Supporting families across the UK

A softer landing for families facing SMAThe Annabelle Rose Foundation for Spinal Muscular Atrophy

Support for families facing SMA

Spinal muscular atrophy changes family life overnight. The Annabelle Rose Foundation steps in with practical help, emotional support and funding for research, for as long as it is needed.

Annabelle Rose as a baby, with a little cream on her face

What we do

Help that reaches the parts of life SMA touches

Around 1 in 6,000 babies is born with spinal muscular atrophy. Every family's needs look different, so our support is shaped around the person, not the paperwork.

How we help in detail
01

Practical relief

Funding home and car adaptations, specialist medical equipment and toys that make everyday life easier, safer and a little more joyful.

02

Time together

Short holidays and memory-making for families facing a short prognosis, so that time together can be spent being together.

03

Beside you

Emotional support for parents, guardians and relatives, help with funeral costs and arrangements, and donations towards research.

A parent's hand holding a child's hand on the armrest of a wheelchair

Our story

Named after a little girl, run by a family who needed help too

The Annabelle Rose Foundation exists because of Annabelle Rose and the family who loved her. They know how quickly a diagnosis turns into appointments, adaptations, hospital stays and hard decisions, and how much difference one practical offer of help can make.

So we fund the things that make daily life easier, give families time away together, and stay close through the hardest moments. We also give to research, because the future should hold more answers than the present does.

Read our story

The shop

Small things that do a lot of good

Thoughtful clothing, keepsakes and awareness gifts. Every order goes straight back into our work with SMA families.

See the full shop
Families walking together on a charity fundraising walk in a park at golden hour

For families

However SMA has touched your life, you do not have to work it out alone

Whether you are newly diagnosed, years into the journey, or grieving, there is someone here who understands. Tell us what would help and we will do our best.

Ways to help

Buy something lovely, or simply give

Shop for a gift with meaning, or make a one-off donation. Both keep our grants, holidays and family support running.