Roots and Wings East Suffolk

Website

Roots and Wings East Suffolk Roots&Wings is a friendly community group in Lowestoft and Waveney supporting ND carers and parents

We still have spaces!
05/11/2026

We still have spaces!

Spoooooky fun at pumpkins and potions 🎃🧪🧙🏻‍♀️
28/10/2026

Spoooooky fun at pumpkins and potions 🎃🧪🧙🏻‍♀️

Adding to our festive fun! 🎄🎅🏽Come and spend a cosy Christmas afternoon making something beautiful together as a family....
25/10/2026

Adding to our festive fun! 🎄🎅🏽

Come and spend a cosy Christmas afternoon making something beautiful together as a family. Adults and children can work together to create one natural family wreath using seasonal foliage and decorations, while children will also have their own smaller wreaths to decorate and take home
With slow cooker hot chocolate and lots of crafts to enjoy, our festive fun session will have something for everyone to get you in that Christmassy spirit 🥰
Family tickets £20-£30 and can be booked via our EEQU

eequ . Org / rootsandwingseastsuffolk

Today!
21/10/2026

Today!

Rant and rave returns!
Joined by our SEN legal facilitators and the lovely ND peer supporters from Lowestoft and Waveney Breastfeeding Support

September 30th
1:00 – 2:30pm
Kirkley Church Hall, St Peter’s Road, NR33 0LJ

A friendly drop-in to listen, be heard and sit alongside parents who just get it
No judgement
No pressure
No formal diagnosis needed
Whether you need to offload, ask questions, or simply drink a cuppa in a room that feels safe this is for you.
We’re also supported by Roots&Wings SEN legal trained facilitators who can guide and assist with EHCP and DLA applications if needed.

If you need DLA/EHCP help then booking a slot with our SEN legal facilitators is essential, this is free support and please DM to book. Whether you’re thinking of applying, need some help advocating, struggle to fill out forms or just want to know more about the process, we are here to help ☺️

16/10/2026

🎃pumpkins and potions🧪

Calling all witches, wizards, ghosts and ghouls you are invited to our sensory spooktacular

-pumpkin painting🎃
-sensory trays🧪
-Halloween themed games👻
-dress up welcome! 👯‍♀️

As always our sessions are send friendly, neuroaffirming and pressure free

Wednesday 27th October
1-2:30
Kirkley church hall, nr33 0lj
£5 per child

Booking link in comments

With October half term, next Wednesday will be a three group day!Starting off in the morning will be our Little Saplings...
15/10/2026

With October half term, next Wednesday will be a three group day!

Starting off in the morning will be our Little Saplings under 5 sensory session, this months theme is teddy bears picnic 10-11:30 🧸

Into the afternoon will me our rant&rave parent support, come for a chat, a cuppa and take a few hours to unwind amongst peers who get it. Our SEND legal team will be present to answer any questions about the EHCP/DLA process as well any any SEND advocacy assistance you will need

Our last group of the day will be our after school wind down at 4-5:30. A after school group full of crafts, sensory trays and games!

Go to our EEQU to book your spaces ❤️

Next week!
15/10/2026

Next week!

Rant and rave returns!
Joined by our SEN legal facilitators and the lovely ND peer supporters from Lowestoft and Waveney Breastfeeding Support

September 30th
1:00 – 2:30pm
Kirkley Church Hall, St Peter’s Road, NR33 0LJ

A friendly drop-in to listen, be heard and sit alongside parents who just get it
No judgement
No pressure
No formal diagnosis needed
Whether you need to offload, ask questions, or simply drink a cuppa in a room that feels safe this is for you.
We’re also supported by Roots&Wings SEN legal trained facilitators who can guide and assist with EHCP and DLA applications if needed.

If you need DLA/EHCP help then booking a slot with our SEN legal facilitators is essential, this is free support and please DM to book. Whether you’re thinking of applying, need some help advocating, struggle to fill out forms or just want to know more about the process, we are here to help ☺️

🌻 LITTLE SAPLINGS🌻Are you a parent living with hEDS, POTS, endometriosis, chronic pain, fatigue, a disability or another...
12/10/2026

🌻 LITTLE SAPLINGS🌻

Are you a parent living with hEDS, POTS, endometriosis, chronic pain, fatigue, a disability or another long-term health condition?
Maybe sitting on the floor isn't always possible, Maybe your energy levels change from one day to the next, Maybe you're neurodivergent yourself and the thought of walking into a busy toddler group, making small talk and navigating all that noise is enough to put you off going altogether.
Perhaps your little one is autistic, has ADHD, sensory differences, developmental delays or simply thrives in a smaller, quieter environment?

