Important info to show your neurologist

Everyday living
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Those lovely MS doctors at Barts have just posted a couple of downloadable resources for PWMS, talking about how important it is to treat MS early and monitor whether the treatment is keeping MS at bay. They suggest that people with less proactive neurologists might want to take these resources in to show to their neurologist.

The resources are here:

http://multiple-sclerosis-research.blogspot.com/2016/07/clinicspeak-brainhealth-finally-version.html

1 Like
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That’s brilliant Sewingchick.

I’ll post the link on the new diagnosis board as well since it’s really important to them as well.

Thanks

Sue

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Great idea.

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How are you getting on sewingchick been waiting for an update x

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All going horribly, I’m afraid. The last day or two particularly, my walking is quite a lot worse - I’m struggling to walk with two sticks, finding it easier to use a walker. Too, too awful.

I’m going to post in a week or two, when I have seen if things continue to get worse. I don’t have much hope that they will get better. Maybe Cladribine might help other people but so far it is not helping me. Like I said, I will post in a completely frank way in a little while, once I have worked what is happening.

I’m sorry about what is happening and that I was so sure that Cladribine would help me.