#speech therapy kit

[speechgears]

Exercises with speech therapy tools enhance communication abilities and overcome speech difficulties. The five exercises in this blog article address articulation, fluency, voice projection, and general communication clarity, among other speech-related issues.

[russellius]

THE SUNDAY TIMES: Molly Hudson, Saturday November 30 2024, 6.00pm GMT

Listening to George Russell field questions about the controversial issues that threaten the future of the sport with clarity and calmness, you would be hard pushed to detect that he was once an unsure and self-conscious child.

Russell as a director of the Grand Prix Drivers’ Association is now one of Formula 1’s leading public voices. But such were his difficulties, he was sent for speech therapy and that focus on clear enunciation has been crucial in helping him progress in a sport that requires concise feedback.

“When I was a young kid, six or seven, my dad used to say he could never understand what I was saying, because I was mumbling all the time,” Russell says as he sits in his team kit in the Mercedes hospitality suite. “As I grew a little bit older, and I started to race in Europe, for three years I had an Italian mechanic. I was in an Italian team. It was a European environment, and you had to talk slow, you had to talk precisely so they could understand.”

“When I was with Force India [now Aston Martin], as a test driver, we did some work with an ex-RAF pilot, just about clear communications and interpretations of people’s words and that really resonated with me.”

The 26-year-old secured his third Formula 1 victory last week in Las Vegas, and that communication came to the fore. He recognised that the track evolution, which meant that lap times were improving as the track was swept clean of dirt by the cars and rubber was laid on the circuit, meant the last car on track would have the best chance of success.

“Vegas was a good example — in qualifying, I was so clear. ‘I want to be the very last car to cross the line.’ It was pretty clear what my requests were. We did that, and we got the pole. I believe in myself this year, especially whenever I’ve trusted my gut,” he says.

Russell was born in King’s Lynn, and attended the private Wisbech Grammar School, before his karting took precedence. He spent his first Formula 1 pay cheque on a new Mercedes for his father, Steve, who ran a business selling seeds and pulses and travelled with his son to races in a motorhome while he was karting.

That family dedication has paid off. Russell is preparing to begin a pivotal new chapter of his career, stepping out of the shadow of seven-times world champion Lewis Hamilton and becoming Mercedes’s lead driver next season, alongside a rookie teenager, the Italian Andrea Kimi Antonelli.

It has been a season of ups and downs for Mercedes, struggling to find a consistent car despite registering four race victories, and managing the departure of Hamilton to Ferrari at the end of the season. Russell has transformed from someone who watched Hamilton race, to being his colleague, and he leads him in the drivers’ championship.

“I definitely looked up to him and admired him,” Russell says. “My hero, honestly, was my brother [Benjy, who also raced under the driver No63 he uses]. “He’s ten years older than me, and he’s who I looked up to when I was go-karting, because that was maybe more relatable for me. He was winning races in go-karts, and he was winning British championships, World Championships, and that’s what I wanted to do, because I could visually see him doing that.

“But without doubt, I’ll always remember my first F1 race for Mercedes [shortly before signing to their young driver development programme] in Abu Dhabi 2016, the Nico [Rosberg] and Lewis race, and just being in the same room as him in the debrief, listening to it all unfold. I was starstruck being there in that moment. So for sure it is surreal that we’ve now been team-mates for three years, and that I know within myself that I can perform at a minimum of his level.”

Russell has raced in 126 grands prix, with three victories, four pole positions and 15 podium finishes, having spent three seasons at a struggling Williams, before stepping up to Mercedes in 2022. His highest finish in the drivers’ championship was fourth, in 2022. This season is his most successful statistically speaking, but he is further down the rankings in sixth because of the spread of drivers claiming wins.

For so long, Hamilton carried the hopes of British fans in F1, and this season Lando Norris has provided the best chance of success. Russell believes next year can be his opportunity, assuming he has the car to do so.

“I’ve been in F1 six years now, next year is my seventh, and my fourth year with the team,” he says. “I feel absolutely ready to take my journey to the next level and I feel ready to fight for a championship. I feel ready to fight against Max [Verstappen] and if we get the opportunity, I’m not going to waste it.

“I feel I’ve been ready for three years. I’m team-mates with the greatest driver of all time and if you’re ever finishing ahead of Lewis Hamilton or beating him in a championship, you know that probably in 12 other seasons that would have been enough to win, or at least fight for a world championship.”

Russell has learnt to celebrate the good times with gusto when they do arrive, cancelling his flight home to party, instead, in Vegas with his girlfriend, Carmen Montero Mundt, and his team members.

The Vegas grand prix is particularly brutal on the body, as it involves travelling to the other side of the world, and then it is held at night. Before claiming his pole position, Russell took a 45-minute nap in his driver’s room.

Those challenges meant extra celebration, and something Russell had been inspired to do by a fellow driver.

“I listened to Fernando [Alonso] when he was on the Jake Humphrey podcast saying he looks back on his victories and regrets not celebrating it more [but] I’ve got to be honest, when I was out in Vegas until the early hours there’s a point of which I thought to myself, ‘You know what, I need to head back now, because I want to experience this feeling again.’ ”

Russell knows that the ability to challenge for titles is dependent on the capability of his car as much as it is a marker of his own talent. His time at Mercedes has coincided with the dominance of Red Bull and Verstappen.

“Arguably, Max shouldn’t have won the championship this year,” he says. “But the others made a few more errors and didn’t capitalise when they had the chance. I feel that we have [won what we could].

“Opportunities don’t come around every single day. This year was Lando’s chance. They [McLaren] might be there again next year. They may not. We just don’t know in this sport; nobody would have predicted Red Bull to fall off form in the manner that they have.

