MS

“Mr.” is the only honorific pronoun used when addressing men, but when addressing women, society still insists we consider her marital status.
It is women’s history month and what better way to honor the past by naming the future? The following 15 female names reflect
Below is a video of what Christina said to 850 people that came to this MS event. The coal that she throws in her stove every
Written by Jamie Hughes I want to justify myself. I want to scream because I shouldn’t have to justify myself. Instead, I
Invisibility presents extraordinary obstacles and risks depending on who is blind to your illness.
By Drs. David Niesel and Norbert Herzog An international trial was recently published revealing the outcomes for 145 patients
Never be afraid to ever say, "I have no idea what you're going through." Try to be someone's perception of light, in an all too often misconceived dim world.
And, Kate believes, if it can work for MS (and it certainly seems to), it can also work for many other illnesses as well
How long will it be before people with MS get well? No way to know. But there is funding for the research. Because California voters said YES to Proposition 71, the Stem Cells for Research and Cures Act, we have a chance to defeat Multiple Sclerosis.
Six years later, at age thirty-three, the MS caught up to him in a fierce way. Jon's body deteriorated rapidly and he was
Wells Fargo, long viewed as one of the strongest and most conservative U.S. banks, was perhaps the most optimistic of the
Follow Elaine Gavalas: Blog Twitter Facebook YouTube Website March has been proclaimed Multiple Sclerosis Awareness Month
Despite the festive season coming around again every year and there being countless occasions throughout the year to dress up and attend great parties, it does seem like party season always tends to sneak up on you and catch you in a moment of unpreparedness.
When Randy Stein was diagnosed with multiple sclerosis, he was far from surprised. After experiencing numbness in his hands
When Dennis Anfuso's wife Linda was told by her doctors that she had muscular dystrophy and a limited number of days left
Many of us living with MS feel this exhaustion and thus feel defeated. I chose not to accept defeat, but to just. stop. exhausting. myself.