At Roots & Wings, we know that finding your village isn't always easy, particularly when your family's needs don't quite fit into the traditional toddler group mould.
That's why we've created little saplings
A gentle, welcoming stay-and-play space

with messy play, sensory exploration, crafts, little adventures and, most importantly, families who just get it.
No pressure to join in.
No expectation for children to sit still, speak or socialise.
No judgement if your child needs to move, stim, explore or take a break.
No awkward explanations if you need to sit down, rest or do things a little differently.
Just connection, understanding and a whole lot of messy fun!
You don't need a diagnosis, a referral or a reason to belong here.
Because sometimes it's not just our little ones who need a safe space to find their people. Sometimes we do, too. 🥹💛

This months theme: Teddy Bears' Picnic!
Next session Wednesday 21st October
Kirkley Church Hall, NR33 0LJ
10:00–11:30am
Every 1st and 3rd Wednesday of the month
Visit our eequ to book, link in the comments 🌻
Bring your little one, their favourite teddy and yourself, exactly as you are.
Little Saplings- little people, big feelings, and a place to grow together 💛

Are we really seeing an epidemic of ADHD and autism diagnoses or are we finally recognising generations of people who we...
10/10/2026

Are we really seeing an epidemic of ADHD and autism diagnoses or are we finally recognising generations of people who were overlooked?
Following the publication of the government-commissioned review into ADHD and autism assessments, we're once again seeing headlines about rising diagnoses, misdiagnosis and concerns that neurodivergence is being over-medicalised and whilst accurate, thorough assessments are absolutely essential, I think we're missing a rather enormous part of this conversation.
For decades, we have been failing to recognise neurodivergence, particularly in women and girls
Let's look at some statistics.
In England:
• In June 2026, there were 294,792 open referrals for suspected autism, with almost 87% having been open for at least 13 weeks.
• In December 2025, NHS figures identified up to 735,157 open referrals potentially relating to ADHD assessments.
• In December 2024, at least 129,179 children aged 0–17 had an open autism referral. Even this was an underestimate because not all children's assessment services were included.
These aren't simply numbers on a spreadsheet. These are children struggling to access education. Families fighting for reasonable adjustments. Adults trying to understand why they've spent their entire lives feeling different and people being told to wait, sometimes for years, before they can access the understanding and support they deserve.
Historically, much of our understanding of autism and ADHD has been shaped by how these neurotypes present in boys and the consequences of that are enormous.
A UK population study found that the average age of autism diagnosis was 12.3 years for males and 14.9 years for females. That's a difference of approximately two and a half years.
A more recent Scottish study found a five-year difference in median diagnosis age across the neurodevelopmental conditions it examined. That’s five years of potentially unmet needs years, of being misunderstood, of being labelled anxious, difficult, dramatic, overly sensitive or simply not trying hard enough and for some women, those five years become twenty, thirty or forty.
And so many woman were diagnosed with other psychiatric conditions before neurodivergence was even thought about so how many women spent years being treated for anxiety, depression, bipolar disorder or borderline personality disorder before anyone considered autism or ADHD?
We know from research that statistically autistic women are more likely than autistic men to have certain psychiatric diagnoses recorded before their autism is identified. We know ADHD in women can be overlooked when difficulties are internalised rather than outwardly disruptive. We know that masking, people-pleasing, perfectionism and years of adapting to expectations can make neurodivergence harder to recognise and and we know that neurodivergent people can experience genuine mental health difficulties alongside their neurodivergence.
This isn't about suggesting that every mental health diagnosis is incorrect.
A 2025 Swedish study of 72,331 autistic people found:
Autistic females 54.2% had a psychiatric diagnosis before their autism diagnosis
Autistic males 40.9% had a psychiatric diagnosis before their autism diagnosis
Among autistic females in the study, before autism was identified:
Previous diagnosis
Percentage
Anxiety disorder
27.0%
Depression
21.4%
Bipolar disorder
2.2%
Borderline personality disorder
1.7%
Two or more psychiatric diagnoses
28.3%