“There’s so much hype around Max. He’s such an exceptional driver, but the fact is, he’s won one race in the last 12 and, it just goes to show everyone is beatable because you are at the mercy of your race car. The difference with him this year is he’s won every occasion that he’s had the chance, and his rivals haven’t.”

Russell will hope that next year he has the chance to show he can capitalise where others have not.

[my-autism-adhd-blog]

Hi there! My friend is going to be opening a toddler / child “play place” and she wants to develop a sensory room to help give a safe space to autistic or other neurodivergent children. She’s enlisted my help, but since I was diagnosed in my early 20’s, I really am not sure what would help autistic children. Not to mention the wide variation of symptoms!

So now, I’m gathering information. I know it’ll never be a “one-size-fits-all” type of thing, but we want to get as close and as inclusive as possible. Do you have experience with places like this? Or, would you have any suggestions? Thanks in advanced <3

Hi there,

I found an article talking about how to build a sensory room. According to this article:

How do you set up a sensory room?

Before designing the room it is important to consider:

1. The individual needs of the clients who will use the room. What are the ages, abilities, and needs of the individuals who will use the room?

2. How many individuals will need to use the room at the same time?

3. How the room will be used. Will the room be a calming area? Will it be used for therapy sessions including occupational therapy, speech, sensory integration therapy, or one on one instruction? 

4. Keep in mind the long term use of the room. If all of your equipment is static, students can become bored. A good goal is to create a flexible space that allows you to create different scenes or moods depending on the emotional, cognitive, and physical needs of the students. How will the room be adapted to meet changing needs and keep it interesting?

Common Components of a Sensory Room

* Bubble tube

* Fiber optic sprays, or lighting

* Beanbag chairs

* Interactive Wall Boards

* Rocking chairs 

* Stereo or MP3 Player with Headphones

* Therapy balls

* Lighting/projector that can display various colors & patterns

* Weighted blankets or weighted lap pads

* A flowing water fountain

* Bins with assorted sensory activities

* Aromatherapy diffuser kit

The full article will be linked below, as it goes into more detail:

I also found another article on what items to include in a sensory room:

What Items To Include in Your Sensory Room

Large crash pillows or mats

Bean bag chair

Body sock

A net swing or therapy sensory swing

Fidget items that allow for a repetitive moment

Weighted blankets or vests – the blankets and vests I linked to here are handmade by a fellow Occupational Therapy Assistant with a small business on Etsy.

Tunnel

Therapy balls

Sensory break cards

Books to read

A stuffed animal or favorite toy – the Soothing Sammy dog and program is a great option for preschool and kindergarten-aged children

Calming, alerting, and organizing activities for kids – free printable included to hang in your sensory room

The article will also be below if you want to read it too.

I hope these help. Thank you for the inbox. I hope you have a wonderful day/night. ❤️

[cosmic-frost-main]

Small info dump on the adoption au while I'm thinking about it and trying to sleep

- Audrey when found by Henry would've been around the age of 3 or 5, she looks way younger due to malnutrition and neglect after Joey's death. Doctors have suspected she drank from ink machine as a source of food but are still bewildered on how she managed to survive, they viewed it as pure luck.

- She became interested in animation when finding Henry's studio sketches of the Bendy cartoons and begging him to teach her.

- It took Linda nearly a month to get Audrey to even get near her without running and hiding, Audrey never does it to Henry and they chalked it up to her just trusting him more.

- Related to the previous fact, Audrey would always hide away in her bed only when Henry is away and only ever goes out when there's food left out for her and Linda being out of sight or when Henry is home.

- Audrey didn't dislike Linda, just nervous around her due to her being the only female figure she's met after only being around male figures.

- Audrey's the reason horror movie night stopped. She saw a scene that involved head turning and redid it happily without trouble, Linda and Henry still have nightmares about it.

- Audrey mostly looks dirtied up due to being adventurous a lot and climbing places she shouldn't, Linda always makes sure to have the med kit ready in case she falls into a bush again.

- Both Henry and Linda have suspicions that Joey used demonic rituals to create Audrey, and the fact she can bleed ink and come out barely hurt after falling many from high heights fuel it.

- Henry gave all the plushies of the Bendy characters he got while working at the studio to Audrey, she frequently uses the large Boris plush as a bed and refuses let go of it when trying to move her to her actual bed.

- Audrey did get taken to therapy to help sort out any problems she had, such as the neglect she endured and get her speech working.

- Her first words were "Papa"

[princess-nell]

