Join my family through Ahnalitas scary journey fighting a rare tumor...
My daughter Ahnalita Gabrielle Mcmillin has been diagnosed with an intraoseous capillary hemangioma in the MAXILLARY region which is a VERY RARE tumor in the mouth ((0.5%-1% chance of acquiring condition based on what I have researched... Think of birth control pills... 99.9% effective)) that began as a congenital condition (
was born with abnormality) this condition consists of an abnormal growth of blood vessels embedded inbetween the soft bone (which explains missing teeth in her mouth that never had a chance to form) and needs extensive treatment at Childrens Hospital in Seattle, where (hopefully) all of the necessary treatments will be available. Now that she has gotten older, the area of problem has expanded and will continue to basically demolish the bone in the way... She may lose bone in her pallate and teeth of areas affected to complete the removal and treatment. Dr klein, the oral surgeon who found this condition, is working hard to get a treatment plan and has finally got childrens hospitals acceptance but since these tumors are so rare & this involves the arterial capillaries, the surgeons are affraid of hemorrhage that could occur while treating her :(
It is known that God does things for a reason... Had she not had braces placed, we would have never immagined that she had a serious life threatening condition... Last summer her braces were placed but that is going to waste because of the area compromised... But money is replaceable and my baby girl is not. YOU ARE MY MOTIVATION TO WAKE UP EVERY DAY AND KEEP GOING IN LIFE!! Believe in him and let him take care of this for you:)
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