@mehaffey
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Helen replied to the topic Transition to Secondary Progressive MS in the forum Living With MS 1 year, 5 months ago
Hi Ed
thank you for your reply to my post. Apologies for delay in getting back to you I haven’t been well and off line for a while.
I have a great neurologist but As you say I wish they would tell us about what can happen as i really didn’t put my increasing memory problems and depression down to My MS at first and honestly thought I was ‘…[Read more]
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Helen started the topic Transition to Secondary Progressive MS in the forum Living With MS 1 year, 5 months ago
I have been very fortunate that I have been pretty stable with my MS since being diagnosed 18 years ago. In the last year I have noticed that I am unable to concentrate and focus on things in work and at home and have really struggled with brain fog; Depression and fatigue in the last nine months. I have now been off work for three months. This h…[Read more]
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Helen replied to the topic Sudden brain fog in the forum Living With MS 1 year, 5 months ago
Hi Micki
I have been diagnosed 18 years and experienced brain fog badly for the first this year. So stressful, debilitating and exhausting.
I was in work and people asking me questions about a job I have done for 10 years and i couldn’t answer. It was like an out of body experience and I was looking done on myself shouting. ‘Answer’. I could…[Read more] -
Tammy and
Helen are now friends 1 year, 5 months ago -
Helen changed their profile picture 1 year, 5 months ago
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Helen posted a new activity comment 1 year, 6 months ago
Hi John and Ed. Many thanks for the lovely welcome. I know I will gain valuable information from this forum and be made to feel part of a community and I hope that I can help contribute to that. -
Helen became a registered member 1 year, 6 months ago
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Hi Helen,Welcome – loads of info, research & experiences on here.
You can also start topics – my fellow mentor Ed explains ‘Posting Items’ at the top of each Forum.
Cheers John -
Hi Helen,
Let me join John in welcoming you. Please reach out to either of us if we can help. I’m on the US side of the “pond,” so we span a lot of hours. 🙂
Ed
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Hi John and Ed. Many thanks for the lovely welcome. I know I will gain valuable information from this forum and be made to feel part of a community and I hope that I can help contribute to that.
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Good luck with the MRI, Helen. Keep us posted on how you’re doing. MS is a strange disease and you never know what it’s going to throw at us next.
Ed