These figures don't mean every earlier diagnosis was incorrect. But they demonstrate how often autistic women had already encountered psychiatric services before autism was recognised It's about asking how many women have been treated for the consequences of unsupported neurodivergence without anyone recognising the underlying neurodevelopmental differences.
So why are diagnoses increasing? It’s because our understanding has changed! Because diagnostic criteria have evolved. Because we now recognise that autism and ADHD can coexist. Because we have a better understanding of less stereotypical presentations, including those seen in girls and women. Because adults who were missed during childhood are finally seeking answers and because communities are sharing information that previous generations simply didn't have access to and we now have confirmed research that it’s genetic. As soon as a parent is seeing signs in their child, they’re recognising them in themselves. An increase in identified neurodivergent people does not automatically mean an increase in the number of neurodivergent people who exist and we cannot assume that every additional diagnosis represents a newly emerging condition. Research suggests a substantial population of autistic adults in England remains undiagnosed and that should be part of the conversation too.
And yes of course diagnosic accuracy matters. Nobody benefits from an incorrect diagnosis, whether that's autism, ADHD, bipolar disorder, anxiety or anything else but concerns about misdiagnosis must not become an excuse to dismiss people seeking assessments or to make already overwhelmed services harder to access. We need properly funded services, appropriately trained professionals, comprehensive assessments and support based on individual needs and another generation of children being told they're simply naughty, not another generation of girls being told they're just anxious, and not another generation of women reaching adulthood believing they have somehow failed at being human.
Perhaps the question shouldn't just be why so many people are being diagnosed now, perhaps we should also be asking why so many people weren't recognised before because neurodivergent people haven't suddenly appeared.
One of the biggest concerns I have about conversations surrounding misdiagnosis is that they focus so heavily on people being incorrectly identified as neurodivergent, whilst overlooking the very real possibility of neurodivergent children being incorrectly assessed as not neurodivergent and masking plays an enormous part in this.
The DSM-5, one of the diagnostic frameworks used to identify autism and ADHD, considers how neurodevelopmental differences present across different contexts. To receive an ADHD diagnosis, adhd signs need to be seen across 3 settings but what happens when a child has spent years learning to suppress those differences in order to survive their school day, what happens when a child makes eye contact because they've learned they're expected to, when they sit perfectly still despite feeling desperate to move?
When they copy their peers, rehearse conversations, suppress their stimming, force themselves to socialise and spend six hours desperately trying to meet expectations that don't come naturally to them but then happens when the very thing that helps a neurodivergent child navigate school is the thing that prevents professionals from recognising their neurodivergence?
Because masking can contribute to a false-negative assessment. A child may appear to cope beautifully in the classroom, only to come home completely dysregulated, exhausted, overwhelmed or unable to manage another demand, And yet, how often do families hear: "They're absolutely fine at school, they have friends, they academically able, as though any of those things automatically exclude autism or ADHD.
They don't. In fact, the DSM-5 explicitly recognises that autistic characteristics may be masked by learned strategies and NICE guidance in England specifically warns professionals that autism may be under-recognised in girls and that coping mechanisms can conceal autistic characteristics. It also advises that autism should not be ruled out simply because a child makes eye contact, smiles, shows affection or has reached typical language milestones. So why are we still treating a child who appears to cope in school as evidence that their parents must be mistaken? Why are we placing so much weight on what adults can observe, rather than what the child is actually experiencing and why are we still confusing compliance with wellbeing?
A child who is masking is not necessarily a child who is coping. They may simply be a child who has learned that expressing their needs is less acceptable than suppressing them. Of course, not every child who masks is autistic or has ADHD, and not every child who struggles at home is neurodivergent but masking should be explored during an assessment, not used as evidence against a diagnosis.
If we're going to have a national conversation about diagnostic accuracy, we need to acknowledge both sides of the equation, The people incorrectly diagnosed with a condition they don't have and the people incorrectly told they don't have a condition they do. The children who don't fit outdated stereotypes. The girls who quietly struggle. The academically successful children whose distress goes unnoticed. The adults who have spent decades compensating for difficulties nobody recognised.
Misdiagnosis doesn't just mean giving somebody the wrong label. Sometimes it means denying them the right one and those consequences can last a lifetime.
If you want to learn more I have included additional research
NHS England — Autism waiting times, June 2026
NHS England — ADHD referral statistics
2025 research — Later diagnosis of neurodivergent girls and women
2025 research — Psychiatric diagnoses preceding autism
NHS ADHD Taskforce — Underdiagnosis and increased demand

Experts say England's ADHD and autism system is under growing strain, with hundreds of thousands waiting for assessments 🧠⏳

It’s situational mutism awareness month and I’ve tried to write this a thousand times but it is something that, at times...
08/10/2026

It’s situational mutism awareness month and I’ve tried to write this a thousand times but it is something that, at times, feels very raw and very heavy.

