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- How Do You Define “FREEDOM” In Living Life?
- …BUT THE HARVARD STUDY SAYS IT’S TRUE…
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- A FICTIONAL LETTER FROM A FICTIONAL PATIENT AND MY FICTIONAL RESPONSE: DOES IT RESONATE WITH YOU?
Althought you provided an alarming statistic (15%), this post makes me feel better. Alzheimers is something that frightens me. It bothers me to think one day I may not recognize my daughter. I have always tried to read, write, and exercise the mind in hopes of fighting off this disease. If diet and exercise helps, well, hopefully I am doing everything I can to avoid this dreaded disease.
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I wrote this article because most people are unaware that lifestyle plays a role in neuro-degenerative conditions. They are also unaware that GOOD medical treatment is available beyond the pharmaceutical option that has proven unsuccessful (by itself.) Finding a doctor willing to evaluate and treat the WHOLE PERSON instead of focusing on “plaque particles” in the brain has proven to IMPROVE cognitive function and has helped countless people return to living their complicated busy lifestyles. People need to understand that pharmaceutical drugs are a tool that addresses a “component” and needs to be utilized in this capacity. It is not (and never will be) the entire answer.
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Understood. I am grateful you posted it, cause I was under the belief there was nothing I could do. Thank you.
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It is common for the average person to believe that Alzheimer’s Disease is a byproduct of “bad luck” with limited benefits offered by the medical community (in the form of a prescription drug.) There is very little information found in every day reading or viewing that expresses a “Functional” approach to this condition and the benefits it offers. If the reader remembers nothing more than “there is a good approach to helping patients especially with early onset, this article has met its goal. People must be made aware of REAL TREATMENTS and the benefits they offer to improving the quality of life.
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I like to read this type of article so that I can keep these ideas in the back of my mind for myself and my family. Thank you, I definitely got something out of this post that will most likely stick with me.
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I started my blog to provide information to the public to help inform them about a side of health rarely revealed in standard reading and viewing material. I have NO INTENTION to tell people the “right” course to follow. I simply want people as informed as possible to make the best decisions for themselves. As a doctor speaking for and against health care policies I offer unbiased credible information obtained mostly from independent sources with no “skin in the game.” I believe solutions often involve better communication and the ability to understand all the “player’s needs in the game.” I am critical in some presentations, but fair and REALISTIC in problem solving.
I always welcome additional views (both supportive and opposed) to generate new thinking and new ideas. Your contribution will continue to add great value to this site. Thank you for sharing your ideas.
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Yes, understood. I don’t go one way or the other too far, everything in moderation ~ which applies for my healthcare as well. Better to have more ideas to consider than less.
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My father-in-law suffered from this disease. My mom, at 83, has altered thinking, but nothing like FIL experienced. I wonder sometimes about her overall health. She suffers horribly from a messed up digestive system (brought on by ingesting diabetes meds for too long???), and I have often wondered if she isn’t nutritionally depleted to the point that her brain cannot function properly. 😦
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Nutritional imbalances can easily lead to digestive (microbiome) imbalances that has a direct relationship to cognitive function. I certainly don’t know if this is the case with your mother, but the circumstances preceding her current presentation are consistent with these underlying causes.
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I keep telling her, “See a dietician, mom!” She doesn’t listen. Typical mother/daughter stuff. 😉
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My father began to listen to my nutrition recommendations when I explained they were not designed to lengthen his life expectancy, but rather to minimize the risk of ongoing damage that would make it impossible to remain independent. I asked him if frequent poor food choices was worth giving up his lifestyle and his condominium for a nursing facility to take care of his essential needs? I think this reality helped focus his attention on the bigger picture. There are times where diplomacy and hard core reality converge and provide an honest vision to the recipient. This was one of those moments with my family.
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sent to my Facebook page….xxxxxxxkat
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Thank you, Kat.
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You offer a lot of very pertinent points/information but I prefer to read shorter articles – I think most do if we are honest. Is it possible to put a summary paragraph at the top so that we can choose if we need to read on? Thanks for your concern, research and dissemination!
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It is refreshing to have constructive criticism thrown my way. I think your suggestion for a summary paragraph makes a lot of sense. I appreciate you offering this suggestion. Understanding the reader’s needs (and respecting their time allowance for reading an article) is just as important as providing information. Thank you again. 🙂
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As you know this subject is of personal interest to me and I really appreciate the information you share in this post. My dad has been on Namenda like forever it seems and I honestly can’t say whether it’s done any good at all.
