• Skip to main content
  • Skip to header right navigation
  • Skip to site footer
  • Who we are
    • Our Vision, Mission, and Values
    • Meet the Trustees
    • Meet the Staff
    • Regional Parent Supporters
    • Our Professional Board
    • Policies and Documents
    • Annual Reports
  • How We Help
    • Carer Support Service
    • Education Support Service
  • Get Involved
    • Family Membership
    • Professional Membership
    • Donate
    • Regular Giving
    • Fundraising & Events
    • Volunteering
      • Become an SMS Awareness Ambassador
      • Become a Regional Parent Supporter
      • Become a Project Volunteer
      • Become a Community Supporter
    • Corporate Support
    • Trusts & Foundations
  • News & Events
Donate
Contact Us
SMS Foundation UK logo

SMS Foundation UK

Supporting SMS families for a positive future

  • What is SMS?
    • New Diagnosis
  • Support & Advice
    • Support for Parents & Carers
    • Support for Professionals
  • Information & Resources
  • SMS Stories
  • Home
  • Contact Us
  • Who we are
    • Our Vision, Mission, and Values
    • Meet the Trustees
    • Meet the Staff
    • Regional Parent Supporters
    • Our Professional Board
    • Policies and Documents
    • Annual Reports
  • How We Help
  • News & Events
  • New Diagnosis
  • SMS Explained
  • Support & Advice
    • Support for Parents & Carers
    • Support for Professionals
  • Information & Resources
  • SMS Stories
  • How You Can Support Us
    • Family Membership
    • Professional Membership
    • Donate
    • Become a Regular Donor
    • Fundraising & Events
    • Volunteering
      • Become a Regional Parent Supporter
      • Become a Project Volunteer
      • Become a Community Supporter
      • Become an SMS Awareness Ambassador
    • Corporate Support
    • Trusts & Foundations
  • Family Membership

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).

Newly Diagnosed?

Rareminds Counselling Service

Living with Smith-Magenis syndrome can bring many unique challenges, and looking after your own wellbeing is just as important as caring for your child or loved one. That’s why the SMS Foundation UK has partnered with Rareminds, a specialist counselling organisation supporting families living with rare conditions.

rareminds logo

Rareminds are highly experienced in offering emotional support to parents, carers, and family members. They understand the particular pressures of caring for someone with complex needs and provide a safe, understanding space to talk.

Why we’ve partnered with Rareminds

We know that emotional wellbeing is often overlooked when families are busy navigating medical appointments, education, and daily life. By working with Rareminds, we can ensure that families living with Smith-Magenis syndrome have access to professional support tailored to their needs.

Confidential and Professional Support

All counselling is completely confidential. Sessions are held directly between you and the Rareminds counsellor. The SMS Foundation is not given any information about referrals or what is discussed — your privacy is fully respected at all times.

Costs Covered by the SMS Foundation

There is no cost to families for accessing this counselling service. The SMS Foundation covers the cost of sessions so that financial worries do not stand in the way of getting support.

This counselling service has limited spaces. If we reach capacity, new referrals will be placed on a waiting list until a place becomes available. At present, we do have capacity to accept referrals.

How it Works

  • The SMS Foundation makes the initial referral via email to Rareminds on your behalf.
  • Once introduced, Rareminds will take care of all communication and arrange your counselling sessions.
  • The service offers both individual counselling (for a parent or carer) and couples/family sessions if you would like to attend together.

Interested in Counselling?

If you think counselling could help you, please fill in our referral form. The Foundation will pass your details directly to Rareminds, who will then contact you to arrange next steps. Please note: this form opens in a new window.

Rareminds counselling referral form
SMS Foundation UK logo

Never feel isolated or alone. Call our helpline: 0300 101 0034

Please note: This is an answer phone service that will alert us as soon as a message is left. A member of the team will call you back as soon as possible – we aim to respond to messages within 48 hours.

  • Facebook
  • Twitter
  • LinkedIn
  • Instagram
  • YouTube
  • Mail

Become a Member of The SMS Foundation UK

Connect with SMS families in your region and be the first to receive updates on any social meetings, conferences, and fundraising events going on!

Family & Carer Membership
Professional Membership

Registered UK Charity (CIO) 1186647

Scottish Charity (SCIO) SC050921

Registered with the Fundraising Regulator

Copyright © 2021 Smith-Magenis Syndrome (SMS) Foundation UK CIO · Registered Charity Address: 61 High Street, Pewsey, Wiltshire SN9 5AF  
Privacy Policy · SMS Disclaimer · Terms and Conditions ·  Media and Logo Usage Guidelines ·  Social Media Usage and Policy · Policies and Documents