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Coming to terms with MS
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carls
Community member Posts: 6 Listener
Hi all, I'm new to this community just roaming about , found by accident trying to get answers and knowledge. I am a Ms sufferer had for the last 20 years now finally after so long coming to terms with it, life doesn't seem so bad now after all.
Comments
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Hello @carls Pleased to meet you welcome.
Thank you for joining and sharing.
I am one of the team of community champions. We guide, advise and help new members who join the community.
You come to the right place for information and support, most of all friendship.
Please have a look around our website. We are friendly, feel free to join in discussions.
Please ask if we can help with anything. Some one will know a member of our community or a member of our team.
Please take care.
@thespiceman
Community Champion
SCOPE Volunteer Award Engaging Communities 2019
Mental Health advice, guidance and information to all members
Nutrition, Diet, Wellbeing, Addiction.
Recipes -
Hi @carls
Good Morning it’s great to meet you today.
I’m also one off the Community Champion’s here at Scope.
Please let me know what questions that you have currently!!!
I would be more than happy in trying to answer them for you.
If I need any further info/advice I will ask forward it onto the rest team for you
@steve51
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Hi @carls welcome to the community! How are you today?Disability Gamechanger - 2019
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Hello @carls. Welcome to the community. I'm glad you found us! How are you doing today?Community Manager
Scope -
Nice to meet you all, hello, I was given information regarding my question about backdated ESA payments did put my mind to rest. I'll be on the community page a bit more now I've found it. Carl's
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Hi @carls and welcome to the Community. It is nice to meet you. I'm glad you found some useful information which helped you and I look forward to seeing you on here. If there is anything else we can help you with then please just ask. All the best.Winner of the Scope New Volunteer Award 2019.
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Welcome to Scope's community! It's great to have you here. Just to get you started we have our Community Guidelines and How to Guide you can see all the latest posts here, jump in and get involved and don't worry we are a friendly bunch!
If you need anything, just let us know.
Scope
Specialist Information Officer and Cerebral Palsy Programme Lead'Concerned about another member's safety or wellbeing? Flag your concerns with us.'
Want to tell us about your experience in the community? Talk to our chatbot and let us know. -
Hi, sorry to read of your diagnosis. I was wrongly diagnosed with PPMS for 10 years some time ago. I read up and learned a lot about it and joined MSUK...they are a great support group.
xxx
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Hi pollyanna thank you for your comment. I dont know when you reached out to my post, was nice to see a response. Have you tried looking up the MS Society? They can be very helpful also have plenty of events going on. I dont know if MSUK is the same organisation. Check it out anyway.
Carl's x -
carls said:Hi pollyanna thank you for your comment. I dont know when you reached out to my post, was nice to see a response. Have you tried looking up the MS Society? They can be very helpful also have plenty of events going on. I dont know if MSUK is the same organisation. Check it out anyway.
Carl's x
Take care xx -
Noooo, ok I see now.thanks for that. Carl's x
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