“It was remarkable and strange how much of the season seemed to be occurring in between episodes or scenes. The worst offender of this was the storyline about Nate, whose rise from kit man to assistant coach was one of the first season’s most successful arcs, and whose descent into aggrieved villainy in Season Two was well-plotted, even if it upset many viewers. Given the empathetic messages of the series, it was obvious that Nate would return to the fold by the end of this season. But pretty much every choice on that journey was mystifying. Rather than show him gradually recognizing what an abusive person he had become, how terribly he had betrayed Ted by leaking his private medical information to the press, etc., the show seemed to view his redemption as a matter of Nate learning to love himself. And the writers’ method of doing that was a bizarre love story involving Jade, the hostess at Nate’s favorite restaurant, who had no personality and no apparent reason for wanting to go out with Nate other than taking pity on him after another woman was mean to him in front of Jade. (Nor were we ever given any reason why Nate was so hung up on Jade, given how repeatedly cold she was to him prior to that moment.) Eventually, it turned out that all Nate really needed was for his emotionally-closed-off father to acknowledge Nate’s genius, and for Nate to play the violin, and suddenly everything was OK. Nate quit his dream job as head coach of an EPL team in between episodes, with no explanation other than his discomfort at club owner Rupert trying to get Nate to cheat on Jade. Early in the season, we saw the entire Richmond squad so incensed by video footage of Nate destroying Ted’s homemade “BELIEVE” sign that they spent an entire half of football being penalized for assaulting various members of Nate’s team. Yet last week, we saw three representatives from the team — two of them, winger Colin and replacement kit man Will, among the most frequent targets of Nate’s abuse in Season Two — arrive at the restaurant with smiles on their faces to tell him the team had voted unanimously to invite him back. Even if you believe Ted’s ethos that forgiveness should not require redemption or atonement, how do you not show a scene where the team — who are in the midst of the winning streak of their lives, have been shown to be a deeply superstitious lot wary of shaking up anything that’s working, and, again, are all furious with Nate for one reason or another — gets together to debate this and vote on it? How do we skip over Nate’s actual return to the building, or the moment when he’s told that he will be — or chooses to be — Will’s assistant, rather than rejoining the coaching staff?”

This whole article, start to finish, sums up everything that had me grinding my teeth about S3. The Nate arc, however, was the worst in my eyes. I rewatched S1&2 over the last week, and I was struck by how well plotted the show was for the first two seasons. Everything was carefully set up and very well acted. Then everything just deteriorated. Nate’s entire arc was set up from the get go — you can see hints of his inner toxicity early on in Season 1. And then, they wasted all this time without showing him doing any of the work. I’m all about a good redemption arc, and I thought Beard’s speech to him was beautiful. But…Nate ends up being the one character who gets everything he wants and needs, and does nothing to earn it. The writing just wasn’t there for it. Why wasn’t he in therapy along with Roy at the end? Of all the characters in Ted Lasso, Nate needed therapy the most.

I also have to say the rewatching the whole thing reminded me of what a toxic, petty little man he was. He didn’t do any real work to work through that and deal with his major relationships, which were always with his father, Ted, and Rupert. Instead he learned to love himself through Jade’s love…and I’m sorry, she has no real personality. What do we know about her, other than she’s sardonic and supports Nate? Oh, and she’s Polish. That’s it. There was a gigantic hole in the middle of that storyline.

[speechgears-india]

Effective Sensory Therapy Tools for Speech and Motor Skill Development

SpeechGears offers a wide range of sensory therapy tools designed to improve oral motor skills, speech clarity, and sensory processing. Ideal for both children and adults, these tools help therapists provide targeted exercises to enhance communication and feeding abilities. The kit includes various equipment to address different sensory needs, making therapy more effective and engaging. Explore our collection of Sensory Therapy Tools at SpeechGears and support better therapy outcomes today!

[nathfiset]

What is Tay-Sachs disease and how cord blood banking can help?

I am ready to enroll in cord blood banking NOW and get my special discount!

By clicking on either buttons, you are agreeing to our TOS and disclaimers and will be redirected to an affiliate cord blood banking provider. We might get financial compensation if you sign up with them through our affiliate links. Unlock your special discounts by adding your promo code.CORD300 in the coupon field to get $300 OFF cord blood and tissue banking. OR cord200 to get $200 OFF if you are getting cord blood banking only. I want more information on cord blood banking

 Tay-Sachs disease is a rare and devastating genetic disorder that primarily affects infants and children. This inherited condition is caused by a genetic mutation that affects the central nervous system, leading to progressive neurological decline and eventual death. Although there is currently no cure for Tay-Sachs disease, there are treatments available that can help alleviate some of the symptoms and improve the quality of life for affected individuals. One potential treatment that has been gaining attention in recent years is cord blood banking. This process involves collecting and preserving the umbilical cord blood of newborns, which contains valuable stem cells that can be used in the treatment of various diseases, including Tay-Sachs. In this article, we will explore the intricacies of Tay-Sachs disease and how cord blood banking can offer hope for affected individuals and their families.

Understanding Tay-Sachs disease: causes and symptoms.

Tay-Sachs disease is a rare genetic disorder that primarily affects the nervous system. It is caused by a genetic mutation that leads to the absence or deficiency of an enzyme called hexosaminidase A (Hex-A). This enzyme is responsible for breaking down a fatty substance called GM2 ganglioside, which accumulates in the nerve cells of individuals with Tay-Sachs disease. As a result, the nerve cells become damaged over time, leading to progressive neurological deterioration. The disease is typically diagnosed in early childhood, and common symptoms include developmental delay, muscle weakness, loss of motor skills, and a cherry-red spot in the eye. Unfortunately, there is currently no cure for Tay-Sachs disease, and it is a devastating condition for affected individuals and their families.

The importance of early diagnosis.

Early diagnosis plays a crucial role in managing and treating Tay-Sachs disease. Identifying the disease in its early stages allows for timely intervention and the implementation of appropriate medical and supportive care. Early detection enables healthcare professionals to provide families with accurate information about the condition, its progression, and available treatment options. It also allows for the initiation of early interventions, such as physical therapy, occupational therapy, and speech therapy, which can help alleviate symptoms and improve the quality of life for affected individuals. Additionally, early diagnosis enables families to access resources and support networks that can provide invaluable emotional and practical assistance throughout their journey with Tay-Sachs disease. By recognizing the importance of early diagnosis, healthcare professionals and families can work together to optimize outcomes and provide the best possible care for individuals affected by this devastating genetic disorder.

How cord blood banking works.

