Travel expenses for Michael’s Dr appointment

Michael was diagnosed with MECP2 duplication syndrome when he was 6 months. MECP2 is a neurodevelopmental genetic mutation that affects boys. It is characterized by low muscle tone during infancy, feeding difficulties, developmental delays, poor or no speech. Half of the boys experience seizures which can lead to developmental regression and spasticity. Some boys learn to walk while others require assistance. Recurrent respiratory infections are also common but can result in death. As of right now there is no cure for MECP2. However, doctors at Texas Children’s in Houston are working to develop a drug to reverse the mutation.

With that being said, we are taking a trip to Houston in April to meet with a neurologist who specializes in MECP2 duplication. They are going to evaluate Michael and hope they can answer our questions.

We are asking for donations to help us with travel expenses to Houston. Any amount is greatly appreciated and we thank you in advance for helping us fund this trip.