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

Additional info: https://youtu.be/811v7RLXP9M
MEBO Karen
at UK Findacure conf 2020

Scroll down and select country
MEBO TMAU TESTING DISCONTINUED
(2012-2017)

MEBO Map Testing & Meetups


Full details : https://goo.gl/TMw8xu
want listed ? contact info@meboresearch.org

MEBO - UBIOME study 2018

'PRESS RELEASE'

NCT03582826
ClinicalTrials.gov

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
& PATM

Started May 2018 - Ongoing

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

NO LONGER RECRUITING

Participation info : LINK English

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

MEBO TMAU Videos

Petitions

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
NCT02683876

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
EURORDIS and
NORD Member Organization
See RareConnect

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MEBO survey for Dr Hazen click here
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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

MEBO Research Clinical Trials

Saturday, June 15, 2013

Gene Patents Eliminated by US Supreme Court & Public database for Hereditary Gene Mutations

As advocates for research and treatment for Rare Diseases, our MEBO international community is very happy to hear the great news of a US Supreme Court Decision. This has revolutionized research propelling it forward to truly provide patients with faster results, by eliminating gene patents and announcing the launch of a public database for hereditary gene mutations!

INTERNATIONAL INITIATIVE APPLAUDS THE SUPREME COURT DECISION ELIMINATING GENE PATENTS AND ANNOUNCES THE LAUNCH OF A PUBLIC DATABASE FOR HEREDITARY GENE MUTATIONS



The Supreme Court's landmark ruling that human genes are not patentable has set the stage for a new era of access to genetic information.
posted by Mark in Genetic Alliance

With this landmark Supreme Court decision, we have an opportunity to pull together and take back our data – as patients, we have the power to change the way our information is shared. I am dedicated to help others free the data and pledge to share my information to help improve patient care and advance the treatment of these diseases that have affected my family for generations.”
Joanna Rudnick, advocate for patients with BRCA mutation
(risk for breast and ovarian cancer) and filmmaker

We know that this will be very well received news by the international research community. Great news!


María

María de la Torre
Founder and Executive Director

A Public Charity
www.meboresearch.org
www.brasil.meboresearch.org
maria.delatorre@meboresearch.org
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