Cord blood banking is a process that involves the collection and preservation of stem cells from the umbilical cord blood of a newborn baby. After the baby is born and the umbilical cord is clamped and cut, the remaining blood in the cord and placenta is collected using a sterile collection kit. This blood is rich in hematopoietic stem cells, which have the potential to develop into various types of blood cells.Once collected, the cord blood is transported to a cord blood bank, where it undergoes processing and cryopreservation. The processing involves separating the stem cells from the other components of the cord blood, such as red blood cells and plasma. This ensures that the preserved cord blood primarily contains the valuable stem cells.After processing, the stem cells are stored in specialized cryogenic tanks, where they are frozen at extremely low temperatures to maintain their viability and effectiveness. These cryopreserved stem cells can be stored for several years, offering a valuable resource that can be accessed in the future if needed.Cord blood banking provides a potential source of stem cells for medical treatments and research. These stem cells have the ability to regenerate and repair damaged cells and tissues, making them valuable in the field of regenerative medicine. They can be used in the treatment of various conditions, such as certain types of cancers, genetic disorders, and blood disorders.By preserving cord blood through banking, parents have the opportunity to secure a potential lifeline for their child's future health. It offers peace of mind, knowing that these precious stem cells are readily available if ever needed for medical interventions or clinical trials.Overall, cord blood banking is a proactive and forward-thinking approach to healthcare, providing families with a valuable resource that may have the potential to significantly impact their child's health and well-being in the years to come.

Potential benefits for Tay-Sachs patients.

Cord blood banking has shown potential benefits for patients with Tay-Sachs disease. Tay-Sachs is a rare genetic disorder that affects the central nervous system, resulting in progressive neurological deterioration. The stem cells preserved in cord blood have the ability to differentiate into various types of cells, including neural cells. This opens up possibilities for their use in potential therapies for Tay-Sachs patients. Stem cell transplantation has shown promise in preclinical studies, with the potential to replace or repair damaged cells in the central nervous system. While further research is needed to fully understand the implications and effectiveness of cord blood stem cell therapy for Tay-Sachs disease, it offers hope for improved treatment options and outcomes for patients and their families.

Availability of cord blood banking.

The availability of cord blood banking has significantly expanded in recent years, providing individuals with the opportunity to preserve and store their newborn's cord blood for potential future use. Cord blood banking involves the collection and storage of the blood found in the umbilical cord and placenta after childbirth. This blood is a rich source of hematopoietic stem cells, which have the ability to develop into various types of blood cells. By preserving this valuable resource, families can have access to a potential source of stem cells for medical treatments and therapies. The increasing availability of cord blood banking services has made it more accessible for families to make this important decision and secure a potential lifeline for their loved ones' future health needs.

The role of stem cells.

Stem cells play a crucial role in various biological processes and hold immense potential for medical research and treatment. These unique cells have the remarkable ability to differentiate into specialized cells and tissues, making them invaluable in regenerative medicine. Stem cells can be harvested from various sources, including bone marrow, adipose tissue, and umbilical cord blood. They have the capacity to repair and regenerate damaged tissues, making them highly sought-after in the field of tissue engineering. Additionally, stem cells have shown promising results in the treatment of various diseases, such as leukemia, spinal cord injuries, and heart disease. The versatility and regenerative properties of stem cells make them a fascinating area of study and a promising avenue for future medical advancements.

Potential for future treatments.

Recent advancements in stem cell research have opened up new possibilities for future treatments. Scientists are exploring the potential of using stem cells to treat a wide range of diseases and conditions, including Tay-Sachs disease. Stem cell therapy holds the promise of replacing or repairing damaged cells and tissues in the body, offering hope for improved outcomes and quality of life for patients. Additionally, ongoing research is focused on enhancing the effectiveness and safety of stem cell treatments, as well as developing new techniques for delivering stem cells to the affected areas. While more research and clinical trials are needed, the potential for stem cell-based therapies to revolutionize the treatment of Tay-Sachs disease and other debilitating conditions is an exciting prospect in the field of regenerative medicine.

Advancements in cord blood research.

Significant advancements in cord blood research have paved the way for promising developments in the field of regenerative medicine. Cord blood, the blood collected from the umbilical cord at birth, is a rich source of stem cells that can differentiate into various types of cells in the body. Researchers have made significant strides in understanding the potential applications of cord blood stem cells in treating a range of diseases and conditions. Studies have shown the effectiveness of cord blood stem cells in the treatment of blood disorders, immune system disorders, and certain types of cancers. Moreover, ongoing research efforts are focused on improving the storage and preservation techniques of cord blood, as well as exploring the use of cord blood stem cells in personalized medicine approaches. With these advancements, cord blood banking has emerged as a valuable option for expectant parents to potentially secure a valuable resource for future medical treatments for their child and family members. The continuous progress in cord blood research holds great promise for the future of regenerative medicine and the potential to improve the health outcomes of individuals facing various medical challenges.

Considerations for families at risk.

When considering the options available for families at risk, it is important to take into account several key factors. First and foremost, it is crucial to consult with a healthcare professional or genetic counselor who can provide personalized guidance based on the specific risks and circumstances involved. Understanding the potential genetic conditions or diseases that may affect your family can help inform decision-making regarding cord blood banking. Additionally, financial considerations play a role, as cord blood banking may involve associated costs for collection, processing, and storage. Evaluating the reputation and accreditation of cord blood banking facilities is essential to ensure the quality and viability of the stored stem cells. It is also important to consider the potential benefits and limitations of cord blood banking, as well as alternative options like public cord blood donation. Ultimately, making an informed decision about cord blood banking can provide families at risk with a sense of security and potential medical options for the future.

