Life is Good: When optimism is part of the MS treatment plan.

Life is Good: When optimism is part of the MS treatment plan.

Tatiana-Haas Castro has Multiple Sclerosis (MS). For 19 years, this shitty disease has tested, challenged, weakened and stolen from her. But the thing that makes Tatiana quite an amazing human and one of our heroes is...she never allows MS to kill her spirit. While, MS has taken so much from Tatiana, it has also inspired, awakened, strengthened and given to her.

The Rare B*tch Project

The Rare B*tch Project

The Rare Bitch Project is a fun way for us to be able to honor some truly awesome women. We make it fun so people will watch it but don't let the quirky concept fool you, we are 100% serious about how much we respect and admire these women. Each woman that we have honored here are amazingly selfless and persistent. They have each persevered... these women are indeed RARE!

Orange is the New Pink

Orange is the New Pink

Even though there are hundreds of thousands of people in the US and millions world-wide with MS, as a community, MS doesn't have that one unifying symbol for those outside of the community to recognize. Not taking anything away from the Breast Cancer Community whatsoever, but we don't see the designated MS orange as a symbol for this amazing group of people like we do with the iconic pink for breast cancer awareness. The MS community doesn't have its Susan-G.-Komen. But it does have Andrea Jackson, a woman who is doing amazing things to help support and honor the orange family! 

Dear Randi, Thank You!

Dear Randi, Thank You!

Yes, I am writing this letter and it is addressed to you but it's purpose and desired impact are much bigger. This letter is on behalf of the people who aren't getting what they need from healthcare. It is for all of the people who are uninformed or unaware with regards to their health. But more specifically, I am writing to you because we want to join forces. Together we can help individuals who have MS become more educated and aware of HSCT and fight to bring greater access to HSCT as a attainable treatment option for all. Basically Randi, we want to make you The Face of HSCT.

You Inspire 'me', Sandi D!

You Inspire 'me', Sandi D!

What if you were told as a kid that you probably wouldn't live to see your 16th birthday? But what if you made it...then you were told that living to 18 yrs old isn't likely? What if you spent the majority of your life in and out of hospitals? What if everything you did in life was 10x harder than it is for pretty much everyone else? Would you have an optimistic outlook on life? I can't say for certain that I would. 

A Heart Warming Story About Staying Cool: Multiple Sclerosis Without AC

A Heart Warming Story About Staying Cool: Multiple Sclerosis Without AC

Sometimes people say "you never know who your reals friends are"...but this could be more FALSE in the case of Yolanda Whitted and Tina Oxendine. Tina and Yolanda are so close they consider each other 'sisters'. The two have been friends since elementary school and Tina has been a huge supporter for Yolanda ever since her MS (Multiple Sclerosis) diagnosis in 2013.