As the end of summer approaches and the new school year draws near, children with special needs and parents alike may experience a mix of excitement and anxiety about the upcoming changes. Transitioning from a laid-back summer schedule to the structured routine of school can be challenging for many children, particularly those with special needs who thrive on predictability and consistency. As parents and caregivers, we want to do our best to ensure our children are as prepared as possible to be successful. Thankfully, there are proactive steps we can take to help ease this transition and ensure a smooth start to the new school year.
What Can you do at Home to Help your Special Needs Child Transition?
Communicate and Prepare:
Open and honest communication is key to helping children with special needs prepare for the school year. Start discussions early, explaining the changes that will occur once school starts. Use visual aids, social stories, or picture schedules to help them understand the daily routine and what to expect in the classroom.
Reestablish Routines:
During the last weeks of summer, gradually reestablish school-year routines. This includes consistent wake-up times, mealtimes, and bedtime schedules. Predictability and familiarity can help reduce anxiety and provide a sense of security for children with special needs.
Visit the School:
If possible, arrange a visit to the school before the first day. Walk through the building, visit the classroom, and meet the teacher. Familiarizing the child with the school environment can alleviate anxiety and help them feel more comfortable on the first day.
Encourage Social Interactions:
For some children with special needs, social interactions can be challenging. Organize playdates with classmates or participate in school-sponsored activities before the start of the school year. Building social connections in a relaxed setting can foster friendships and ease the transition into the school community.
Develop a Transition Plan:
Collaborate with the child’s teachers and school staff to develop a personalized transition plan. This plan may include gradual integration into the school setting, shorter school days initially, or additional support services as needed. Individualized attention and support can significantly reduce the stress of starting a new school year.
Address Specific Concerns:
Identify any specific concerns the child may have and work together to find solutions. For instance, if the child is worried about changes in the daily routine, create a visual schedule they can refer to throughout the day. Addressing these concerns proactively can help alleviate anxiety and promote a positive mindset.
Create a Back-to-School Countdown:
Use a visual or interactive countdown to the first day of school. This can be a fun and engaging way to build excitement and anticipation for the upcoming school year.
Encourage Expressing Emotions:
Let the child know that it’s normal to have mixed feelings about starting a new school year. Encourage them to express their emotions and actively listen to their concerns. Offering support and understanding can help validate their feelings and build their confidence.
Positive Reinforcement:
Offer positive reinforcement and praise for any efforts the child makes during this transition period. Celebrate small victories, such as successful playdates or positive interactions with classmates. Positive reinforcement can boost their self-esteem and motivate them to face new challenges.
Conclusion
The transition from summer ending to school starting can be a significant milestone for children with special needs and their families. By implementing these practical strategies and providing consistent support, parents and caregivers can help ease the anxiety and uncertainty that may accompany this transition. Through open communication, personalized planning, and a nurturing environment, children with special needs can embark on the new school year with confidence and enthusiasm, ready to embrace the opportunities for growth and learning that lie ahead. At The Oxford Center, our BCBA’s are knowledgeable and experienced with helping your child transition from summertime to school time and are ready to help your child achieve all of their goals. To learn more about our ABA program, click the link below.
The Oxford Center has a very exciting new addition- an approximately 960 square feet indoor playscape for our Brighton location! This playscape has been a long process of picking out the perfect model and features, patiently tracking its shipment process, and then watching excitedly as it was being built! We know this playscape is going to be so much fun for our kiddos! Our playscape features a climbing rock wall, multiple slides, a ball pit, a swing, an obstacle course, and more! With so many great, fun features, we know this playscape is going to be a great addition. But is there any point to it beyond just being fun? Absolutely! The playscape is going to be a huge asset to our ARTS programs.
What is our ARTS Program?
Our ARTS program stands for Autism Recovery Thru Synergy. At The Oxford Center, our synergistic approach to autism is unlike any other ABA center. We use every tool in our belt to help our kids grow and develop as much as possible. We know that many kids coming to us for ABA services will also benefit from services like Physical Therapy, Speech Therapy, and Occupational Therapy. So, we have incorporated all of these therapies into one program so that we can provide each of our kids with the best possible individualized experience.
How will the playscape be used in ARTS?
When picking out our playscape and all its features, we made sure to put careful thought into how the playscape would be able to benefit each therapy in our ARTS program. We want our kids to have fun and enjoy their time here- but it is also important to us that they are learning, and that we are doing everything we can to help them as well. Here are the benefits and learning opportunities our playscape will have for our ARTS program:
-Applied Behavioral Analysis Therapy:
ABA offers a huge wealth of opportunities for growth through our playscape. Our kids will be able to practice waiting, requesting preferring locations, shoes and socks on and off, turn taking, peer play, requesting actions, requesting actions from peers, transitions from preferred locations, requesting help, identifying emotions, and more!