Making an informed decision.

When making an informed decision regarding any medical procedure or intervention, it is crucial to gather as much relevant and reliable information as possible. This includes conducting thorough research, seeking guidance from trusted healthcare professionals, and considering the potential risks and benefits involved. It is important to weigh all available options, taking into account factors such as personal circumstances, medical history, and individual preferences. By seeking out reputable sources of information and engaging in thoughtful deliberation, individuals and families can make informed decisions that align with their values and goals.In conclusion, Tay-Sachs disease is a devastating genetic disorder that affects the central nervous system and can significantly impact a child's development and quality of life. However, with the advancements in technology and medical research, cord blood banking has emerged as a potential solution for families at risk of passing on this disease to their children. By storing a newborn's cord blood, which contains valuable stem cells, families now have the option to potentially treat or even cure Tay-Sachs disease in the future. This is an exciting development in the fight against genetic disorders, and it is essential for families to educate themselves and consider cord blood banking as a proactive measure.

FAQ

What is Tay-Sachs disease and how does it impact individuals who are affected by it?Tay-Sachs disease is a genetic disorder that progressively destroys nerve cells in the brain and spinal cord. It primarily affects infants and young children, leading to developmental regression, seizures, loss of motor skills, muscle weakness, and eventually death. Individuals affected by Tay-Sachs disease often experience a rapid decline in physical and mental abilities, requiring extensive medical care and support. There is currently no cure for Tay-Sachs disease, and treatment focuses on managing symptoms and improving quality of life.How does cord blood banking play a role in potentially treating or managing Tay-Sachs disease?Cord blood banking can potentially play a role in treating Tay-Sachs disease through stem cell transplantation. Stem cells from umbilical cord blood can be utilized in replacing damaged cells in individuals with Tay-Sachs disease. This can assist in restoring functions that are impaired by the disease. Additionally, cord blood banking allows for the preservation of a potential source of stem cells for future therapies that might be developed for managing Tay-Sachs disease.What are the potential benefits of using cord blood stem cells in the treatment of Tay-Sachs disease?Cord blood stem cells have the potential to treat Tay-Sachs disease by replacing damaged cells in the brain and nervous system, potentially slowing or halting disease progression. These stem cells can differentiate into various cell types needed for tissue repair and regeneration, offering a promising therapeutic approach for managing this devastating genetic disorder. Additionally, using cord blood stem cells eliminates the risk of rejection commonly associated with other types of stem cell transplants, making it a safer and more effective treatment option for Tay-Sachs disease.Are there any limitations or challenges associated with using cord blood banking for Tay-Sachs disease treatment?One limitation of using cord blood banking for Tay-Sachs disease treatment is the potential difficulty in finding a suitable match for transplantation due to genetic variability. Additionally, the amount of cord blood collected at birth may not always be sufficient for treatment. Furthermore, the effectiveness of the treatment in reversing or halting the progression of Tay-Sachs disease remains uncertain and requires further research. Additionally, there are ethical considerations regarding the commercialization of cord blood banking and access to treatments for all individuals.How does the process of cord blood banking work and how can individuals or families affected by Tay-Sachs disease get involved?Cord blood banking involves collecting and storing the blood from a newborn's umbilical cord for future medical use. Families affected by Tay-Sachs disease can get involved by choosing to store their baby's cord blood, which may contain stem cells that could potentially be used for treatments in the future. This process can be arranged through private cord blood banking facilities. Additionally, families can participate in research studies and clinical trials related to Tay-Sachs disease to further contribute to advancements in treatment options.  Read the full article

[phonologix-1]

Exploring promising therapies for children with autism and speech delays

In the field of supporting children with autism and speech delay, innovative therapies and interventions are constantly emerging, bringing hope and progress kit for families on this journey. Speech-language pathologists play a key role in identifying and implementing these promising approaches, working alongside families to support communication development of children.

One innovative therapy that is gaining ground is augmentative and alternative communication (AAC). AAC includes a range of tools and techniques, including picture boards, communication devices, and sign language, designed to help people with limited verbal communication skills. By providing alternative means of expression, AAC allows children with autism and speech delays to effectively communicate their needs, interests, and thoughts.

Another promising intervention is social skills training (SST), which focuses on teaching children with autism the essential social skills and behaviors needed to successfully interact with peers and adults. Through structured activities and role-playing exercises, SST helps children learn how to initiate conversations, interpret social cues, and confidently navigate social situations.

Additionally, sensory integration therapy has shown promise in addressing the sensory processing challenges often associated with autism. This therapy aims to help children regulate their responses to sensory input, such as touch, sound and movement, through structured activities and sensory experiences. By promoting sensory integration, children are better able to cope with sensory stimuli and participate more effectively in daily activities.

In addition, parent-implemented intervention (PII) programs are increasingly recognized for their effectiveness in supporting child development in the home environment. These programs enable parents to become active participants in their child's therapy journey, equipping them with strategies and techniques to promote communication, socialization, and behavioral skills in daily interactions with your child.

In summary, a range of innovative therapies and interventions promise to support children with autism and speech delays on their journey towards communication and social success. By applying these approaches and working collaboratively with speech-language pathologists and other professionals, families can help their children reach their full potential and thrive.

[speechgearss]

Discover a curated selection of sensory integration therapy tools at Speech Gears' Therapeutic Special Kit. Our range of meticulously chosen products aims to provide comprehensive support for individuals seeking sensory integration therapy. From tactile stimulation to proprioceptive aids and vestibular tools, our collection offers diverse options to assist therapists, educators, and caregivers in facilitating effective sensory integration sessions. Explore our assortment today to find innovative tools that promote sensory processing, aiding individuals in achieving improved focus, coordination, and sensory regulation.

