
Helping Autistic Children with Transitions and Change
Did you know that moving from one activity to another can require up to three times more mental energy for an autistic young person? This simple fact highlights why daily transitions often feel overwhelming for many individuals on the spectrum.
Autism is a neurodivergent condition that affects how someone thinks and interacts with the world. It’s crucial to understand this is not a mental health issue, but rather a different way of experiencing life.
As a spectrum condition, autism presents uniquely in each person. Some young people need more support with certain aspects of daily life than others. Common characteristics include different social interaction styles, sensory processing needs, and a strong preference for routine.
This guide provides practical, evidence-based strategies for families. We focus on helping autistic children navigate changes more smoothly. Our approach considers individual needs, communication styles, and sensory profiles.
With the right support, parents and carers can build their child’s resilience. This helps them cope more effectively with daily transitions and unexpected changes.
Understanding Why Transitions Can Be Challenging for Autistic Children
Several key factors contribute to these challenges. Each young person’s experience is unique, but common themes emerge across the spectrum. Recognising these helps in providing tailored support.
The Need for Routine and Predictability
For many on the autism spectrum, a predictable routine provides essential security. Knowing what comes next reduces uncertainty and significantly lowers anxiety. Familiar patterns create a comfortable structure for the day.
Unexpected alterations can feel deeply unsettling. A change in schedule or an unplanned event disrupts this sense of safety. This disruption often triggers stress responses that others might find surprising.
As one expert notes,
“Routine isn’t just preference; for many autistic individuals, it’s a fundamental coping strategy for navigating a confusing world.”
Sensory Processing Differences
Sensory experiences are often intensified or diminished. A young person might be hypersensitive to certain sounds, lights, or textures. Others may seek more sensory input, appearing under-responsive.
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Transitions frequently involve a shift in sensory environment. Moving from a calm space to a bustling one can be overwhelming. This sensory overload uses up mental resources needed to cope with the change itself.
Common transitions like leaving home for school or switching lessons present multiple sensory challenges. The cumulative effect can lead to withdrawal or distress. Understanding a child’s specific sensory profile is therefore crucial.
Communication and Social Understanding
Abstract language and social cues can be hard to interpret. Instructions like “We’ll go soon” are vague and lack clear timeframes. Literal thinking means metaphors and idioms often cause confusion.
Transitions involve unspoken social rules and expectations. Knowing when to pack up, how to line up, or reading a teacher’s body language for cues isn’t always intuitive. This adds a hidden layer of complexity to every change.
Expressing their own feelings about an upcoming change can also be difficult. A child may not have the words to say they feel worried or need more time. This communication gap can increase frustration for everyone involved.
These challenges don’t exist in isolation. Sensory overload can make it harder to process verbal instructions. Anxiety about communication can heighten sensitivity to environmental changes. This interconnectedness means support must be holistic.
With compassionate understanding of these core needs, adults can begin to build effective strategies. The next sections explore practical approaches based on this foundation.
Foundational Strategies for Effective Communication
Clear communication forms the bedrock of supporting a young person through daily changes. When a child understands what is expected and what will happen next, their anxiety can decrease significantly. This section outlines core techniques to make your interactions more effective and less stressful for everyone involved.
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Using Clear, Literal Language
For many individuals on the spectrum, language is processed literally. Idioms, metaphors, and sarcasm can be confusing. Phrases like “pull your socks up” or “cat got your tongue?” may be taken at face value.
Instead, use direct and concrete statements. If you want a task completed, say exactly that. For example, “Please put your shoes on now” is clearer than “Let’s get a move on.”
Starting a sentence with the child’s name, like “Sam, it’s time for lunch,” ensures they know the instruction is for them. This simple tip cuts through background noise and grabs their attention.
Allowing Ample Processing Time
After you speak, a pause is essential. Processing verbal information often takes longer for autistic children. They need time to interpret the words, decide on a response, and then act.
Count to ten silently after giving an instruction before repeating it. This allows time for the message to sink in. Rushing can increase pressure and lead to shutdowns.
When you ask your child a question, pose it one at a time. “What would you like to drink?” is manageable. “What do you want to drink and shall we go to the park later?” is two separate requests that can overload working memory.