Our playscape will help to develop key skills in both physical therapy and occupational therapy. These include practicing skills like vestibular input which will allow kids to practice for changes in their position, movement, or direction of the head. They will also be able to practice motor planning while playing which allows them to remember and perform body movements to fulfill a task, dynamic balance which will allow our kids to practice remaining standing and stable while engaging in play, practicing coordination, kinesthetic awareness which allows practice sensing the position and movement of their own body, strengthening muscles, and lots of practice with sensory processing and visual-spatial awareness skills through each of our playscape features.
In speech therapy, our playscape will offer fantastic opportunities for peer-to-peer interactions involving turn-taking and sharing. They will be able to increase functional play skills by sharing and taking turns in things like waiting their turn to go down the slide, use the ball pit, sharing balls, etc. They will also be able to increase their expressive language skills through utterance length and labeling skills to express their wants and needs, whether that be verbally or through an AAC device.
In conclusion, the addition of our indoor playscape at The Oxford Center’s Brighton location signifies more than just a physical expansion; it symbolizes a commitment to innovative and holistic autism therapy. Through this vibrant playscape, we are exemplifying how learning and development can be intertwined with play and fun. By providing a nurturing environment that sparks curiosity and excitement, we are able to foster an atmosphere where children can flourish and reach their fullest potential. As we look ahead, the playscape represents a bright future for autism therapy, where innovation, compassion, and the power of play combine to create a world of possibilities for the children in our care.
Check out our timelapse video of the playscape being built!
Our Camp ABA program is in full swing for the 2023 summer season! Our Camp ABA program is a summer program designed for children with autism spectrum disorder (ASD). This program offers a fun and educational way to spend the summer practicing social, emotional, and learning skills. Camp ABA is a summer Applied Behavioral Analysis (ABA) program that aims to give kids all the experiences of a camp-like atmosphere while still going through a top-notch ABA program! We have had some really fun and educational themed weeks so far and we are so excited for the weeks we have in store still!
Week One: “Saved by the Bell”
We kicked off our first week of Camp ABA with a “Saved by the Bell” theme! This week kids truly celebrated the start of summer by making graduation caps and friendship bracelets, playing with water balloons, playing basketball, having story time and freeze-dance parties, and more! The kids had a great time starting camp and officially kicking off the summer!
Week Two: “Gardening Week”
Going into our second week of camp, the kids had a great time continuing their fun and learning. We enjoyed a gardening theme this week, and I think it’s safe to say the kids had a great time! For gardening week, the kids had fun with a flower scavenger hunt, veggie tasting, painting garden stones, learning to weed a garden, making fairy jars, and more! Move over Mom, we saw a few green thumbs starting to come out!
Week Three: “Down on the Farm”
Week three of Camp ABA was dedicated to a “Down on the Farm” theme! The kids had a great time experiencing some country-living activities and we loved seeing how much they enjoyed it! Our kids got to imitate shearing sheep and milking a cow, playing kickball, making Juneteenth flags, line dancing to Old MacDonald Had a Farm, and more! These kids are ready to move into some nice country-living!
Week Four: “Under the Sea”
Finally, week four of Camp ABA is going to the ocean with a “Under the Sea” theme! Our little sea creatures are going to have a great time diving into all of the activities we have planned. The kids are going to get to go on a sea creature scavenger hunt, learn about ocean layers and currents, coral reef sponge paintings, painting sea turtles and a deep-sea diver, having a Just Dance “Under the Sea” Disney Party, and more! We are so excited to see how much fun the kids have learning about the ocean and everything in it!
We Can’t Wait for More!
With about half of Camp ABA in the books, it’s safe to say we are off to a fantastic start! The kids are having so much fun learning and socializing with their fellow Camp ABA-ers! But, even with everything we have already done we are still just getting started! We have loads of fun themes left for the kids to experience and we can’t wait to share all of the fun with you!
Summer is usually a time full of relaxation, time to spend with family and friends, and plans for great vacations. This isn’t usually the case for parents of children with cognitive impairments, though. For these parents, they know that summer is going to be much more difficult for their child and their family.
What Difficulties do Children with Cognitive Impairments Face During Summer?
Routine: Children with cognitive impairments thrive under a regular schedule where they, at least roughly, know what to expect and when. So, when a child has been in school for 8 months out of the year they get very used to their routine while in school. Then, once summer begins, they suddenly have to learn a whole new routine! The sudden change can feel uncomfortable, unfamiliar, and intimidating. This dysregulation can cause them mental and emotional stress, making this a difficult transition period.
Lack of Social Opportunities: Many children with cognitive impairments have some challenges associated with their communication and social skills. While in school, they have ample opportunities to grow and practice these skills but once they are home for the summer, those opportunities are most likely going to be very few and far between. This sudden decline in opportunities to socialize may cause their overall social skills to decline and they may lose some of the progress they made during the school year.
Loss of Education/Learning: As with any child, the summer months are often filled with deficits and losses of learning. While in school, students are regularly reading, constantly being exposed to new materials and concepts, and gaining new academic skills. Summer is a disruption to this learning that often results in students losing some of the knowledge they gained during the school year simply because they are no longer practicing and thinking about those skills.
