Baby Charlotte Pierre Robin Syndrome

Hi, my name is Meghan and Charlotte is my wonderful beautiful daughter. She has not had it easy so far in her young life. Yet she is always smiling and in good spirits and is the sunshine of my life. Charlotte will be 1 year old on September 2nd and she has been diagnosed with Pierre Robin Syndrome.

Pierre Robin Syndrome is a rare congenital birth defect characterized by an underdeveloped jaw, backward displacement of the tongue and upper airway obstruction. Cleft palate is also another defect present in children with Pierre Robin.

She has to have a Jaw Distraction, Cleft Palate Repair Surgery and Removal of Jaw Brackets. 2 separate procedures with a total of 3 weeks in the Hospital and over 2 months of Recovery time..

As a self employed sourdough bakery owner I will be out of work for at least a month and have to stay in San Diego at a Hotel/Air BnB for that time.

The donations would go toward- Food, Gas, Hotel & Loss of income for Bills/Rent

Any help would be greatly appreciated and would go a long way for us.

Charlotte and I thank you so very much!!!