The MS Project

When my mom was diagnosed with MS the only two public figures who has come out about the disease at that time were Richard Pryor and Annette Funicello. My mom identified more closely with Annette on […]

Thank you so much for your interest in being a part of Orange is the new pink – raising awareness for Multiple Sclerosis.

In 2011 & 2012 we put out a compilation of stories by people with MS about their journey […]

Life is like a game of cards. The hand that is dealt you represents determinism; the way you play it is free will.
Jawaharal Nehru

Read the full original post here.

New father Jack Osbourne has been hit with devastating news just as he’s easing into parenthood.

The 26-year-old son of rock legend Ozzy Osbourne, who welcomed daughter […]

The MS Project   The MS Project is a collection of things created to raise awareness for Multiple Sclerosis . Consisting of a book, a website, apparel, and an iPhone app these elements work together to bring more attention to the disease, teach people, and create a strong community.   The book – Volume 1 was released in March, 2011 [...]

Another great blog I came across. Read here.   WHY BULLY A PERSON WITH A DISABILITY   Or why bully anyone at all. I’ve never understood why some people belittle or bully other people. But when they do it to a person with a disability to me it’s beyond being mean it’s cruel.There was a recent article “Children With [...]

This was a fun blog I came across. Please check it out here.

I came across this amazing post. Please read full post here. Although I am a relatively smart person, I can admit to having done some pretty dumb things in my life. A lot of the dumbest things came after finding out I had MS. I thought if I listed the top five, it might save someone from repeating [...]

World MS Day  is coming soon on Wednesday May 30th, 2012. If you’re not familiar please go check the site out and see how you can be one of the 1000 faces.

I came across this amazing site called Kiss Goodbye to MS. It’s an initiative based out of Australia that works with people to raise money to go towards MS research and services for people with MS.

They have some amazing things going on so I encourage you to check them out.

I Really Need to Pee! read original post here. Let’s talk bladders. It’s a big topic on my mind right now because in the last few weeks I’ve been feeling the effects of bladder dysfunction — an MS symptom that’s plagued me since my early 30s. I’ll admit that this isn’t something I love to discuss, but it’s an [...]

A great new blog I found in my search for MS related blogs. Relative MS . Catharsis Posted on April 28, 2012 by John It was interesting that I got some comments back on the post about dignity. For me it was cathartic to write. Since I’m an “old softie,” I found myself tearing up while writing it. We are all [...]

A great blog I came across -  PasstheMSplease Gibberish I saw this on Facebook the other day: “Every time I see a math word problem it looks like this: If I have 10 ice cubes and you have 11 apples, how many pancakes will fit on the roof? Answer: Purple, because aliens don’t wear hats.” Unfortunately, this [...]

Read full blog post here. Good news and bad news So the good news is that my medicine finally came today! It’s a shot for five days of a hormone that will make my body produce more of it’s own natural steroid. In turn, hopefully making me feel like a new woman! Fingers are crossed. Another good thing [...]

by Lisa Emrich What Does MS Equal To You? MS = a twisted roller coaster, spiraling and without brakes . I can’t recall the last “real” roller coaster I rode.  Honestly, I’m trying to rack my brain.  Was it during a visit to Disney World in 1985?  Or could it have been in a car driven by a speed [...]

Subscribe in a reader by Pamela Bascio I came across this blog post and although it is almost a year old I just felt it was right from the heart and you would find it meaningful…….. After ten years – not all happy, my husband and I are going to divorce. It’s ok. We still get [...]

A great blog you can read here. To show that living with Multiple Sclerosis can be simple when we find our way of living with it.I love my family,and know that without their PUSH I could not do any of what I post on here.I do have a good support team,and that matters.So I do hope that [...]