[pranay-234]

Down Syndrome Market Strategic Imperatives for Success and Rising Demand Till 2032

Introduction:

Down syndrome, a genetic disorder caused by the presence of an extra copy of chromosome 21, presents unique healthcare challenges and opportunities. This article delves into a comprehensive analysis of the global Down Syndrome market, offering insights into the latest trends and an outlook that highlights both the existing challenges and emerging prospects within this evolving healthcare landscape.

𝐑𝐞𝐪𝐮𝐞𝐬𝐭 𝐒𝐚𝐦𝐩𝐥𝐞 𝐂𝐨𝐩𝐲 𝐎𝐟 𝐑𝐞𝐩𝐨𝐫𝐭: https://www.alliedmarketresearch.com/request-toc-and-sample/11914 

Understanding Down Syndrome:

Down syndrome, also known as trisomy 21, affects individuals from birth and can lead to developmental and cognitive delays. While it remains a lifelong condition, advancements in medical care, therapy, and social support have improved the quality of life for those with Down syndrome.

COVID-19 Impact Analysis:

COVID-19, which originated in Wuhan, China, has had profound global implications since its emergence in December 2019. The highly contagious disease, caused by the SARS-CoV-2 virus, swiftly spread to nearly 213 countries, prompting the World Health Organization to declare it a public health emergency on March 11th, 2020.

The initial stages of the pandemic were marked by a lack of specific diagnostic tests for COVID-19, leading to the use of alternative, less effective diagnostic methods. This gap in specific diagnostic tests presented a lucrative opportunity for diagnostic manufacturers to introduce their COVID-19 diagnostic kits. Many established players and innovative start-ups from across the globe seized this opportunity and introduced COVID-19 diagnostic kits into both local and global markets. This strategic move not only allowed them to contribute to the fight against the pandemic but also helped in sustaining their revenues during a time of crisis.

However, the pandemic's impact rippled through global supply chains, disrupting the procurement of raw materials necessary for the manufacturing of diagnostic devices and products, including those used in the diagnosis and management of Down syndrome. Manufacturers of these diagnostic products also faced challenges as they reduced their production due to the pandemic's constraints. Consequently, the Down syndrome market has been significantly affected by these disruptions, with potential consequences for the industry.

In conclusion, while the swift response of diagnostic manufacturers to the COVID-19 crisis showcased innovation and adaptability, the broader healthcare industry faced disruptions and challenges in its supply chain and production processes due to the pandemic's ongoing impact. The Down syndrome market, like many other healthcare sectors, has not been immune to these challenges, and the path to recovery remains a critical consideration.

𝐏𝐫𝐞-𝐛𝐨𝐨𝐤 𝐭𝐡𝐢𝐬 𝐑𝐞𝐩𝐨𝐫𝐭 𝐍𝐨𝐰: https://www.alliedmarketresearch.com/down-syndrome-market/purchase-options

Market Overview:

The global Down Syndrome market encompasses a broad spectrum of products and services aimed at improving the well-being and potential of individuals with this condition. These range from medical therapies to educational and social programs.

Key Market Trends:

Early Intervention Programs: Early diagnosis and intervention programs have gained prominence, offering essential support for children with Down syndrome to achieve their full potential.

Genetic Testing and Counseling: Advances in genetic testing have enabled better prenatal detection, giving expectant parents more information and support in making informed decisions.

Inclusive Education: Inclusive education practices and tailored learning programs have expanded opportunities for children and adults with Down syndrome.

Market Drivers:

Advancements in Medical Therapies: Progress in medical therapies, including speech and physical therapy, has improved the quality of life for those with Down syndrome.

Growing Awareness and Advocacy: Increased awareness and advocacy efforts have led to improved support systems and social integration for individuals with Down syndrome.

Outlook:

The global Down Syndrome market is expected to continue evolving with an emphasis on early diagnosis and intervention, enhanced medical therapies, and increased opportunities for education and social integration. As society becomes more inclusive and aware, the prospects for individuals with Down syndrome

have brightened. While challenges remain, the concerted efforts of healthcare professionals, researchers, advocates, and affected families are reshaping the landscape for individuals with Down syndrome.

𝐈𝐧𝐭𝐞𝐫𝐞𝐬𝐭𝐞𝐝 𝐭𝐨 𝐏𝐫𝐨𝐜𝐮𝐫𝐞 𝐭𝐡𝐞 𝐑𝐞𝐬𝐞𝐚𝐫𝐜𝐡 𝐑𝐞𝐩𝐨𝐫𝐭? 𝐈𝐧𝐪𝐮𝐢𝐫𝐞 𝐁𝐞𝐟𝐨𝐫𝐞 𝐁𝐮𝐲𝐢𝐧𝐠: https://www.alliedmarketresearch.com/purchase-enquiry/11914  

Conclusion:

The global Down Syndrome market, driven by a commitment to improving the lives of those affected by the condition, is undergoing a transformation. With early interventions, advanced therapies, and inclusive education, individuals with Down syndrome are finding greater opportunities and support than ever before. As research continues and awareness grows, the outlook for the Down Syndrome market is marked by optimism, highlighting the ongoing commitment to enhancing the quality of life and potential of those with Down syndrome.

About Us

Allied Market Research (AMR) is a full-service market research and business-consulting wing of Allied Analytics LLP based in Portland, Oregon. Allied Market Research provides global enterprises as well as medium and small businesses with unmatched quality of "Market Research Reports" and "Business Intelligence Solutions." AMR has a targeted view to provide business insights and consulting to assist its clients to make strategic business decisions and achieve sustainable growth in their respective market domain.

