You might be asking do the ME/CFS and FM communities need yet another Forum? Our answer is an emphatic yes. There are great Forums out there but none of them provide the options that we do, and none are committed like we are to utilizing the full power that modern Forum packages present. Our guess is that you’ve never experienced a fully “realized” Forum – that you’ve never seen a Forum like ours – and we’ve just gotten started. The next step for our Forums is going to blow your mind.
Containing sections that allow you to review doctors, treatments, view recovery stories, identify resources, add and view video’s, create bookmarks, browse a Prohealth store, pick your own theme (I’m running out of breath) – we can confidently say they’re the most effective and complete Forum package you’ve ever encountered.
The ME/CFS Buzz group are our first testers. We’d love it if you’d check them out, put them through their paces and give us suggestions before we open them up fully. Over the next two days I will be filling in the Forums more: adding more recovery stories, treatments to review, clinical trials, posts, etc. If all goes well, we’re going to open the Forums up to the public on Wednesday.
You can find Health Rising’s ME/CFS and FM Forums here and learn more about some of it’s features here. You can make suggestions in the Forums here.
Thanks for listening. Hope to see you on the Forums..
Great news! thanks so much for pulling this together. I look forward to checking it out.
all the best
Thanks Beth. Hope you like it 🙂
Thank you so much! I am running into brick walls with lack of care provided in the UK NHS gp surgery. Looking into ways to get some advocacy.
Im so looking forward to browsing through, yeh like you say i prrsonally feel like im always hitting a brick wall and the fact im also basically am a tech dummy which my kids tease me about lol havent really been able to find much or get much info but by the sounds if it you are going to be really helpfull, thankyou for taking the time out to help others like myself and i wish you all the best
🙂
thanks…Jakk
Jakki,
Maybe the “kids” can help out by printing information off the Internet that you’re interested in. Just a thought.
Terrie W.
I’m sorry but I cannot to understand what do you mean with ME/CFS & FM Buzz. I imagine they are acronyms but…could you please explain it to me? Thanks
ME/CFS – chronic fatigue syndrome FM – fibromyalgia
Thank you so much