Sunday, May 3, 2009

Tri-County Education Center Needs Your Help!

Tri-County Education Center in Noblesville, IN is in danger of closing it's doors. This may be our last hope to save the school. Below is a letter from one of the parents on the current situation and the school districts response.



We have been nominated for Extreme Makeover Home Edition and were recently contacted and asked to complete an application and send in video. We mailed the application materials on 04/24 and sent extensive footage of the school asking Extreme Makeover to do what it can to help these children and possibly save our school.


Please take a moment & leave a message on the coporate line 323-785-2262 of Extreme Makeover Home Edition and ask them to help Savannah Ropke, her mother Sheri Reece and the Tri-County Education Center of Indiana.

To learn more about Tri-County and how it serves the needs of these children CLICK HERE. Her school serves special needs children with a variety of therapies that improve their daily lives and goes far beyond the level of a regular school to address their needs. The school is in danger of losing funding and closing it's doors.

Over the winter I appeared on Channel 6 in Indy with other Mothers with students at TCEC.



Dear Ms. Reece,

Thank you for videotaping our Tri County Education Center building for the application to Extreme Makeover Home Edition. Unfortunately, it appears that our children’s school is in imminent danger of being closed within the next year or two.

I was present at the most recent meeting of the Governing Board for the Hamilton-Boone-Madison Special Services Cooperative on Friday, April 17, 2009. As you are aware, the Governing Board is composed of the Superintendents of the seven school districts that participate in the Co-op for special education services, which includes our school (TCEC). A plan for the use of the economic stimulus funds was proposed, which you have a copy of. Despite the fact that a complete, in-depth review of the state of our school facility and the recommended repairs was presented to the Governing Board a year ago, there is absolutely no mention of using stimulus fund money (the ARRA grants) for repairs and renovations of the Tri County Education Center in the proposal, despite the fact that new projects such as the needed repairs would qualify for those funds.

Even more alarming was the proposal to use the ARRA stimulus grants to fix up one building so that one other facility could be eliminated. Here I am quoting the proposal that was presented at the meeting: “Combining facilities and administrative staff: HBM currently maintains two facilities, HBMEC and TCEC. Long-range efficiency could be reduced by combining the facilities during the two year grant period. Successfully combining facilities is contingent upon a commitment to increase the effectiveness and efficiency of HBM programs and programs in local districts. Potential short-term cost: Small scale renovation costs of one of the facilities which could be funded through the ARRA funds or CPF.”

Since the all of the HBM administrative offices (as well as Mosaics School) are currently located at the HBMEC site, guess which one of the facilities would be closed? Certainly not the administrative office site at HBMEC, which the Governing Board, at this very same meeting, just approved a $30,000 technology upgrade for so that there would be wireless internet access at their building!!!!!

Unfortunately, there is not enough room at the HBMEC site for all of the offices that are currently at TCEC, as well as the 5 classrooms, home living center, sensory room, and gymnasium (and of course, there is no pool or playground there, either). I fear that our school is in imminent danger of closure without any workable plans to relocate it.

In addition to these other issues that I have listed is the fact that the Noblesville School District recently lost their referendum for funds for new building projects. They need more school space and have no funds to build with. I know that the Noblesville Schools Superintendent is requesting the use of space in our TCEC school building for at least two Early Childhood classrooms. The previously open discussions about reimbursements for classroom space and nursing staff suddenly went “under the table” at the meeting this past Friday, with the Noblesville Superintendent and the Co-op Administrator agreeing to discuss the issue of use of space at TCEC at a private meeting. I am very disturbed by that, since these are all public facilities that are being discussed and should not be decided upon at a private meeting without public accountability. I have a very strong suspicion that Noblesville Schools wants to purchase our TCEC building for their own use, and need to do so as quickly as possible.

During a phone conversation on Friday, the Co-op administrator told me that there were no plans to relocate the school to the HBMEC site. He said that he could not comment on any plans regarding the TCEC school until after the Program Review is completed. However, his proposal recommends “expanding options for students with severe disabilities in local districts”. Since we are already aware that the special education literature supports the placement of disabled children in community schools with their non-disabled peers, I suspect that the Program Review will support disbanding the TCEC altogether and placing our students into various existing community schools. However, due to the fact that ours is not the only Special Education facility in existence for children with severe disabilities, and it was obviously a good idea for this school to exist in the first place, I have to question the wisdom of not having an alternative to community placement for children who are medically fragile, or (as is the case with many of the children at TCEC) are not adequately served by their community placement in the first place.

I really wish that I had better news about the fate of our children’s school. If the Governing Board votes to close TCEC, which they appear to be taking active steps toward, then our children will very likely not have a school at all. Renovation and expansion of the HBMEC site, which previously was a school building before housing the administrative offices, may be our only chance to preserve the very special, and very effective, educational experience that our children currently benefit from at TCEC. However, with the current climate of budget cuts in all seven of the co-op’s school districts, I suspect that this will not happen, since the Superintendents all seem to be very resistant to using the stimulus fund grants for anything other than trying to ease the shortfalls in their own districts’ general funds budgets. I fear that if they are left to their own devices, the Superintendents will only pay attention to financial considerations and take the least expensive option, which is putting our disabled children into existing community classrooms. But even that is a poor option, considering the fact that our communities have seen a huge influx of new residents and the existing schools are currently unable to keep up with their own expanding populations and will not be able to adequately house these additional special education classrooms to serve our severely disabled students.

