Beautiful Miss Poppy

This is our daughter Poppy, with the award winning smile.

Poppy was born in 2010 and suffered severe brain damage caused by a lack of oxygen supply to the brain during her traumatic birth. As a result of this, our little girl is severely disabled.

She is registered blind, epileptic, learning disabled and has quadriplegic cerebral palsy, needing full trunk support, and her condition is classed as life limiting.  Cerebral palsy affects 1 in 400 live births in the UK, however Poppy is at the most severe end of the spectrum.

To date Poppy continues to impress doctors with her progress, as it was originally thought that due to the extensive brain damage she incurred during at birth, she might be in a persistent coma. Poppy has overcome massive hurdles, shows alertness and is responsive to her environment.

Our little girl will, however, face further difficulties as she grows, including stiff muscle tone in both her arms and legs, making normal movements difficult and painful. Her head and trunk stability are poor at present, and do not allow her to sit independently or raise her head fully when lying on her stomach.

Despite this, Poppy enjoys different sensory experiences and we try and make every day count for her. She has even been surfing, an experience she just loved! Poppy is able to smile when she is happy and has even started to giggle on occasions, but she is unable to speak or communicate through signing due to her condition. She is currently trialling eye gazing equipment as a means to communicate at school.

We are fundraising for specialist equipment and therapies that will give Poppy the best opportunity to maximise her potential and improve her quality of life. We have a real chance to make a difference to Poppy’s functional outcome, but needs access to the right interventions and equipment.

Poppy is now 10 and will be starting secondary school next year. She continues to grow and has out grown her wheelchair. 

She has been trialling eye gaze equipment as a way to communicate which has been going really well. We really want Poppy to have her own equipment so she can practice daily so she can maximise her ability and to enable her to possibly use this to communicate in the future. 

The first three items we are fundraising for are:

•A new specialist wheelchair- 

•Eye gaze equipment which includes a computer, specialist eye gaze  Software and a specialist camera which tracks her eye movements. -

•A specialist car seat as Poppy finds it uncomfortable travelling for long periods of time, which is necessary when we travel for her specialist appointments in her wheelchair. This car seat has trunk and hip support and is also safer than travelling in her wheelchair. The cost is £3323.00

Have access to these vital pieces of equipment will mean more than words can say. It will enable us to continue to care for Poppy at home, where all little girls should be.

Follow Poppy's story on Instagram @beautifulmisspandme 

Tree of Hope reserves to use these funds for any purpose stated in
the parents charter, including but not limited to, medical treatment, surgery and therapies and related travel expenses, medical and exercise equipment, childcare, home adaptations and the cost of vehicles designed for the disabled.







 



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