A partnership that’s finding answers in Lyme and other tick-borne diseases
By Bay Area Lyme Foundation Many different groups comprise the Lyme disease community including patients,…
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The physical and financial devastation of unrecognized Lyme disease
Caroline Ciocca delivered the following public comment to the federal Tick-Borne Disease Working Group on…
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What you need to know about the new Lyme ICD-11 diagnostic codes
By Kris Newby, Invisible International The World Health Organization (WHO) has added 15 new medical…
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Things not to say to people with Lyme and other invisible illnesses
By Vicki Novinsky, aka “Miss Diagnoses” How many times have you been asked whether you…
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Tulane researcher asks, “Could chronic Lyme contribute to Alzheimer’s dementia?”
By Kris Newby, Invisible International In 2019, the late-great-science-writer Sharon Begley wrote an insightful article,…
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“Pain scale” often inflicts extra pain on suffering patients
By Meg Huber For six and a half years of my life, I was in…
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Treating Bartonella cleared most of my son’s symptoms of autism
By Debbie Kimberg For years, I had no idea that I was infected with Lyme…
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What connection between Lyme disease and teen suicide?
By Dr. Rosalie Greenberg As I was looking at a recent edition of the New…
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Screenwriter turns a couple’s courageous Lyme fight into a film script
By Steve Doherty I was bitten on the neck by a tick in 1996, while…
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Patient story: Lyme disease deserves more than “mediocre attention”
By Casey Fillian Thirty-seven years ago, I went to summer camp in a heavily wooded…
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