Thank you again for your work on the application to Extreme Makeover Home Edition. Maybe there is some way that they can help us to keep from losing our children’s school. Good luck, and thanks for trying to preserve the quality of the education that our very special children receive.

Sincerely,

Theresa Treep, MD, FAAP
President, TCEC Parent Teacher Association


Please contact Extreme Makeover Home Edition and tell them that TCEC needs their help.

Thursday, January 8, 2009

Help Us Pass Savannah's Law!! (Updated)


SAVANNAH'S LAW INTRODUCED BUT WE NEED YOUR HELP!! We can not get this bill pushed through without massive amounts of support, so WE NEED YOU!

I have been speaking and meeting with state and federal legislators about our situation in attempt to get laws changed that truly impact and devastate the American people. It is a minority group of folks that continually get overlooked and swept under the carpet.

Some potential changes I am proposing will not benefit our family, but will prevent families in the future from experiencing the same devastation our family has as a result of a tragic situation. Therefore, I will not stop this endeavor until changes are made.

Update:Thus far, a bill has been introduced into the 110th Congress entitled "Savannah's Law" HR 5494. It did not make it through the stages it needed to get the attention it deserves. It is currently being re-introduced into the 111th Congress as has yet to be assigned a new number.

I truly feel this should coincide with another proposal I have been discussing with the State legislators regarding auto insurance requirements on a state level. However, I am having much difficulty reaching those that can make it happen.

We can't get their attention unless enough senators and congressmen and women have heard of HR5494 it won't make any progress.

Please visit the previous post in the blog to read our story and help us get Savannah's Law passed. This law will help countless victims and children.

Please take a moment to contact your local senators and congressmen and women and ask them to support Savannah's Law.

Contact your senator(s) here

Contact info for governors, congressmen and senators for all 50 states including fax numbers

Thank you for taking the time to visit.

Wednesday, January 7, 2009

RAISING A CHILD WITH A DISABILITY : "Welcome to Holland"

BY Emily Perl Kingsley



I am often asked to describe the experience of raising a child with a disability - to try to help people who have not shared that unique experience to understand it, to imagine how it would feel. It's like this...

When you're going to have a baby, it's like planning a fabulous vacation trip - to Italy. You buy a bunch of guide books and make your wonderful plans. The coliseum. The Michelangelo David. The gondolas in Venice. You may learn some handy phrases in Italian. It's all very exciting.

After months of eager anticipation, the day finally arrives. You pack your bags and off you go. Several hours later, the plane lands. The stewardess comes in and says, "Welcome To Holland".

"Holland?!?" you say, "What do you mean "Holland"??? I signed up for Italy! I'm supposed to be in Italy. All my life I've dreamed of going to Italy"

But there's been a change in the flight plan. They've landed in Holland and there you must stay.

The important thing is that they haven't taken you to a horrible, disgusting, filthy place, full of pestilence, famine and disease. It's just a different place.

So you must go and buy new guide books. And you must learn a whole new language. And you will meet a whole new group of people you would never have met.

It's just a different place. It's slower-paced than Italy, less flashy than Italy. But after you've been there for a while and you catch your breath, you look around…and you begin to notice that Holland has windmills...Holland has tulips. Holland even has Rembrandts.

But everyone you know is busy coming and going from Italy...and they're all bragging about what a wonderful time they had there. And for the rest of your life, you will say "Yes that's where I was supposed to go. That's what I had planned".

And the pain of that will never, ever, ever, ever go away...because the loss of that dream is a very significant loss.

But...if you spend your life mourning the fact that you didn't get to Italy, you may never be free to enjoy the very special, the very lovely things...about Holland

Tuesday, January 6, 2009

HELP US PASS SAVANNAH'S LAW!!

SAVANNAH'S LAW INTRODUCED BUT WE NEED YOUR HELP!! We can not get this bill pushed through without massive amounts of support, so WE NEED YOU!

Please take a few moments to e-mail or call and tell them Savannah's story and tell them to support the bill HR5494 "Savannah's Law". The links for contact information can be found below.

This could possibly help our family get justice for our sweet little girl and help other families that may be suffering from the same situation.

If passed, it will be a FEDERAL Law so it will benefit all families in situations like ours and allow our children to live fuller lives and ease the burdens on families throughout the country. You can read all about the bill below.

You will also find links below to the contact information for EVERY senator in congress and contact information for all congressmen across the country. Just visit the link to find the contact info for your state.

Please also take a few moments and refer your friends to this group page or invite them to join.

WHAT IS SAVANNAH'S LAW?
Congressman Dan Burton [R-IN-05] announced that he has introduced H.R. 5494 known as ‘Savannah’s Law’ to revise the bankruptcy code in order to ensure that an individual can not file bankruptcy in cases where permanent disability results from personal injury. Currently, the bankruptcy code does not make exceptions for cases of permanent disability.

