Although it’s too late to participate in the Walk To End Lupus, which will take place later today in New York City, those of you who care deeply about this issue can still contribute to the cause. One of the main ways, of course, being education and outreach. The Lupus Foundation of America is a...
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Next Saturday The Lupus Foundation of America will hold its annual walk in New York City. As most of you probably know, I care about this issue on a personal level and have tried to spread awareness of this disease to people who might not otherwise be aware of its impact upon society.
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The New York/Tri-State lupus support group which we’ve promoted recently is having a meeting in less than two weeks, which you can attend! You can find out the location of the regular meeting by registering at Lupus Friends & Family Foundation’s Meetup page.
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Earlier this month, we brought to your attention the existence of a new non-profit called Lupus Friends & Family. Founded earlier this year with the purpose of empowering those with lupus and their loved ones, it intends to hold a Lupus Day sometime this coming September.
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One of the unfortunate realities of clinical research is that much of it doesn’t bear fruit in the way its intended beneficiaries would like it to, i.e. resulting in cures for the diseases from which they suffer. It often leads researchers into blind alleys and cul-de-sacs rather than transformative medical breakthroughs. Even so,...
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