Research Project for Lyme Patients that have done the 23 and Me Test

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From NutriGenetic Research Institute:

We need as many participants as possible for this study to be presented at the ILADS Summit in Europe! Please share this information and please take a few minutes to fill out and e-mail the forms and your raw data.

We do need at least 500 Lyme patients data for the study to be conclusive. So far we have 15, so please send us your results!

Lyme Disease Research needs you!

If you have your 23 and me results… we NEED you! This is 100% free and will take a few minutes of your time. ANd you will get a free genetics report about how you detox!

The NutriGenetic Research Institute is conducting a study investigating the possible correlation of genetic variants with those dealing with chronic Lyme disease. The findings will be presented at the ILADS (International Lyme and Associated Diseases Society) Conference in Helsinki, Finland this June.

Participating is easy – if you have chronic Lyme and have done the 23andMe test, simply complete a short survey, read and sign the consent form and email back both of those forms and your raw 23andMe data to research@tolhealth.com.

Or visit https://vimeo.com/156214813 to watch an informative video that details the research project in greater detail.

To find the survey and consent form, click here –https://www.facebook.com/groups/1061595410570584/files/

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Other Related Links

Where to order your 23andMe tests?

MTHFR and What Does it Mean?

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13 thoughts on “Research Project for Lyme Patients that have done the 23 and Me Test”

  1. I am interested in the study – I have congenital Lyme only diagnosed 8 years ago. I do NOT do Facebook, so I need someone to email me with LYME STUDY in the subject.

    1. The study is over now.. but if you are interested in any future ones with this group you can contact them directly if you are not on Facebook.

  2. I am interested in the study – I have congenital Lyme only diagnosed 8 years ago. I do NOT do Facebook, so someone will have to email me.

  3. Are they still wanting results for this study? I saw in the video that they were only taking them through the 10th of March.

    1. Yes, still awaiting news. You can follow them in their facebook page listed above too to keep an eye if they want more help in the future.

  4. I’m more than willing to share my data but I need something in return. I need more than the “detox” rest. I already have the MTHFR report. I need a. Ore complete report of ALL my genes from the raw data. I did the MTHFR and GeneticGenie reports. They are not inclusive. Give me more results data from my raw data and I will gladly share it.

  5. You should ask the following websites for their support –
    LymeNinja.com — Mackay Rippey
    Lyme Success stories
    MTHR.com
    Buhner Lyme

  6. If you are in remission but had it for 20 years before you treated it, does that count or they only looking for patients that have it right now… I mean I’ll still have the genes that might have contributed to it being a problem.

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