By the time Finn was 8 months old, we’d really come a long way since those early days after his birth. Doctor’s appointments were less frequent. The surgeries were behind us. We were on the same page. We were engrained in the every day job of parenting our son. As most new mothers do, I imagine, I was spending any free time I had immersing myself in books — “how to get your baby to sleep through the night”, “how to raise a kind human”, “how to make your own baby food” (a short-lived phase), “how the hell to get your baby to sleep through the night?!?!” among others.
On top of the usual parenting books, I was also reading anything I could find about how to raise a blind child. As rare as our situation is, the amount of literature published on the topic is scarce to say the least. I did find one book that was extremely old and extremely technical. But, I took what I could get. The first few chapters were a biology lesson in how the eyes work and communicate with the brain. Helpful information I suppose, but I was well past any interest in the mechanics of it all — just tell me what my son needs already! It turned out that a lot of what Finn needed was no different from what any other infant needs with a few modifications. We learned to talk to him A LOT — for example, I never just swoop in and pick him up without saying first, “Mama’s going to pick you up.” This is to prevent startling him. Or, anytime I carry him throughout the house I describe where we’re going, how we’re getting there, the directions we’re taking. I’m sure a lot of parents do this too, but for Finn it has to be pretty constant and consistent as he depends on these descriptions to learn about his environment.
But when I came upon the chapter in this book entitled “Early Intervention” a lightbulb went off. I studied Early Childhood Education alongside Psychology as an undergrad in college. I even went on to get a Master’s degree in Education Policy. None of this do I use directly in my job in Event Marketing, which has sometimes led me to look back and wonder if I had let my education go to waste. But, now I think perhaps the education path I chose wasn’t meant for my professional career at all — that perhaps it was meant to give me a solid foundation for my career in parenting Finn. All of that is to say, the concept of Early Intervention was not new to me. I knew the basics — that any child born with disabilities or delays is entitled to free government services to help them achieve and succeed to the best of their abilities. I knew this was protected by the Individuals with Disabilities Act (IDEA). Yet, not until I read that chapter had it really dawned on me that we needed to apply for services for Finn. I’m not sure why it took so long — I had accepted Finn’s blindness for sure, but perhaps I was still in a bit of denial that I was in fact, a special needs mom. And though I had basic knowledge of what Early Intervention entailed, I really had no knowledge of what services a blind child would qualify for or need. From what I remember of my course studies, blindness was not one of the typically identified “disabilities” on the list.
Luckily this book laid it all out there for me — the two most important services Finn would need would be a TVI (Teacher for the Visually Impaired) and an O&M (Orientation and Mobility Specialist). A TVI provides tools and education specifically for those with visual impairment or blindness. An O&M teaches those with visual impairment to move safely and independently throughout their environment — for example, how to properly use a cane. I’d never heard either of these terms before, or if I had it had been years ago in school and it didn’t sink in. If only I’d known then that I’d have a blind son 15 years later, I’d have listened a bit more closely! After reading up on these services, I was a bit dismayed that no one — none of the doctors we’d seen — had yet suggested to us that we should apply for these services. Luckily, I read this book and luckily I had the base background education that I did or we may have gone many months or even years longer without getting Finn the services he needed. From there I asked our pediatrician, our retinal surgeon and Miss H their thoughts about Finn’s needs. They all agreed that we needed to apply for services through the state as soon as possible, though none seemed particularly familiar with what the services would be or the process. We were on our own.
I found the Tennessee Early Intervention Services (TEIS) phone number online and called them three times before receiving a call back. When I finally got someone on the phone, I was asked a slew of questions regarding Finn’s medical history. From there, we had to have all of his records transferred to the TEIS offices to prove need. Once they established that there was in fact a need for services, we’d be assigned a Coordinator. This process took about a month. I told the lady on the phone that my son was completely blind. I’d sent her all of his medical records proving this fact. Yet, a month passed before they confirmed and approved this all to be true.
We were assigned a coordinator, we’ll call her Miss C. Our first meeting with Miss C was pretty simple — she came to the house, met Finn, had us fill out some paperwork and let us know that we’d been preliminarily approved for services pending one other medical record they needed. I was annoyed, but things seemed to be moving along. She let us know that we’d then be assigned a Developmental Therapist and we would soon know how many days a month they would allow us to see him/her. I started to ask a few questions that went something like this: “The Developmental Therapist — what is his/her role?” “What is his/her background in vision impairment?” “Would we also be given a TVI and an O&M?”
This is where things went south for Miss C and myself, we’ll call me Mama Bear. She told me that the Developmental Therapist (DT) is meant to ensure that Finn achieves his developmental milestones, but that he/she would have no background in visual impairment. She said she knew of one DT with a background in O&M, but that she was assigned to another county. She went on to say that TEIS had no TVI or O&Ms on staff in my county so those services would not be available for Finn. I’m sorry, WHAT?!?!?! My follow up questions went a bit like this: “You’re telling me that my blind child is approved for services, but none of those services are specific to visual impairment?” “You’re telling me that there are no TVIs or O&Ms in the state of Tennessee available to help him?” “You’re telling me he’s only been approved to see a Developmental Therapist even though he thus far has shown no signs of developmental delays?” Her first answer was “yes”. Her second answer was “well, there are TVIs and O&Ms, but not on our staff so you’re welcome to obtain those services privately and pay for them on your own.” Her last answer, “yes”. As you can imagine, I had some follow up questions: “What about parents of children like Finn who can’t afford to pay for services on their own?” “What about those who don’t have the means to take their child to said services?” Are they just left to fall through the cracks?” Her answers were again, yes, and my response was a simple, unacceptable. Things got pretty tense with the Miss C. I don’t think she was prepared for me to break out the book I’d just read. Or for me to reference the IDEA act. I was armed with knowledge and I wasn’t taking no for an answer.