What Can You Do at Home During Summer?
Create a Schedule & Stick to it:
One of the best things you can do for your child with a cognitive impairment is to create a schedule for the summer months so that they have something to stick to. This schedule could include eating breakfast at a specific time, reading time, educational time, games time, outdoor time, etc. No matter what schedule you decide to create for your child, it is essential that you are consistent and stick to it as much as possible. Being inconsistent with a schedule will lead to poor results and will not help to regulate how your child feels after experiencing disruption from their school schedule. If possible, prepping your child ahead of time to make them aware before a schedule change will help them to adjust to new situations with ease and comfort.
Plan Social Activities:
To help your child continue to maintain and grow their social skills, try to plan different social activities that il allow them to continue practicing these skills. These activities could be things like meeting with a friend to play a game, attending community events at libraries or other public areas, or signing up for summer activities like bowling, gardening, swimming, etc. These opportunities will help improve your child’s communication skills, ensure your child maintains any social and emotional learning they gained throughout the school year, and will help them to feel more confident in themselves and around others.
Plan Educational Activities:
Finally, planning educational activities can help make sure your child does not experience the loss of learning that is common for school-age children over the summer. Reading with your child and then discussing the book can be a great way to help them practice their reading comprehension skills, doing different science experiments can be a great way to engage your child’s curiosity and learn new science skills, having scheduled match times can help your child advance their match capabilities, etc. The possibilities are truly endless!
Conclusion
In conclusion, the summer months can present unique challenges for children with cognitive impairments and their families. The disruption of routines, limited social opportunities, and potential learning loss can create additional stress and difficulties during this time. However, there are proactive steps that parents can take to support their child’s well-being and promote continued growth. By creating a structured schedule, planning social activities, and incorporating educational experiences, parents can help their child navigate the summer successfully. These strategies not only provide a sense of stability and familiarity but also offer opportunities for skill development and maintaining progress made during the school year. With thoughtful planning and consistent implementation, parents can empower their children with cognitive impairments to have a fulfilling and enriching summer that contributes to their overall development and happiness.
Cooking for children who are picky eaters can be challenging, especially when it obtains to children with food aversions such as many children with autism. A child’s diet plays a crucial role in their overall health and development. In turn, this diet plays a huge role in your child’s life and if your child is a picky eater or has food aversions, they may not be getting everything they need from their diet to be healthy. Children with autism spectrum disorder (ASD) often have sensory sensitivities and rigid eating patterns, leading to limited food preferences. Some children with ASD may have heightened sensitivities to taste, texture, and smell, which can contribute to their aversions. Ensuring a well-rounded diet is crucial in maintaining your child’s health, promoting their growth, and supporting overall development.
Common Food Aversions in Children with Autism:
While food preferences can vary among individuals, there are some common food aversions that frequently appear in children with autism:
Textural Challenges: Many children with autism struggle with certain textures, such as crunchy or slimy foods, leading them to avoid fruits, vegetables, or meats.
Limited Food Groups: Some children with autism may stick to a few preferred food groups, such as carbohydrates or processed foods, neglecting the necessary nutrients.
Sensory Sensitivities: Strong flavors or smells may trigger aversions in children with autism, making it challenging to introduce new or unfamiliar foods.
Color or Presentation: A child’s preference for specific colors or food presentation styles may limit their choices, affecting the variety in their diet.
Incorporating Nutrient-Rich Foods:
Ensuring children with autism receive a balanced diet is essential for their growth and development. Here are some nutrient-rich foods to include in their meals:
Protein Sources: Offer lean meats, poultry, fish, or plant-based alternatives like beans and lentils to provide essential amino acids and support muscle development.
Colorful Fruits and Vegetables: Incorporate a variety of fruits and vegetables, such as berries, oranges, leafy greens, and sweet potatoes, to provide vitamins, minerals, and antioxidants.
Healthy Fats: Include sources like avocados, nuts, seeds, and olive oil, which provide omega-3 fatty acids and support brain function.
Whole Grains: Opt for gluten-free whole grains like quinoa, brown rice, and gluten-free oats to provide fiber, vitamins, and minerals.
Dairy Alternatives: If your child is lactose intolerant or has dairy aversions, consider providing plant-based milks such as almond, cashew, or coconut milks that are rich in vitamins!
Tricks to Work Around Food Aversions:
Here are some helpful strategies to navigate food aversions and encourage a healthier eating experience:
Gradual Exposure: Introduce new foods gradually, allowing your child to explore them through sight, touch, and smell before attempting to taste.
Food Pairing: Combine less preferred foods with favorite choices to increase acceptance and familiarity.
Food Modifications: Alter the texture or presentation of a food to make it more appealing, such as blending vegetables into sauces or purees.
Food Chaining: Build upon preferred foods by gradually introducing similar alternatives, expanding their palate over time.
