The Broadway League announced that Broadway performances in New York City will be suspended through the remainder of 2020 due to COVID-19. They released updated information regarding performance cancellations and ticketing. Broadway theaters are now offering refunds and exchanges for tickets purchased for all performances through Jan. 3, 2021.

Broadway

While continuing to work with city and state officials along with leaders in science, technology and medicine The Broadway league is trying to formulate the best plan to restart the industry. Some of the logistics being reviewed include screening and testing, cleaning and sanitizing, wayfinding in theaters, backstage protocol and much more. 

Returning productions are currently projected to resume performances over a series of rolling dates in early 2021. Tickets for performances for next winter and spring are expected to go on sale in the coming weeks. For regular updates on ticket sales, individual show announcements, performance dates, and more, please check Broadway.org for information as it becomes available.

“The Broadway experience can be deeply personal but it is also, crucially, communal,” said Chairman of the Board of The Broadway League Thomas Schumacher.  “The alchemy of 1000 strangers bonding into a single audience fueling each performer on stage and behind the scenes will be possible again when Broadway theatres can safely host full houses.  Every single member of our community is eager to get back to work sharing stories that inspire our audience through the transformative power of a shared live experience.  The safety of our cast, crew, orchestra and audience is our highest priority and we look forward to returning to our stages only when it’s safe to do so. One thing is for sure, when we return we will be stronger and more needed than ever.”

“Our membership is working closely with the theatrical unions and in concert with key experts and some of the greatest minds inside and outside of the industry to explore protocols for all aspects of reopening. We are focused on identifying and implementing necessary measures that will enable us to resume performances safely for Broadway audiences and employees,” said Charlotte St. Martin, President of the Broadway League. “We are determined to bring back the people who rely on this industry for their livelihood, and to welcome back all those who love this vital part of New York City, as soon as it is safe to do so.  As so many of us in the Broadway community have been saying during this time – We’ll be back, and we have so many more stories to tell.”

Those holding tickets for performances through Jan. 3, 2021 will receive an e-mail from their point of purchase with detailed information regarding refund and exchange options. Any customers holding tickets through Jan. 3, 2021 that have not received an e-mail by Jul. 13 are advised to contact their point of purchase for assistance after this date.

—Jennifer Swartvagher

Featured photo: Sudan Ouyang on Unsplash

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Persistent attention issues have a significant impact on the daily lives of millions of people. Today Akili announced that the U.S. Food and Drug Administration (FDA) has granted clearance for EndeavorRxTM (AKL-T01) as a prescription treatment for children with attention deficit hyperactivity disorder (ADHD). Delivered through a captivating video game experience, EndeavorRx is indicated to improve attention function as measured by computer-based testing in children ages 8-12 years old with primarily inattentive or combined-type ADHD, who have a demonstrated attention issue. 

Akili ADHD

Attention impairments are a key component of ADHD for many children yet are often overshadowed by more overt symptoms of ADHD.

EndeavorRx was reviewed through FDA’s de novo pathway and its clearance creates a new class of digital therapeutics. EndeavorRx is designed to directly target and activate neural systems through the presentation of sensory stimuli and motor challenges to improve cognitive functioning.

“We’re proud to make history today with FDA’s decision,” said Eddie Martucci, Ph.D., chief executive officer of Akili. “With EndeavorRx, we’re using technology to help treat a condition in an entirely new way as we directly target neurological function through medicine that feels like entertainment. Families are looking for new ways to help their children with ADHD. With today’s decision by FDA, we’re excited to offer families a first-of-its-kind non-drug treatment option and take an important first step toward our goal to help all people living with cognitive issues.”

EndeavorRx was granted clearance based on data from five clinical studies in more than 600 children diagnosed with ADHD, including a prospective, randomized, controlled study published in The Lancet Digital Health journal, which showed EndeavorRx improved objective measures of attention in children with ADHD. After four weeks of EndeavorRx treatment, one-third of children no longer had a measurable attention deficit on at least one measure of objective attention. Further, about half of parents saw a clinically meaningful change in their child’s day-to-day impairments after one month of treatment with EndeavorRx; this increased to 68% after a second month of treatment. Improvements in ADHD impairments following a month of treatment with EndeavorRx were maintained for up to a month.

