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March20 podcast Dr Hazen
anti-TMA pill in a year or 2 ? (scroll 12 mins)

Additional info:
MEBO Karen
at UK Findacure conf 2020

Scroll down and select country

MEBO Map Testing & Meetups

Full details :
want listed ? contact

MEBO - UBIOME study 2018



MEBO Gut Microbiome Study
"Microbial Basis of Systemic Malodor and PATM Conditions (PATM)"
Funded by uBiome Research Grant

"Microbial Basis of Systemic Malodor and PATM Conditions (PATM)"

Dynamics of the Gut Microbiota in
Idiopathic Malodor Production

Started May 2018 - Ongoing

Current people sent kits : 100/100
3 kits per person


Participation info : LINK English

MEBO Private Facebook Group
to join : go to
or contact
Join/Watch the weekly
BO Sufferers Podcasts



TMAU Petition world
TMAU UK end total:262
TMAU UK ends 23/01/20
TMAU Petition USA end total 204
USA : Moveon open
TMAU (Dominican)
Metabolomic Profiling Study

Start : Aug 2016
Stage 1 : 27 Canadian volunteers to test
Latest click here (26 oct) :
17 samples returned

Note : Stage 1 is Canada only.
Return cut-off date : passed
Analysis can take 6/8 weeks
Analysis start in/before Nov
MEBO Research is a
NORD Member Organization
See RareConnect TMAU

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MEBO Metabolic Malodor Survey (international) for Dr Hazen click here
click to Read more/less

survey for ANYONE who identifies with METABOLIC MALODOR

begun : Oct20
end : no ending for now

Regular readers will know that Dr Stan Hazen et al at Cleveland Clinic are developing a TMA-blocker pill, as they proposed in a 2011 paper that TMAO is a factor in CVD. Recently Dr Hazen and colleagues contacted MEBO as they have always thought they could also help with TMAU. This survey is to give them an idea of the 'state of the community'. It is a "version 1". They may not even look (though they have access permission), but it could be useful to give them an overview of the community

MEBO had a zoom call with Dr Hazen and his team in October. Another zoom call is planned when they have time

This is a GOOGLE FORMS survey

short url for survey :

current participants : 113 (update 18dec20)

Thursday, September 18, 2008

Member of TMAU Foundation in Thames Festival 2008 Meet-up

One of the beautiful young ladies who attended our Thames Festival 2008 Meet-up dictated an audio presentation for us, which is herein transcribed. She would also like to extend the following invitation to us:
I would like to invite all of you to contact me if you require membership of the Renewal newsletters which are produced in the US and distributed locally in the UK with contribution from people with TMAU and other odour conditions. In addition, if you would like me to address any questions to Dr. Lachmann when I get around to interviewing him, please let me know so that I may advise him of these issues beforehand so that he would know what our concerns are. You may read about this interview in our Renewal newsletter afterwards.
Transcription of her audio message:

Hello, I’m here to talk about the UK Meet-up on Sunday, 14 September 2008. I live and work in London and study for a psychology degree with The Open University, and I have been diagnosed with Secondary TMAU, and in my spare time, I am involved in a support group network for people living with Trimethylaminuria.

I am also a member of the TMAU Foundation, which is coordinated in the US/New York, and we produce a newsletter called ‘Renewal’ globally. Since being a member, I have come across various other support groups for body odour conditions, one being the MSN Body Odor. One of the main coordinators, Arun Nagrath, from that site organized a Meet-up this weekend in London during the Thames Festival, which you could probably hear in the background.

I did not attend on Saturday, but Sunday, there were about 8 of us. We spoke openly about our experiences and had some good fun and good food. I met lovely people who I intend to keep in contact with, so hopefully good friendships can develop. I am honored to be part of this group and grateful to Arun for organizing.


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