Cooking Together: Involve your child in meal preparation and make it a fun and interactive experience to increase their interest in trying new foods.
Kid-Friendly Gluten-Free Recipes:
Here are a few delicious and nutritious recipes that cater to picky eaters, including those on a gluten-free diet:
Mini Veggie Frittatas: Combine whisked eggs, chopped vegetables (such as bell peppers, spinach, and mushrooms), and shredded cheese. Bake in a muffin tin until set and golden brown.
Chicken and Vegetable Skewers: Alternate marinated chicken cubes with colorful vegetables like cherry tomatoes, zucchini, and bell peppers on skewers. Grill or bake until cooked through.
Cauliflower Pizza Bites: Blend cooked cauliflower florets with eggs, gluten-free breadcrumbs, and seasoning. Form into small patties and bake until golden. Top with tomato sauce and cheese.
Quinoa Stuffed Bell Peppers: Cook quinoa according to package instructions and mix with sautéed vegetables, ground meat (optional), and spices. Stuff the mixture into halved bell peppers and bake until tender.
Banana Oat Cookies: Mash ripe bananas and mix with gluten-free oats, nut butter, and a touch of honey. Shape into cookies and bake until lightly golden.
Have Lunch at The Oxford Center!
Cooking for picky eaters, especially those with autism and food aversions, requires patience, creativity, and a focus on nutrient-rich foods. By understanding the concerns, incorporating essential nutrients, implementing tricks to work around aversions, and exploring kid-friendly, gluten-free recipes, parents and caregivers can promote healthy eating habits while catering to their child’s unique needs. At The Oxford Center, we understand how important it is to make sure your child is getting everything they need to grow up happy and healthy. That’s why our lunch program is completely individualized to what will be best for you and your child!
In this Episode of TOC Talks, Andrew sits down with Officer Edward Blackburn, The Oxford Center’s security officer! Together, they discuss Officer Edward’s background, some of his prior experiences, and what he does at The Oxford Center. Listen to find out who Edward is, how he found The Oxford Center, the ways he is improving the safety of The Oxford Center, and why Edward loves what he does!
Check It Out!
Want to learn more about some of our other security features at The Oxford Center? Check out our security video!
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Check out our episode and don’t forget to subscribe to TOC Talks! We can be found on all your favorite Audio or Podcast platforms as well as video podcasts on our YouTube and Facebook pages! Find us at the links below!
Want to stay connected and up to date on what is happening at The Oxford Center? Make sure to follow our Social Media Pages! If you would like to find our TOC Talks Podcast page, click on the link below.
“I don’t think you realize you’ve lost hope until you find it again.”
-Emily Kistner
If you have been to our Brighton location of The Oxford Center or if you have visited our website, you are probably familiar with Grace Kistner. For those who are not familiar with Gracie, she is an adorable little girl who loves exploring, watching Candy Crush, watching the minnow in the Axolotl tank, and giving hugs. Gracie’s journey began long before discovering The Oxford Center, but it changed her life and her family’s life once treatment began here.
Gracie’s Beginning
Born at 5lbs 1oz, Gracie was tiny, but always happy and healthy. At 6 months old, she began missing milestones and the doctor noticed low tone. At 9 months old, she still had low tone, head lag, and was not meeting milestones. Gracie began Physical Therapy, and her parents, Andrew and Emily, were encouraged not to worry. Gracie’s parents were often told that every child is different, they grow at their own pace, and that she would probably just catch up one day.
At 12 months, the developmental delays and low tone continued, and Gracie’s parents found a new Physical Therapy clinic to try, as not much progress was made with the current PT they were in. After several months, Gracie began to make progress, eventually sitting up on her own, but it was slow, and Gracie hated every minute of Physical Therapy. Watching their baby cry through 45 minutes a week of therapy was devastating to Gracie’s parents, but they pushed on, knowing it was what she needed. Aquatic Therapy was mentioned to Gracie’s parents, and as Gracie had loved the water since she was an infant, they enrolled her. Gracie loved it from the first session, and seeing Gracie’s joy and not one tear during this new Physical Therapy brought her mom to tears.
Diagnosing Gracie
At 24 months, Gracie was still developmentally delayed, still missing milestones, and started displaying spasms and twitches. This led to a new part of Gracie’s journey, with consults to Neurology, Genetics, and Physical Medicine and Rehab. Blood tests were done and an MRI of the brain, but everything came back normal. The lack of answers to explain Gracie’s delays and spasms was frustrating but was the start of a pattern that would be repeated often throughout Gracie’s journey.
At 3 years old, Gracie was still delayed, still not speaking, and progress was slow, so a new consult was placed to a Developmental Delay Pediatrician. Within minutes of walking into the doctor’s office, Gracie was given a diagnosis of Hypotonic Cerebral Palsy. As Gracie’s parents had been told for years to be patient and that Gracie may still just catch up one day on her own, this was devastating. They were told that there was no cure for Cerebral Palsy, and the only treatment was therapies. After learning this, Gracie’s parents began every therapy they could find for her, eventually adding OT, Speech, and Hippotherapy to her current aquatic and clinic Physical Therapy. Gracie began to gain strength in her core, using a gait trainer, and a reverse walker with a seat sling and pelvic stabilizer. Gracie’s parents took her everywhere to let her explore with her newfound mobility using this equipment. Gracie’s parents tried alternative therapies to help as well, including chiropractor and cranial sacral massage.