I did not know that about the plaques being a result of the inflammation but it sure makes a lot of sense. What in the heck causes that in the first place is the big question. You’re right that diet and nutrition must be playing a role. Caring for loved ones with dementia as I know you know, is just horrible. Demographics and longer life spans will bring it to epidemic levels and we need better treatments.
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There are many factors that allow the body to become susceptible to disease and dysfunction. We are in control of some of the most important factors, but many do not realize the essential roles we play in the disease process. Naturally there are factors outside our controls as well (such as genetics and environmental,) but as more people begin to recognize the need to follow a healthier approach to life, diseases (in general) will be greatly impacted.
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The technical paper is surprisingly accessible, in terms of both availability for free reading online and understandability by nonspecialists. Thanks for calling attention to it.
While Dr B’s clinical experience with 9 of the 10 patients clearly justifies a large study with effort to prevent distortion by wishful thinking, it is hard to see how a double-blind trial could be designed. Sadly, some people are so devoted to DBT-s that they remind me of the joke about a guy looking for his dropped key at night under a street light, well away from where he dropped it. (“The light is better here.”) Maybe the entrenched bias in favor of taking 1 or 2 drugs is reinforced by misguided insistence on DBT-s. Dunno how to approximate the virtues of a DBT for something like Dr B’s protocol. Does anybody have any ideas?
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As a clinician, I used to mandate quality research before implementing treatment protocols. With experience, I came to realize the double blind studies were much more relevant to me than my patients. Even if a placebo creates clinical change in awareness and or function is there no value in its utilization. We currently know the pharmaceutical drugs are minimally beneficial at best addressing cognitive impairment. If a functional protocol demonstrates improved performance based on a person returning to work or safely driving a vehicle, I am no longer concerned about the science before implementing the treatment plan. It becomes sciences responsibility to explain the “WHY” it works, not the patient’s responsibility. I no longer believe in delaying protocols that potentially offer greater function and control for an individual suffering cognitive impairment because science hasn’t quite figured the best design for the study. How many years was aspirin used without fully understanding how it worked.
“Bayer launched acetylsalicylic acid as a commercial drug in 1899 under the name Aspirin. People knew from experience that aspirin worked, but lacked scientific knowledge about how it worked and why it worked. The New York Times Magazine called it in 1966: “The wonder drug nobody understands.” (Reference Source: Mann and Plummer, Aspirin Wars, p. 273.)
If there is hope for a better quality of life (without potential harm to the patient) and alternative options provide little if any hope, I believe it makes sense to follow this path. There is a good chance the politics of business will interfere with the research design and skew the results anyway.
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[…] my blog posted on April 12, 2016? You see, I wrote the following paragraph IN MY POST entitled, ARE THERE BETTER TREATMENTS FOR ALZHEIMER’S PATIENTS? before this study was ever […]
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[…] Are There Better Treatments For Alzheimer’s Patients […]
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My husband has Alzheimer’s and it is a different journey from the one we prepared for in our lives.
We have had 53 years of a great life, good and bad, and we will continue as far as we can. Your work is greatly appreciated and we pray that a cause and cure will be found soon.
Thank you.
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It is a blessing to have had the opportunity to experience 53 years of life in a relationship with a person that means the world to you. Although the journey has taken an unforeseen turn, the commitment the two you share will provide the strength and courage necessary to see it through. It is certainly a difficult condition (disease,) but caring doctors willing to set aside profit in exchange for qualitative treatments will find alternative approaches to help people overcome the factors that contribute to this difficult condition. Your willingness to share your situation shows the character you possess. My thoughts and prayers are with you and your family for the best quality of life possible. Answers are slow, but persistence will uncover new truths to help resolve this difficult diagnosis.
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[…] via ARE THERE BETTER TREATMENTS FOR ALZHEIMERS PATIENTS? — All About Healthy Choices […]
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Thank you Doctor Jonathan – This disease is horrible and scary and tragic, robbing people who should otherwise be living a long life of a normal lifespan. Finding a cure should be of utmost importance. Very informative post – thank you for all the great information and hopeful attitude.
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Thank you Joan. As people begin to understand that “cures” are less about substances and more about integration and implementation of necessary lifestyle habits, debilitating diseases will become less prevalent.
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