Said Burton, "This bill is designed to make sure that Americans permanently injured because of someone else’s mistake get the care they need."

Burton introduced this legislation responding to the concerns of his constituent Sheri Reece and her daughter Savannah. In 2003, Sheri was in a terrible automobile accident while she was pregnant with Savannah. Sheri suffered multiple injuries, but unborn Savannah suffered severe brain damage.

Savannah, now 4 years old, is unable to sit, stand, walk, dress or feed herself and requires around the clock care. Sheri was offered a settlement by the insurance company which was severely insufficient to provide Savannah the care she requires and prohibits any further legal action. If the Reece family declines the settlement and moves forward with a lawsuit, the federal bankruptcy court can discharge any judgment she might get from the state civil courts and Savannah would again be denied the necessary care.

Concluded Burton, "I was very upset when I heard the story of the Reece family. The individual that caused this wreck has caused irreparable harm to an entire family. It is important that our laws protect those unfortunate victims of personal injury that results in permanent disability."


Please help today, we can't get this through without the help of caring citizens like you. Your time and interest is greatly appreciated.

Contact your senator(s) here

Contact info for governors, congressmen and senators for all 50 states including fax numbers.

This is our story and how we got here!

Hi everyone....I wanted to give you details of the journey Savannah and our family has had the past five years.

THE ACCIDENT
It was a clear January day. The news had been talking about a blizzard type storm coming in sometime that morning. However, when I headed out to work that morning the skies were clear and the roads were dry. It was cold. I dropped my children off at their schools and went on my way. Rush hour traffic is always a bear to tackle every morning. I was always trying to find a route that was quicker and easier. I thought I found it.....but this ended up being the route that would change me and my family’s life forever.

I was driving the speed limit and following the flow of traffic on a two lane state road. I was headed for the exit that would take me closer to my workplace. I came upon a slight curve in the road and a guard rail that out lined the curve. I never quite understood why that guardrail was there. It seemed to be more of a hazard than anything. Both ends of the guard rail “ramped” down to the pavement rather than a straight edge and they were never marked well. Plus each end of the guardrail seemed to be flattened from cars running into them on many different occasions. Out of nowhere I heard some clanging, crashing type of noises, but could not see in front of the car ahead of me to see what was going on, because of the curve. It all happened so fast, but at the same time seemed to last forever.

Out of the blue I see a car actually flying through the air. The initial thought was “Wow, it’s like something you see in the movies”, not realizing what would happen next. I thought the car was going to fly right by me. Instead, it flew into my driver’s side door. It was like a slow motion feeling. Quickly, the surroundings came back to real time. I immediately took off my seat belt to get out and make sure everyone was alright. Then it hit me…I wasn’t going anywhere. The dash was in my lap and what was left of the driver's side door was laying on top of me. I was trapped. Soon thereafter a woman came to my window frantically telling me “hang in there, someone is on their way”. I couldn’t quite understand why she was so panicky. Quickly, I realized why. I couldn’t feel my left arm or move it. It felt very heavy. I couldn’t feel my legs. My entire body was numb as I was going into shock. The main worry was difficulty breathing as if I was gasping for air. I will never forget the distinct smells while I was gasping for my next breath. I immediately turned to her and said “Please tell them I am pregnant and please tell them to hurry" as I could feel myself fading. I felt as though I was going to black out. I kept telling myself to calm down and concentrate on breathing. All of a sudden everything went black. I could still hear what was going on around me. My experience from nursing kicked in reminding myself that hearing is the last thing to go. I was still alive and I need to fight. I started to think of the last thing I said to each of my children and saw pictures of them in my mind. How I had to stay in this world for them. I thought of my unborn child and wanted to live to see her face and meet her in person. I HAD to make it through this for my children.

The next thing I heard was the sound of a man’s voice asking me for phone numbers. I for the life of me could not think of any numbers. I couldn't think straight like my mind was drifting in and out on a cloud. Then I heard him say “life-line”. I knew then how serious this was. I heard glass breaking while they were trying to extract me from the car, still unable to see and very confused about what was going on around me. "Keep breathing, keep breathing" I kept telling myself. After that, I do not remember a thing. I lost consciousness. Was I dead? I woke up in the Emergency Room at a level one trauma hospital while the nurse was trying to put a chest tube in to re-inflate my lung that had collapsed. She could not get between the five broken ribs that had collapsed with the lung. Once the chest tube was in I began to breathe a little easier but began to feel intense pain in my leg. What was wrong with it? Apparently the bones had broken and were protruding through the skin and muscle. I heard mention of possible amputation. I think I remember saying “I don’t care, just please stop the pain”. I’m not sure what happened after that until I woke up in the Intensive Care Unit feeling very nauseated. I was hooked up to several machines not sure what had just happened and still very fuzzy headed. Unsure of what "parts" I still had or what needed to be done during surgery. I just remember thinking "I'm alive" But what about the baby?