Finding The Oxford Center
In December 2019, Gracie’s parents discovered The Oxford Center after a family member heard an ad on the radio about Hyperbaric Oxygen Therapy (HBOT) for Cerebral Palsy. Willing to try anything that could help Gracie, a Discovery Session was scheduled, and an hour drive was made from Toledo, Ohio to Brighton, Michigan to learn more about it. From the moment Gracie’s parents walked into The Oxford Center, they were made to feel at home. Gracie connected instantly with the staff, and this was so important to her parents as they knew she needed to trust and love the people who would be working with her. After learning how HBOT could help with Cerebral Palsy, Gracie’s parents were told about Intensive Physical Therapy that used TheraSuit. Willing to try anything, appointments were scheduled, and arrangements were made to relocate for eight weeks to begin this new journey in February 2020, and oh, what a journey it was. Gracie’s parents found something they didn’t realize they had lost. Hope.
Wanting to document the therapy sessions and the progress hoped for, Gracie’s parents took pictures and videos to share with family and friends back home who were praying for Gracie. The progress that Gracie made was phenomenal, both from HBOT and TheraSuit. Cognitive improvements were seen as Gracie learned how to safely slide down the stairs, something her parents had worked on for months. Physical progress was seen as she learned to take steps with parallel bars and push from sitting to standing. Gracie’s trip was cut short due to COVID, but her parents scheduled her to return for another round of both therapies in September of 2020, and again saw much progress both physically and cognitively.
Oxford Kids Foundation
After the second trip for therapies in September 2020, Gracie’s parents wanted to schedule another trip, but as they had paid out of pocket for two rounds of each therapy already in addition to housing and living costs, they were out of money. That was when they heard about the Oxford Kids Foundation. The Oxford Kids Foundation is a 501(3)c non-profit organization run entirely by volunteers that helps provide funding and access to essential therapies that are not covered by insurance in the state of Michigan. Immediately, Gracie’s parents applied for a grant to help with costs for another trip. They were approved for a grant and with the help of a GoFund me started by Andrew’s sister, a third round of therapies began in January 2021 and eventually a fourth round in May of 2021. Gracie’s parents are so incredibly grateful for the opportunities that were made possible for Gracie through the help from the Oxford Kids Foundation.
Autism Diagnosis
Gracie made incredible progress during her therapies at The Oxford Center, but her parents noticed some things that were concerning. Gracie seemed to be very sensitive to certain sounds, was overly focused on spinning objects, would crawl or walk away from her parents, and many more. She had been evaluated for Autism at age two, but as she looked at the psychologist and reached for her, a diagnosis was dismissed, and her parents were told “Autistic kids don’t do that”. If you are unfamiliar with Autism Spectrum Disorder (ASD), it presents differently in girls than it does for boys. Girls tend to be more social naturally, while boys may not be. After learning more about ASD, Gracie’s parents decided to have her evaluated again in June of 2021. This new specialist was experienced in evaluating girls for concerns of Autism, but also separating the characteristics of Cerebral Palsy and developmental delay from ASD. After many questions and an in-person evaluation with Gracie, it was confirmed that Grace was on the Autism Spectrum. This diagnosis added a new path to Gracie’s journey in the form of Applied Behavior Analysis (ABA).
Gracie is Walking!
During Gracie’s Discovery Session in December of 2019, a nurse asked her parents what their goals were for her. While they had many goals, the primary goal was for Gracie to be able to walk. While she was small at that point, they knew there would come a time when they would no longer be able to carry her, and the ability to walk would greatly change all of their lives. In the fall of 2021, Gracie began walking independently. Her parents will forever remember the “firsts” that happened at The Oxford Center. The first time she stood up from sitting, the first time she stood independently, and the first time she walked across the lobby of The Oxford Center to get to her favorite nurse, Elizabeth. So many firsts that at one point Gracie’s parents weren’t sure they would ever see, and so many “firsts” to come.
What is Gracie up to Now?
Gracie attends ABA and also has Physical Therapy, Occupational Therapy, and Speech Therapy. While she is still nonverbal, she is learning to communicate on a “talker” and has been able to make her need and wants known this way. She is continuing to gain strength and new skills, and her parents can’t wait to see what else is in her future.
Want to Learn More About the Oxford Kids Foundation?
The Oxford Kids Foundation helps hundreds of children, like Grace, get access to the therapies they need every year! This Foundation has the power to change the life of a child, a parent, and an entire family. This mission is one that is close to the heart of us all here at The Oxford Center. That is why The Oxford Center is hosting the Oxford Kids Foundation’s 13th annual ‘Be The Change’ Fundraising Gala!
