Getting Hudson a band & trips
Donation protected
First and foremost, thank you for taking the time to read this. Some know Hudsons story some of you are unaware of my sweet Hudson. Let me give you short version.
March 22,2017 Hudson was born via C-section at 33 weeks due to several problems we were unaware of until 3 weeks prior. Hudson was born at 2lbs 9oz, later to find out he has a very rare chromosome deletion. So rare he is the only one in Texas. Hudson was in the nicu for 3 months and continues to go to Dr.s and specialist monthly in Fortworth @ Cooks.. Along with the chromosome deletion Hudson has missing parts in his brain,he's had 2 surgeries(G-button & spine) & countless procedures & test.. He is finally 12lbs,is on oxygen at night and nap times..He is fed by g-button only due to aspiration & is still physically and mentally like a 2 month old! We will be getting hearing aids in may & hopefully eye surgery soon..(not sure what % blind he is yet) kidney issues and the list goes on.
Now, for this go fund me account.
Hudson was approved for a head band to help fix this sweet melon of his as it is growing up and out on the left side and we are trying to prevent any more neurological issues..To my surprise His insurance did not approve paying for the band as they do not cover his diagnosis... As family and friends know I became a single mother and am doing this crazy life with Hudson and older brother the best I can and with the best help from family & friends at the best of their abilities..Unfortunately, I am unable to work due to all his appointments in fort worth,therapy weekly and he has to have someone watching him 24/7 due to the breathing issues.
Asking for help is not the easiest for me to do.. But, I have to put my pride aside and ask... This band is crucial for him, and due to his slow growth they are estimating us traveling every 2/3 weeks to fort worth for the next 2 years just to check his growth in the band. I know that financially getting him there for these trips and the band its self is not something I can financially do myself..
This would help pay for his band,gas,food and any emergency that pops up (you never know what will happen with a SN kiddo).
Please, if you are in any spot to help this momma out I would be forever grateful.. If you are not ,please just send a prayer our way as I am always grateful for prayers for my sweet boy!!
If you don't already, please follow Hudson and his story at #HudsonStrong on fb!
March 22,2017 Hudson was born via C-section at 33 weeks due to several problems we were unaware of until 3 weeks prior. Hudson was born at 2lbs 9oz, later to find out he has a very rare chromosome deletion. So rare he is the only one in Texas. Hudson was in the nicu for 3 months and continues to go to Dr.s and specialist monthly in Fortworth @ Cooks.. Along with the chromosome deletion Hudson has missing parts in his brain,he's had 2 surgeries(G-button & spine) & countless procedures & test.. He is finally 12lbs,is on oxygen at night and nap times..He is fed by g-button only due to aspiration & is still physically and mentally like a 2 month old! We will be getting hearing aids in may & hopefully eye surgery soon..(not sure what % blind he is yet) kidney issues and the list goes on.
Now, for this go fund me account.
Hudson was approved for a head band to help fix this sweet melon of his as it is growing up and out on the left side and we are trying to prevent any more neurological issues..To my surprise His insurance did not approve paying for the band as they do not cover his diagnosis... As family and friends know I became a single mother and am doing this crazy life with Hudson and older brother the best I can and with the best help from family & friends at the best of their abilities..Unfortunately, I am unable to work due to all his appointments in fort worth,therapy weekly and he has to have someone watching him 24/7 due to the breathing issues.
Asking for help is not the easiest for me to do.. But, I have to put my pride aside and ask... This band is crucial for him, and due to his slow growth they are estimating us traveling every 2/3 weeks to fort worth for the next 2 years just to check his growth in the band. I know that financially getting him there for these trips and the band its self is not something I can financially do myself..
This would help pay for his band,gas,food and any emergency that pops up (you never know what will happen with a SN kiddo).
Please, if you are in any spot to help this momma out I would be forever grateful.. If you are not ,please just send a prayer our way as I am always grateful for prayers for my sweet boy!!
If you don't already, please follow Hudson and his story at #HudsonStrong on fb!
Organizer
Megan Price
Organizer
Wink, TX
