Non-Insulin Dependent Diabetes Type 2, according to the Cambridge University Press. August 31, 2017

between 90 and 95 % of all individuals with diabetes have type 2 diabetes and are over the age of 35 years. (Page 667).

     It is Cambridge University Press, the Cambridge World History of Human Disease, 1993. It is how they published and how they present what is diabetes?
     So, really what is this about? There are pediatric diabetes and adult diabetes, right? Why it is DM type 1 or DM type2? Still not clear.

In contrast to type 1 diabetes cases, there are many cases (type2), (up to 50%) that remain in-diagnosed.

So, if diabetic type 2 had already insufficient insulin secretion when one was under age of 16, but was not diagnosed with DT1 then why today it is type 2 diabetic? Just because of age 35+? Sounds very in-professional, and really far away from being Academic.

Type 2 produce insulin but may require more of it in order to manage their glucose levels.

Still not clear, how much insulin humans need to meet demand for body to function? Type 1 diabetic's pancreas  does not secret insulin at all, and they need less insulin then type 2 diabetic, right? So how it is discovered that one is type 1 diabetic whose pancreas does not secret insulin, or type 2 diabetic, whose pancreas secrete insulin , but the amount of insulin secreted is not sufficient for body to function?
So, if diabetic type 2 need more insulin to control blood sugar then why this type of diabetes classified as "Non-Insulin_Dependent Diabetes (Type 2 )? I Still do not get the point.

The majority of all patients are treated with dietary modifications, often with caloric reductions for weight loss, and with hypoglycemic tablets.

So, if diabetic need insulin due to low insulin secretion, then .... then what? No insulin for type 2 diabetic, why? We are non-insulin dependent. I posted many times, reason  does not apply for medical pro. They do have own logic, and no one without mental problems is able to get it.
      This is book, text book, published by Cambridge University Press to teach student the History of Disease. It is more then 1000 pages. After poor student read all this professional logic, there is no room for reason. Brain perfectly washed.

Those symptoms, which include excessive urination,urine containing sugar, hunger, thirst, fatigue, and weight loss, are common to all types of DM.

 True? It depend. Say me, how diabetes diagnosed? According to the level of sugar in blood, regardless of what type of diabetes it is. How effectiveness of treatment checked up? A1c level, other blood test, the sugar in blood. At the same time diabetes, according to the Cambrige University Press, is :   

"Diabetes Mellitus (DM) is an endocrine disorder characterized by lack of insufficient production of insulin by the pancreases." (Page 665)

       So, why diagnose based on the level of sugar in blood?  If any types of DM is endocrine disorder then why do not check up, how healthy pancreas before force it with SU to secret more insulin? What if pancreas is already in final stage of diabetes development and progression?
       Also there is another problem. How to find out if treatment work or not? Sugar in blood cannot show is pancreas getting better or with treatment is is getting down. This is why diabetics type 2 gone less then withing ten years after treatment started, and type 1 diabetic who are on insulin therapy, live long and healthy lives. It is diabetes type 2 which stand on the spot number 7 on the row of leading causes of Death.
       BTW, is this really true that we all do have DM? Not really. The sugar in urine is the stage when sugar in blood is very very high. If sugar in blood is above the normal it does not mean that there is sugar in urine. This is why when we come to hospital they found, sugar in blood is elevated, and can be really high, but there is still no sugar in urine, so we are not DM. At the same time when type 1 diabetic's urine would be tested, there is no sugar in urine. So, diabetes type 1 perfectly cured, right? They even do not have elevated level of sugar in blood, honeymoon phase. Many of them in this phase for the rest of the lives. They are type 1 diabetics, and they control blood sugar with right diet and work out. The question is why they did not control sugar before they started to take insulin shots but rushed to ER?
      Well, to make long story shorter, why do not stop to diagnose diabetes with some symptoms which are difficult to apply to the abnormality in tissue, and start any diagnose with the health of pancreas, endocrine system? At least, it is diabetes, Endocrine System Disorder, according to Cambridge University presentation of diabetes. First thinks first. Let us at first diagnose what to treat, and only after that to apply medicine needed to fix the problem. Not vice versa.

via Ravenvoron

Big War on Little Pond. August 30, 2017

It was our trip to campground in Catskills, Little Pond. We use to camp on this ground every season. I love this camp. We used to be there when I was able to hike. Now I just sit on the waterfront, and enjoy the camping. No longer. Two days after this shot was taken camp ranger demanded I no longer can use my set up. It is prohibited by DEC.  Well, I tried to contact DEC and I tried to be reasonable. Why cannot I use my set up? 