The ‘Be The Change’ Gala will take place on April 22nd at 5 P.M. Buying a ticket to the Gala will get you access to an elegant multi-course plated dinner, access to our live auction, and amazing entertainment. Plus, you’ll have a chance to make a difference in the lives of children with disabilities. All proceeds from the event go directly towards helping children receive the therapies they desperately need!
We’re also offering an online auction, open to the public, which includes unique and exciting baskets, vacations, experiences, and more! Even if you can’t make it to the event, you can still bid on some amazing items and help support a great cause. Don’t miss out on this incredible opportunity to give back and have a great time doing it. Visit theoxfordkidsfoundation.org to get your tickets and access the auction today!
Although law enforcement is tasked with keeping the public safe, interactions between first responders and those with autism spectrum disorder (ASD) or other psychiatric conditions can be contentious, and in some cases, deadly. At The Oxford Center, we care about the safety of everyone in our building, so we want to make everyone is as prepared as possible if we ever had an emergency… including the police officers.
That’s why Officer Ed, our security officer for The Oxford Center, is holding a “Autism & Law Enforcement Workshop“! This workshop is open to police officers who would like to learn more about how to respond to a situation where individuals with Autism and other psychiatric conditions might be present. We have invited officers from the city of Brighton, Green Oak Township, Livingston County, and the Michigan State Police. Officers in attendance will receive training in identifying characteristics of people with autism, de-escalation techniques, techniques when responding to an emergency at The Oxford Center, interactions with a person(s) with Autism, and communication techniques.
This workshop will take place at The Oxford Center on Wednesday, May 3rd from 11 AM to 1:30 PM. If you know of any police officers who could benefit from this workshop, please direct them to register at the link below.
Welcome to CP Awareness month! CP stands for Cerebral Palsy, and all of March is dedicated to raising awareness about this condition, so The Oxford Center is going to join in this endeavor. Many of us may have a family member or know someone with Cerebral Palsy, but we might not actually know much about the condition. Thankfully, The Oxford Center is here to help you learn more and raise awareness about this condition!
Cerebral Palsy is a neurological disorder that affects movement, posture, and muscle coordination. It is caused by damage to the developing brain, which can occur during pregnancy, childbirth, or early childhood. At this point, Cerebral Palsy affects roughly 1 in 500 children worldwide, and its severity can vary widely from person to person.
Every week, The Oxford Center will be posting different graphics, articles, and podcast episodes that will help to educate and raise awareness about this condition. Look out for our updates every week on our website and social media platforms!
ABA Academy has been busy this past month with art projects, science experiments, music, gym, reading, writing, and math lessons that follow a weekly theme. Some of our themes so far have been National Library Lovers Week, Dental Health, and Time.
During National Library Lovers Week, we learned all about books! We learned the parts of a book, the jobs of an author and illustrator, genres, and of course all about what libraries have to offer. We were even visited by two librarians from The Brighton Public Library!
During Dental Health week, we visited our very own Oxford Center Dino Dentist chair and made elephant toothpaste in a science group. We started March off with the theme of Time by making clocks, learning how to tell time, and playing What Time is it Mr. Fox? in gym.
Stay tuned for our upcoming themes and adventures for the rest of the month of March like Weather, St. Patrick’s, and The Five Senses.
The ‘Be the Change’ Fundraising Gala is Fast Approaching!
Don’t forget The Oxford Center will be hosting the 13th Annual Fundraising Gala Dinner and Auction for the Oxford Kids Foundation on April 22nd! This event is a longstanding and beloved tradition in raising funds to support children with disabilities, chronic illness, and traumatic injuries.
Tickets for the Gala are available for purchase now. Tickets will feature fine dining, access to our silent/live auction, and drinks will be available. For more information on the Gala and how to purchase tickets, please click here.
If you or anyone you know is interested in sponsoring the “Be the Change” gala event, please click here for more information or contact andrew@oxfordkidsfoundation.org to look over a sponsorship packet. The Oxford Kids Foundation is also accepting donations of any unique quality to be included in the Gala’s silent/live auction. If you would like to make any item donations to the Gala auction, please contact Andrew Kistner at andrew@oxfordkidsfoundation.org.
We can’t wait to be a part of the change with you!
If you are interested in helping with the Oxford Kids Foundation, we are looking into adding even more ways to make that possible! For years, we were a proud partner of Amazon Smile, which allowed a portion of proceeds to be donated to the Oxford Kids Foundation every time you shopped. Regrettably, Amazon is closing its’ Amazon Smile program to focus on other philanthropic ventures.
Thankfully, there are still ways to give! We are happy to share that we are partnered with Kroger to make giving easy and convenient for you every time you shop. You can now link your Kroger card to The Oxford Kids Foundation! You can help provide life-changing therapies to children that need them, and Kroger will donate funds based on the shopping you do every day. There’s no cost to you and all you have to do is enter your Kroger Shoppers card at checkout!