“Effective communication isn’t about fluency of speech; it’s about the successful exchange of information and understanding. Forcing a quick response can block that exchange entirely.”
Exploring Alternative Communication Methods
Words are not the only way to communicate. Many young people benefit from visual or physical supports. These methods provide a concrete reference that can reduce frustration.
Visual prompts are a powerful tool. A picture of a toothbrush can signal brushing time. A symbol for “car” can show the next activity is a journey. Using these alongside your words creates a multi-channel approach that reinforces meaning.
Systems like Makaton (sign-supported English) or Picture Exchange Communication Systems (PECS) offer structured alternatives. They give the child a clear way to express needs, wants, and feelings without relying solely on speech.
The care you take in setting the scene also matters. Choose a quiet place for important chats. Minimising background noise and visual clutter helps the child focus on your message. This thoughtful preparation is a key part of your support.
By observing which methods your child responds to best, you can tailor your approach. This personalised advice for autistic young people builds a bridge of understanding, making every transition that follows much smoother.
Implementing Visual Supports and Timetables
Visual supports transform the intangible concept of ‘next’ into something a child can see, touch, and understand. For many young people, processing a steady stream of verbal instructions during a busy day is challenging. Pictures and symbols offer a static, concrete reference that reduces cognitive load.
This method provides clarity and predictability. It hands control back to the individual, showing them the sequence of events in a clear way. Let’s explore how to build these essential tools.
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Creating a ‘Now and Next’ Board
This simple tool is brilliant for breaking down the immediate future. It visually shows the current activity and the one that follows. You only need two columns or pockets labelled ‘Now’ and ‘Next’.
Use picture cards, symbols, or photographs to represent tasks. For example, a photo of a toothbrush for brushing teeth, or a symbol of a car for a journey. Involve your child in choosing these images. This involvement helps them feel ownership and control.
Consistency is key. Always use the board to signal a change. When one activity finishes, physically move the ‘Now’ card away and bring the ‘Next’ card into its place. This action provides a clear, visual cue that the transition is happening.
Using Visual Schedules for Daily Routines
For a broader view of the day, a visual timetable is invaluable. It maps out the main events in sequence. You can create these for morning routines, the school day, or weekend plans.
Tailor the schedule to your child’s comprehension. Younger children may respond best to photographs. Others might prefer simple symbols or written words. Display it in a central area, like the kitchen fridge or a bedroom wall.
As each task is completed, your child can remove the picture or tick it off. This gives a satisfying sense of progress. It also makes abstract concepts like ‘later’ or ‘after lunch’ visually concrete.
“Visual schedules act as an external memory aid. They free up mental energy that would otherwise be spent worrying about ‘what comes next’, allowing that energy to be used for engaging in the activity itself.”
Preparing for Future Changes Visually
Visual systems are not just for routine things. They are crucial for preparing for new or unexpected events. A ‘surprise’ card can be used to denote an unplanned activity, reducing the shock of the unknown.
Before a new experience, like a dentist visit, create a short visual story. Use pictures to show the sequence: travel to the clinic, wait in the chair, open mouth, then leave. This pre-teaching builds a mental map.
The same principle applies across settings. A mini-schedule for the classroom or a visual checklist for a shopping trip provides consistency. This helps the young person feel secure wherever they are.
Remember, these supports should evolve. As your child grows, their needs and interests change. Update the images and complexity of the timetable accordingly. Online symbol libraries and speech therapists can offer excellent resources and tips.
By making the unseen seen, you empower them. You provide a roadmap for the day, reducing anxiety and building the confidence to navigate their world.
Managing Sensory Needs During Changes
The sensory environment surrounding a change can determine whether it proceeds smoothly or becomes overwhelming. For many young people, sensory processing differences mean everyday transitions involve navigating a minefield of potential triggers.
These sensory experiences are not just background noise. They directly impact a person’s ability to shift focus and adapt to new situations. Effective management of these needs is therefore essential.
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Identifying Personal Sensory Triggers
Every individual has a unique sensory profile. Some seek more stimulation, while others actively avoid certain sensations. Observation is your most powerful tool for understanding these differences.
Watch for patterns during difficult transitions. Does your child cover their ears in noisy corridors? Do they become distressed under bright fluorescent lights? These reactions point to specific sensitivities.
