Meet Michaela, my sweet, happy, inspiring niece. Michaela lights up any room with her beautiful and sincere smile and she has brought so much joy and happiness to all those around her since she came into this world. Unfortunately, at 6 months, Michaela had multiple seizures called infantile spasms, she was rushed to the hospital where after many testing they diagnosed her with Lissencephaly; a rare brain abnormality cause by a chromosome deletion. Because of the Lissencephaly, it does not allow her to develop like other children or live the life we hoped and dreamed for her. It comes with global delays and seizures that affect her both intellectually and physically. Unfortunately, Michaela has a life limiting condition which is devastating to the family and those around her. We want her to have the best quality of life which is very costly as her family is paying for all of it. This includes lots of different types of therapies. With all the therapies, Michaela has shown some much progress that doctors said she may never do! She continues to show her strength and determination and to stay with us for as long as she can! She will fight any battle that comes her way! Please support Michaela and her family fight this battle! Your generosity will help pay for her all her medical/therapy treatments and many adaptive equipment which are costly.
Money raised through this go fund me page will be dedicated to her ongoing care and legacy.
Please open your hearts for this sweet girl who deserves every chance at normalcy while she is with us. Every penny counts.
Michaela is a princess with the strength of a warrior!
She needs all your help to continue to be that warrior princess!
Follow her journey through Instagram: @miksroks
Thank you in advance for your generosity!