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No Warranties or Representations
Lyme Disease symptoms vary from person to person. (lymes disease lyme's disease lime disease limes disease)
The data and information presented in this web site are presented in good faith and believed to be accurate regarding Lyme disease (commonly misspelled lymes disease lyme's disease lime disease limes disease) and other related diseases. Any and all liability for the content or any omissions including any inaccuracies, errors, or misstatements in such data or information is expressly disclaimed. The web site is compiled for the sole purpose of informing community members of resources and information pertaining to Lyme Borreliosis Disease and its coinfections. Lyme disease symptoms may vary from person to person.
The Canadian Lyme Disease Foundation, Directors and members are not liable for any direct or indirect damages or any damages whatsoever resulting from loss of use, data or profits, whether in an action of contract, negligence or other tortious action arising out of or in connection with the use or performance of information available from this website.
Consult a qualified Lyme ( Borreliosis ) Disease literate doctor for medical advice if Lyme Disease is suspect to discuss your Lymes Disease Symptoms.
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Dr. E. Murakami Centre for Lyme Research, Education & Assistance Society
April 6, 2009
It is with great excitement that we announce the official opening of the Dr. E. Murakami Centre for Lyme Research, Education & Assistance Society.
It is Dr. Murakami's life work to make a difference for those suffering with Lyme. Up until now, Dr. Murakami has been fighting this fight as a lone doctor. Now he has a Society to fall back on, representative of all he believes in. He is the founder and president of this society. This will now be his lasting legacy.
The Society is registered with the Government of Canada as a Not-for-profit Society. It is currently run by a board of nine directors. There is a good line up of experiences within the board members to assist in achieving the goals of the Society.
As the Society is a not-for-profit organization, it relies heavily on donations, grants and outside funding. The society website has been set up to accept donations from anyone interested. Memberships are also available, for those who are able, which will allow them to be part of the Society and assist with fundraising activities and efforts.
Up until now, Dr. Murakami has been funding his efforts on his own. As all of you know, he does all of his communications with sufferers au gratis. We hope you will join the official Society of Dr. M in some way, shape or form that suits you best.
The first priorities of the Society is to advance the research efforts as quickly as possible. There is a plethora of information and data that has been gathered from patients just like you. This information and the work of cooperative laboratories will fuel the truth forward.
We are looking forward to a positive future and some exponential changes for those with Lyme and co-infections.
Please visit the Society website and bookmark it.
We hope you will be able to help out anyway you can. http://www.murakamicentreforlyme.org
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