Encouraging study on Alzheimer's!
11 years ago
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Alzheimer's is the cruelest thing ever...having a hard time
Comments (23)"I still believe it is the culprit and I researched AZ when my husband was diagnosed and found a document written by one of the top immunologist in this country saying he thought it was alum and said it was rampant in this country and one day there would AZ patients in the streets because there would not be enough homes for them. Aluminum enhances meds and it is in almost every shot you get, it's in 95%of all anti acids meds, etc." I agree. I also think we are getting too many toxic chemicals from vaccines. Emma, do you have the link to the document by the immunologist? I'd like to read it. Here are some more thoughts on this subject. "Studies confirm fluoride enhances 'bioavailability' of aluminum What apparently happens when individuals with aluminum-induced neural degeneration are exposed to fluoride is that the fluoride enhances the toxicity of aluminum. In terms of bioavailability, or the ability of aluminum to cause harm, fluoride greatly increases the overall toxic burden of this pervasive metal, rendering it exceptionally more toxic. "[A]luminum-induced neural degeneration in rats is greatly enhanced when the animals were fed low doses of fluoride," reads the news release for a 1998 study published in the peer-reviewed medical journal Brain Research. "The presence of fluoride enhanced the bio-availability of aluminum (Al) causing more aluminum to cross the blood-brain barrier and become deposited in the brain. The aluminum level in the brains of the fluoride-treated group was double that of the controls." Links that might be useful. www.naturalnews.com/044366_fluoride_aluminum_brain_damage.html http://www.realfarmacy.com/22-medical-studies-that-show-vaccines-can-cause-autism/...See MoreReally great breakthroughs in Alzheimers research
Comments (17)I'm with rob on this, it was what I was trying to say but my explanation wasn't very good. Her link was to an article about a Merck product that just got pulled. The publication also had an article about an Eli Lilly drug that was similarly in late stage trials and got pulled in November. Lilly was said to have spent hundreds of millions of dollars on that project, an amount hugely in excess of the funds that academic labs have to spend. That article also said "Over the past decade, 99 percent of experimental drugs for the disease have failed in clinical trials". Here's another project that was terminated. These drug projects would have received a lot of media attention about their promise and may have caused many to have false hope. Research has a lot of ups and downs and is a very long process. False conclusions and misdirection are far more frequently the outcome of research work than silver bullets....See MorePotential treatment for Alzheimer's
Comments (0)This article from Yale seems encouraging--although when the subjects are mice it must be hard to tell what side effects might be taking place. http://news.yale.edu/2017/07/05/drug-restores-cells-and-memories-alzheimer-s-mouse-models?utm_source=YNemail&utm_medium=email&utm_campaign=ynalumni-07-06-17...See MoreQuestion about Alzheimer’s
Comments (26)Chisue, you raise some very good questions. In my 40+ years of hospital nursing, I have seen heartbreaking instances of people with advanced dementia being forced to undergo life extending procedures -- such as open heart surgery! -- because their family members felt that it was the right thing to do. But, they fail to see the terror, the pain, the combativeness, the inability to leave drains and IVs and wounds alone, the patient sometimes injuring themselves or a staff member, and so on, because he/she is unable to comprehend what is being done to them or why, and unable to feel safe in such a foreign environment. Then those family members come in and demand that the patient not be receiving sedation or pain medication because it leaves them drowsy when the family wants to interact with them. And, those families often have failed to understand that Alzheimer's, for one, is itself a fatal disease. One of the ways that medicine has changed in the past 40 years is the way that we respond to fatal illness -- back then, we wouldn't put terminally ill or advanced dementia patients on life support, or ask families if they wanted us to "do everything, including CPR", when we knew that would be futile or merely extending their dying process. We just didn't (and I think society in general didn't) consider it a reasonable option: Now, we are obligated to do just that. I made the decision on the behalf of both of my parents -- who each had dementia of different types, my mother from repeated cerebellar strokes, my father from microvascular ischemia -- that they would receive comfort care only in the event of a major illness. Therefore, any treatment would be solely for the sake of relieving pain, shortness of breath, and so forth; not to extend life just for the sake of extending life. I feel strongly that we need to respect the gift of life, however we are designed to have our lives end and we need to respect that and recognize that death is sometimes a gift also....See More- 11 years ago
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