Amelia’s Walk For Cerebral Palsy
Donation protected
Hi everyone if you could all give this a we read it would be so much appreciated.
As most of you may no me and Morgan had a baby at such a young age we were just aged 14 & 15 big shock to everyone it was... 15th of November 2014 came and our beautiful daughter came into this world weighing 5lb 4oz at 6 weeks early. We named her Amelia-Rose. Amelia was the most beautiful contented funniest we girl throughout her baby years & still up untill now... while amelia was growing up we had noticed her milestones weren’t meeting she wasn’t doing the things other baby’s were doing she was delayed in her mobility etc walking & crawling. Fast forward age 2 and half amelia was still not doing these things. We were sick of telling the doctors something wasn’t right here and no one was listening to us.. Finally after the constant running about begging for people just to look at her, age 3 and 9 months amelia was seen by a pedestrian who had sent for Amelia to get an MRI scan to see what and why was there something there that was causing this & yes there was... 11th September 2017 We got told that amelia had a disability named CEREBRAL PALSY... I’ve never ever heard of this name ever! me and her daddy was so confused, what? how?why? Cerebral palsy is a disability that effects the brain to send signals to parts of your body, there are so many forms and different types of this disability. Amelia had gotten CP by premature birth & a lack of oxygen that had went to her brain... cerebral palsy is a life time disability.. how cerebral palsy effects amelia? Amelia suffers with her lower limbs (legs knees and ankles) amelia can only walk so much before her legs will cramp and cause pain to her.. amelia also takes constant spasms in her legs day/night, constant appointments after appointments physio after physio.. . amelia is on medication and injections to try and help the spasms to stop although we are still trying to find the right one. It’s things amelia cannot do that other kids can do witch is very heartbreaking to watch day in & out. Amelias dream is to do what other kids do... (jump, to run super fast, not to have sore legs the list could go on) our daughter is such a funny happy, kind hearted most independent we girl you would ever meet and loves to help others out I have came on here to tell you all what Amelia and me spoke about on Wednesday night. Amelia has decided that she wants to raise money for kids/ adults with cerebral palsy, she has precisely said her self she will walk the divis black mountain. This is a 3 mile walk... to say we as a family are so so proud of her as it is she comes of with this. She our girl is a ROCK STAR!!!
All donations will go to all the doctors and nursers, physiotherapist, pedestrians, OT’s surgents and many many more that help Amelia with her daily days and that they will also continue to do so throughout her life dealing with CP. thank you so much everyone for taking the time to read this it means so much. All donations are welcome. Amelia’s walk will take place on the 3rd of July❤️
As most of you may no me and Morgan had a baby at such a young age we were just aged 14 & 15 big shock to everyone it was... 15th of November 2014 came and our beautiful daughter came into this world weighing 5lb 4oz at 6 weeks early. We named her Amelia-Rose. Amelia was the most beautiful contented funniest we girl throughout her baby years & still up untill now... while amelia was growing up we had noticed her milestones weren’t meeting she wasn’t doing the things other baby’s were doing she was delayed in her mobility etc walking & crawling. Fast forward age 2 and half amelia was still not doing these things. We were sick of telling the doctors something wasn’t right here and no one was listening to us.. Finally after the constant running about begging for people just to look at her, age 3 and 9 months amelia was seen by a pedestrian who had sent for Amelia to get an MRI scan to see what and why was there something there that was causing this & yes there was... 11th September 2017 We got told that amelia had a disability named CEREBRAL PALSY... I’ve never ever heard of this name ever! me and her daddy was so confused, what? how?why? Cerebral palsy is a disability that effects the brain to send signals to parts of your body, there are so many forms and different types of this disability. Amelia had gotten CP by premature birth & a lack of oxygen that had went to her brain... cerebral palsy is a life time disability.. how cerebral palsy effects amelia? Amelia suffers with her lower limbs (legs knees and ankles) amelia can only walk so much before her legs will cramp and cause pain to her.. amelia also takes constant spasms in her legs day/night, constant appointments after appointments physio after physio.. . amelia is on medication and injections to try and help the spasms to stop although we are still trying to find the right one. It’s things amelia cannot do that other kids can do witch is very heartbreaking to watch day in & out. Amelias dream is to do what other kids do... (jump, to run super fast, not to have sore legs the list could go on) our daughter is such a funny happy, kind hearted most independent we girl you would ever meet and loves to help others out I have came on here to tell you all what Amelia and me spoke about on Wednesday night. Amelia has decided that she wants to raise money for kids/ adults with cerebral palsy, she has precisely said her self she will walk the divis black mountain. This is a 3 mile walk... to say we as a family are so so proud of her as it is she comes of with this. She our girl is a ROCK STAR!!!
All donations will go to all the doctors and nursers, physiotherapist, pedestrians, OT’s surgents and many many more that help Amelia with her daily days and that they will also continue to do so throughout her life dealing with CP. thank you so much everyone for taking the time to read this it means so much. All donations are welcome. Amelia’s walk will take place on the 3rd of July❤️
Organizer
Demileigh Bennett
Organizer
Northern Ireland