“For children living with ADHD, improving their ability to focus and resist distraction is critical to their daily functioning and performance in school,” said Elysa Marco, M.D., cognitive and behavioral child neurologist and Clinical Executive for Neurodevelopmental Medicine at Cortica Healthcare. “Unlike traditional ADHD medications, EndeavorRx is designed to specifically target inattention. Based on the benefits my research participants and patients have experienced, I am thrilled that EndeavorRx is moving from the lab to the clinic to play an essential role as part of a comprehensive treatment plan for children with ADHD.”

The EndeavorRx treatment will be available with a prescription to families soon. Akili believes that cognitive impairments require the same constant attention and care as with any other chronic condition. EndeavorRx will be released as the centerpiece of the Endeavor Care Program, which includes the EndeavorRx treatment and Akili Care,TM a mobile tracking app and personal support services for caregivers. Easily accessible from home, EndeavorRx is downloaded from the App Store by families on their mobile devices and does not require any additional equipment.

“The clearance of EndeavorRx marks the culmination of nearly a decade of research and development and was fueled by the commitment of our team and collaborators to challenge the status quo of medicine. This would not have been possible without the dedication of our clinical research partners and hundreds of families who gave their time and energy to participate in our clinical trials,” said Scott Kellogg, senior vice president of medical devices at Akili.

EndeavorRx is built on the Akili Selective Stimulus Management engine (SSMETM) core technology, a proprietary technology designed for the targeted activation of specific neural systems in the brain to treat diseases with associated cognitive dysfunction. SSME presents specific sensory stimuli and simultaneous motor challenges designed to target and activate the neural systems that play a key role in attention function while using adaptive algorithms to personalize the treatment experience for each individual patient. This enables second by second monitoring of patient progress completing the treatment sessions, and continuously challenges each patient to an optimized level, encouraging patients to improve their performance. Driven by the core belief at Akili that effective medicine can also be fun and engaging, EndeavorRx is delivered through an action video game experience. The captivating experience of EndeavorRx is designed to drive engagement and compliance.

—Jennifer Swartvagher

Featured photo: Akili

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Once a picky eater, always a picky eater? Science says that may be the case. If your little one often pushes away or refuses to take a bite of a veggie they don’t like, don’t expect them to grow out of it anytime in the near future. 

According to a study by the University of Michigan, by four-years-old children could be established picky eaters. Additionally, controlling or trying to restrict your child’s diet may backfire causing them to become more finicky. 

baby eating watermelon

“Picky eating is common during childhood and parents often hear that their children will eventually ‘grow out of it.’ But that’s not always the case,” says senior author Megan Pesch, M.D., a developmental behavioral pediatrician at Michigan Medicine C.S. Mott Children’s Hospital.

Researchers found that fussy eaters tend to have a lower body mass index and are not underweight. It is also less likely that they will be overweight or experience obesity. 

“We still want parents to encourage varied diets at young ages, but our study suggests that they can take a less controlling approach,” Pesch says. That being said “we need more research to better understand how children’s limited food choices impact healthy weight gain and growth long term.”

The study followed 317 mother-child pairs from low-income homes over a four-year period. Families reported on children’s eating habits and mothers’ behaviors and attitudes about feeding when children were four, five, six, eight and nine.

From preschool to school-age, picky eating habits were stable which indicates that any attempt to expand food choices may need to happen during the toddler or preschool years in order to be effective. High picky eating was associated with lower BMIs and low picky eating with higher BMIs. 

Increased pressure to eat and food restrictions was closely associated with reinforcing picky eating habits. This backs up the research conducted by Mott Children’s Hospital. Pressuring children to eat foods they dislike will not lead to a well-rounded diet later in life. 

Certain child characteristics, including sex, birth order, and socioeconomic status, also have been associated with persistence of picky eating.

“We found that children who were pickier had mothers who reported more restriction of unhealthy foods and sweets,” Pesch says. “These mothers of picky eaters may be trying to shape their children’s preferences for more palatable and selective diets to be more healthful. But it may not always have the desired effect.”

It is unknown if children who are picky eaters would have become even more selective if they did not receive higher levels of controlling feeding behaviors, Pesch says. She says future studies should investigate interventions around maternal feeding and child picky eating.

