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Forum - LISOMS Network

Update: Forum No Longer Active

Closed sign - No longer active

Thank you to all who supported the LISOMS Network and our past forums. We appreciate your willingness to engage with us. We do, however, regret to inform you that the network is no longer active. We did have subscribers, so we saw that the need for a place to connect was there, however, the forum has not been very active for quite awhile now.

With the popularity of social media platforms, forums are no longer the best way to connect with visitors. We may attempt to start a FB group if that is something you would like. We do have a page there, however it is not a group. If you would like a group, please don't hesitate to let us know here

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!

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.

What can you do?

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.

And again, here's a link to our new social media page, LISOMS Network. (Link will open in a new window.)

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.

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Cir & Akrista

You are reading original content written by Akrista or Cir L'Bert of Life in Spite of MS. If you enjoyed reading this blog, please consider following us on Facebook, Twitter, Pinterest, and Instagram. See you there!

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