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Ongoing Medical Expenses

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Please help us get Logan Kline to his medical procedure!!

Nine year old Logan Kline was born in March of 2006 in New Haven, Connecticut. Since his birth, Logan  gets treated for his rare disease, Eosinophilic Esophagitis/Eosinophilic Colitis.  Aside from his rare disease, Logan also has a cardiac arrythmia, craniosynostosis, Ehler Danlos syndrome, obstructive sleep apnea, a small mass in his sphenoid bone and partial paraylsis to his palate due to repair for his cleft palate. 

Logan started treatment with Yale-New Haven Hospital, then CT Childrens Medical in Connecticut. Childrens Hospital of Boston was next, they were more advanced with Logans disease, a two hour drive from home.  After a long wait, Logan was accepted to be seen at the Cincinnati Childrens Hospital in Cincinnati , Ohio. Cincinnati Childrens Hospital has offered him huge promise for the future as they are the leading research hospital for his disease! Although  there is no cure for his disease, Logan is a happy 9 year old boy that tries to be there for others, especially his friends that are ill. 

We lost our funding for medical transport to and from Cincinnati Children's Hospital where our son is seen by a team of doctors. We fly to Cincinnati for his biopsies and treatments every 6 months and the trips are very expensive.  We cannot afford to fly and must drive, as it is the least expensive of the two means of transportation, it will be an 11 hour drive.  Logan has been overdue for his scope to check for damage to his esophagus and colon and we  cannot wait any longer.  We are hoping to raise money to defer the cost of these trips. 

Thank you in advance for your help.
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Donations 

  • Michael Cousins
    • $50 
    • 7 yrs
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Organizer

Kelly Kline
Organizer
New Haven, CT

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