Those of you who have come along to our groups or sessions and met my magical little poppets will know that situational mutism is something very close to my heart. For my littlest one, speaking can feel impossible in places where her body doesn’t feel safe or settled. She may have all the words in her head and desperately want to join in, but anxiety can make them feel completely out of reach. It isn’t a choice, stubbornness or a child refusing to answer. Situational mutism is an anxiety condition. it’s known clinically as selective mutism but that for me feels like it sounds as if it’s an active choice she is making.
For a long time, I didn’t know that. I thought she was shy. She would ignore peers who said good morning in the line before nursery, or sit on my lap during playgroups, and I told myself she needed time. I thought perhaps she was a Covid baby who hadn’t had enough chances to be around people.
And then came all the questions I asked myself.

Did I not take her to enough groups? Did I not socialise her enough? Was I doing the right thing when I answered for her? Should I have waited longer for her to speak? Was I helping, or making it harder?

I replayed so many moments, wondering if I had missed something or made the wrong choice. I wanted to protect her, but I also wanted to help her find her voice. I didn’t always know what the kindest or most helpful thing to do was and I still don’t have a perfect answer for every moment.
What I know now is that this wasn’t caused by me failing to take her to enough groups, or by not socialising her “properly.” She wasn’t being difficult, and she wasn’t choosing to keep her words from people. She was anxious and unable to speak in those situations. I was a parent trying to understand what my child needed with the knowledge I had at the time.
Answering for her was something I did because I could see she was struggling. Sometimes she needed me to make sure people understood what she was trying to communicate. Sometimes the most supportive thing I could do was take the pressure off. I’ve learned that I can give her space and time, accept other ways of communicating, and still help her feel heard. I don’t have to make her speak to prove that she can.

Situational mutism can be hard to understand because a child may talk freely at home, then be unable to speak with certain people or in particular places. They may still be listening, understanding and wanting to be part of what’s happening. They might communicate through gestures, pointing, writing, facial expressions (which If you’ve met my babe, you know exactly what she’s thinking my the cheeky look on her face) or other ways. A child not answering doesn’t mean they haven’t heard you, doesn’t like you or doesn’t want to join in.

At school, my little one can struggle to communicate basic needs like hunger, thirst or pain. I’ve watched her struggle just to say “good morning.” There was been times she’s been very unwell but can’t express or communicate which part of her body is causing her discomfort so is therefore dismissed. There are friends and family who love her dearly who have never heard her speak. They’re yet to hear her wicked sense of humour that makes her older sister roll about laughing or that dirty laugh that fills every corner of our home. Sometimes there’s a particular kind of grief in knowing that, not because she owes anyone her voice, but because I wish the people who love her could share those moments with her.
But she is so much more than the words she can or can’t say. Her humour is still there. Her thoughts and feelings are still there. She is still taking everything in, making connections and finding her own ways to be part of the world. We celebrate the small steps, but I don’t want her to feel that speaking is the measure of her progress or the price of being included instead we celebrate those small wins, her giving a bag of crisps to a familiar person to open, her pointing to what she would like in a cafe, her accepting praise without shutting down after.
The best support is gentle and low pressure: give her time, don’t put her on the spot, don’t make a big deal of whether she answers, and let her communicate in whatever way feels possible. Most of all, keep including her! Help the people around her understand that quiet does not mean uncaring, uninterested or unaware.

If you’re a parent asking yourself the same questions I did, I wish I could reach back and tell the earlier version of me: you weren’t supposed to know everything straight away. You were learning your child, trying to help, and doing the best you could with what you understood then. Your child didn’t need you to get every moment perfect. They needed you to keep listening, keep learning and keep showing them that they belong.

Awareness matters. Patience matters. And every child deserves communication, whether or not they can use their voice there.

Address

Lowestoft

Alerts

Be the first to know and let us send you an email when Roots and Wings East Suffolk posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Shortcuts

Share