A Quote by Teri Garr

Speaking out about multiple sclerosis to others who may be dealing with this disease is actually helpful to me as well as, I hope, to others. It builds community, helps bring awareness to MS, and strengthens the MS movement that will ultimately lead to the end of this disease.
Multiple Sclerosis is obviously close to my heart and I'm determined to make a difference in the lives of people who suffer from the disease by raising the profile of MS, as well as raising funds for advocacy and research.
I think eventually they're going to find out that MS is like 10 different things. I have a neurological disease something like MS, and it's MS, so let's take medicine for it
I think eventually they're going to find out that MS is like 10 different things. I have a neurological disease something like MS, and it's MS, so let's take medicine for it.
As I travel across the country speaking about MS, perhaps I can offer others comfort and hope.
physical disability looms pretty large in one's life. But it doesn't devour one wholly. I'm not, for instance, Ms. MS, a walking, talking embodiment of a chronic incurable degenerative disease.
Y'all really think Ms. Shakur, or Ms. Wallace, Or Ms. Mizell from out in Hollis Wouldn't exchange the love and fame Attached to their loved ones' names Just to have 'em still alive in their arms?
When I got diagnosed, the more research I did about it - MS overall, as a subject, as a disease - there's a lot of misconceptions and there's a lot of unknowns about it, and there wasn't anyone out that was close to my age or close to anything like me out there.
My mother started to suffer from multiple sclerosis, but nobody knew what MS was then. My father didn't - and later he suffered a great deal of guilt over that. It was an awful business and very fraught.
The bottom line is that this author, a practicing neurologist dealing with Alzheimer's disease on a daily basis, believes we need to expand the public awareness that modifiable lifestyle factors have a profound role to play in determining who will or won't get this disease.
People still think of AIDS as a shame-based disease, it's a sexually transmitted disease, and you're either gay or you're a prostitute or an intravenous drug user. And so a lot of people are still very bigoted about this disease. It's such a treatable disease. It's so - the end is in sight for this disease, medically.
The best compliment for me is when someone says they'll pay to watch me play, And I can say that I'll pay to watch MS Dhoni bat. MS is not the next Gilchrist. He's the first MS Dhoni
Well, Clive, it's all about the two Ms - movement and positioning.
I have late-stage Lyme disease. I was misdiagnosed for many, many years and told I had lupus, MS, Crohn's disease, even degenerative arthritis. And finally in 2010, I got the correct diagnosis, because on the last Le Tigre tour, I was having several seizures a day and at times not being able to brush my own teeth.
We are aware that the order of God requires the exercise of humility, but not of servility of slaves; but a humility that can be associated with undoubted courage and unflinching integrity; at the same time there is no room for pride, self-sufficient pride, that rests solely upon its own capabilities, and refuses to look for the support and countenance of others.--MS 7:91 [MS is the Millenial Star]
You can keep it to yourself, but you could also call a support team like the team at MS LifeLines. They are there to support the MS community and give good advice.
I have a deadly disease called Sickle Cell Anemia that I was born with that affects millions of others - primarily in the Black and Latino cultures. I feel I can inspire others with this Sickle Cell disease to be strong and believe in themselves.
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