It was shortly after when I discovered the extent of my injuries. I had open fracture of my leg, five broken ribs, lacerated spleen, internal bleeding, hemo-pneumothroax (punctured lung with blood filling the cavity), shattered fracture in my upper arm, fractured scapula, and a concussion. The surgery involved a lot of metal, rods, plates, pins, screws, you name it I had it in the left side of my body. I became half a bionic woman. I also received five blood transfusions due to the internal bleeding. I had several CT scans, MRI's, Xrays, etc. But the most important of all was the status of my unborn child. Was she still with us? I was told that they monitored the baby’s heart beat once I was in the Emergency Room and it was determined that I was somewhat stable. They found a heartbeat...hallelujah!!!! She was still with me!! Not thinking of the complications that she could have experienced as a result of the accident, surgeries, medications,etc. I felt so blessed knowing she was still alive. "She must be a fighter like her mommy" was my first thought.

I was on a morphine drip for pain. I was moved to Progressive Care in two days then to a regular room after that with the chest tube in place the entire time. I can’t describe the pain or horror I felt during my stay. I remember a doctor telling me that if I were to get in an accident I picked a good time to do it, because all of the baby's vital organs had developed and she wasn't big enough to get the impact of the crash......(he failed to mention she could potentially have brain damage). So I held onto this little bit of hope. I was told That my insurance had run out and no further days would be covered in the hospital. I had three children at home to care for and stairs to climb when I got there. I was in no condition to take that on. I couldn’t walk even with a walker let alone climb stairs so I was transferred to a Rehabilitation Hospital so I could learn how to walk again and to climb stairs. After a week it was time to go home.

The next couple of weeks were horrific. Being a nurse, I was always the caregiver not the receiver so it was very difficult to be helpless. I know I was not a good patient. I was frustrated with the fact that I couldn't take care of myself. After all, I had three children I needed to care for but I could barely care for myself. I wanted to get back to being a mommy. I didn't have time for this. I had a shower chair with rollers on it to maneuver from the bed to the bathroom using my one good leg to "scootch". The entire task took quite a bit of time to accomplish. At times I wouldn't make it. I was embarrassed and humiliated. I was isolated to the second level of the home for a while because I wasn't confident in my ability to climb stairs. I had to fold my walker and use it as a crutch as I traveled up and down. Each time I laid down or tried to get up from lying down I would experience an almost complete "blackout" followed by the room spinning. My children were wonderful and wanted to help but I was the one that wanted to take care of them. I wanted them to continue on with their lives. I wanted them to keep being kids because they would never get that time back. I didn't want them feeling like they needed to care for me. After all, that isn't supposed to happen until I am elderly right? I went to my children's sporting events after building my confidence with the stairs but had to attend in a wheelchair due to the amount of walking it took to get in and out of the buildings. I had to be driven by others anywhere I wanted to go. I didn't want to go many places but my kids events have always been important to me. My parents were my saving grace those first couple of weeks.

I went back to work on my walker approximately four weeks after the accident. I was highly advised by my nurse case manager to reconsider returning to work based on my injuries. But, I had planned on taking the full time off for my new baby after delivery. The time I had already taken for the accident had cut into my plan. I did have an extensive ultrasound after I got home from the hospital. The results did not reveal any significant findings which gave me further hope. However, being a nurse, especially a Labor and Delivery OB/GYN nurse, I was still a little worried. After all, physicians advise not to even take an advil during pregnancy much less what we just went through. I had also enrolled into college prior to the accident so I could further my degree in nursing. The classes began about six weeks after the accident. Once again, I attended in my walker. Clasess were held once a week for three hours a night. I attended after work one day a week.

Some time during my recovery I also learned that I was taken to the hospital by ambulance instead of life line due to incoming weather conditions. Life line helicopter was called to come to the scene of the accident to fly me in to the hospital due to the extent of my injuries and most likely because I was also pregnant. However, I also learned that the helicopter took flight to come to the scene and had to return to their take off point due to bad visibility. Apparently the storm the news had been talking about had reached downtown Indianapolis. We were northeast of there and the storm has not approached our area at that time. I wonder to this day if there would have been a different outcome for Savannah had they flown me to the hospital. Life line typically has a very skilled experienced staff on board more familiar with serious injuries. I wonder if getting to the hospital quicker and placing the chest tube would have allowed less time for decreased oxygen to my baby girl. I guess I will never know.

In the midst of all this I had to find out how to pay the bills, what I needed to do to get my medical bills covered by the guy that hit me. The immediate need was to get a car to replace the one that was totaled during the accident. I had just purchased a SUV four months before the accident. I was in love with this vehicle. It was the first automobile that was nice and big enough for the family including the new addition on the way. However, since it was a new purchase, the insurance did not value the car at what I had left to pay on it. Therefore I had to roll the difference into another car. Not to mention the fact that I had not been working so was receiving no compensation and my credit was going downhill during the time it took to find a lawyer that wouldn't screw me over. This was a cut and dry case. Black and White. No question who was at fault and no question that the policy limits would be met if not exceeded from this accident. I wanted a lawyer that was willing to take less than a third for writing a letter to the company of the other driver's insurance and cashing in for very little effort. I found one and it was exactly the case. Once the settlement was done I was able to pay off the car I had purchased with the additional funds that I had to roll over into the new loan. I paid approximately sixteen thousand dollars for a nine thousand dollar vehicle. By the time the medical expenses were covered and the lawyer took his cut, there was little to none left. But this didn't bother me. All I wanted was the results of this accident covered. After all, had this not happened I would have continued to coast through life as I had been. Always striving to reach the American dream. Furthering my degree to open doors for my career so I could take care of my children and give them the best lifestyle I could offer.