Communication also provides vital clues. Ask simple questions about what feels uncomfortable. A young person might describe certain textures as “scratchy” or noises as “too sharp.”
Common triggers include loud, sudden sounds and harsh lighting. Crowded spaces and specific clothing textures also frequently cause distress. Professional assessment by an occupational therapist can offer deeper insight.
They use standardised assessments to map sensory preferences. This creates a detailed profile highlighting areas of sensitivity and seeking behaviour.
Creating a Supportive ‘Sensory Diet’
A sensory diet is a personalised plan of activities. It helps regulate the nervous system throughout the day. Think of it as nutritional support for sensory processing.
The goal is to maintain optimal arousal levels. This makes transitions feel more manageable. Activities are scheduled before, during, or after expected changes.
Deep pressure activities often provide calming input. Weighted blankets or firm hugs can ground an anxious nervous system. Movement breaks offer another valuable way to regulate.
Swinging, jumping, or even simple stretches release energy. Fidget tools provide discreet sensory feedback during waiting times. Chewy necklaces or textured putty work well for some people.
“A well-designed sensory diet doesn’t eliminate sensory challenges. Instead, it builds the individual’s capacity to tolerate and recover from sensory experiences that cannot be avoided.”
Consistency is crucial for these strategies to work over time. Integrate them into daily routines at home and school. This builds resilience within the nervous system.
Adapting Environments to Reduce Overload
Environmental modifications create safer spaces for transitions. The first step is eliminating unnecessary sensory stimuli. This might mean dimming lights or reducing background noise.
Create designated quiet zones in busy areas. A calming corner with soft seating and low lighting offers refuge. Noise-cancelling headphones are a simple but effective tool for many.
Prepare for new environments by researching venues in advance. Look for sensory-friendly sessions at cinemas or museums. Bring familiar sensory tools as comfort objects.
Always have an exit strategy if overload occurs. Knowing there’s a place to retreat reduces anticipatory anxiety. This planning empowers both the child and their supporters.
Specific adaptations help at common transition points. Visual timetables reduce cognitive load in classrooms. Transition objects carried between activities provide continuity.
Waiting areas can be made more comfortable with simple adjustments. Reducing clutter and providing seating options makes a significant difference. These tips benefit everyone in the environment.
Collaboration across settings ensures consistency. Share successful strategies with teachers and club leaders. This creates a unified approach to meeting sensory needs.
Older young people can learn self-regulation techniques. Teach them to recognise their own signs of sensory overwhelm. Provide them with appropriate coping strategies they can implement independently.
Professional support is available through occupational therapists. They specialise in sensory integration therapy. Organisations like the National Autistic Society offer guidance on equipment and environmental assessments.
Remember, small adjustments often yield significant results. Asking the young person what would help shows respect for their experience. This collaborative way of working builds trust and effectiveness.
Reducing Anxiety and Preventing Overwhelm
Building resilience against anxiety involves understanding both preventative strategies and supportive responses to overwhelm. For many neurodivergent individuals, the world feels unpredictable and full of hidden social rules. This can create a constant background of worry that intensifies during transitions.
Difficulties with predictability, sensory sensitivities, and social understanding make young people particularly vulnerable. When they cannot make sense of what is happening around them, anxiety naturally rises. This emotional state affects both mental health and daily functioning.
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Effective support means recognising early warning signs. It also means having practical tools ready before distress escalates. This proactive approach benefits the entire family and helps build long-term coping skills.
Recognising the Signs of Rising Anxiety
Every young person shows anxiety differently. Learning their unique signals is the first step in providing timely support. Early intervention can prevent a minor worry from becoming overwhelming distress.
Common signs include increased self-stimulatory behaviours, often called stimming. This might involve more hand-flapping, rocking, or repetitive vocalisations. Withdrawal from social interaction is another key indicator.
Some children express their discomfort through verbal protests or questions. They might repeatedly ask about timelines or seek reassurance. Physical signs often accompany these behavioural changes.
Flushed cheeks, rapid breathing, or clenched fists can signal rising stress. Changes in posture or facial expression provide valuable information. Noticing these subtle cues requires careful observation over time.
“Anxiety in neurodivergent individuals often manifests through changes in behaviour or physiology rather than verbal expression. Learning to read these non-verbal signals is crucial for timely support.”
