Dal Dwylo CIC

04/09/2026

All welcome
Comment below if you would like to come

03/09/2026

✨ Cuppa and a chat for parents and carers of autistic children and children with additional needs ✨

Come along for an informal chat over a cuppa to share experiences, and receive advice and confidential support.

⏰ 10:00am - 12:00pm
📆 07/09/2026
📍 Conference Room, Alltwen Hospital
🗣️ Guest Speaker: Autistic UK

Open to families across Gwynedd. Priority will be given to parents and carers of children and young people who are not currently receiving support from specialist services.

02/09/2026

Pob lwc I pawb heddiw
Good luck to everyone to day

02/09/2026

📣Rydyn ni'n falch o gyhoeddi bod Dal Dwylo bellach yn gyswllt cymunedol Gogledd Cymru ar gyfer Unique.

Bydd cyfleoedd i deuluoedd yn y gymuned sy'n delio â chyflwr cromosom prin ar draws Gogledd Cymru gwrdd â chysylltu â phobl eraill, a chael eu hwyluso gan Dal Dwylo.☕️🍰
Rydyn ni'n hynod gyffrous i wneud y cam hwn ymlaen wrth gefnogi teuluoedd. Os hoffech fwy o wybodaeth, cysylltwch am sgwrs.
—-
📣We are proud to announce that Dal Dwylo is now the N Wales community contact for Unique.

There will be opportunities for families in the rare chromosome disorder community across North Wales, to meet and connect with others, facilitated by Dal Dwylo. ☕️🍰

We are very excited to be taking this step forward in supporting families. If you would like more information please get in touch for a chat.

You can learn more about Unique - Rare Chromosome Disorder Support Group at https://rarechromo.org/who-we-are/

28/08/2026

27/08/2026

💻 Must Watch: RARE REV-inar Next Wednesday 2nd September 💻

The transition from paediatric to adult healthcare services in Rett syndrome is a critical milestone for families, yet it remains a significant challenge.

Join RARE Revolution for RARE REV-inar Episode 028 as they discuss the gaps in care and how we can bridge them 💜

This educational webinar is relevant to healthcare professionals involved in the care of people with Rett syndrome and related neurodevelopmental disorders, including paediatric and adult clinicians, specialist nurses, allied health professionals as well as parents and caregivers of those living with Rett syndrome.

Register for free here:
🔗 https://bit.ly/RARE-REV-inar-Rett

27/08/2026

To the Parent/Caregiver of a Person with a Disability Experiencing Guilt-

The what if’s tend to pile high for parents/caregivers of people with disabilities.
What if- I had just read with them more?
What if- I had just paid out of pocket for that therapy they didn’t qualify for?
What if- I should be doing more so their life can be…more?
What if- I didn’t do enough?
What if- I am not doing enough?
What if- I am not enough?

What if their struggles are my fault?
When the guilt makes our shoulders heavy, too heavy, may we remember that parenting/caregiving is only so difficult for the ones who care.
May we remember that parenting is the hardest job in the world to do well.

May we remember that there are even more layers of complexity when it comes to raising/caring for people with disabilities.

Because we are bringing up people in a world that is not built for them.
It is, at times, exhausting, overwhelming, isolating and confusing.
&
May we remember that the guilt we carry is only present because our love is so great.

We want the very best for them and have advocated in so many different ways.
Some of those endeavors have been successful and others not so much.
But we tried.
We are trying.
We keep trying.
Because we care. Because we love. Because they are worth the fight.

May we remember that we are in the ring for them so often.
& and may we remember to step out of the ropes for the battles we are not intended to fight.
May we not beat ourselves up in the process.

Because we need our strength.
&
We also need to rest.
Just like they need their strength & their rest, too..

Because life is not meant to be a constant self-improvement project.
We can push when we need to.
& we are allowed to just be.

May we find the balance of both pushing for change, for progress, for more
&
May we embrace what is, who they are, who we are too.

May we let this be enough.

25/08/2026

⚠️ GŴYL HAF ANTUR WAUNFAWR – WEDI’I GOHIRIO ⚠️

Yn anffodus, oherwydd y rhybudd tywydd melyn am stormydd sydd mewn lle ddydd Iau, rydym wedi gorfod gwneud y penderfyniad anodd i ohirio Gŵyl Haf Antur Waunfawr.

Roeddem yn edrych ymlaen yn fawr at groesawu pawb i’n safle i fwynhau’r diwrnod gyda ni, ac rydym yn siomedig iawn na fydd modd cynnal y digwyddiad fel y cynlluniwyd.

Gobeithiwn y byddwch yn gallu ymuno â ni yn ein digwyddiad nesaf! Cadwch lygad allan am ragor o fanylion yn ystod yr wythnosau nesaf. Diolch yn fawr am eich dealltwriaeth a’ch cefnogaeth.

⚠️ ANTUR WAUNFAWR SUMMER FAIR – POSTPONED ⚠️

Unfortunately, due to the yellow weather warning for thunderstorms which is in force on Thursday, we have had to make the difficult decision to postpone the Antur Waunfawr Summer Fair.

We were really looking forward to welcoming everyone to our site and having you join us for what was set to be a fantastic day, and we’re very disappointed that we won’t be able to go ahead as planned.

We hope you’ll be able to join us at our next event! Keep an eye out for more news over the coming weeks. Thank you so much for your understanding and continued support.

Cor Arwyddo Lleisiau Llawen DJ Stretch Disco / SelfieStation / DIY Disco / Equipment Hire. Llwybrau Llesiant

22/08/2026

*People with Profound and Multiple Learning Disabilities in the UK Research*

A group of university researchers (from the University of Birmingham, Manchester Metropolitan University, The University of South Wales, The University of Glasgow, and Queens University Belfast) and we have partnered with Learning Disability England, PAMIS, Positive Futures, and The All Wales Forum.

We would like to invite you to take part in ‘The Lives of People with Profound and Multiple Learning Disabilities in the UK’ survey.

The survey is specifically about the lives of people with profound and multiple learning disabilities (PMLD) across the UK.

We want to know more about the lifestyle of people with PMLD, and how we can better support them going forward in the future.

This research is funded by the Baily Thomas Charity.

Please find more information and how to apply on the website - https://www.pmld-survey.ac.uk/