—Jennifer Swartvagher

Featured photo: Dazzle Jam from Pexels

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We sat down with Raquel Nieves, MD, of Stanford Children’s Health and Bayside Medical Group to talk about special needs children in her practice, including those with Down syndrome. As a medical professional and mom to a special-needs child, Dr. Nieves has a unique perspective. Read on to hear her take on what to look for in a pediatrician, how her daughter has informed her practice and what parents of special needs kids can do to best advocate for their children.

From your experience, what different skills might a parent look for when choosing a pediatrician for his or her child with special needs?

Dr. Nieves: Essentially, a pediatrician who’s willing to listen, who’s open minded and who has an attitude to serve others. In addition, you need to find a doctor that fits your personality since this will hopefully be a long-term relationship. The doctor also should be knowledgeable about children with special needs or, more importantly, be willing to learn from others who are more experienced.

 

I know that you have a personal interest in special needs children. Can you tell us a little bit about your daughter Anna and her special needs?

Dr. Nieves: We knew when I was 14 weeks pregnant that she was going to have Down syndrome. The whole first year for me was a big blur since she had three surgeries and five hospitalizations all within the first year of life. I felt like I was living in the hospital, and it was a rough time because I also had two others to care for, her older sister and brother. Now, (at age 4), Anna continues to have multiple appointments and therapies that we manage five times a week to include speech, occupational and physical therapies. Additionally, she participates in extracurricular activities that build her core strength and balance such as swimming and horseback riding. It all keeps me very busy, however, seeing her progress brings me such joy and that is what keeps me motivated.

How do you feel raising Anna has changed how you practice medicine?

Dr. Nieves: It has definitely made me more patient in general and much more compassionate toward families with children with special needs. Now that I’ve been on the patient end of things, I feel like I can truly relate to parents. I can understand the frustrations. I want to know what each individual parent or caregiver is dealing with in regards to their special needs child. Being in the unique position of understanding the medical side as well, I look for opportunities to identify the barriers that our families face and try to fix them with the goal of making our medical system better equipped to help our families.

What lessons have you learned as a physician raising a child with special needs?

Dr. Nieves: What we say as doctors truly matters. Parents are listening and we need to be very careful with our communication. The other lesson that I learned is that the parent of a child with special needs should be an advocate for his or her child. As long as you advocate in a respectful manner, then everyone benefits and this is because the doctors who are delivering the care also care about your child. Ultimately, we all have the same goal in mind as the caregivers: to do what’s in the best interest of our children.

What has Anna taught the rest of the family?

Dr. Nieves: Anna has taught our family so many lessons, to include love and compassion for all. Her friendly demeanor wherever we go spreads cheer and joy to all who are around her. She has taught our family about compassion in a way that is beyond learning it in a book. You can say, “be kind to people,” but it’s different when you have to live it day in and day out. My children, whether they wanted to or not, had to learn to give and sacrifice for another. They had to learn early on that life is not just about them, but about loving, helping, and serving others. They learn so much from Anna and they, too, teach so much to Anna.

How can parents advocate for their child with special needs, especially when it comes to health care?

Dr. Nieves: The best way to advocate is to speak up. If something bothers you, speak up about it. You are your child’s voice. Another thing that I feel very passionate about is to advocate for your child, not only in the medical setting, but in every setting, especially in an educational setting as well. I am a strong advocate for inclusion in schools. Done correctly, everyone, including the children without special needs, benefits with more cooperation, better behaviors, a sense of purpose, and higher test scores. I really feel that this is what humanity is all about. A final thought: we need to be expecting a lot out of our children, no matter what the disability is and no matter how severe. It doesn’t matter what IQ or what special needs a child has, all children have the ability to learn and progress, and it is our job as caregivers and medical providers to try to move them forward one step at a time.

Raquel Nieves, MD, is a board certified pediatrician and a fellow of the American Academy of Pediatrics. She graduated Summa Cum Laude from Vanderbilt University and received her medical degree from Boston University School of Medicine. She completed her residency at Travis Air Force Base, and served our United States Air Force for eight years. In addition to her general pediatrics practice in the military, Dr. Nieves was the Medical Director at Dover Air Force Base as well as a certified allergy extender. She is fluent in Japanese and speaks basic Spanish. She holds a special interest in caring for children with Down syndrome. She is married with three children. Her goal is to deliver the highest quality care to children in the most compassionate way.

photos: Stanford Children’s Health

When kiddo is sick you’ll do anything to make them feel better. But do so-called “folk remedies” actually work?

