According to an ms email yesterday we are all moving to a new forum this month. Anyone else got this email from Oliver from the MS Society?
Below is part of the email:
We want everyone using our forum to have the best possible experience. So we’ve been working with the forum community to find out what can be improved and make sure it’s a great space.
That’s why we’re excited to announce the launch of a new forum. We really hope you’ll like it.
Don’t worry, all your existing threads will be on the new forum. And you’ll be able to access your account, private messages, threads and comments as usual.
When will this happen?
Our new forum will go live at the end of April.
Your account will move over to the new forum.
At the end of April, we’ll send you an email with a link to change your password.
Click on the link, and it will take you to a webpage where you will need to change your password.
Once you’ve changed your password, you’ll be back in your account and you can use the forum as usual.
Please note: a few days before the launch, our current forum will no longer be available.
I can’t remember what version of the forum this will be for me now 3 or 4. How about you?
I got the email. Personally I am looking forward to some new software and I’m hopeful that we will be moving to a more modern platform. I own and run a very large online forum (not MS related) and the format of this forum I find very frustrating.
Has anyone been asked what they would like to gain in the new forum?
or indeed anything they would like to lose?
The forum is much better than the stream of consciousness provided by facebook.
when first diagnosed I found searching old posts useful. I have started very few posts, but have received some useful recommendations. I try to make useful comments when I think I have some useful input.
I wonder how people use the forum compared to using the website.
Hi Jen, there will be avatars on the new forum, and as well as receiving a notification for threads you subscribe to or comment on, you can also tag members on a post and they will receive a notification that you mentioned them.
Hi crd, there will be a new and improved search function, making it easier to find the threads that are important to you.
We gathered feedback from two surveys, asking for your thoughts on the forum and about using forums for online support more generally. Over 1,350 people with and affected by MS completed the survey and that feedback helped us shape the requirements for the new forum. We also asked members recently to help shape the new category boards, which we will offer on the new forum.
Thank you for the supportive comments, crd. We ran surveys via this forum to gauge our members opinions and understanding of what works best and what is needed to improve the current offering.
As well as this, we also ran a discovery phase which looked at both forum and website analytics to help shape this understanding.
The forum will remain as a peer to peer support space, and as such will not supplement our MS Helpline service.