Ally Cadence Trust for Spinal Muscular Atrophy
0800 23 43 762
0333 44 43 762
" Supporting families affected
  by SMA Type 1 "
" Supporting families affected
  by SMA Type 1 "
0800 23 43 762
0333 44 43 762
0800 23 43 762
0333 44 43 762
" Supporting families affected by SMA Type 1 "

How Your Money Helps

ACT for SMA Butterfly Logo
How Your Money Helps
We are very appreciative of all donations received, however much its for.  We always try to keep our overheads as low as possible.  We receive low cost storage facilities and free office space, and all our staff are volunteers so there are no wages to pay.  If you would like to know how your money helps this should give you an idea..
Apnea Monitor image
£ 10
Provides a newly diagnosed family with leaflets, an information pack and both telephone and email support.  We have a dedicated freephone number.
£ 20
Provides a cot wedge to be sure that your child can be propped at the correct angle, to help reduce secretion levels.
£ 75
Funds a sensory toy pack and bubble tube.  Many of these items are very visual, noisy or simply lightweight, meaning your child can still enjoy playtime.
Funds an apnea monitor which alerts parents/carers if the child stops breathing.
Funds a set of fibre optic lights. Being lightweight and colourful these always seem to be a firm favourite.
Funds a home visit to a newly diagnosed family anywhere in the UK.
Sensory Toys
Funds an Underwater GoPro for families which is typically used during Hydrotherapy Sessions.

Funds a DSLR Camera.  With both photo and video options this simple to use camera can capture the most precious, high quality, memories.
Funds a specialist car seat with pushchair for loan to families. These enable the child to sit at the correct angle, safely, in the car and whilst out and about.  Typically the car seats are suitable from birth until 18 months (dependant on weight)
Funds a Pulse Oxymeter with alarm.  Being battery operated these can be great as a backup incase of a power cut. 

We have had some sensory toys donated by a family that lost their child to SMA Type 1. We are always so greatful to receive donations like this and will ensure they are passed on for other children to enjoy and benefit from.
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