Andrew's Hope: HURRY UP OCTOBER!!!

Wednesday, September 22, 2010

HURRY UP OCTOBER!!!

Well, we just completed a 2 day stint in Boston. Andrew went through an outpatient 24 hr EEG. We won't have any results until next week. Not that I am about to get my hopes up, or get excited but....Andrew has had no drop seizures or clonic jerks for at least 5 days now! I have this feeling in me that says it's just the calm before the storm. Of course Andrew's Neurologist in Boston says OH, NO don't think like that! This is very "typical" of him. I can only hope that we are not in for a grand mal type seizure next. Other than that he is doing well and enjoying his 2 weeks off from school. He starts back on August 31. I have HUGE reservations about whether this fall class will be any better than the summer one. He now has a new teacher and the school it supposed to be getting themsleves specialized training so they can learn how to teach Andrew.

We are very anxious for Andrew to get his seizure dog!!

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About Andrew

Andrew is a very handsome wonderful 6 year old boy. He gives us so much joy to have him in our life and, just like any parents, we want to do everything we can to make his life better.

Andrew has bilateral hearing loss and a difficult to control seizure disorder. Andrew also has a visual processing disorder which essentially makes him "blind". While he can visualize objects, he can not process and identify what he is seeing. On top of this, Andrew also has a swallowing disorder which makes it necessary for specialized feeding.

The seizures Andrew has been diagnosed with have also included Infantile Spasms, which is a very serious diagnosis in a child. Due to the severity and frequency of Andrew's seizures, he is termed as "Global Delay" because of the interruption they cause in his daily learning and processing of information. This is despite of being on multiple medications and therapies.

At 3 years of age, Andrew took his first steps. We are still waiting for the day he says his first word. Andrew has come a long ways in the last 3 years. Having Carina enhance her training to include tethering will be wonderful for Andrew. We have fought long and hard to get him walking, including fighting the school when they wanted to put him in a wheelchair. Andrew should be indepdendent as safely possible and noone should ever hold him back.

Carina has improved Andrew's long term quality of life by alerting and providing comfort before, during and after seizures. She can also help to be Andrew's eyes and ears and provide a much needed source of support and comfort to him as he meets the upcoming challenges in his life. We heard about a great organization that places highly trained dogs.

4 Paws for Ability is a non-profit organization dedicated to helping children and adults with disabilities. The dogs are specially chosen and trained specific to each individual's needs. Our previous fundraising was on behalf of 4 Paws For Ability in order to minimize the wait time and allow us to participate in the process of placing a dog with Andrew.

Why 4 Paws For Ability?

4 Paws For Ability specializes in training service dogs for children with special needs and has a very high success rate. We encourage you to visit their site at http://www.4pawsforability.org/ to learn more about this wonderful organization. 4 Paws For Ability is a 501(C) Non-Profit Agency and all donations are tax deductible. 4 Paws for Ability's mission is to "Enrich the lives of people with disabilities by the training and placement of service dogs to provide individuals with companionship and promote independent living." and "Assist with animal rescue whenever possible by obtaining many of our animals from shelters and rescue groups." Through a family friend, we heard of another family currently undergoing the training and placement process of a seizure response dog for their 4 year old daughter Caitlin. 4 Paws For Ability is very highly recommended and has placed over 500 service dogs!