Analisa Latchman

Analisa Latchman is a 24 year old female patient who was born with a cranial deformity that has now become very symptomatic. Her condition is called frontal bone dysplasia and has started to show defects since she was 10 years old. However as she grew the defect became more pronounced and more symptomatic.

Her symptoms include :
Constant
Headaches

A visible defect of her left eye known as endothalmus where her left orbit is slowly receding into her skull. Causing increase pressure to her brain in that left side.

Frontal bone thining and bulky extraoccular muscles on the left side.

Recently she has started to have loss of consciousness.

She has had consultations with the ophthalmologist and the maxillofacial surgeons as well as
Dr. Dukhi the neurosurgeon in Guyana. His major concern is as the disease progress it will cause her entire left side of the face to receed inward along with the left eye and continue to squeeze on her brain even furthur. This can then lead to a stroke and seizures that cannot be controlled.

As a result of this Analisa requires a surgery to be done by 3 specialities in order to reconstruct the left side of her face and have a microfilm placed that will stop the progression of the left side of her face inward. This surgery requires the neurosurgeon the ophthalmologist as well as the maxillofacial surgeon and it is very technical. It is also tremendously expensive.

We are kindly asking for your support to save this young lady's life. She is a mom and the only child for her parents. Please assist in whatever way you can. You can contact her mom on #592 [phone redacted]. Thank you very much.