What people say about LymeNet Europe

For everything that is related to Lyme and/or Lymeland, but doesn't fit in the other forums. Speak your mind, connect, ask help, etc.
Martian
Posts: 1944
Joined: Thu 26 Jul 2007 18:29
Location: Friesland, the Netherlands

Re: What people say about LymeNet Europe

Post by Martian » Thu 5 Nov 2015 21:55

Source: https://www.mywot.com/en/scorecard/lyme ... t-87979533
drpyron 10/25/2015

I don't trust
  • Misleading claims or unethical
  • Hate, discrimination
Medical nonsense and conspiracy theories. Ignore unless you are researching ignorance.

Camp Other
Posts: 996
Joined: Wed 2 Mar 2011 4:32
Contact:

Re: What people say about LymeNet Europe

Post by Camp Other » Fri 6 Nov 2015 6:00

Martian wrote:Source: https://www.mywot.com/en/scorecard/lyme ... t-87979533
drpyron 10/25/2015

I don't trust
  • Misleading claims or unethical
  • Hate, discrimination
Medical nonsense and conspiracy theories. Ignore unless you are researching ignorance.
Dr. Pyron? Who's that? I searched Google and the top 3 doctors who came back were a family doctor, a radiologist, and an osteopath. However, there were other doctors after that - some MDs, some PhDs - so who knows?

I love how they leave a critique yet don't actually take the time to give examples of which specific claims were misleading or unethical on the site. That, and where they observed hateful or discriminatory behavior.

Hit and run, folks. If you're going to criticize, at least say something substantive.

(Conspiracy theories? Really? I wonder what they think of some other Lyme disease websites...)

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