A few years ago, San Diego mom Debbie Vigan posted her unusual cold cure on Facebook, namely, putting sliced potatoes in her son’s socks as he slept. After a night sleeping with potato socks, her son had stopped coughing and his runny nose dried up. While Vigan mentioned she “saw an article” touting the cough and cold home remedy, she didn’t include her source—but the idea isn’t entirely out of left field.

According to Healthline, putting onions in your socks is an old folk remedy for kicking the common cold or flu to the curb. While it might smell awful, the reasoning behind this trick comes from several different sources. In the 14th century, people believed onions could ward off the Black Plague.

But why stick onions or potatoes in your socks? According to Chinese reflexology—an ancient form of complementary medicine—the feet are covered in “access points” that connect to all other areas of your body, via your qi, or life force energy. Basically, treat the feet to treat the whole body.

Photo: Rawpixel

Western medicine and science have shown that sulphuric compounds in onions have the ability to kill bacteria and viruses—but only when ingested, and in very limited studies. There isn’t data to back those results you apply those same onion compounds externally to your skin, as myth-busting website Snopes notes. When it comes down to it, there’s no solid scientific evidence that onions on your feet can cure a cold. Then again, there’s also no evidence that they don’t, either.

Ditto all of the above for potatoes.

Please note, we don’t advocate using this remedy in place of consulting a medical professional when your child is ill.

—Erica Loop, Keiko Zoll

 

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Trying again is the secret. I do believe that God leads us by the desires of our hearts. After my cervical cancer, my ovaries were saved and I had all the faith in the world that we could have another baby.

So, in August 1996, just nine months after my radical hysterectomy, Rick and I met our surrogate mother, Gwen, along with her candid and very easygoing family in Sacramento, California. In 1996 surrogacy was a bit of a mystery, especially in Virginia. As much as we had read and researched, we sought the comfort of the most accomplished hands within this delicate field.

The morning of our flight out to the West Coast was somewhat typical of a travel day, with the obvious exception of my whirling excitement. I checked through all of the last-minute details and was ready to give Yogi and Baloo their “going on a trip” hugs and treats when a pain struck my lower abdomen so hard that it brought me to my knees. My breath was taken away. My face flushed with heat. I had never felt anything like this before, not even after my recent surgery. This was something new, something full of power and something that wanted my attention. Minutes later, it was gone for the most part. I still felt exhausted. I stood up slowly, feeling like the wind had been knocked out of me. My heart pounded with joy for the inspirited blessing. Once again, a higher power had made an entrance into my life, and I knew it.

Later that day, at the surrogacy center in California, Rick and I sat talking with the doctor. I mentioned to him that I had a very strong feeling that I was at the beginning of my cycle and running some blood work might be a good idea. The doctor suggested that my earlier abdominal pains could have been from nerves. I knew otherwise, and he was kind enough to support my intuition. I realized how complex this whole process would be, and every little bit of blessed favor was not only welcomed, but honored. He ordered an ultrasound and blood work.

Later in the afternoon, after meeting with the doctors, we met Gwen for the first time. I was so excited! We felt an instant closeness. It was comfortable and effortless. There were no awkward spaces to fill with small talk; we fell right into each other. I told her about the incredible cramps I had that morning before leaving home in Virginia, and I shared my hunch that I was at the beginning of my cycle.

The next morning, she excitedly called to tell me that she had just started her period. I’ve never been so delighted about a period in my life! My hopes were sky high. When we arrived at the fertility center the doctor told us that the ultrasound showed that I had already ovulated and the blood work confirmed that I was also at the beginning of my cycle. The doctors were amazed that our cycles were perfectly aligned. They had never seen this happen without manipulation. This was a confirmation to me that I was exactly where I needed to be. I had made the intended connection.

With our cycles perfectly in sync, we were able to move forward immediately. There would be no time spent finding my cycle and taking medicine to align mine with Gwen’s. Had I not been attuned and opened to my soul and the Divine at work, who knows how long the road would have been and where it would have taken us. Trusting my intuitions and listening to the gentle voice inside of me allowed so many blessings in. Feeling and experiencing God and Universe communicate directly with me elevated my life to a place of expansive harmony that I never want to forsake.

