• Skip to main content
  • Skip to header right navigation
  • Skip to site footer
  • Home
  • 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?

Are you considering adopting a child with Smith-Magenis syndrome?

March 9, 2022

Western Bay Adoption Service has approached us to help them find a forever home for a little girl with Smith-Magenis syndrome. They are looking for a two-parent family, or a one-parent family with a close and active support network. Details about this very special little girl can be found below or downloaded here.

Adoption Profile

I was born in 2019 and was recently diagnosed with Smith-Magenis Syndrome (SMS). I need a family who understands my needs, will celebrate my successes, advocate on my behalf and who can offer me time patience and love.

I’ve been described as a very special and rewarding child to care for. I really love swimming and kicking my legs in the bath. I love sensory toys with buttons, noises and bright colours – and cuddles.

I also enjoy being outside, going to the park, having a drive in the car and going on long walks in my pram. At home I like songs and nursery rhymes, my soft ball pit and watching Blue’s Clues.  I am learning new skills all the time. I can now crawl, stand and cruise the furniture and walk with a walking frame. My vision is impaired but I am very aware of my surroundings and can follow bright lights, colours and shadows around the room or on the TV. 

Oh and I REALLY love the colour blue.

I enjoy my specialist playgroup, going out and about with my carers and lots of playtime at home, which really encourages my sociability and my development. I can babble, screech and blow raspberries to make myself understood. I’m also learning sign language. I am likely to need specialist school provision in the future.

My foster carers say, “It is so rewarding seeing her coming on, and the determination and appetite she has for learning new skills. Her adoptive family will need to be prepared for a lot of uncertainties around her future development and to give her lots and lots of time. In return, she will make the most of their love, support and patience to develop her abilities – and, of course, give them so much love back.”

I thrive on being given time, love and attention. Equally, I love to watch other children and there is a baby in my foster placement, so I’m open to a family with or without other children. It might be nice to have a sibling!?

Due to my unique needs I am looking for a two-parent family or one parent with a close and active supportive support network. If you would like to know more about me or think you could be the family I’m looking for; please get in touch, I would love to hear from you.

Contact: Melanie Oates

www.westernbayadoption.org

0300 365 22 22

Share:

Share on Facebook Share on LinkedIn Share on E-mail
Category: News
Previous Post:OJRD logoCaregivers’ experience of sleep management in SMS: research study published on Orphanet Journal of Rare Diseases
Next Post:Education Survey for Primary Carers in the UKperson filling out a survey
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