Savannah-Amelia Moulds hopes and dreams
Thanks for taking the time to visit my JustGiving page. Our baby girl Savannah has been diagnosed with a very rare brain condition called lissencephaly. It only affects 1 in 100,000 and the prognosis is poor. Doctors have told us she may not live past the age of 10 and she will likely never walk or talk or meet any of the other milestones most babies do. She will remain at the mental age of around 6 months old. So every day now is a blessing with savannah, doctors said that the pote9flr life threatening seizures and infections are just around the corner and we are living on pins, fearing for the worst but hoping for the best. We just want to give her her best shot at life, getting her all the physio and treatment available to her, we want to prove the doctors wrong. I want to see my baby girl take her first steps and I need to hear her call me mummy, however long that takes. Whatever it takes. We want to fill her life with amazing experiences so we never have to look back and wish we had done things differently with her.
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7.5% of all donations to Tree of Hope in relation to this appeal will be allocated to the general charitable purposes of Tree of Hope to cover our core operating costs