Every mom dreams of the moment when she delivers her baby and the doctor hands her that sweet, perfect little newborn. That first moment when a mom gets to see the tiny human she's been carrying for nine months is incredible. She hopes her new child will be free of pain and stay out of harm's way, because she loves them more than anything in the world.
But when Rhiannon Atkinson gave birth to her sweet baby girl Pippa she never could have imagined the heartache she would go through because of a rare genetic skin condition she was born with.
She was missing most of the skin on her hands and feet
When little Pippa was born, she was missing 90 percent of the skin on her hands and feet. She was constantly in excruciating pain, and the doctors diagnosed her with epidermolysis bullosa. According to Little Things, "Whenever anyone touched Pippa's skin a blister and tear would emerge."
Atkinson said that when Pippa was born it looked like her hands and feet had been dipped in boiling water. Atkinson was heartbroken.
"Being told your child has an incurable condition is incomprehensible," Atkinson said. "It broke my heart ... But then not being able to touch her or cuddle her for five months was torture."
Pippa had to spend the first months of her life lying down on a pillow, and no one could touch her skin or she would feel extreme pain. She was eventually able to come home from the hospital, and her condition improved since her diagnosis. Her mom also learned how to clean her wounds and change her bandages.
Constantly caring for the blisters is difficult, but it was especially difficult when Pippa was still a newborn. Atkinson said she had to clean the house 10 times per day so the blisters wouldn't get infected and worsen.
Intense pain isn't the only terrible thing about this condition. Because of her skin sensitivity, Pippa hasn't learned to crawl or walk, and she's 14 months old. Her mom wrote on Facebook, "Seconds on her feet fully supported by me results in two blisters on her right foot and one on her left."
The family is doing everything they can to find a way to make their daughter more comfortable. They're looking into putting another room in their home to house a Microsilk bath, which exfoliates the skin "to remove dead skin and scabs." They set up a JustGiving account to raise money for the expenses.
Until the family is able to add this extension, they will continue to care for Pippa and keep her pain under control. They're keeping a positive attitude, and won't give up hope until a treatment works for Pippa.
Lindsey loves traveling and shopping, and her favorite place in the whole world is Disneyland. She also loves spending time with her family and cute husband. She is studying Professional and Technical Writing and is part of the content team for FamilyShare.