Three months later, in November 1996, my embryos were transferred into our surrogate. Ten days after the transfer we received the amazing news that the implant was successful—we were pregnant on our very first try! This year, Thanksgiving brought even more for us to be grateful for, and this year, we celebrated. The next nine months were magical. Rick and I wanted to be as much a part of this pregnancy as possible. We flew out to Sacramento for each and every doctor visit, and I was Gwen’s coach during our birthing classes. Over the next ten months, Gwen and I became so close. We spent a lot of time together. Neither one of us held back: we were both willing and open. I was older than her by several years. Our trust in each other created an intimacy and an incomparable bond. She would ask for advice, and in answering, I was as discerning as I would be with my own daughter or close friend. I truly cared about her and loved her.

We were brought together by this miraculous undertaking, but our focus wasn’t always the pregnancy. She had a life despite her benevolent commitment. Together she and her husband, Bruce, had four children. Their personalities were distinctive. Each of the kids was welcoming, warm and fun. Their enthusiastic interest and support of us was another blessing. We shared family dinners with non-stop boisterous conversation swirling around the table as the kids let their voices ring loud and clear. The pre-teen sense of humor on display was entertaining and invigorating. The girls loved to sing for us while we relaxed outside in the warm California evenings after dinner. Each one of us was openhearted and engaged in these new friendships. Each one of us had something to give and something to receive.

I wanted to stay there—in this place where God and Universe were reaching out and leading me forward. Drop by drop, blessing by blessing, my heart filled with light and love.

 

Julianne Haycox is an artist, photographer, lover of all things in nature, and a fearless traveler. She is the author of Be Still and Know, a book filled with her photography and meditative quotes and Conversations with Grace (Koehler, March 2020), a book of inspiration and personal growth.  

If taking care of kids is hard work, then taking care of sick kids is indentured servitude.

It starts out innocently enough. Your poor baby has a fever and the look on his tired, pale little face is enough to send you running for his every heart’s desire. You cook, clean, launder, check temperatures, buy bulk Ibuprofen and Tylenol and administer it around the clock. You change sheets, empty wastebaskets filled with tissues, call the doctor, take him to appointments, follow up appointments and end-result appointments. You play board games and craft, you puzzle, read and watch movies. You lay next to him until he falls asleep and check the fan and humidifier before leaving the room.

You fall into a deep slumber the moment your head hits the pillow knowing you must wake up every three hours during the night to check his temperature in the dark. You stumble blindly, half asleep down the hall with your iPhone light as your guide and silently try to stick the thermometer in his ear. In the dark, you squint as you try to make sense of the numbers blinking on the thermometer and then try to remember if you gave Ibuprofen or Tylenol as his last dose. You may have to stumble back down the hall to check the list you made with every temp taken along with medicine dispensed at any given time throughout the day. Once the correct medicine is determined you wake your fever-induced, groggy child and ask them to guzzle 10 ML of a syrupy, cherry-flavored liquid that will hopefully secure him and you a few more hours of desperately needed shut-eye.

Now imagine that you have not one but two little boys, both equally sick with the flu. Take everything I’ve said and multiply it times two. I know…its not a pretty picture. The truth is that as hard as it is to manage two sick kids….that’s not the hardest part. Oh no, the real fun begins when one of them begins to feel better. Not, go back to school better, but well enough to be out of bed. The homemade chicken broth you so lovingly tried to spoon into their mouths is now turned away for “real food.”

“Mom, what I’d really like is a burger from the Habit”, my 7-year-old told me on one such afternoon. “How about a turkey sandwich?” I countered, hoping it might sound equally as appetizing. But alas, after four days of little to no food, nothing was going to go down as smoothly as a burger from the Habit. I looked down at the same sweatpants I’d been wearing for four days and figured wearing slippers wasn’t going to be my worst crime and climbed into the car.

Now most people might have told their sick child no, but after four days of being inside, the short ride felt like freedom. I rolled down the windows, turned up the music and sped off into the warm day. Once I returned home and the meal had been consumed, my son wanted to know what we were going to do. As though neither of us had been doing anything for the last several days. I suggested puzzles, coloring, past due homework, games, reading. Any independent activity that I could think of. But none seemed to appease him. What he really wanted was for me to come up with something amazing that we could do together. The problem was that nothing I suggested was hitting the mark. As fun as this game was, I sill had another sicker child that needed my attention, so I parked my younger son in front of our electronic babysitter and hightailed it upstairs to attend to his every need.

