News break! Well, actually a cancellation - we won't be able to keep The Link II going any longer. Even with 600+ members, we will have to put it on hold. We do have a solution though - LISOMS Network - simply click on the link, and you'll be taken right there. We think it will be more engaging, or at least easier.
If you are looking for our forum, please note that our old social media network - The Link II - (shown below) will be closing it's doors shortly. If you are a member there, please consider joining here instead. And if you haven't yet become a member of The Link II, then now's the perfect time to join LISOMS Network!
(NOTE: Above image link will open in a new window).
This network is more of a social media type set up, one that we are all a little more familiar with. It will be easier to engage with us, as well as with one another. So come on over and check it out and we'll be there more often, too!
Adding a forum, though doable, was something I felt unsure about, until now. I surprised myself when it actually worked. The Link II is a message board with lots of bells and whistles, and a chat room to boot. You asked for one, so please jump right in and enjoy it.
You'll be able to add photos, videos, links. You can chat with other members.
There will soon be a caregivers corner, if you care for someone with MS and would like to connect with others who also have a loved one with multiple sclerosis. Whether you are a parent of a child with MS, a wife or husband of a spouse, a child caring for a parent, or a sibling caring for a brother or sister, you are welcome.
Share your stories, get advice, or just connect with one another. We all need support and who better than someone who understands what we're going through.
So, come join us now at the LISOMS Network! Help us make it one of the best groups for MSers, their families, and their friends. Join us now and then invite your family members, and friends.
After you join, be sure to share, tweet, or otherwise, get the word out that we're here and would love to have all who have MS or are supporters of those who have multiple sclerosis. Without you, there would be no Life in Spite of MS, so we hope you will enjoy this new addition.