From Environmental Conservation Law Part 190 8 (w) No person shall erect, construct, install, maintain, store, discard or abandon any structure or any other property on State lands or subsequently use such structure or property on State lands, except if the structure or property is authorized by the department or is:

(1) a geocache that is labeled with the owner’s name and address and installed in a manner that does not disturb the natural conditions of the site or injure a tree;

(2) a camping structure or equipment that is placed and used legally pursuant to this Part;

How this set up disturb or injure any site on camp? 
 It is very typical set up. No trees involved, no any injuries to the land.Just say me, why I have to have special permit from Albany to use this set up?
 Well, let us take another look at the camp
 on Little Pond. As it is demand according to the People With Disability Act Little Pond has accessible toilet. On day use area. Only one on the all campground. No one campsite around. 

Generally the DEC Recreation program does not allow the use of portable toilets or showers. We make ever attempt to provide our guests with restrooms, shower buildings or bathhouse changing rooms throughout our facilities. Our guidance rules on these topics were created in an effort to provide a reasonable measure of privacy for not only the site occupants, but also for the neighboring campers and visitors. The guidance was also created to ensure the safety of the general public and the environment by providing sanitary conditions in our facilities. The risks of an unintentional discharge from these type of units are a real possibility. In addition, the New York State Environmental Conservation Law Part 190, Use of State Lands has a section that prohibits the installation and setup of unauthorized structures like portable toilet and changing facilities.

Just think for a moment, what if all campers must use camping restrooms as changing facilities? Not reasonable, right?  Why camper who cannot use public restrooms must be prohibited to use own portable toilet rather then go to day use area every time when one have to go? Why this does not sound stupid? Because of I am not
 Buzzelli, Mike J (DEC) <mike.buzzelli@dec.ny.gov>
or
Fraser, Carole A (DEC) <carole.fraser@dec.ny.gov>
or any other official who demand I have no right to use my private portable toilet or shade to hide it.  
       As it is presented they use all attempt. The question is, what if campground still have no shower building for family where I can have shower? What I have to do? At least Little Pond has no family shower, all toilets be accessible, or site which can be accessible. So, before demand that camped must put down own set up, why do not look around, if there is place where camped can be?
      Well, there was suggestion. Around toilets there are all the time free sites. Reason? I am sure no one will take this site if there are other sites available. So, these sites put aside for people with disability.  How these sites done? They are just closer to the toilet. Is this site well developed? No. It is wet. In case of rain I may have free bed-ride right to the lake. 
     Really, I am interesting, is this really true that people with special needs need to be as closer to toilet as DEC can provide? I do not think so. I can be even closer to toilet if I stay home. It is next door from my bedroom. Really, why I need to go to Little Pond and have fun to fight with fly? 
       When I book my site I take a look at the very specific info I need. 
Site must be on waterfront with good access to the water.   For me now it is very difficult to sit on my boat. I am very poor in control my body, so boat must be stable, no move. My man hold it, and I take first step in it.  Then he helps me to take a sit. Now when I am in I will not go out till we return to the site. On some places there is good access to the water. In others it is not. 
      As I  was suggested I have to take site away from water, why? Do they prohibit me to take water trips on lakes and rivers? Good question. But if I can take these trips then why I cannot camp on water front? 
       Next look at the distance from toilets. I do not like smell of toilets. I do have asthma. Very often I do have Asthma attacks.  Also I do have headache , very often it is very severe. So, door flopping is not the choice for me.
       There still no answer what is wrong with my set up. How my set up, this set up, hurt trees or land? After we put down our tent and shade and fold our tables and put all in our car there is no evidence we had been there, just campfire place need to be cleaned. Looks like DEC never see how campers put on tarps all around the trees, and BTW, children's diapers go were? Does Little Pond ranger ever saw tarps tied to the trees?