But this dream turned into a nightmare...

I carried the pregnancy to term while working full time and attending school. The delivery went without much incident. She was in the newborn nursery and had APGAR scores of 6 and 9. The doctor did a newborn assessment on her and found everything to check out fine. Being a nurse and working in Labor and Delivery and Newborn Nursery, AND knowing what she had been through with the accident, I was leary. I asked the doctor several questions about my concerns. She had slightly overlapping suture lines and a small fontannel. But he told me not to worry. In hindsight I also remember the nurses in the nursery concerned with her being "jittery" so they drew blood sugars and, of course, they were fine. I also remember getting her newborn pictures in the hospital and the photographer having difficulty positioning her due to "stiffness". These were all signs that no one picked up on...and of course I overlooked because I wanted to hang on to the "hope" the medical professionals were giving me. I took her home and began to notice she was very irritable. I thought she might have colic.....but , again, in hindsight I figured out that was not the case. I also noticed a poor suck reflex, which I expressed to the doctor during her newborn visits and I was told not to worry. Another symptom was constipation. Her bowel movements were hard and sometime the size of softballs (how miserable that must have been for her).

Once she started into the developmental milestones at around 4 months of age, I noticed she wasn't holding her head up very well. I also mentioned this to the doctor. his response was "just give her a couple of months, some kids are just a little delayed". That was it for me...I just had a bad feeling that something was really wrong. I made an appointment with First Steps to have her evaluated . I also made an appointment with a developmental pediatrician to get a baseline assessment. First Steps came in, did an evaluation, and determined that Savannah qualified for services. All the while I was doing research on what could possibly be wrong. I was never a pediatric nurse so I was not familiar with pediatric conditions. Nor did I realize that there was a brain condition out there that didn't eventually lead to an early death. I thought all disabilities were degenerative and typically none of them had a long lifespan. During the research phase I realized how wrong I was. There was no evidence of ANY genetic or hereditary problems on either side of my or her father's families....which is what I was running into during my search. The ONLY thing I could come up with was cerebral palsy. I asked the First Steps evaluators if this is what they thought was going on with my child...I asked them to please help me try to understand what was going on with my daughter. Their response was "we can not diagnose children".. I told them I understood, but this was totally off the record. I needed to understand what was going on so I could help my daughter. They would not budge.

Then came the appointment with the pediatric developmental doctor, which I could not get for two months from the time of the call. I will NEVER forget this day. I took her in and the doctor did an assessment and told me "I am glad you picked up on this, I share your concerns for your daughter. We need to get an MRI". Once they received the films, a neurologist came to the office to read them. The setting of this meeting will forever be ingrained in my mind . The films were on the "light board" both doctors were standing on each side of them. We were taken into a room where it looked like staff members were taking a break around a table. The neurologist then told us the news...."this area right here is abnormal" After the initial shock we reconvened in the exam room and the questions began.....how bad was it...how will this affect her life? What will she be able or not able to do? It was like pulling teeth to get information. I couldn't believe that they couldn't be more forthcoming with information about what was going on with my daughter.....

Then the REAL journey started...now I had to set up appointments with SEVERAL different types of services....arm braces, foot braces, new doctors, medications, injections, a physiatrist, a neurologist, an orthopedist , cardiologist, opthamologist, gastroenterologist etc etc etc....I was lost. I was caught in a whirl wind. As a nurse I had always worked around doctors and all of them said the same thing..."there is no doubt in my mind that the accident caused your daughter's condition"...however, I could not get any of the doctors that evaluated her to commit to this...they would state what her condition /diagnosis was and also mentioned the accident in their documentation but they didn't link the two. I finally asked one of her doctors to address causation. She informed me that this was not a typical service she provided but did know a very reputable pediatric neurologist that provided this service. It was the main objective of his practice. However, he was located in South Bend. I didn't care if he was at the North Pole...I needed this..I needed to know.

A cardiologist saw Savannah for one visit for a heart murmur concern to which he determined was benign. During the visit I discussed with him the accident and how I had been on a quest to confirm my suspicions that the accident was the cause of her condition. He explained to me that typically if cerebral palsy is related to a genetic disorder it is metabolic in nature. He went on to say that if a genetic condition is diagnosed it is considered the primary diagnosis and the cause of developmental delay. He then said that cerebral palsy in these cases is a secondary diagnosis. Otherwise, if cerebral palsy is a primary diagnosis it is typically a result of an event that happened in utero, during birth , a premature birth, or the first five years of life. He said that the event causes decreased or lack of oxygen to the brain resulting in damage or death of brain tissue. He performed a test the day of Savannah’s office visit that could determine if her condition was due to metabolic factors or not. The test proved it was NOT metabolic in nature. Therefore, his feeling was that the accident was most likely the cause of her condition, but encouraged me to take Savannah to the pediatric neurologist as this would be a more specialized evaluation and would provide a more definitive diagnosis.

