SMS Foundation UK
Supporting SMS families for a positive future
We are a small charity that supports families living with Smith-Magenis syndrome (SMS)
Never feel isolated or alone. Call our helpline and leave a message: 0300 101 0034 (we aim to respond to messages within 48 hours).
Author: George Fox brings over 25 years of specialist education and SEND leadership experience, alongside a deep, practice-based professional understanding of SMS…. Read more This article is the …
When we think of therapy, we often imagine one-to-one sessions where a therapist works directly with the child. This can be the case, but we also need a clear understanding of the model of support …
We are all awaiting the government’s next steps on special education and are keen to understand what future changes may come. While the system may shift in the coming years, the core purpose of the …
Transitions can be difficult for children and young people with special educational needs and disabilities (SEND). The move to a new class, a new teacher, or a new school needs time, planning, and …
Transition planning isn’t just about moving school, it’s about carrying forward everything that’s helped your child thrive and making sure they won’t be left behind. Why This Matters The …
How this statement can be used: parents and carers may include this statement in applications for DWP benefits (such as PIP), EHCP processes, social care assessments, housing or adaptations requests, …
Navigating the Education, Health, and Care Plan (EHCP) process can be confusing and frustrating—especially if you’re caring for a child with Smith-Magenis Syndrome (SMS). The legal language, …
Details A guide to navigating the process and pathways in the development of an Education Health and Care Plan (EHCP) for children and young people requiring additional support. Speaker …
What Every Parent and Carer Needs to Know Don’t forget to register for your space to a SEND education webinar hosted by the SMS Foundation UK. The webinar will be taking place …
