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Play Ball!

Updated: Apr 20

Obviously, there is a lot of press this month in honor of Autism Acceptance and Awareness month. I have a lot of feelings about some of the things I see on social media about these topics but I’ll save that for another time. This is saved for something I'm very excited about!

It's springtime and we know what that means, right? It's flowers, spring cleaning, new hope and BASEBALL! Rochester is a great place to catch a game, one of the very best as a matter of fact. Frontier field is a great ballpark as many of us know. Beautiful Park, great food, awesome local drinks, and family friendly. The General Manager of the Red Wings, Dan Mason, is a local guy. He's also a hockey player and I won't hold the fact that he played at one of the other Catholic Schools against him anymore. But the one thing he and the whole organization are awesome at is promotion and community! Minor league baseball is a hard sell, especially in this post COVID world. They were hurting after a season off and I’m excited to get back to the ballpark myself.

But, as a family with a special needs kiddo it's not as easy as grabbing some tickets, getting to the park and just kicking back. There are all kinds of considerations for us. For Gavin it's food and drinks, it's space to be G, it's keeping him safe and with us. There is also the unknowns like how will he be with the crowd or the loud sounds? So, it takes a bit more thought and consideration for sure! But it's spring and I want to take my boy to the ballpark just like my dad did.

Well, enter the Rochester Red Wings! This past week they made a formal announcement and debuted their brand new Sensory Suite! A great ballpark just got so much better! This is a beautiful suite that’s outfitted with a lot to help families like ours and our kiddos. Sensory toys, perfect decor, and other enhancements to make the game fun for us, safe and enjoyable for Gavin and truly a service to our community! I personally cannot wait to see the space in person!



It's one thing to be aware and accepting but, to run with it and make a difference in so many lives, that's all you can ask for from your hometown club! To say we are blessed with the services offered in Rochester would be disservice to what really is available to us. The Red Wings just upped the ante with this contribution to our community!


Thank you to the whole Red Wing organization for this awesome gift. We appreciate it so much. Someone please grab me a beer, some peanuts, a plate and lets PLAY BALL!


#rochesterredwings

#rocredwings

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Happy belated Thanksgiving everyone! The 2022 Thanksgiving at the Varecka home will certainly never be forgotten! Let me tell you why! As I’ve said before, with Gavin, it’s just easier to host maj

So... they say it takes a Village.

More like a whole county!

Every parent knows what it takes to get by day to day with a 5-year-old boy.    It’s high energy, loud and always interesting for sure...   They’re dirty, they’re strong enough to break lots of stuff and smart enough to get into plenty of trouble, right?     Well, add ASD into the mix and it’s like turning the volume up to 11!   Thankfully, we have some great people around us to help with all this fun!


Thought I’d try to take you through a little piece of the undertaking that is team G.    We will be the first to tell you that since the day we received the diagnosis of Gavin being autistic our team has been nothing short of incredible.    We’ve had a couple of bumps or members that just didn’t click with G but it was not anything to get too twisted about.   Well, there is one situation where the “Varecka” came out of dad but I’ll tell that story another day or anytime you’d like to join me for a bourbon.  So in short, we’re a very lucky bunch!


Ok, so below is the roster of positions on Gavin’s team right now and some quick descriptions.   These are the people who are with him to teach, ensure his safety, provide some good stuff and just love on him.     

  • Mom and Dad – Yup, I’ll put us here because, well we kinda started this whole thing.

  • Gavin’s Sisters (4) – They all fill various roles but most important is that they have been at his side from day one and always will be the best teammates he can have.  They truly care about everything G is involved in.    

  • Gavin’s respite provider – Our 5th daughter and an honorary member of the clan.    She loves his boy as if he was her own.    We’ve had a few people fill this role and not until she did we have the right one!     Lucked out here, too!

  • School – Gavin’s team at Hilton Village Elementary and the district are above amazing.   The administration for the special needs program is top-notch and I’ve never felt we didn’t get exactly what Gavin needs.  We’d heard horror stories and ours sure isn’t one.    We are so lucky to live here.

    • Gavin’s Special Ed Teacher – Ring leader at school and someone we trust to always shoot straight with us about his progression and keep us on point of her expectations for the US.   Communication is so important and they rock it!     I have to also say, Gavin’s experience with the BOCES Pre-K was outstanding too.     Leaving there was hard for all of us and they truly love G.    Making it all happen during COVID was impressive.  

