
Spasticity offers its own set of challenges for someone with MS.
However, the best—and simplest—message about spasticity and MS is that there are ways of controlling it.
Because it needs individual management, you should seek advice and assessment early. You can call on your GP, neurologist and/or hospital-based services.
We can also help. Regional MS Societies have trained and experienced Field Workers who provide a wide variety of services and practical support to people with MS, their carers and families, as well as advice on all matters concerning MS.