Sabrina Jean Marie Herrera Memorial Fund
of $3,000 goal
Raised by 43 people in 77 months
Sabrina Jean Marie Herrera was born on September 8, 2010 and was taken from this world on March 14, 2013, entirely too soon. Her family is now faced with not only dealing with the loss of her young life, but the expenses that come with laying her to rest. This fund is to help them with funeral and cremation costs. Any amount is appreciated! Sabrina is loved and missed and made a huge impact on everyone who watched her grow.
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Sabrina's story (taken from her grandma's blog)
She is the child of my oldest daughter who was almost 17 when she found out she was pregnant. I was saddened that she had a child so young but loved her and have supported her with my whole heart. When she was 20 weeks pregnant she was urged by several doctors to get an abortion because the baby had a stroke in utero. They tried to solve the issue of the bleeding when my daughter refused to abort the baby.
The treatment they gave her made matters worse and by the time she was 25 weeks pregnant the baby had several more strokes. They did not want to take the baby early ( which in hindsight probably would have made her life better). They pushed her until her skin could stretch no more and delivered a very sick baby at 37 weeks.
She was still bleeding and the strokes had obliterated probably 85 % of her brain. We were told to prepare her funeral. At a few months old she had brain surgery to put in a shunt due to her hydrocephalus. A month or so later, she had to have it redone because it malfunctioned.
She has had months of therapy and a few more strokes, and it took forever to get appropriate diagnosis' of her illnesses. She has several disorders: MTHFR ( a genetic mutation), Lipo protein alpha deficiency (difficult to explain), epilepsy, failure to thrive, severe cerebral palsy in all muscles in her body, and she is blind.
We have had lots of ups and downs in her short two years of life and she has spent more time in the hospital than she has out of it. We know that our time with her is limited not only because of her illnesses but because of the errors the doctors have made in her care as well.
We struggle financially, that is to be expected. We also struggle emotionally as well. This little girl is the light of our life. Her smile can brighten even our worst days. I can remember her being on life support a few short months ago, we spoke and knew she was going to be okay by the huge smile she gave us. She cannot speak or walk or eat like your average 2 year old child, but she is our Sabrina.
I love sharing her with everyone because she is such a joy to be around. This is why I share her with you. My daughter is almost 20 now and her life revolves around Sabrina, because she has to have 24 hour care. We help her take care of her, all of us do.