facebook.com/Hunters-Journey-435058996908005/
Hi everyone! Thanks for taking a look at this. This account is to help the Davidson family. Their youngest, Hunter, has been diagnosed with FPIES. It is “Food Protein-Induced Enterocolitis Syndrome (FPIES) is a type of food allergy affecting the gastrointestinal (GI) tract. Classic symptoms of FPIES include profound vomiting, diarrhea, and dehydration. These symptoms can lead to severe lethargy, change in body temperature and blood pressure.” Hunter just turned two and gets his main source of nutrients from formula (which is also very expensive, as it has to be a certain type of formula) He has very few known “safe foods” that he is just now able to put in his mouth and occasionally known to swallow them. Currently they are headed to Colorado to visit a team of doctors who specialize in FPIES, and syndromes like it (which as you can imagine is also very expensive) Katie, Hunter’s mom, quit her job to be able to focus more on Hunter and all the therapy and doctors appointments he needs. She’s also able to practice sensory skills with him at home too. She is selling all kinds of old toys, and things she doesn’t use to help raise money. She has a MASSIVE prayer team behind her, backing her up through Christ— and He has been delivering! I am setting this account up in case anyone out there is willing to help their situation, no matter how small. She may kill me for this because she is not one to ask for money, and rarely do I see her even ask for help- so I decided to do this FOR them. Love you guys!
https://m.facebook.com/Hunters-Journey-435058996908005/
Organizer and beneficiary
Kirsten Smith
Organizer
Broken Arrow, OK
Katie Davidson
Beneficiary
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