Documenting patterns helps identify specific triggers. Keep notes about what preceded anxious episodes. This advice helps create personalised prevention plans.
Developing a Toolkit of Calming Strategies
Proactive management means implementing calming strategies before anxiety escalates. Waiting for crisis points reduces effectiveness and increases distress. A personalised ‘calming toolkit’ provides ready-to-use resources.
This toolkit should contain items and strategies that help the young person self-regulate. Favourite sensory items often form the foundation. Weighted blankets, textured fabrics, or favourite scents can be comforting.
Calming visuals might include photographs of peaceful places or favourite characters. Comfort objects from home provide familiarity in unfamiliar settings. The toolkit should be portable for use across different environments.
Effective strategies vary between individuals. Deep pressure activities like firm hugs or compression garments help some people. Rhythmic movement such as swinging or rocking benefits others.
Favourite music with predictable rhythms can regulate the nervous system. Quiet spaces with reduced sensory input offer essential retreats. Predictable repetitive activities provide a sense of control.
Encourage young people to contribute their own ideas based on what works for them. This collaborative approach builds ownership and self-awareness. It teaches valuable self-regulation skills for lifelong health.
Structured downtime should be scheduled into daily routines. Predictable quiet periods prevent cumulative overwhelm. Advance preparation for known stressors reduces anticipatory anxiety.
Understanding Meltdowns vs. Tantrums
It is crucial to distinguish between meltdowns and tantrums. This distinction determines the appropriate response and support needed. Confusing the two can lead to ineffective or harmful interventions.
Meltdowns are neurological responses to overwhelming sensory or emotional experiences. They represent a loss of behavioural control due to system overload. The individual cannot ‘snap out of it’ through willpower alone.
In contrast, tantrums are goal-directed behaviours aimed at achieving a specific outcome. They typically stop when the desired result is obtained or when the strategy proves ineffective. Tantrums involve more conscious control.
“Meltdowns are not behavioural choices but rather the brain’s emergency response to being overwhelmed. Supporting someone through a meltdown requires compassion, not discipline.”
During a meltdown, the priority is safety and de-escalation. Reduce sensory input by moving to a quieter space if possible. Use calm, minimal communication without making demands.
Allow time for the nervous system to recover without pressure to ‘move on’. Afterward, focus on reconnection rather than discussion of the episode. This approach respects the person‘s experience and preserves dignity.
Teaching anxiety management skills follows a gradual progression. Start with co-regulation where the adult provides external support. Slowly move toward self-regulation as the young person develops these skills.
Collaboration between home, school, and other settings ensures consistency. Share successful strategies across all environments where the child spends time. This unified approach provides security and reinforces learning.
For example, if deep breathing helps at home, teachers can offer the same technique at school. Sensory tools should be available in multiple settings. Consistent responses to anxiety build trust and effectiveness.
This comprehensive approach addresses emotional wellbeing proactively. It recognises that preventing overwhelm requires understanding individual needs. With the right support, young people can develop resilience against daily challenges.
Building a Foundation for Resilience: Daily Wellbeing
The fundamental elements of daily life – sleep, nutrition, movement, and rest – directly shape resilience against transition challenges. When these core needs are met consistently, young people have greater internal resources to handle change. This creates a stable platform from which they can engage with the world more confidently.
Good physical health supports better emotional regulation and cognitive function. This directly impacts mental health and the capacity to adapt. Building daily habits around these areas is therefore not just about wellbeing, but about developing essential life skills.
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Establishing Healthy Sleep Routines
Sleep disturbances are common among individuals on the spectrum. Many children struggle to fall asleep or wake frequently during the night. This can stem from anxiety, sensory sensitivities, or differences in melatonin production.
Creating a consistent bedtime ritual signals to the body that it’s time to wind down. This might include a warm bath, reading a story, or listening to calming music. The sequence should be predictable and occur at the same time each evening.
The sleep environment itself requires careful attention. Consider blackout curtains to block light and weighted blankets for deep pressure. Reducing screen exposure before bed minimises blue light that disrupts natural sleep cycles.
“Sleep is the foundation upon which all other daily coping strategies are built. Without adequate rest, even the most carefully planned transitions become significantly more challenging.”
