Logan's pulmonary hypertension medicine

Hi, our names are Garrett and Tayler, and we're the parents of Logan. Logan was born 3 months early, and had a myriad of health problems in just his first few months of being alive. First his kidneys weren't working, then his liver stopped working. Now he has pulmonary hypertension. Thankfully, the first two problems have fixed themselves, but the pulmonary hypertension is where we're facing the most difficulty. His medicine is $250 per month AFTER insurance kicks in. There's no other alternatives for the medicine he's on unfortunately. Once he's transferred to his next (and hopefully last) hospital, the medicine can't be shipped to them. So we have to order it every month and bring it to him in the hospital. They said he will be on this medication for at least 3 years so we are asking for help for a years worth.

We're anxiously awaiting the day Logan can come home to his twin brother Caleb. Not having to stress about Logan's medicine every month will help us get to enjoy our time together as a family.

We appreciate you all and any help you are able to give.

Thank you!