Recent Lyme Developments and Parent Advocacy
Guest Dorothy Kupcha Leland, the co-author of When Your Child Has Lyme Disease, joins me in discussing the latest from LymeDisease.org and MyLymeData.com. This is something every person diagnosed with Lyme disease should take part in, ASAP! Why?
- 14,000+ patients registered their journey of Lyme disease in order to have a national registry of symptoms and issues.
- The data is condensed and analyzed in a comprehensive database in order to help scientists and researchers gain a better understanding of how it works and evolves.
- It covers patients who did have a rash, others that didn’t, how many consider themselves well, how many are still sick, etc.
- Every sufferer should consider signing up in order to gain a better understanding of where people are finding relief and stay up-to-date with the latest news.
It only takes about 30 minutes to register and begin working together. Advocacy is medicine! Feel instantly better knowing you are helping the cause and doing something helpful with your disease. This is really big stuff and you might be surprised by what the results are showing so far.
To register for MyLymeData, click HERE.
And to listen to Dorothy’s story and hear the latest from LymeDisease.org, click HERE.
As always, stay informed. Your health depends on it!
Love,
Ali
