#HopeForIsabel
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Hello everyone I just want to thank you for taking the time to read this.
Andrew dunning will be jumping out of a plane to help raise money for our special miracle daughter Isabel.
This is the first of many fundraisers we are hoping to do for her and if anyone would like to raise money we would be eternally greatfull.
please share this page and if at all possible please donate...Isabel has been diagnosed with..
Microcephaly
Necrotising enterocolitis
Short bowel syndrome
Cerebral palsy
Cystic periventricular leukomalacia
Gastroesophageal reflux disease
Grade 2 Retinopathy of prematurely
Continuous pump fed
Unsafe swallow
As many of you know Isabel dunning was born extremely premature at 25+4 weeks weighing only 830g.
Throughout Isabel's 5 and a half month stay in the neonatal intensive care unit she's been ventilated, three laparotomy operations to remove her dead small intestine caused by NEC.
She caught septicaemia at the same time and was on full life support, steroids and had seizures.
I could go on for hours talking about everything she went through and everything she still is and will have to go through but hopefully I can keep it short and sweet.
From everything that has happened sadly she has been diagnosed with a lot and is now severely disabled.
Over half her brain has been damaged and gone.
We were told many times to she wouldn't have any quality of life and to turn machines off.
We always believed she was a fighter.
We need to raise money for specialist equipment and sensory equipment.
Sadly the things Isabel will need throughout her life is easily going to rack in to the tens of thousands.
We need to get her seating equipment, sensory toys, go to seat, a specialist car seat, specialist bath.
We need to pay for private splints to be made, the list just goes on and will get even more longer and expensive as she gets older.
We have another beautiful older daughter Chloe and we've tried to be a normal happy family but it's very hard on us all.
Isabel has had 3 operations so far and has to have another major operation this year 2017 to place gastrostomy then gastrojejunostomy extension tube. She will be peg fed continuously through out the day and night.
Thank you for reading
And anyone that wants to come and watch Andrews jump I will put details on my Facebook Page.
https://www.facebook.com/hopeforisabeldunning/
Xx
Andrew dunning will be jumping out of a plane to help raise money for our special miracle daughter Isabel.
This is the first of many fundraisers we are hoping to do for her and if anyone would like to raise money we would be eternally greatfull.
please share this page and if at all possible please donate...Isabel has been diagnosed with..
Microcephaly
Necrotising enterocolitis
Short bowel syndrome
Cerebral palsy
Cystic periventricular leukomalacia
Gastroesophageal reflux disease
Grade 2 Retinopathy of prematurely
Continuous pump fed
Unsafe swallow
As many of you know Isabel dunning was born extremely premature at 25+4 weeks weighing only 830g.
Throughout Isabel's 5 and a half month stay in the neonatal intensive care unit she's been ventilated, three laparotomy operations to remove her dead small intestine caused by NEC.
She caught septicaemia at the same time and was on full life support, steroids and had seizures.
I could go on for hours talking about everything she went through and everything she still is and will have to go through but hopefully I can keep it short and sweet.
From everything that has happened sadly she has been diagnosed with a lot and is now severely disabled.
Over half her brain has been damaged and gone.
We were told many times to she wouldn't have any quality of life and to turn machines off.
We always believed she was a fighter.
We need to raise money for specialist equipment and sensory equipment.
Sadly the things Isabel will need throughout her life is easily going to rack in to the tens of thousands.
We need to get her seating equipment, sensory toys, go to seat, a specialist car seat, specialist bath.
We need to pay for private splints to be made, the list just goes on and will get even more longer and expensive as she gets older.
We have another beautiful older daughter Chloe and we've tried to be a normal happy family but it's very hard on us all.
Isabel has had 3 operations so far and has to have another major operation this year 2017 to place gastrostomy then gastrojejunostomy extension tube. She will be peg fed continuously through out the day and night.
Thank you for reading
And anyone that wants to come and watch Andrews jump I will put details on my Facebook Page.
https://www.facebook.com/hopeforisabeldunning/
Xx
Organizer
Shelley Colclough
Organizer