Pawan Kumar, the CEO of Allied Market Research, is leading the organization toward providing high-quality data and insights. We are in professional corporate relations with various companies and this helps us in digging out market data that helps us generate accurate research data tables and confirms utmost accuracy in our market forecasting. Each and every data presented in the reports published by us is extracted through primary interviews with top officials from leading companies of domain concerned. Our secondary data procurement methodology includes deep online and offline research and discussion with knowledgeable professionals and analysts in the industry.

[globaljobalert-blog]

Infant/Toddler Development Specialist & Content Writer - Remote(USA)

Company: Lovevery About Lovevery Lovevery is a fast-growing digitally native brand co-founded by successful serial entrepreneurs and based in Boise, Idaho. Our customers are parents, and our mission is to help them feel confident they are giving their children meaningful development experiences in the critical early years of life. Taking a science-based approach, Lovevery products have won awards from Red Dot, Parents’ Choice, and NAPPA. TIME Magazine named The Play Kits subscription offering as one of the Best Inventions of 2018. The Role Lovevery seeks a knowledgeable and passionate Infant/Toddler Development Specialist & Content Writer to join our mobile app team. In this role, you will answer questions and provide expert advice and support to parents and caregivers of children ages 0 to 3. You’ll also work with experts in different fields to provide thoughtful and nuanced responses to a wide range of early child development and parenting questions. To be considered for this position, you must have significant clinical experience working closely with infants and/or toddlers (as opposed to K-12 education or a daycare setting). Excellent writing skills are essential to produce high-quality content under tight deadlines. Responsibilities: - Serve as operations lead for Ask & Learn feature of the app, working closely with mobile development team to ensure functionality - Coordinate and manage question and answer content (write and/or assign, review, and publish) for Lovevery’s mobile app - Collaborate with experts in different fields, such as Sleep, Feeding, Occupational Therapy, Physical Therapy, Speech and Language, and more - Write in a conversational style with empathy, warmth, and authority - Select questions and answers for publication to a broader audience - Work with editors to format and publish content pieces that align with the Lovevery philosophy and voice - Work with other teams to maximize the value and reach of content informed by the Lovevery community About you: - Master's degree in Early Childhood Development or a related field (minimum requirement) - Minimum of 5 years experience working in early child development, with a focus on ages 0 to 3 - Strong knowledge of a range of early child development topics - Excellent written and verbal communication skills - Exceptional organizational skills, attention to detail, and the ability to manage multiple responsibilities effectively against timelines - Ability to work with technology and software, including Google Suite and other programs - Ability to work collaboratively with teams across different departments If you are passionate about early child development and have a desire to help families support their children's growth and development, we encourage you to apply for this position. The Benefits/Perks You’ll Enjoy - Competitive salary, benefits and stock option package - 3 weeks PTO in year 1 +14 paid holidays - Generous parental leave - Any equipment you need to get the job done - Free/discounted Lovevery products Salary Range Information Based on market data and other factors, the salary range for this position is $90,000-$120,000. However, a salary higher or lower than this range may be appropriate for a candidate whose qualifications differ meaningfully from those listed in the job description. Lovevery is proud to be an equal opportunity employer that values diversity in all forms. All employment decisions at Lovevery are based on business needs, job requirements, and individual qualifications, without regard to race, religion, national origin, sexual orientation, gender identity, HIV status, marital status, or any other status protected by the laws or regulations in the locations where we operate. APPLY ON THE COMPANY WEBSITE To get free remote job alerts, please join our telegram channel “Global Job Alerts” or follow us on Twitter for latest job updates. Disclaimer:  - This job opening is available on the respective company website as of 8thJuly 2023. The job openings may get expired by the time you check the post. - Candidates are requested to study and verify all the job details before applying and contact the respective company representative in case they have any queries. - The owner of this site has provided all the available information regarding the location of the job i.e. work from anywhere, work from home, fully remote, remote, etc. However, if you would like to have any clarification regarding the location of the job or have any further queries or doubts; please contact the respective company representative. Viewers are advised to do full requisite enquiries regarding job location before applying for each job.   - Authentic companies never ask for payments for any job-related processes. Please carry out financial transactions (if any) at your own risk. - All the information and logos are taken from the respective company website. Read the full article

[warriorsbutnotreally]

OC Showcase - Buzzshine

a silver tabby tolly with ragged black stripes, a short, stumpy black tail, a white underside, white hind paws, a white nose, white chin, thick fur around their neck, and copper eyes

/

Buzzshine here is nonbinary [they/them] who is a large admirer of flowers and helping others. They dedicate most of their time to helping around camp but they have been known to go out hunting.

They have a huge dislike of violence and will only fight if they need to, but even then the idea is enough to set off their anxiety

Patient, kind, yet nervous and struggles when placed in any sort of spotlight - they are more comfortable being a pleasant face in the background than to be any sort of hero or notable figure.

They are also very drawn to the idea of one day having their own family - a loving mate and maybe even kits to care for. When I've used them they had their kits call them parry cause I thought it was adorable.

A smaller thing to note is their stutter, which they've struggled with from the time they were a kit. They work hard with their own speech therapy and goes out of their way to help others who struggle speaking like they do.

/

in canon Clans they'd be in RiverClan, as their decorative nature would be better used there. They would be a dry-paw, not liking the water that much.

/

they're a nonbinary bisexual tolly with no preference when it comes to the gender of their partner.