When I called the pediatric neurologist office I was asked if I had a lawyer. I told them I wanted to be sure this was linked before I made this step. I had a lawyer immediately after the accident but wasn't sure I was going to use him again.....even though I had been talking to him about the possibility of a claim for my daughter.....The doctor's office would not see her unless she A) had a lawyer's recommendation or B) a referral from a doctor.... I thought WOW he really does only see these type of patients...I called the doctor's office that recommended him...she immediately sent a referral...

The pediatric neurologist was the most intelligent medical professional I had talked to since the beginning of her medical journey. He ordered multiple tests and went through an extensive and very thorough history on Savannah and myself. After reviewing one hundred and eighty seven MRI images with me describing areas of the brain that had been damaged or did not develop at all, and explaining every wave form on several EEG studies, he was able to pinpoint her brain damage to her gestational age…..which happened to be at the time of the accident. He also stated “this little girl deserves some compensation, and you need a good lawyer”. He recommended a lawyer he was familiar with.

Thus began our long painful legal battle with the system. Not only the legal system, but the start of fighting legislation who set the laws currently out there that work AGAINST the American people. The same laws that prevent those of us that have or lives stripped away from us keeping us from reaching the American dream.


more to come about our battle with the system!!!! This part of the story will baffle all of you. It is unbelievable how America can let what happened to us happen at all to ANYONE. It is amazing and will leave you with your mouths on the floor and your heads shaking in disbelief. Because....until you live through it you will never understand it or even know that it is going on in the world!!!

WILL POST MORE ABOUT OUR LEGAL BATTLE WITH THE SYSTEM LATER THIS WILL INCLUDE THE MEDICAID SYSTEM THE AUTO INSURANCE SYSTEM THE LAWS THAT IMPEDE ABILITY TO GET THE PROPER HELP AFTER A CATASTROPHIC SITUATION, THE LAWS THAT DON'T ALLOW PROPER COVERAGE FOR COST OF LIVING FOR A FAMILY THE LAWS THAT PREVENT PEOPLE FROM REACHING THE AMERICAN DREAM AFTER EXPERIENCING A CATASTROPHIC SITUATION....ETC ETC ETC

Friday, December 12, 2008

If you would like to help Save Tri-County School

CALL THIS NUMBER TO HELP US SAVE THE SCHOOL. YOU HAVE TO LEAVE A MESSAGE. THIS IS THE NUMBER TO THE PRODUCTION OFFICE AT EXTREME MAKEOVER.
1-323-785-2262
Please stress the importance of how this will help several communities, families, and especially a group of children that truly deserve what this school has to offer them.
If Extreme Makeover could renovate or re-build the school, the board would have NO REASON to close because of lack of funding

e-mail the penningtont@abc.com address

The more influx of calls we give them at the production office the better

There is an application process to Extreme Makeover however it is 20 pages and a video needs to accompany it...with the upcoming meetings to decide the fate of the school..I am not sure we can accomplish it that quickly...please inform them we will gladly do the application process however we are in a bit of a time crunch and would like to give the "board" a resolution so they won't even have to vote on this!!!


Please read and listen to the new stories below to find out more about the potential closing of a school that serves a vital role in our children's lives who face challenges from their disabilities.

PLEASE HELP THE KIDS!!

Saturday, December 6, 2008

Savannah and I join other families on Indianapolis FOX59

Savannah and I were recently guests on FOX59 along with other families of Tri-County Schools.



If you'd like more information on how you can help please contact me at ForSavannahsSake@gmail.com. Thanks for watching!

Call 6 For Help with Rafael Sanchez Steps in to Help Save Tri-County Opportunity School in Noblesville, IN Thanks WRTV!!

Savannah's school is in danger of closing. They are facing budget problems. Please watch the video and see how important it is for us to save this school for the kids. We urgently need your help.



Please take a moment and send a message School Board President Steven Wornhoff at swornhof@ccs.k12.in.us and let him know how important it is that let them know how important it is to keep Tri-County Opportunity School open for all of our children.


If you'd like to help or want to learn more please contact me at ForSavannahsSake@gmail.com.

Tuesday, December 2, 2008

SAVANNAH'S STORY /Blogging


Just wanted to let people know I intend to share more of my story when I find the time. I'm currently now worrying about and working to stop the closure of Savannah's school. In addition to Savannah's needs I of course have 4 other children so my time is always limited, but I want to share our story with the world. The last five years of our lives have extremely challenging and filled with the constant struggle of trying to find the resources to meet Savannah's needs. Not just her daily needs but her needs for the future.

Thank you for visiting the page and when there is time I promise to share more of our journey.