She did agree to do what she could to get me the one DT in the area with an O&M background even though she was not currently an actively practicing O&M. I took a deep breath and held it together until she left. I was angry. I was in full-fledged mom advocacy mode. As confident as I’d been while she was in my living room, as soon as she left I was deflated and afraid. Afraid that there was nothing I could do to get my son the services he needed.
Though I knew enough about the IDEA act as a whole, I didn’t know much about Tennessee’s interpretation of that law. I did as much research as I could online, but that only took me so far. I started researching TVI and O&M’s in the area to see what kind of information I could gather. I then came across a TVI training program at Vanderbilt University. I emailed the head of the department and explained my situation, and asked if there were any TVI’s on staff who might know more about the Early Intervention system. Candidly, my husband and I have the means and were willing to pay for services privately if necessary, but I wasn’t about to come out and say this in my email. I knew for all the other mothers in my situation out there who don’t have the means, this just wasn’t right. The person I emailed at Vanderbilt immediately responded and gave me another contact there who she said had extensive experience in the field. She followed up a day later with two other contacts. Just when you get discouraged by one person’s seeming disregard to help, you turn around to find another who goes above and beyond!
I reached out to all three contacts and the first one to respond, we’ll call her Miss D, was a certified vision teacher, O&M instructor as well as an early interventionist. Bingo! She could not have been more helpful or sympathetic. She explained to me that having specific vision services for Finn was an absolute necessity and needed to start sooner rather than later. Furthermore, and as I’d suspected, that it was the state’s responsibility to provide them. She offered to come to our house, do an evaluation of Finn at no charge, and meet with him weekly until we could get services from the state. She didn’t want him to fall through the cracks for even a minute. People are so wonderful sometimes!! Miss D came to do her evaluation the next week and put together a full report that spelled out Finn’s developmental status and needs. A lot of children with visual impairments have delays related to development. Thus far, Finn had exhibited no other issues — he’d hit every milestone “on time”. That’s not to say he didn’t need a DT — he was only 8 months at this point and who knew if his development would continue on this path. But, the DT was more of a preventative need for Finn than an immediate one. The need for a vision teacher, someone who could ensure he had the proper tools to learn without visual input, was a true, immediate need for our son. Miss D gave us the name of the head of TEIS for a neighboring county — she told us that she knew of a similar situation to have had happened years prior and that this man had secured a private vision teacher to be paid for by the state of TN for a little boy, also blind. She told me to send her report to him and give the background. She also agreed to call him herself and let him know I’d be reaching out. I heard back from him immediately — he said he’d be sending all of his paperwork from the family he’d worked with years back to my Coordinator and her boss, his counterpart for my county, as evidence of a precedent and what needed to be done. Within days of his email, we were approved a vision teacher to come meet with Finn once a week! We were also approved the DT with O&M background to come 2-4 times a month. Hallelujah! The persistence and help of others had prevailed!
We started the process of applying for services in May. Finn was approved for a vision teacher and began seeing her in late July. It took three months of phone calls, waiting, emails, and most of all, people who cared, to help us to get there.
What I learned from all of this was that my most important job as Finn’s mother is going to be working as his advocate. Being his Mama Bear. At the same time, I’ll be working as an advocate for all other mothers in my shoes just as that one mother in Tennessee had done years before me when I’m sure she had to go through an even harder battle to get her son a vision teacher with no precedent yet set. I think of other mothers out there who don’t have a background knowledge about Early Intervention or have never heard of the IDEA Act and are starting on this journey; who may not have access to or know where to find the books I’ve read; who may take no for an answer simply because they don’t have the knowledge, time or energy to put up a fight that they may view as a losing battle.
As a side note, I don’t want to bash TEIS or even my original Coordinator (we have since moved counties and have been assigned a new Coordinator which I think we were both happy about since we never fully recovered from that initial first impression). For all the stress it caused me for those few months, they have provided really wonderful specialists who work with my son every week in the comfort of our own home. He is now in his 7th month of service and it has truly been invaluable. Though they are here for Finn, they are really here to teach Patrick and I how to equip him with the tools he needs to succeed. I’ve learned so much! So, Early Intervention is an amazing service any special needs parent should take advantage of — just don’t be afraid to fight for what your child needs, what you think and know they need, despite what you may be told. The more precedents we can set, the better for those who come after us. And most of all, know that there are people out there who can help and who are eager to help. Including me!
7 thoughts on “Mama Bears Unite”
This needs to be posted in the family forum at the Federation of the Blind and other pertinent places. Very helpful info for new families in this situation.
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Another remarkable post, Alison. What you are doing is greatly to be admired. Keep it up, and keep on writing!
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You continue to amaze me, dear girl. I love you.
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No surprise you are the perfect advocate for your son and have a meaningful background. Great work momma bear!
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Don’t mess with mama!! So proud of you!
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You are a fantastic mom, advocate and writer! Can you present to the County Board of Supervisors or State Legislature? 🙂
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I’m so sorry that you have to deal with this. Not that your son is blind, but that you have to deal with the overwhelmingly uninformed, unorganized, and misunderstanding system and society. It will continue to be like that. You are right, in addition to the job of mom, you also have been given the job of advocate. It is absolutely essential, as you can see. I am so glad you are writing about it. And I am so proud that another child has been fortunate enough to have a mother that doesn’t trust blindly and accept what is, but instead fights to give her child everything they can have. It’s such a shame that it has to be such a fight just to get basic things, but is it, and your son’s life and well being would suffer greatly if you weren’t a fighter. Proud of your hard work.
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