Their parents are Dewbreeze [mother] and Featherheart [father] - Featherheart being from another Clan and moving over to be with Dewbreeze and their newborn kit.

they're one of the ones with a TH link

[bughead-in-the-comics]

Bughead Trivia: Some of Jughead’s Hobbies were Influenced by Betty.

During a regular hangout at the chock’lit shoppe in Thought For Food (Jughead’s Double Digest #167, 2011), Betty complained that Jughead only talks about food so she decided that what he needs is a new hobby to help him expand his interests. After leaving Pop’s, Jughead immediately visited the Riverdale hobby shop to buy a kit for model building. Of course, the scale model he built was later revealed to still be food-related (a sort of fast food town with a pizzeria and a burger joint, among other things), but it is sweet that he took Betty’s suggestion seriously. She is one of the few people in Riverdale who can actually influence the very individualistic Jughead in some way and it is very evident in the number of hobbies he has taken up over the years.

While reading a book in The Unfolding Crisis (Archie’s Pal Jughead #124, 2000), Betty suddenly asked Jughead about his opinion on origami. Jughead was unfamiliar with it, so Betty tried to explain that origami is the art of paper folding and showed him the page with a how-to guide. Jughead tried following the instructions out of curiosity, but he ended up discovering that he has a natural talent for it when he successfully folded a “pretty paper ballerina” on his first try. He became so obsessed with origami that he started folding every piece of paper he sees: Coach Clayton and Coach Kleat’s game plan, Dilton’s Blue & Gold layout, Professor Flutesnoot’s test forms, Ms. Beazley’s menus, Principal Weatherbee’s speech notes, Mr. Svenson’s paper towels, and even Reggie’s candy bar wrapper.

In Summer Fun.. and Some 'R Not (Jughead #316 1981), Jughead took Betty’s suggestions even seriously when he put his trademark laziness aside to try a bunch of summer sports. He tried everything from windsurfing and beach volleyball to diving and surf boarding. Although he proved to be quite inadequate when it comes to all those sports and he eventually resorted to what he does best (eating, of course!), Jughead still showed in this particular story how much he valued Betty’s opinion by trying out all of her ideas without any hesitations.

Another Jughead hobby that was influenced by Betty is cake decorating, which was featured in Cake Mistake (Archie’s Pal Jughead #135, 2001). In the story, Jughead became interested in the art of cake decorating after Betty told him that she taught herself how to do it by simply watching an instructional video by Marta Stewmeat. Jughead, who decided he wanted to learn how to “adorn a cake so festively” like Betty, borrowed the said video, bought a multi-nozzle pneumatic decorator, and went on to ice every random thing he lays his eyes on (much to the Riverdale townsfolk’s dismay, of course). 

Betty's influence over Jughead also made him change his mind about certain activities that he would otherwise not touch with a ten-foot pole. In The Quiet Man (PEP Comics #266, 1972), Jughead was very vocal about his dislike of miming. He even went as far as making fun of the people who perform it. A furious Betty, who flat-out accused him of having no culture, insisted that miming is an ancient art form that is very difficult to pull off. Years later, in the story Mime Your Own Business (Jughead #39, 1992), Jughead went full-on Marcel Marceau by performing a mime act at the park: he entertained passers-by while sporting the stereotypical mime outfit consisting of white facial makeup, black suspenders, and a silk opera hat. To say that Betty approved of this change is an understatement. The girl was charmed.

Volunteering is not exactly considered as a hobby, but Jughead has developed a habit of offering his services to help the needy because of Betty. Thanks to her, he has gotten involved in a string of charitable acts that include donating books for a charity drive, signing up Hot Dog as a therapy dog to comfort hospital patients and nursing home residents, painting a mural for senior prom, working at the chock’lit shoppe for a day to give Pop Tate a much-deserved vacation, coaching a pee-wee baseball team, building a sand castle inside a mall, preparing dinner at the community center, running a marathon to help raise funds for hospital equipment, donating toys to the orphanage, doing a bunch of chores to help celebrate Svenson Appreciation Day, raising a Christmas fund for the senior citizens of Riverdale, taking photographs for the retirement community’s prom-themed dance, serving food at the homeless shelter, and a bunch of other things. He even donated his prize money to The Goodwill Girls, the philanthropic group founded by Betty. ♥

[squirrelcrow-po3]

okay i almost forgot i changed snowkit a lot

so what never made sense to me is how snowkit could speak when he was born deaf. yes i know this is a kids book and some people born deaf can speak but like. these are cats with no technology obvious or goddamn speech therapy so he really SHOULDNT be able to speak bc babies learn to speak through imitating sounds around them

and besides. i changed him to be the kit of goldenflower and tigerclaw (bramble and tawny’s littermate) and he looks different than in canon. he’s mostly white with golden spotted tabby patches

so i believe ill make it so he gets an infection when he’s fairly young, which leaves him totally deaf. during the time he’s born, there is a sickness that infects ashkit that snowkit could have gotten and could have affected his hearing

also he lives in this au! but unfortunately speckledawn (speckletail) dies fighting off the hawk to save her grandkit. he is later named snowspeckle to honor her

he is apprenticed to brackenshade (brackenfur). which is nice to speckledawn was bracken’s foster mother. while snowkit has some limited speech, i do imagine him forming a sort of body language to communicate. which he develops with brackenshade, who probably is like an interpreter for him. the clan probably learns the basics of their sign language, but bracken knows it in its entirety. and snowspeckle can do some limited “lip” reading as well, but it isn’t entirely reliable. the two are incredibly close throughout their lives

[speechgears-india]

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