via Ravenvoron

Day-by-Day. August 30, 2017

My hands getting better. Yesterday I took off bandage from my fingers. Today fingers still do not work very well, but still, they are all dry. It is good. Swelling still painful. New skin is sensitive.
       My man wrap my legs in brown bandage and the wight bandage above the brown. When we try to use only one, white bandage, it fall out right to the next morning. Swelling decreased, and bandage fall.The brown bandage usually applied for the full week. But I do have allergy on the brown bandage, and my man has his problem with skin when he applied it to my legs. Another downside of brown bandage, it is too expensive. We can use white bandage and re-use it for many times. Brown bandage can be used only once. Then it is trash. The cost is between $3 and $5 for every roll. I need two at once, one to every leg. Do your math. It is most effective way to treat edema, as I do see so far, but it is also way too expensive.
        Doctor Rx some stoking and I still not able to find where to get it. It is edema. When water decreased, no one size still the same. This is why bandage fall, Even brown bandage fall. But when edema increased, the pain is not bearable. Bandage cut the skin as it is knife. Not that there are visible cut, not at all. But pain, and skin became as waves. In some degree it is not possible to hold, and I cut the bandage. I just cannot take this pain any longer. So, as I do think, there are no any stockings that will work for me. Anyway, I still not able to find where to get them. Good job. Doctor Rx some treatment, and probably this treatment does not have place to be.
      Legs are dry by now. No wounds. I am capable to walk, not far but around apartment I can.
      I am very very dizzy. I do not know why it is so, but I am very very dizzy. I try to stay home. I try do not move too much when I am alone.
      Asthma getting worse. I no longer do have medicine to use to work it out. Symbicort I do have, and it is medicine which makes me very dizzy. I try to take it as less as I can. There is no other medicine to curb Asthma. I even do not remember when last time I was in clinic to check up how it is progressed. My primary is specialist in this department. So, there are never any attention to this problem. Looks like he ignore all the problem I do have and push only one agenda, weight. Anyway, there is no any visit to clinic in visible distance. He simple refuse to give any appointments to me. I do have this situation not first time. I am ill person. Doctors usually happy to work 'to prevent' all what possible to happen, but when anything happened, and one got ill, they are hiding all around, and never around of the patient. Disgusting.

via Ravenvoron

Diabetes Emoji

Do you think that diabetes is trying to tell me 

that it wants its own official Diabetes emoji/emojis?  

No joke and this is NOT photoshop guys. 

THIS is what I saw when I looked down at my fingers 

after I checking my blood sugar this morning (it was 111😁.) 

FTR, that's my blood, not a Sharpie drawn smiley face~

Pretty damn trippy! 

via Diabetesaliciousness

Toilet War on Little Pond public camp. To Carole Fraser Opened Letter.

This is e-mail from New York State Department public lands 

Hello *********

Thank you for speaking with me today about your request for accommodation under the Americans with Disabilities Act. As I explained on the phone, we usually do not allow people to use the portable toilets or structures other than tents and campers.  However, since Mr. Buzzelli had offered to consider special circumstances in your case, I called to talk to you about that. As I explained, we would like for you to have a letter, that explains the accommodations that we agree on, so that you can continue to go camping.  You told me that you did not want a letter and you did not want to discuss any accommodations further.

If you reconsider, please let us know.

 

Carole Fraser

Universal Access Coordinator

Division of Operations

NYS DEC

625 Broadway

Albany, NY 12233-5254

518-402-9437

 Sorry, I really still do not get the explanation. If this so then why it is not in rules we all do have to sing when we come to camp? What wrong with portable toilet?
At the same time Ms. Fraser ask me if I can put this toilet in tent. So, then I can use it? What is difference if it is outside tent but under the same tarp?

Really, what is wrong with my set up?
     Still, it is war, and now for what  I am prohibited? and why?
 

"From Environmental Conservation Law Part 190 8 (w) No person shall erect, construct, install, maintain, store, discard or abandon any structure or any other property on State lands or subsequently use such structure or property on State lands, except if the structure or property is authorized by the department or is:

(1) a geocache that is labeled with the owner’s name and address and installed in a manner that does not disturb the natural conditions of the site or injure a tree;

(2) a camping structure or equipment that is placed and used legally pursuant to this Part;"

What is important that she try to present I ask about special accommodations. I do not ask about anything special. What I ask is, send me mail that my portable toilet cannot be used on public lands. It is so simple. 
Now, there is another issue. 

