Help baby Nash !
Donation protected
Hi ~ my name is Haley and I am posting this in hopes to raise money for the family of a special little baby boy named Nash. This handsome little man is so special he is 1 in 160 million! I just adore him and his family so much that I want to do anything I can to help them out. Seeing my friend Angie go through this with her son has really touched my heart. Having to see her son poked and prodded, scanned and tested, scary surgeries, all of this while knowing it is not going to end anytime soon is heart wrenching! As a mother myself I know she would do anything to make her lil man feel better. That is why I am doing what I can to help. Below is a little summary of Nash and what he is going through. 
Nash Hensley was born on 11/04/14 to his mother Angela and father Nick. He also has a beautiful 4 year old big sister named Aleigha. Since shortly after birth they knew there were some problems and ever since Nash has been in and out of hospitals and has a long road of doctors ahead of him.
Nash has 2 genetic disorders. One is called PKU which means that his body is missing an enzyme that helps break down protein. He will be on a very strict diet for life. Very little protein. Basically a vegetarian. He has been on a special formula strictly for patients with PKU since a few weeks after birth and will have to continue drinking this for life. His parents have to draw weekly blood samples that are sent to Riley Childrens Hospital to monitor his protein levels. They will be learning so much more about this genetic disorder as he continues to grow.
Nash also has what is called Achondroplasia. Meaning he will be a little person. There are things that are being closely monitored during his growth development.
He has also been on oxygen since birth but neither Riley or Cinncinatti Childrens Hospital can tell his family exactly why. They are hoping in due time he will no longer need it.
It has been a long 8 months for Nash and his family, but if you were to meet him you could understand that it is worth every minute of it. I know they still have a long ride ahead of them but they will continue to plug away to give him the best care they possibly can and continue to seek the answers needed to provide him with the most normal life as possible.
Please help us raise money for the Hensley family so they can get Nash the best care possible! Help them ease the finacial struggle of hospital bills, travel exspenses to and from Riley and Cinncinatti Childrens Hospitals and the everyday expenses of oxygen and special foods. If you can please donate! Nick, Angie, Aleigha, and Nash will be forever greatful!
If you cannot donate please SHARE Nash's story to spread the hope and love!
Nash's mom said "One thing I think we have learned more than anything from this and I hope everyone along his journey of life with him will also learn is that you can never judge a book by its cover. Because that book can give you the best story you have ever read. "
I hope reading about Nash's story has touched you in some way. His little smile has permantly touched my heart and I pray things will get better for him soon and that these donations can help that in anyway possible!
Thank you from the bottom of my heart!
Haley Morris
Nash Hensley was born on 11/04/14 to his mother Angela and father Nick. He also has a beautiful 4 year old big sister named Aleigha. Since shortly after birth they knew there were some problems and ever since Nash has been in and out of hospitals and has a long road of doctors ahead of him. Nash has 2 genetic disorders. One is called PKU which means that his body is missing an enzyme that helps break down protein. He will be on a very strict diet for life. Very little protein. Basically a vegetarian. He has been on a special formula strictly for patients with PKU since a few weeks after birth and will have to continue drinking this for life. His parents have to draw weekly blood samples that are sent to Riley Childrens Hospital to monitor his protein levels. They will be learning so much more about this genetic disorder as he continues to grow.
Nash also has what is called Achondroplasia. Meaning he will be a little person. There are things that are being closely monitored during his growth development.
He has also been on oxygen since birth but neither Riley or Cinncinatti Childrens Hospital can tell his family exactly why. They are hoping in due time he will no longer need it.
It has been a long 8 months for Nash and his family, but if you were to meet him you could understand that it is worth every minute of it. I know they still have a long ride ahead of them but they will continue to plug away to give him the best care they possibly can and continue to seek the answers needed to provide him with the most normal life as possible.
Please help us raise money for the Hensley family so they can get Nash the best care possible! Help them ease the finacial struggle of hospital bills, travel exspenses to and from Riley and Cinncinatti Childrens Hospitals and the everyday expenses of oxygen and special foods. If you can please donate! Nick, Angie, Aleigha, and Nash will be forever greatful!
If you cannot donate please SHARE Nash's story to spread the hope and love!
Nash's mom said "One thing I think we have learned more than anything from this and I hope everyone along his journey of life with him will also learn is that you can never judge a book by its cover. Because that book can give you the best story you have ever read. "
I hope reading about Nash's story has touched you in some way. His little smile has permantly touched my heart and I pray things will get better for him soon and that these donations can help that in anyway possible!
Thank you from the bottom of my heart!
Haley Morris
Organizer and beneficiary
Haley Morris
Organizer
South Bend, IN
Angela Hensley
Beneficiary