When sleep issues persist, collaborate with healthcare professionals. A GP can rule out underlying health conditions or refer to a paediatric sleep specialist. They may discuss melatonin supplements if natural production is insufficient.
Navigating Eating Difficulties
Eating challenges often arise from sensory processing differences. Some autistic children prefer foods of specific colours, textures, or temperatures. Others may experience genuine distress when presented with unfamiliar items.
Medical factors can also influence eating patterns. Issues like constipation or acid reflux make eating uncomfortable. It’s essential to address these with a doctor, as they affect nutritional intake and overall wellbeing.
Gradual exposure offers a gentle way to expand food repertoires. Present a tiny portion of a new food alongside familiar favourites. Celebrate any interaction with the food, even if it’s just touching or smelling it initially.
Create positive mealtime environments by reducing pressure. Avoid battles over food and focus on making the experiences enjoyable. Some others benefit from having their own dedicated cutlery or plates with compartments.
For significant concerns like limited intake or pica (eating non-food items), seek professional support. Dietitians specialising in neurodiversity can provide tailored advice. They help ensure nutritional needs are met while respecting sensory preferences.
Incorporating Movement and Downtime
Regular physical activity helps regulate the sensory system and reduce anxiety. Movement provides proprioceptive input that grounds the nervous system. This makes subsequent transitions feel more manageable.
Incorporate movement in ways that align with the child‘s interests. This might be trampolining, swimming, or simply walking in nature. The goal is enjoyable engagement rather than rigorous exercise.
Downtime is equally crucial for recovery. After demanding transitions or social interactions, the nervous system needs to reset. Schedule predictable quiet periods into each day to prevent cumulative overwhelm.
Create balanced daily schedules that include both structure and flexibility. Visual timetables should show not just activities but also rest breaks. This teaches the valuable skill of pacing oneself.
Regular medical check-ups support overall care. Prepare for dentist or optician visits using social stories and visual schedules. Many practices now offer specific appointments for neurodivergent patients.
Building resilience happens through consistent practice over time. Celebrate small successes in trying new foods or managing bedtime independently. Positive reinforcement strengthens these emerging skills.
The interconnected nature of wellbeing means each area supports the others. Poor sleep affects appetite and energy for movement. Good nutrition provides fuel for daily activities and supports mental health.
When families prioritise these foundational elements, they create a virtuous cycle. The child feels better physically, which improves their emotional state. This enhanced wellbeing then increases their capacity to handle life’s inevitable changes.
Parents and carers play a vital role in modelling and supporting these habits. Sharing information and strategies with the wider support network creates consistency. This collaborative approach benefits the entire family unit.
Remember that progress may be gradual and non-linear. What works for one young person may not suit others. Be prepared to adapt approaches as children grow and their needs evolve.
Local support groups often share practical examples of what has worked for their young people. Connecting with these communities provides both practical advice and emotional support for parents navigating similar challenges.
How to Access Support and Professional Help in the UK
The journey to secure appropriate help for a neurodivergent child in the United Kingdom follows specific statutory routes. Understanding how health, education, and social care systems interconnect provides a roadmap for accessing vital support.
These services work together to create comprehensive assistance for families. Each pathway has distinct procedures and professionals who can offer specialised advice.
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Working with Your GP and Health Visitors
Your general practitioner serves as the primary gateway to healthcare support. They assess your concerns and explain available options around treatment and assistance.
Preparation enhances these appointments significantly. Create a concise list of observations about your child’s experiences and needs. Include specific examples of challenges during transitions or daily routines.
You can request reasonable adjustments to make visits more comfortable. Ask about dimming lights in the consultation room or providing a quieter waiting area. Some practices offer home visits for children who find clinical settings overwhelming.
GPs can refer to Child and Adolescent Mental Health Services when needed. They may also connect families with community paediatricians or occupational therapists. Health visitors provide valuable early years support for younger children.
“A prepared parent is an effective advocate. Bring notes, dates, and specific observations to medical appointments. This concrete information helps professionals understand your child’s needs more clearly.”
Collaborating with Your Child’s School and SENCO
Educational settings play a crucial role in supporting neurodivergent young people. Every maintained school has a Special Educational Needs Coordinator. This professional oversees provision for pupils with additional needs.
