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by marjorie on 12 April 2012 - 12:04
by beetree on 12 April 2012 - 12:04
by Blitzen on 12 April 2012 - 12:04
The selected dogs were cadaver and SAR dogs from all over the country. Their owners had responded to the request for trained dogs to search the debris for bodies. The average time served by each dog and handler was 12 days and no NY PD or other K9 dogs were included although some of them served for a year or more and a large percentage of those dogs had already died from one of the leukemias, other cancers and many had respiratory issues. Why were those dog excluded from the study? It turned out to be a political thing (IMO), it looked like someone with one of those SAR dogs worked for someone who was a generous donor to the AKC CHF foundation. When I asked why the dogs that served there longterm weren't tracked I never got a straight answer. When I asked if any of the researchers considered the fact that more than a few of the K9's that served there had already died from lymphosarcoma, they said that was anecdotal and not relevant to the study.
I will no longer contribute one cent to the AKC CHF.A million dollars spent to track a handful of dogs that served for an average of 12 days at Ground Zero was not IMO money well spent that benefted dogs in general.
A friend worked for the NIH in DC and said statistics there were manupulated all the time in order to receive funding for politician's pet projects.
by beetree on 12 April 2012 - 12:04
by Blitzen on 12 April 2012 - 12:04
I don't intend to stop DNA testing for DM until I am convinced there is something better. I will err on the side of caution and use those results accordingly so I reduce the odds of producing dogs that test at risk. Can they still get DM, maybe, maybe not. Right now no one knows that for sure. If the Flash test were still aviailable, I'd use it in conjunction with the Coates test. Maybe DM in the GSD is different from other breeds, maybe it's more like ALS, maybe it's more like MS, I don't know for sure. Like the rest of you, I'm just doing the best I can. Right now we are cutting the baby in half.
I think it's was a terrible blow to the breed when Clemmons lost his funding.
by Blitzen on 12 April 2012 - 12:04
by beetree on 12 April 2012 - 13:04
by Blitzen on 12 April 2012 - 13:04
When my first breed was proven to be a model for a human disease, we had to retain professionals to apply for and administer the grants. It turned out to not be a whole lot of money, but it did help to establish the mode of inheritance and to identify other markers that were exclusive to the effected population.
by hillelunteren on 12 April 2012 - 17:04
A post from over the ocean, as most postings seem to be US posts.
First; everybody, try to be polite to each one, even when disagreeing.
Second; I too have doubts as to the SOD1 test and nevertheless I keep on testing. As a neurologist told me after the OFA test became available: I do not consider the cause of DM to house in the SOD1, but by lack of better we recommend it.
A geneticist, elderly already and not afraid to speak his mind in public on TV and radio and very much involved in animal-welfare, put it like this: The boys and girls at the uni's want to publish, so they research. After having found out something it is being published as fast as possible. Thereafter they are no longer interested in more research because the outcome of their own research may be questioned. So they try to block any new research.
Whether DM is to be compared with ALS or MS I don't know, I am no neurologist. However reading about it in the Wikipedia I personally consider it more likely to be like MS.
The Wiki about ALS says; degeneration of upper and lower neurons, located in the ventral horn of the spinal cord and the cortical neurons that provide their efferent input. Futhermore: characterized by rapidly progressive weakness, muscle atrophy and fasciculations, spasticity, dysarthria, dysphagia, and respiratory compromise.
This doesn't comply with my experience with DM and by now I have had, unfortunately, quite a bit of it. I have seen no impairement of the brainstem but in my opinion a clear degradation of the nerves in the backbone caused by the myolin being affected.
The Wiki about MS says; an inflammatory disease in which the fatty myelin sheaths around the axons of the brain and spinal cord are damaged, leading to demyelination, which is more in line with my own observations.
ALS affects the nerves of the brainstem, our dogs only showed a progressive weakness of the hind legs, daily massage of the spinal cord at about 2/3 of the backbone kept them going for quite a while, even though the end was inevitable.
What it all comes down to is that more research is warranted, it's a pity that Dr. Clemmons has been denied funds to continue, but what about Texas A&M, they were doing research as well. What I mean to say is; one shouldn't be blind to other, maybe radically different, points of view. No one, not Dr Coates nor Dr. Clemmons nor anyone else should rule out anything. It could very well be that the cause of DM differs by breed. Maybe DM is not the one disease as we label it and should we consider to alter it into DM-syndrome which would open our minds to more possible solutions.
Blitzen mentioned a one million dollar project, I only wish we could have funds like that over here, what could we accomplish with so much money! Our scientists at the university have only limited fixed salaries (yes, that is socialist allright), but that results in the best outcome for the least of money.
by Abby Normal on 12 April 2012 - 17:04
Is Dr Clemmons still applying for funding in this field or for the research into the 'treatment' of DM (which appears to me to be a different thing to finding a genetic marker or causal factor) for it?
When I had a dog involved in a treatment trial for AF in the UK, the cost of treatment itself was not funded by the researching body, that still had to be paid by the recipient (ie me).
I totally agree that screaming and pulling ones hair will never achieve anything. The way forward Marjorie I can see is collection and analysis of data, discussion with all organisations (including those hated researchers at UofM and OFA to keep abreast and understand exactly what is currently happening) researching funding options, and contacting other research organisations. It will be slow, it will not help Missie T in the meantime sadly, nor many other dogs currently suffering this disease, it would seem that ship has sailed, and that must be painful to accept. That is one path. The other is for UofM and others to continue their research. They are re-looking at Bernese, they are looking at the 2 GSD carriers, these things are not always right first time, nor do they stand still. It is not sensible to block one pathway to follow another. All options need to stay open. In the meantime, if breeders stop testing the money will not go to alternative research, it will just stay in the breeders pocket.
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