The entertaining and nurse-maiding went on for another two days until suddenly, one fine morning, my older son announced he too was ready to leave the land of his bedroom. Now suddenly, I had two half-well kids who both wanted me to entertain them at the same time and were suddenly well enough to fight about every single menial thing throughout the day. One wanted grilled cheese and the other pasta. One wanted to play Xbox and the other wanted the tv. And where they didn’t align, an argument would erupt. Arguing between two sick children sounds something like this “I (cough cough cough) am telling (blow nose) mom (cough, blow, repeat). You’re (hack up a lung) the worst (sniffle, sniffle, suck up snot) brother ever (dissolve into a fit of tears from the energy expended during the argument).”

When four people have been stuck inside together for six days the chance to leave is a coveted prize. My husband had to fly out for work on the 6th day and couldn’t contain his excitement over leaving. He hopped into that chauffeured sedan with barely a backward glace and drove off into a land where people get to go not only outside, but outside of the country. As we head into day seven, I am losing my ability to cope. I can no longer keep track of the Tamiflu doses and the fever reducers. My lists are tossed carelessly aside, jumbled up in the wastebasket with the used tissues. The soup now comes from a packet I mixed with some lukewarm water. The only thing holding me together is the hope that they will be well enough on Monday to go to school.

 

I am the proud mom of 2 energetic little boys, an 11 year old dog and sometimes my husband! Life moves pretty fast, if you dont look around once in a while...then you can pretend you dont see the piled up dirty laundry, dishes and never ending trails of toys!

Researchers from the Weizmann Institute of Science may have a way to predict a mother-to-be’s risk for gestational diabetes—and it’s all thanks to some serious math!

The study, which was published in the journal Nature Medicine, analyzed data on almost 600,000 pregnancies from Israel’s Clalit Health Services. Using a computer algorithm, the researchers were able to find nine parameters that could predict the risk for gestational diabetes.

photo: Nappy via Pexels

So what does this mean for you and other pregnant mamas? It’s possible with nine questions (the nine parameters) medical providers could accurately pinpoint risk for the disease well before the expectant mother shows signs of gestational diabetes.

Of the research, senior author Prof. Eran Segal of the Computer Science and Applied Mathematics and the Molecular Cell Biology Departments, said, “Our ultimate goal has been to help the health system take measures so as to prevent diabetes from occurring in pregnancy.”

—Erica Loop

 

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You already know the way a serious case of the tireds or total frustration can affect your tot, but now recent research from Northwestern University may have found another reason behind toddler temper tantrums.

According to the study published in the Journal of Applied Developmental Psychology, expressive language (the words your child says) may have an impact, too.

photo: Ryan Franco via Unsplash

Researchers surveyed more than 2,000 parents who all had toddlers between 12 and 38 months of age. The parents answered questions about their toddlers’ tantrum behaviors, as well as how many words the children could speak.

So what did the researchers find? The data showed a connection between late talkers (toddlers who had less than 50 words or weren’t stringing words together by two years) and severe tantrums.

Elizabeth Norton, an assistant professor in the department of communication sciences and disorders at Northwestern said, “We totally expect toddlers to have temper tantrums if they’re tired or frustrated, and most parents know a tantrum when they see it.” Norton continued, “But not many parents know that certain kinds of frequent or severe tantrums can indicate risk for later mental health problems, such as anxiety, depression ADHD and behavior problems.”

Before you start to worry about your kiddo’s lag in language, co-principal investigator Lauren Wakschlag, professor and vice chair in the department of medical social sciences at Northwestern University Feinberg School of Medicine and the DevSci director said of toddler tantrums, language delays and later issues, “All these behaviors must be understood within developmental context.”

Wakschlag continued, “Parents should not overreact just because the child next door has more words or because their child had a day from The Wild Things with many out-of-control tantrums. The key reliable indicators of concern in both these domains is a persistent pattern of problems and/or delays. When these go hand in hand, they exacerbate each other and increase risk, partly because these problems interfere with healthy interactions with those around them.”

—Erica Loop

 

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