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Suzanne Edholm: What it’s Like to Live With An Aggressive Form of MS

Suzanne Edholm: What it’s Like to Live With An Aggressive Form of MS

by Kate Milliken | Nov 23, 2015 | Meet The Users Of MCP

In all my conversations with MS’ers, I have rarely come across someone who had such a crazy time getting diagnosed as Suzanne Edholm. A rabid NY Mets fan, it took two years of severe symptoms and three neurologists to finally determine her MS. In that stretch of time,...
Q&A: Are There Any New Treatment Therapies For Progressive MS?

Q&A: Are There Any New Treatment Therapies For Progressive MS?

by Kate Milliken | Nov 10, 2015 | MCP Interviews

MyCounterpane Founder Kate Milliken sat down with Dr. Timothy Coetzee, PhD, the Chief Advocacy, Services & Research Officer for The National MS Society to answer questions submitted by people online who are living with MS. One question focused on the status...
Q&A: Do All MS Doctors Profit From The Drugs They Prescribe?

Q&A: Do All MS Doctors Profit From The Drugs They Prescribe?

by Kate Milliken | Nov 2, 2015 | MCP Interviews

One of the most important questions that emerged was about the connection between doctors and pharma.  There is a large population of people with MS who feel wary of big pharma.  The question is:  Do doctors go so far as to make a profit when they write you a...
What is the Cost and Length of a Clinical Trial for a New MS Drug?

What is the Cost and Length of a Clinical Trial for a New MS Drug?

by Kate Milliken | Oct 26, 2015 | MCP Interviews

The second question in the interview was this: What is the cost and length of a clinical trial for a new MS drug? If you’ve ever wondered why MS drugs are so expensive, watch this video to see Dr. Coetzee’s explanation. MyCounterpane Founder Kate Milliken...

How a blog, book, & stroppy teenager helped one mother thrive with MS

by Admin Account | Oct 21, 2015 | Real Stories

Without my teenager, I probably wouldn’t be where I am right now. MS crashed unexpectedly into our lives in 2011 – a destructive meteor. Neither of us were prepared and life as we knew it disappeared as the sun set and I lay on a hospital bed contemplating the future,...
Q&A: 400,000 People Are Estimated To Have MS. Is That True?

Q&A: 400,000 People Are Estimated To Have MS. Is That True?

by Diana Frustaci | Oct 16, 2015 | MCP Interviews

MyCounterpane Founder Kate Milliken sat down with Dr. Timothy Coetzee, PhD, the Chief Advocacy, Services & Research Officer for The National MS Society to answer questions submitted by people online who are living with MS. The first questions was this:  They say...

What Do You Think About The New Biogen Tecfidera Commercial?

by Kate Milliken | Oct 8, 2015 | MCP Interactive

The new Biogen Tecfidera commercial: Love it? Loathe it? In-between? MyCounterpane and MSPals have joined forces to bring you a platform to share your thoughts. Record your feelings below!  ...

What Was the Best Thing a Neurologist Ever Said To You?

by Kate Milliken | Oct 5, 2015 | MCP Interactive

What was the best thing a neurologist ever said to you and how has it affected the way you live with MS? It’s hard to find a good neurologist. But when you find one you connect with, the bond is strong. At MyCounterpane, many users describe their neurologist as part...
How Your Neurologist Impacts Your MS

How Your Neurologist Impacts Your MS

by Kate Milliken | Oct 1, 2015 | Powerful Moments, Real Stories

The Hippocratic Oath states “I will remember that I do not treat a fever chart, a cancerous growth, but a sick human being”. Does your doctor treat you like a human being? Multiple sclerosis, commonly known as MS, has symptoms that are easily quantified as well as...

The Week In (Awesome!) Multiple Sclerosis News – 9/1/2015

by Kate Milliken | Sep 1, 2015 | News

Hey, there. Thanks for stopping by to read about awesome MS news. We hope you’re having a great week. We’ve been pretty busy planning an exciting new campaign about your MS (details to come soon) but we’re thrilled with the news we’ve read these past...
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MyCounterpane provides a platform for patients and caregivers dealing with a chronic illness to tell their story based on how they feel. By doing so, each personal journey is broken into moments, and those moments can be easily searched.
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