tag:blogger.com,1999:blog-3652036210877702504.post1218107811435903672..comments2024-03-26T08:33:06.926-04:00Comments on The MEBO Blog: Message from Karen - New CampaignUnknownnoreply@blogger.comBlogger4125tag:blogger.com,1999:blog-3652036210877702504.post-51911746209217630142013-08-19T09:25:45.997-04:002013-08-19T09:25:45.997-04:00Thank you very much for your support for this caus...Thank you very much for your support for this cause and your donation. Anyone wishing to make a donation for this research project, can click on the PayPal button found on the right sidebar of the Front Page of this blog, under MEBO For Trinzyme Project. It is tax deductible in the US because MEBO is a Public Charity in this country. We will soon be a registered Charity in the UK as well.<br />Maria de la Torrehttps://www.blogger.com/profile/17315221071837223412noreply@blogger.comtag:blogger.com,1999:blog-3652036210877702504.post-65841703557409659902013-08-19T09:20:29.998-04:002013-08-19T09:20:29.998-04:00i did already realize those of us without diagnosi...i did already realize those of us without diagnosis can help. i donated money to trinzyme out of my own pocket, and i stopped eating ALL foods and liquids for 2 weeks.....i consumed nothing but boost nutrition shakes and water, no morning coffee nothing, to see if diet would impact my odor condition....im just saying reaching the masses in the public and trying to raise money will unfortunatly Anonymousnoreply@blogger.comtag:blogger.com,1999:blog-3652036210877702504.post-78685456023667210042013-07-24T00:49:09.545-04:002013-07-24T00:49:09.545-04:00This might need to be the next webinar to get the ...This might need to be the next webinar to get the word out more effectively . Its also past time for people with no diagnosis to recognize that these studies Do actually affect how the medical community views All malodor conditions more seriously ,not only TMAU. Jimi is asking for some documentation that legitimizes the need and use of donations . His and others rightful skepticism can be Jojohttp://www.badbreathhalitosis.com/noreply@blogger.comtag:blogger.com,1999:blog-3652036210877702504.post-13444291253960429662013-07-05T11:43:33.497-04:002013-07-05T11:43:33.497-04:00My suggestion realize how lucky you are to have a ...My suggestion realize how lucky you are to have a diagnosis.......only people who HAVE tmau can advocate and fundraise.......call popular tv shows email them numerous times a day.....get on a show ask for donations......contact agencies that run the fundraisers for private charities.......its the rest of us without a diagnosis who not only need to fight for funding but also to be taken seriuosly.Anonymousnoreply@blogger.com