    • Other teachers at school for G.     Physical Therapy, Occupational Therapy, PE, Music, and Speech.    He has individual and group activities during the week with all these teams.   Here again, their ability to communicate to us exactly what’s going on is priceless.

  • Applied behavioral analysis (ABA) – This is a behavioral therapy in our home.    There is controversy around ABA as some feel it does nothing but teach habits or try to force those with ASD to comply with “commonly accepted” behavior.    We’ve not experienced this at all and Gavin has done very well with the day-to-day skills they help with.   He is engaged and our experiences have, for the most part, been awesome.     One experience with a potential provider company was horrible, but, we dealt with that quickly and we love the team he’s on now.    Gavin has these services up to 5 days a week!     He has 2 providers as well as a supervising provider too.     All bring something different but all come together for his plan.    The truly amazing thing for us is that they are now pushing into school!    This is big, very very big.    To have the providers that work at home with him allowed to be in the classroom isn’t a regular occurrence.    Our school and ABA team worked hard to make it happen and everyone is on board and we’re already seeing returns we may never have before.

    By having ABA push into school we, as a team, have a better chance to ensure his lessons support one another at every session.   Using common terms and methods makes it so much easier to ensure consistency which is a big deal to our kiddos.    As a matter of fact, we’re working on a meeting now for just that very thing.    We feel we may be able to push G harder at home than we are.    We have a feeling his ability is beyond some of the stuff we do here and we want to be sure we continue to challenge him.   

    ABA is a self-pay thing and I’m so thankful for my employer and the very strong benefits they provide for our family.    Without that, we’d have to make some hard choices.

  • Medicaid services – We all look at our deductions on a paycheck and you can’t help feeling upset at the money taken out of our checks.    Well, I can tell you my feelings on this have changed, even on my property taxes.    Being reliant on some government programs now makes me thankful for where we are.    While there is plenty in NY I’m not fond of, I can say it’s the best place to be for Gavin right now.   

    • Self Direction – GAME CHANGER!     Yep, I said that.    This program allows us a lot of help when it comes to G and some direct costs for things to improve his life.    While it’s a huge list of services available some of the biggest for us is Respite, Memberships for places like the Strong Museum and the Zoo, assistance that allows us to take Gavin’s respite provider along on our vacations.    Gavin also gets some help with classes like his current swim lessons!  We’re even offered the opportunity to purchase equipment for our home to help his development and get assistance in the costs.    We were so amazed by this that G’s momma has made a career out of being a Broker for this program.    Now she helps other families just like ours too!

    • So for people under this program, Gavin has his Broker and a Fiscal Intermediary to keep an eye on the money….   

  • State Services – His Care Coordinator helps us with everything we do with the  New York State’s Office for People With Developmental Disabilities.   This is a huge bag of stuff but, she’s kind of like the QB for Gavin’s overall program.    She’s even helping us with some modifications at our home to ensure Gavin’s safety.     In the past, they helped us get a fence for our back yard too.    Gavin is an elopement risk and keeping him home is obviously important.    This allowed us a little extra help in ensuring his safety.

  • The Assistive Technology Team at Monroe BOCES 2 – WOW!     We say Gavin’s voice but this team is truly responsible for his voice.   Starting with the study to
    see if Gavin was a candidate for an augmentative and alternative communication (AAC) device through the process with insurance approval, delivery, deployment and repair they have been outstanding.  For those of you who don’t know much about them that is what Gavin is using at the beginning of this post!


So, as you can see it’s a pretty big village for G.   We can’t thank these amazing people enough.    I’m sure I missed a couple along the way and if so, I’m sorry!   In our effort to share our world I thought it would be interesting to see what a machine it is for families like ours.  These are not easy jobs or easy money for the providers.     They do it out of love and concern for everyone they work with.    What’s really cool is that even as Gavin moves on, as he gets older we can call all of our past providers when we need a little help.   We were struggling with some behaviors during COVID and reached out to one of our very favorite providers from the earliest days of Gavin’s early intervention program.    She offered to come by the house just to see what’s up in G’s world and point us back down the path.    Can’t put a price on that!


For our family members, it amazes me the love and willingness to help they all show us.    Always ready to help and listen when the days are hard.    It makes things so much better.   As a side note, Gavin’s sister Julia has decided to study Occupational Therapy when she heads to college in the fall.    Inspired by the people who have helped her baby brother, she wants to do the same for others.    She may have the biggest heart I’ve ever seen…


Thanks for coming along for a small part of the ride and stay tuned!


Love,

David