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Newsletter
Archive:
MyLymeDataBlog Posts
Clinician Barriers to Providing Care: Why Patients Can’t Get the Care They Need
29
SEP
2022
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COVID Vaccination Side Effects – Lyme patients similar to general population
01
MAY
2021
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Why We need Patient-Partnered Research
30
APR
2021
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How much does the CDC undercount Lyme cases? It depends on where you live.
02
FEB
2021
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We Need to Embrace All Forms of Evidence to Accelerate the Pace of Research in Lyme Disease
13
NOV
2020
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Are antibiotics useful for treating chronic Lyme disease patients? MyLymeData study provides some answers.
09
OCT
2020
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COVID-19 Impact on Lyme Patients: Survey Results through September 10, 2020
15
SEP
2020
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Lyme Disease Prevalence: Does Sex Matter?
06
JAN
2020
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MyLymeData: My Data, My Trust
21
NOV
2019
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2019 MyLymeData Chart Book released
30
APR
2019
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Lyme Disease Stigma and Privacy Survey Results
21
FEB
2019
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What alternative treatments work for Lyme disease? What are their side effects?
06
JAN
2019
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Prevalence of Lyme disease is a big and growing problem — let’s look at the numbers.
03
JAN
2019
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Using MyLymeData to Build a Lyme Disease Research Engine
05
DEC
2018
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The problem of Lyme disease misdiagnosis
27
NOV
2018
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“Chronic Lyme disease” remains a contentious term
12
NOV
2018
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“Super responders” are key to personalized Lyme disease treatment
19
OCT
2018
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Why Doesn’t the CDC Count Lyme Disease Cases in the South and the West? Everybody Else Does.
03
AUG
2017
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Do antibiotics help patients with Lyme disease who are also diagnosed with MS?
17
JAN
2017
Read More »
The importance of early diagnosis of Lyme disease
27
DEC
2016
Read More »
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