Link your card to The Oxford Kids Foundation today by clicking the link below.
The Oxford Center is excited to say that we have successfully launched our new podcast and it is going great! Our new podcast is released once a week and is released every Thursday. Our TOC Talks podcast can be found on all streaming platforms with a video podcast on our Facebook and YouTube page. Every week, follow our Marketing Director Andrew Kistner as he dives into different issues and stories here at The Oxford Center with a new special guest every week! In our podcast, you can hear the personal stories of some of our patients and their journey with The Oxford Center, learn more about how some of our services can benefit different conditions, learn more about some of our staff here at The Oxford Center, discover new techniques and tips to help improve your life, and more!
If you have any topics or ideas you’d like to hear about in our podcast, let us know! You can submit any thoughts, suggestions, or questions by emailing our podcast host himself, Andrew Kistner, at andrew@theoxfordcenter.com.
Check out our episodes below and don’t forget to subscribe!
The Oxford Center is thrilled to welcome Nicole Cunningham to our team as the head of our nutritional services program. Nicole is a certified Functional Nutrition Therapy Practitioner (FNTP) and Restorative Wellness Practitioner (RWP). Nicole offers individual and whole group nutrition classes that are highly personalized and customizable to what will best suit each individual. Our nutrition coaching seeks to help you learn more about food and how it interacts with your body, learn what foods and diets will work best for you and your specific needs, and support you on your journey to making ever-healthier nutritional choices. Clients will find that it is empowering knowing that you can change and improve your health without needing help from anything else.
Nicole’s journey with nutrition began 10 years ago with the birth of her son, Cameron. Cameron was born with over seven true food allergies and about a dozen food sensitivities that caused his body to break out in rashes and made eating exceedingly difficult. She spent countless hours poring over research, trying different foods, and tracking the effects different foods had on her and her son’s body. Eventually Nicole’s efforts paid off, and she eliminated all but one of her son’s food allergies. Through this journey, Nicole discovered a passion for nutrition and understanding the effects someone’s diet might have on their body and overall health.
Nicole has personally gone through everything a client would go through and is here to help guide every client on their way to understanding food and their body and improving their overall quality of life.
The Oxford Center is excited to launch our new podcast, “The Oxford Center Talks” (or TOC Talks for short!). Our new podcast will be released on Thursdays once a week and will be able to be found on all streaming platforms with a video podcast on our Facebook and YouTube page. Every week, follow our Marketing Director Andrew Kistner as he dives into different issues and stories here at The Oxford Center with a new special guest every week! In our podcast, you can hear the personal stories of some of our patients and their journey with The Oxford Center, learn more about how some of our services can benefit different conditions, learn more about some of our staff here at The Oxford Center, discover new techniques and tips to help improve your life, and more! If you have any topics or ideas you’d like to hear about in our podcast, let us know! You can submit any thoughts, suggestions, or questions by emailing our podcast host himself, Andrew Kistner, at andrew@theoxfordcenter.com.
Check out our first episode below and don’t forget to subscribe!
Any parent of a child with autism spectrum disorder (ASD) knows what a challenge it can be to manage the condition at home, ON TOP of managing everything else at home. Being a parent is such a wonderful gift, but it is also a full-time job and can be exhausting at times. Adding on managing an ASD diagnosis could very easily prove to be exhausting for many parents. Thankfully, The Oxford Center can share some tips and tricks to help you manage while providing the best environment possible for your children and yourself.
Jessica Dodson, our ABA Program Director, says “At The Oxford Center, we help create routines within a successful environment to not only help the child grow, but the whole family. I have so many parents that focus on comparing how their child is doing against how another child is doing, so I always remind my parents and caregivers that everyone has their own separate path and journey. Most importantly, remember that we will all make it through our paths with a little teamwork and perseverance.”
Our COMPASS program is underway! All of our students have been working very hard this past month. Our COMPASS program is targeted towards teens and adults diagnosed with autism and other developmental disorders. In this program, we help these individuals learn the skills needed to move on to the next stage of their life whether that be going to and succeeding in higher education, living independently, obtaining and maintaining meaningful employment, and more.
We talked to Matt Nivison, our COMPASS Coordinator, and he has this to say about the first class of COMPASS students. “The first class is going excellent. I am so incredibly proud of them all. You can see how hard they’re working, how quickly they’re picking things up, and just how much they want this. Every day, they’re actively taking steps to succeed and grow and it’s so cool to watch it happen in an environment where they don’t have to worry about the negative consequences that we all faced in our first jobs. They’re learning what works for them while gaining experience and confidence! It’s really, very cool”.
The program will run for approximately 6 months, 5 days per week, for 3 hours per day. If you would like to learn more about the program or ask about enrollment, please feel free to contact us at 248-486-3636.
Don’t forget The Oxford Center will be hosting the 13th Annual Fundraising Gala Dinner and Auction for the Oxford Kids Foundation on April 22nd! This event is a longstanding and beloved tradition in raising funds to support children with disabilities, chronic illness, and traumatic injuries.