The SENCO can arrange SEN support through a graduated approach. This begins with assessing needs and planning appropriate interventions. Schools may develop an Individual Education Plan outlining specific strategies.
Effective collaboration requires regular communication. Share successful approaches used at home with teaching staff. Request meetings to discuss your child’s progress and any emerging challenges.
Many schools implement visual timetables and quiet spaces. They may provide sensory breaks or alternative communication methods. Discuss how these can be consistently applied across different classroom environments.
If a school cannot meet needs through their available resources, you can request an EHC assessment. This formal process evaluates whether statutory provision is necessary. The SENCO typically initiates this request in partnership with parents.
Understanding Education, Health and Care (EHC) Plans
These statutory documents outline special educational provision for children and young people with complex needs. They bring education, health and social care services together in a coordinated way.
Eligibility requires that special educational needs cannot be reasonably met through usual school resources. The child’s learning difficulties must significantly impact their educational progress. The plan must be necessary for accessing appropriate education.
Assessment begins with a formal request to your local authority. This can come from parents, the school, or a professional. The authority has six weeks to decide whether to proceed with a full assessment.
During assessment, various professionals contribute reports. These might include educational psychologists, speech therapists, or paediatricians. The process examines all aspects of the child’s development and needs.
If approved, the EHC plan specifies outcomes and provision across education, health, and social care. It names the educational setting and details specific support requirements. Annual reviews ensure the plan remains relevant as the child develops.
You have appeal rights if the local authority refuses an assessment or issues an inadequate plan. The First-tier Tribunal (Special Educational Needs and Disability) hears these cases. Many parents seek advice from SENDIAS services before proceeding.
“An EHC plan is not about labelling a child, but about securing the right resources to support their learning and development. It’s a practical tool for ensuring needs are properly met across all settings.”
Utilising Your Local Offer and SENDIAS Services
Every local authority must publish a Local Offer detailing SEND services in their area. This online resource lists available provision from early years through to adulthood. It includes both statutory services and community support groups.
The Local Offer helps families understand what’s available locally. It covers education, leisure activities, and health services suitable for neurodivergent young people. Checking this resource provides valuable information about local opportunities.
SENDIAS services offer free, impartial advice completely independent from local authorities. Every area has such a service providing guidance on the SEND system. They help parents understand their rights and navigate complex procedures.
These services can explain EHC processes, prepare for meetings, and support mediation. They offer templates for letters and help organise documentation. Their independence ensures advice focuses solely on the child’s best interests.
Specialist organisations provide additional resources and support. The National Autistic Society offers detailed information on EHC plans and school strategies. Local autism charities often run parent support groups and social activities.
Accessing mental health support typically involves referral to CAMHS. Waiting times vary across regions, so early referral is advisable. Seek autism-informed therapeutic approaches that respect neurodivergent thinking styles.
Navigating these systems requires organisation. Maintain records of all assessments, reports, and correspondence. Create a dedicated folder for educational and medical documentation. This preparation makes meetings more productive and ensures nothing is overlooked.
Building a comprehensive support network involves connecting with various groups. Professional support comes from healthcare and education services. Peer support connects you with others sharing similar experiences.
Community resources include leisure activities aligned with your child’s interests. These provide valuable social opportunities in supportive environments. A strong network benefits both the child and their entire family.
Remember that accessing support is an ongoing process. Needs evolve as children young people develop new skills and face different challenges. Regular review ensures provision remains appropriate over times.
These UK systems, while complex, provide structured pathways to assistance. With persistence and the right information, families can secure meaningful support for their neurodivergent child’s journey.
Conclusion
Every journey with a neurodivergent young person is unique, filled with both challenges and remarkable growth. This guide has explored key strategies: understanding transition difficulties, using clear communication, and implementing visual supports.
Managing sensory needs and reducing anxiety are crucial. Maintaining daily wellbeing and accessing professional support complete the picture. Remember, what works for one child may differ for others.
Trust your instincts as a parent or carer. You know your family best. It’s okay to ask for help when needed. Connecting with other parents through support groups can provide valuable shared experiences.
Progress may be gradual. Celebrate small successes along the way. With patience and the right advice, you can help build resilience for all the changes ahead.
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