Medical Expenses for Isabella.

Isabella Malia is our beautiful 22 month old daughter. At around 10 months of age, we started to see specialist's for Isabella's neck and head anomolies, facial assymetry and other abnormalities present. We see 2 different children's hospitals, of which diagnosed her with torticollis, plagiocephaly, hypotonia and Congenital Unilateral Hypoplasia of Depressor Anguli Oris, or in more familiar terms, a paralyzed muscle in the face., a rare and permanent conditon. At times, isabella' suffers from a noticeable lip droop(causes gravity to pull her tounge outward and to the right)and left sided arm and hand tightness. Because of her young age, the specialists we have seen did not want her to undergo an MRI. Isabella's delay in gross motor skills(at almost 2 years of age she cannot walk unassisted) and other cosmetic deformities have left her doctors and specialist baffled and without certain tests she cannot be properly cared for and diagnosed.
We have seen a handful of medical professionals, all of which came up short. Most of her signs and symptoms point to a Stroke during birth... We now see a pediatrician on molokai who is helping us to run the tests she needs to be diagnosed and the equiptment she needs to provide quality of life. The medical bills are now starting to come in and will only increase with time.
I would not ask for a dime unless it was for her.. Every penny raised would go to travel expenses, co-payment for her AFO's to assist in walking, her genetics testing, and MRI, Specialist Visits, X-Rays etc. Anything helps, prayers and all. Thank you and God Bless❤