MS Society Medical Advisers release consensus statement on going outside while shielding
We know these announcements have been concerning for people with MS who are shielding, as they don't feel clear about the risks of going outside or increasing social contact during the pandemic. So we asked our Medical Advisers, who are some of the leading clinicians for MS in the UK, to agree a consensus statement about it.
This is a new version of their previous consensus statement on shielding from 2 June, updated to reflect the new Government advice.
MS Society Medical Advisers' consensus statement
Our MS Medical Advisers agreed:
“Where the relevant national government (in England, Wales, Scotland, or Northern Ireland) has decided that the risk from COVID-19 is low enough to recommend that those shielding can go outside and resume social contact, then we would generally agree that a person with MS can do so.
“In this scenario, the physical and mental health benefits of going outside would generally be likely to outweigh the risk of infection, for someone who has been shielding for a number of weeks already.
“However, it is important to note that everyone’s risk is different and that people may be comfortable with different levels of risk. If you are feeling unsure you can consult our previous advice on the wider risk factors for people with MS from COVID-19.
“People should be particularly cautious for at least 12 weeks after courses of alemtuzumab and cladribine, which significantly increase the risk of infection. If this applies to you, you should discuss the most appropriate social distancing with your MS team.
“When going outside, there are a few important points to remember:
- the advice still very clearly says you should stick strictly to social distancing rules if you do go outside – and when meeting others outside your household or support bubble
- you should minimise time in enclosed spaces like shops and public transport
- open spaces like parks or fields will generally be safest, rather than for example urban pavements
“We also emphasise the importance of attending appointments with healthcare professionals, or seeking help if you feel seriously unwell. The consequences of not getting regular or emergency healthcare can be very serious for people with MS.
“If you are still feeling uncertain after having considered the risks and the precautions that you can take, you can contact the MS Society Helpline to talk over your situation.”
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