Monday, December 1, 2008

Tri-County School in Danger of Closing

I recently received an e-mail from a mother of a child with special needs that attends the same school that Savannah does...and the board is thinking of closing the school...this is a facility that specializes in the needs of our kids...we need to fight to keep it open and need as much support as we can get...apparently they are having a meeting on December 12th to begin the decision process.

I have already tried to contact the media..but the more support we have the better.

Here is the copy of the e-mail the parent send out to all the kids parents:

Hi Tri County Parents,

My name is Meredith Serpas, my daughter Olivia is a student at Tri County. I am sending you some disturbing news regarding our school. This past month Tri County received a financial review from the Superintendents of the eight school districts. Led by Dr. Barbara Underwood from Carmel, a push is being made to close the school. You read that correctly. THEY WANT TO CLOSE THE SCHOOL.

They have done all of this as quietly as they can and hope to have a meeting December 12th to decide. All this without informing the community or parents. Afterall to them, it is basically only effecting 40 plus students. I believe it is much more than that.

To save money, they want to mainstream the children to their local school districts. The cost of running Tri County is shared between three counties(Hamilton, Boone & Madison), within those counties, there are eight school districts. Tri County school handles those children who have been classified as severe or profound. It is my belief that within the spectrum of children classified as "special needs" there is a group that will not benefit from mainstreaming. The typical special needs classroom in a mainstream setting is not prepared nor equipped to handle these children. Children at this level are not learning colors and numbers they are learning "life skills". Their parents want them to communicate, feed themselves, walk . The school districts are trying to save money at the expense of what is in the best interest of the kids. They will simply Warehouse our children to save a buck. As a parent of a child in this "special category" I am appalled at how this is being handled. I am disgusted that in this age we have a group of pencil pushers who simply care about the bottom line. What will happen when you take this group and place them, some will be declared too disruptive and will have to final alternative choices. For many parents they will simply keep their kids home, isolating them and keeping them from reaching their potential.

We are the voice for our children. I am but one mom, but together we can be heard. Please contact your local Superintendent. Call the Govenor, Congressman and Senators. What they want to have happen is that they hold a meeting, make a decision and simply let us know. We do not have a lot of time. If you have any ideas let me know. I am currently trying to reach (over the holiday) and attorney for disability issues.

Meredith Serpas

Sunday, November 23, 2008

We've been nominated to Extreme Makeover Home Edition!

Back in July we were nominated for Extreme Makeover Home Edition. Below is the letter that was submitted on our behalf.




Please wish us luck and keep us in your prayers.


Hello Extreme Makeover Home Edition,

My name is April Sjoholm and I would like to nominate Sheri Reece and her family who truly deserve an Extreme Makeover. Before I go into detail, I would hope you would take into account Savannah 's story and all the trials this little girl and her family have had to endure and will continue to endure as they battle together this lifelong disability. Their home may not look like it is ready to fall down on its own, but it is in desperate need of a makeover since it does not even come close to meeting Savannah's needs.

Savannah's Story

Sheri Reece is a single mother of 5 children. Over 4 years ago, she was involved in a life threatening car accident. The individual responsible was air borne in his vehicle when it struck her driver's side door. Sheri was life lined to the nearest level one trauma hospital with multiple injuries fighting not only for her life, but the life of her unborn child. Sheri did carry her pregnancy to term, however being a nurse herself she looked for possible complications due to the high level of trauma and near death experience. Four months after Savannah was born, she was diagnosed with Cerebral Palsy. She is unable to sit, stand, walk, dress or even feed herself.

Sheri is not only struggling with the day to day battles of being a single mother of 5, but she also faces the challenge of providing the best possible care for Savannah . She struggles financially for several reasons according to Indiana Law, insurance companies are only obligated to offer policy limits (whatever is purchased by the policy holder). Policy limits do not even come close to covering Savannah 's life-long disability. Throughout her quest to find proper care, single parent of 5 and juggle work, Savannah 's health began to deteriorate and she lost a significant amount of weight.

Sheri was forced to quit job as a registered nurse because she could not find qualified care for Savannah . Private insurance companies do not cover home care and no facilities offer care for special needs children, so she had to quite her job to provide the proper care for Savannah not to mention transporting her to 3-5 medical appointments a week. Now Sheri has no health insurance for herself because she can not secure employment.

Before this tragic accident that has left Sheri and her family devastated and at risk of losing everything, she built a home and provided the best possible care for her family. They moved into a 2-story home in Noblesville. Now this home once a foundation for love and nurturing has become a challenge and an obstacle.

Savannah's disability will last a lifetime, but the struggle this family is facing right now does not have to be. With the help of Extreme Makeover Home Edition, this family can learn to enjoy life more and worry less about some of the obstacles they are currently facing with their home. By building a home for this family, you can not only change their lives forever, but be an inspiration to the entire community.

