Hi everyone, my name is Kate Milliken and I’ve had RRMS since 2006. In 2009, I made a documentary about my journey called (I can't post a link here as it is my first thread, but you can Google it if you want to watch!). I threw out my story in the most emotionally honest way I could and since creating it, I’ve had over 50,000 unique visitors view the site and still get 2-3 phone calls a week from people with MS wanting to talk about it. This, along with my own experiences, has made one thing very clear: as a community, we need a better way to connect not only by our individual experiences, but how we’re feeling about them.
For over a year I’ve been working on a solution and it is here - once again, I'm unable to post the link directly
I will post again here with more information soon! In the meantime, please check out , and feel free to email me directly to learn more about my newest venture.
**Moderators note: Per MS World rules you can not post your email or reference to your personal website in the body of a text. You may post your email in your personal profile and reference it in your text as well as your personal website**
I'm deeply grateful!
Kate Milliken
For over a year I’ve been working on a solution and it is here - once again, I'm unable to post the link directly
I will post again here with more information soon! In the meantime, please check out , and feel free to email me directly to learn more about my newest venture.
**Moderators note: Per MS World rules you can not post your email or reference to your personal website in the body of a text. You may post your email in your personal profile and reference it in your text as well as your personal website**
I'm deeply grateful!
Kate Milliken
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