Tickets for the Gala are available for purchase now. Tickets will feature fine dining, access to our silent/live auction, and drinks will be available. For more information on the Gala and how to purchase tickets, please click here.
If you or anyone you know is interested in sponsoring the “Be the Change” gala event, please click here for more information or contact andrew@oxfordkidsfoundation.org to look over a sponsorship packet. The Oxford Kids Foundation is also accepting donations of any unique quality to be included in the Gala’s silent/live auction. If you would like to make any item donations to the Gala auction, please contact Andrew Kistner at andrew@oxfordkidsfoundation.org.
We can’t wait to be a part of the change with you!
Any parent of a child with autism spectrum disorder (ASD) knows what a challenge it can be to manage the condition at home, ON TOP of managing everything else at home. Being a parent is such a wonderful gift, but it is also a full-time job and can be exhausting at times. Adding on managing an ASD diagnosis could very easily prove to be exhausting for many parents. Thankfully, The Oxford Center can share some tips and tricks to help you manage while providing the best environment possible for your children and yourself.
Tips and Tricks to Help you Manage ASD at Home
Establish a routine: Having a structured routine can provide comfort and stability for individuals with autism. Keep a consistent schedule for daily activities, such as mealtimes and bedtime.
Create a sensory-friendly environment: Autistic individuals may have sensitivities to light, sound, and touch. Try to minimize sensory triggers by using soft lighting, avoiding loud noises, and incorporating soft textures in the home.
Use visual aids: Visual aids, such as schedules and diagrams, can help individuals with autism understand and follow routines. Use pictures, symbols, and charts to help with communication and organization.
Encourage independence: Autistic individuals often benefit from learning and practicing new skills. Encourage independence by allowing them to participate in daily activities, such as cooking and cleaning.
Provide a quiet space: It is important for individuals with autism to have a quiet space to retreat to when they become overwhelmed. A designated quiet room or corner can provide a calming environment.
Practice social skills: Autistic individuals may have difficulties with social interaction. Encourage and practice social skills at home by playing games and engaging in conversation.
Implement calming strategies: Autistic individuals may become overwhelmed and need to calm down. Implement calming strategies, such as deep breathing exercises, to help manage emotions.
Seek professional help: If necessary, seek the help of professionals, such as therapists or behavior specialists, to support individuals with autism and provide resources for managing autism at home.
Managing autism spectrum disorder at home can be a challenge, but with patience, understanding, and the right strategies, individuals with autism can lead happy and fulfilling lives.
How to Practice Self-Care While Managing ASD at Home
As parents, we love our children and always want the best for them. Sometimes, we get so focused on taking care of our children and families that we forget about taking care of ourselves too. We all know that self-care is the first step in being able to care for someone else, so let’s look at some ways to help take care of yourself first!
Prioritize self-care: Make time for activities that bring you joy and relaxation, such as exercise, hobbies, or spending time with friends.
Seek support: Connect with other parents in similar situations through support groups or online communities and consider seeing a therapist or counselor for individual support.
Practice mindfulness: Incorporate mindfulness techniques, such as meditation or yoga, into your daily routine to reduce stress and increase self-awareness.
Take breaks: Make time for short breaks throughout the day, even if it’s just a few minutes of quiet time.
Set realistic expectations: Be realistic about what you can accomplish and delegate responsibilities to other family members or caregivers when possible.
Use respite services: Consider using respite services to provide temporary relief and allow for some personal time.
Take vacations: Plan and take regular vacations to recharge and refresh.
Remember, taking care of yourself is crucial for being able to provide the best care for your child with autism. Prioritizing self-care can help improve your physical and emotional well-being and increase your ability to manage autism at home.
How Can The Oxford Center Help?
The Oxford Center is dedicated to providing the best possible services for each of our children and helping parents be as successful as possible. In our Applied Behavioral Analysis (ABA) program, we place a focus on not only working with your child to ensure success, but we focus on working with you too. We know that consistency is important for a child with ASD, so we want to make sure we spend time working with parents to go over what their child is learning during ABA therapy and how parents can best support that learning at home.
Jessica Dodson, our ABA Program Director, says “At The Oxford Center, we help create routines within a successful environment to not only help the child grow, but the whole family. I have so many parents that focus on comparing how their child is doing against how another child is doing, so I always remind my parents and caregivers that everyone has their own separate path and journey. Most importantly, remember that we will all make it through our paths with a little teamwork and perseverance.”
Contact us today to find out how we can help you and your child be successful at 248-486-3636.
What is a Discovery Session, and why do I need one?
The purpose of the Discovery Session is for one of our team members to better understand your situation and what your journey has been like so far. From there, our team member can discuss COMPASS in more detail and how it can help give you success in your next states of meaningful employment.
Please fill out the form below if you would like our staff to contact you, answer your questions, or get you scheduled for a free Discovery Session.
