In my past experience as a pediatric physical therapist, I followed the traditional path, which involved patient treatments one time per week. I often thought to myself, “Am I really making a difference in this child’s life?” I then learned about an intensive therapy treatment approach that showed promise in pediatric population, and I made an effort to learn more about this program. With the encouragement and support of family and friends, I began the Richmond Hope Therapy Center in 2006, providing the Richmond area with the TheraSuit method of intensive physical therapy.
We are South River Compounding Pharmacy, Richmond’s trusted resource for customized medications, quality natural supplements, and personal health consultations. Our pharmacists work in conjunction with prescribers and their patients to decide on the most appropriate therapy for each individual.
Families find that a personalized form of treatment, including compounded medicines, can be of great benefit to a patient with autism. Nutritional supplements and biomedical treatments are effective in treating common ailments that children with autism may experience. These may be administered in the form of a gel that is easily absorbed by the skin. We are also able to produce custom medications that omit irritating or allergy-inducing inactive additives such as red dye and gluten.
We take pride in our community and thrive on giving back, building trusting relationships with practitioners, patients, customers, and friends. We welcome anyone and everyone to attend our free seminar series, Achieving Wellness with Baylor Rice, where we discuss topics such as thyroid health, BHRT, autism, and ADHD.
Have a question? Come in and see us!
Twelve years ago, our lives changed instantly when our vibrant and healthy three-year-old son suffered a traumatic brain injury. He fell head-first from a second-story window onto the asphalt driveway at our home in Powhatan, VA.
Caregivers who want to plan for the financial future of their adult dependent over the age of twenty-two who has special needs often have different issues to consider than caregivers of younger dependents. Special needs planning is sometimes very different for caregivers who have dependents in these two age groups.
We love it so much that we not only want to experience it ourselves, but we want to bring it to as many people in and around Richmond as we can. We believe that play is an integral part of life, and can be the best motivator for good behavior, good character development, and even hard work that there is. Even so, we also know that it can be a little hard to come by in our day-to-day lives.
Hello, Internet! My name is Cole Szymonik, and I have autism Asperger’s Syndrome. Normally, the term “syndrome” implies a debilitating mental condition that the victim must deal with for his or her entire life, but Asperger’s is different; Asperger’s is a debilitating mental condition that the victim must deal with for his or her entire life that can make him or her smarter. That’s right – Asperger’s has pros (like making me a nerd) and cons (like making me a nerd). Of course, in order for this passage to make sense, I will have to elaborate on this idea.
One of the greatest benefits of having Asperger’s syndrome is a boost in cognitive ability and learning skills. I find this very useful when going to school, playing video games, or interpreting modern art (Okay, that blob is red and weird, so… does it represent the artist’s anxieties, or…). The ability to learn quickly is very useful in a workplace environment, so Asperger’s helps in that regard, as well.
That said, Asperger’s syndrome has its downsides, too. One of the biggest problems caused by Asperger’s is the intensification of natural emotions – good for watching drama, but bad for keeping quiet in school. I sometimes get in trouble because of my feelings, so I have to go to a special class called “Social Skills”. The class is an uncomfortable tradeoff – It helps me deal with my emotions at the cost of my intelligence and my sanity. It is also very difficult to find people similar to myself, so I feel like a social outcast.
But you kind of are a social outcast.
Oh yeah, punk?
And what makes you think I’m a social outcast?
Well, for one thing, you’re talking to yourself. Typing to yourself, even.
Why, you —
…Thanks, I needed that. Anyway, I often feel like a social outcast, so…there’s that.
As can be seen, Asperger’s syndrome has both upsides and downsides. Insert good conclusion sentence here. See ya!
An increasing number of children are experiencing developmental challenges, and autism spectrum disorder is often being identified as the culprit. Dr. Evelyn Frazier, who specializes in autism spectrum disorder at Bon Secours Developmental and Special Needs Pediatrics at St. Mary’s Hospital, notes that the onset of autism can be
indicated by a delay in language development, a lack of eye contact or very little interest in caregivers or other children.
To be happy, to have fun, to learn, to sing, to talk with their kids, they are all expectations of every mother. No one would say that these are hard things to do, but for a mom of a child with autism, it isn´t that easy. For two years I’ve been struggling with communication and some behavior issues with my little 4 years old boy with autism.
As a family, we tried to go to the movies several times, but we failed. Me or my husband had to go outside the theater because our baby was noisy, or anxious, or trying to eat someone else´s popcorn or soda. We tried to keep him in a regular school, but some misses declared incapable to keep him, so we had to make changes. We tried to teach him to say some words, but he just brings what he wants or pushes us to get it. That made us feel frustrated, angry and worried. We started to visit specialists, to test him, and spending more time and money trying to find out what was wrong with him. At the beginning, we saw those expectations falling down. We stopped to try for a while.
However, after researching and meeting new people, we realized that we can still be happy, learn, sing, communicate, and have fun with him and his brother. And guess what? It’s not that difficult now! I mean, we cannot do everything as we want it, but we try to find new ways that works for him and for us. For now, we don’t go to the movies together, my husband and I take turns to go with our oldest boy and the other stays home eating popcorn with Andy. We looked for therapy institutions and special needs schools from the government in order to not to spend money we don’t have, and still help our boy. We enjoy doing those activities he enjoys like swimming, running, riding bikes, and jumping. We can go to restaurants or some other public places carrying an electronic device with us so he can watch his favorite series, and songs as well as play educational games. We can travel longer distances and change the route being aware of his emotions and mood. We can buy enough food he likes so he can eat well. And, of course, we can talk to people around us about how important it is their help. All these adjustments have made us notice how much happier our baby boy is. In conclusion, we can still be happy. Not only BE HAPPY IN SPITE OF our circumstances, but BECAUSE of them.
I´m happy when looks at me and, even though he doesn´t speak, he lets me know how much he loves me. I’m happy when he dares to do something new, and he learns. I’m happy to know more than before, to be more human, to be wiser, and stronger than ever. I believe in Happiness. This is our life, this is what we have, and what we love. I just would want it other way.
“What is happening in his head, ooh, I wish I knew, I wish I knew”
— from “Go To The Mirror!”, by Pete Townshend
In January 2003, my wife Carissa was pregnant with our last child. At the time, I remember thinking how little I cared about the triviality of the baby’s gender, and only caring about having a healthy baby. This was in part due to my profession as a pediatrician and in part due to being an older parent at 40. Both experiences had me realize that so many things could go wrong, I never did take for granted the gift of having a healthy, happy, “typical” child. My son was delivered via elective c-section, and, after having respiratory difficulties that resolved within 24 hours of life, seemed perfectly healthy.