The MS society launched this campaign on behalf of thousands of MS patients who are unable to get Sativex due to their location in the country. This campaign calls on people suffering from muscle spasms, regardless of where they find themselves in the UK. It also calls on every other person with friends and family members that are suffering from muscle spasms. The MS Society is begging for all to take action by contacting the local health service and also putting pressure on policymakers to enact a change in the health system.
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