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There are many ways in which Marrowforums can develop and grow. You can help by letting us know your ideas and suggestions.
In return, we can help you by answering questions about use of the site. To ask a question about Marrowforums, make a comment or suggestion, report a problem, or tell us what you like or don't like, start a new thread here in the Site Comments forum. If you prefer to communicate with us privately, send a Private Message to Neil Cuadra or to the next available Administrator. Thank you for your participation! Neil Cuadra, site owner |
? on Marrowforums
Hi Neil,
Thanks for all your work on this forum. We need to get everyone on it and of the email one - which has been quite busy lately. Question, is there a way that a new post in Marrowforums, for example in MDS; could generate a notification in my email that a new post has occurred? Thanks again, Kirby |
You aren't the first to ask about email, Kirby, so we've put together a small tutorial about the choices.
The Finding what's new at Marrowforums thread explains ways to get email when new posts are made, and other ways to learn what new threads and posts have been made. If you or others have more questions about this, just let us know by starting new threads here in the Site Comments section. |
Thanks
Thanks for working on this. I am very interested in reading information from the archives.
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MDS convention in Los Angeles?
Can you please tell us the dates and the hotel of the MDS convention to be held in Los Angeles next August. Thank You very much.
Monica Meyer Quote:
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Quote:
At this time, dates are known but the hotel is not. You can watch that news thread (or subscribe to it) for further announcements. |
thanks
Thanks to everyone here...
this site gives me hope.. :) |
FB
Hi just wondering if there was a button (not tech savy its prob called something eles?) that could be added to post this site onto facebook to continue raising awareness?
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Heather,
We've talked about creating a Marrowforums Facebook presence but haven't made it a priority yet. Unlike many other websites, we're not interested in attracting as many site visitors as possible, only people who are affected by bone marrow failure diseases. So people tend to hear about us through their medical sources, support groups, or through word of mouth rather than through social networks. |
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