Description of the major challenges within the home:
Savannah was just an infant at the time Sheri bought her home. It was difficult to determine at that time what challenges lied ahead as she had not enter her developmental phases of life yet. As she started entering these developmental milestones, Sheri discovered her physical challenges and have been trying ever since to help her overcome them. Some things are in God's hands. As Savannah grew it was apparent that her physical challenges would make her severely dependent on others for all aspects of her care. Physicians have indicated to Sheri that she will most likely never walk independently. She is unable to bear weight independently either. She is reliant on adaptive devices and individuals around her to function. The adaptive devices have been very difficult to obtain, not to mention the obstacles that we must overcome in the home.

All bedrooms and bathrooms are located on the second level of the home. Thus, carrying Savannah up and down stairs several times a day. As she grows this becomes more and more difficult. Bathing has also become somewhat of an obstacle. She is a total lift.. Bending over to place her into the bathtub has proven to be a challenge. The first floor of the home does not allow enough space for a bedroom and bath for Savannah , unless an addition is built onto the home. Sheri has looked into this and realized she is unable to afford it. She is also unable to find a program that will assist with funding to make this happen. Savannah utilizes a gait trainer (walker) in attempt to ambulate. She does require assistance with this.

Sheri is diligently trying to get her to initiate steps on her own. She is able to make the motions but requires someone to push the walker in order for her to take a step. Hopefully someday she will be able to perform this on her own. Carpeting on the first level and the enclosed areas impede this goal to some degree. It is much easier for her to use the walker on solid ground. She has also looked into solid flooring for the first level and , again, simply can not afford it. Savannah is practicing potty training at school but Sheri does not have the proper accessible toilet to practice at home. It will be difficult to master this without the proper equipment and, again, have been unable to obtain.

When Savannah is cradled through the hallways and stair well, at times, her little feet bump into the walls because there is not enough room this will continue to get worse as she continues to grow. The stair well is not conducive for a chair lift (this has also been looked into) and no room for an elevator...none the less the inability to absorb the expense.

Currently Savannah is in a chair that can be transported into a vehicle, however, the chair and Savannah have to be transferred together. This is also becoming difficult. This creates safety concerns for Sheri because she has almost dropped her a couple of times with transferring her not only in and out of a vehicle but indoors as well.


A NOTE FROM SHERI:
I have only been able to have the pleasure of watching one episode of Extreme Home Makeover and it was a true miracle. Our family doesn't need the "bells and whistles" We just humbly ask for accessibility for our precious Savannah in order to make her life as she grows as independent as possible so she won't have to struggle performing tasks that all of us do every day that we unfortunately take for granted. She didn't ask for this and deserves a fighting chance. We all have choices in life that can "make us or break us". Savannah will be limited in opportunities but I, as her mother, believe that with a little help from those that care and A LOT of love, all things are possible. Savannah and I came very close to losing our lives one tragic day. She may have ended up with challenges, but God put her here on this earth for a reason and I know I would not be the person I am today without her in my life. She, along with all my children, are a precious gift. Savannah truly deserves the opportunity to live life to its fullest even with her challenges. Thank you for taking the time to consider helping Savannah .....it is folks like you that give me a glimmer of hope that miracles still exist. If you are unable to help our family at this time, I understand, but would appreciate prayer for my beautiful Savannah , our family, and the families out there that face the same challenges.

Dan Burton Introduces Savannah's Law

Dan Burton introduces Savannah's Law

Indiana Legislative Insight covered some legislation Dan introduced in last week's issue:
U.S. Rep. Dan Burton (R) introduces H.R. 5494, known as "Savannah's Law," to revise the U.S. Bankruptcy Code to ensure that an individual cannot file bankruptcy in cases where permanent disability results from personal injury. The bankruptcy code does not currently offer exceptions for cases of permanent disability. Rep. Burton introduced this legislation responding to the concerns of constituent Sheri Reece and her daughter, Savannah Reece.

In 2003, Sheri was in an automobile accident while pregnant with Savannah. Sheri suffered multiple injuries, but unborn Savannah suffered severe brain damage. Savannah, now four years old, requires around the clock care. Sheri is also a single mother to four other children and a neo-natal intensive care nurse. Sheri was offered a settlement by the insurance company which she contends was insufficient to provide Savannah the care she requires, and which would bar any further legal action.If the Reece family declines the settlement and moves forward with a lawsuit, the federal bankruptcy court can discharge any judgment she might get from the state civil courts, and Savannah would again be denied the necessary care.

Crossposted at Dan Burton's Healthcare Blog:
http://www.danburtonblog.com/health_care/

Saturday, November 22, 2008

Savannah's Story

Savannah's Story
I am currently working on providing readers of this site all the details of our journey from the date of the accident to present day..It is long, detailed and complicated. I should probably write a book.

In the meantime, while I am busy with this, please view the Channel 6 news story below. I struggled for over 9 months with private insurance companies trying to get Savannah the much needed medical equipment/adaptive devices required so she could sit, stand and potentially walk. The insurance company wanted to deny the equipment due to it not being "medically necessary" ...what a crazy world we live in!!!




THANKS TO CHANNEL 6 FOR THEIR HELP!! They made one phone call to the insurance company I had been battling for over 9 months and were able to get this equipment not only authorized, but delivered to our home within 2 weeks!! We will be forever indebted to them for making this happen for Savannah!