"I believe that we have the ability to authorize the use of your equpiment but it must be done in writing from the Albany office so you could use the letter for future camping. If you reconsider, please let me know and I will draft up the letter you willl need.  I am working out of the office tomorrow and Friday."

 What I do believe, they do not have this authorization. How this authorization can fit into Americans With Disability Act?  That I have to go where Ms. Fraser let my go? Sorry. It does not work in this way. She  has no such authority. It is she, who must work out the way that I can live well. At least she said so.
Next what I wish to say, there must be rules that campers cannot use portable toilets, and these rules must be enforced to all campers. So, campers with little one should not be on public lands. Dogs. No dogs. Ms. Carole Fraser suggested to me that I can book sites away from water. But there is no rules that campers cannot book sites around water if they bring pets, dogs, or have little one.  So, why it is only for me that I have to ask letter how to camp? I follow all rules. But Little Pond camp ranger is abusive person. I think she is unhappy. This is why she come to our site to start this war. What I wish to ask Albany Office, is this really true that any staff has right to get in communication with campers outside their duty? I do not think so. There is perfect time to shine. My tent. My private cabin.

Usually it is under tarp. But when tarp put down tent and cabin stay apart. Well, if I will use this cabin to cover firewood, then it is OK as I hope.  If I do use my portable toilet in tent, then it is also OK, as Carole Fraser said. What I cannot do is, put them together.Sorry, still not able to get why?
     On Little Pond late in night in deep darkness there is light around my tent, and footsteps. It is Catskills, it is Black Bear country. My man is out of site, went to take shower in public building. I scared to Death.
       It is not Black Bear. It is camp ranger sneaking around. Only in Catskills. No one in Adirondack. They do the same job, but without scaring campers.
      It is easy to see, we do not injury trees. Our tarp is on the top of tent and on the top of cabin. My man has set up camp without my help, so we use as easy way as we can. No one camp ranger see how tarps and nails injury trees. No one pay any attention for the sites on opposite road where human wast all around.  Why state Department so active in my toilet deal and no any attention to the cleanses around camps and on closer to the hiking spots?  I think it would be better if camp ranger clean all around the camp, so she know better if my toilet benefit to cleanness or destroy public lands.
So simple, just send her to clean up all dirty spots on Little Pond, so she would see difference between go-bushes and using portable toilets.

via Ravenvoron

Disable person use of NY State pubilc land, try it if you can. August 23, 2017

       Right now I do have call from Fraser, Carole A (DEC) <carole.fraser@dec.ny.gov> What is the problem? It is my camping. Some years ago on some public camp sanitation took trash, and human wast poped up. So, now there is low (as she tried to say to me) that I cannot use my portable toilet on site. On every site there are little one, dogs, and it is rule to clean after dog. So, wast go to where? But in stead to do the job NY State Public Land protection issued Law to prevent people like myself to use portable toilets and portable cabins. So easy to boost active life style! With Invokana which is widely spread among diabetics type 2, and diuretics which most people use, this is best way to prevent cleanses of our lands. 
      Really, be reasonable. In stead of create more stop with restrooms it is easy to put fence around the highways, and let people to carry on pee and ka-ka right to the home. There is better suggestion. Is someone saw sometimes that in urban streets there are smell, and human wast go out? Yes, it is not often but happen. So, to prevent this from being happened, let us prohibit people from doing natural way of leave. 
       As I said, dogs have right to be on site next to water. Little one play in water all day long. Disable person who is not capable to walk to distance longer then site size, must book site ... or simple stay home. Of cause, really why we are ill? Because of lifestyle! 

        I said, No! Sorry, Mr. Carile. I prefer you send police to put down my tent and arrest my portable toilet! I let my camera ready!

We are willing to consider special circumstances and conditions to provide for reasonable accommodations for all of our visitors. May we suggest possibly reserving campsites closer to our restroom facilities? Also, many of our locations have newer toilet and shower buildings that provide family, unisex and/or have accessible features. 
 Buzzelli, Mike J (DEC) <mike.buzzelli@dec.ny.gov>

 Thank you for writing us and expressing your concern regarding the use of portable toilets and changing cabins at your campsite.

Generally the DEC Recreation program does not allow the use of portable toilets or showers.

But I am not general population. I am disable person. Person like myself very often use portable toilets even at home, because it is too long trip ti take to go bathroom. Also we do have bed-bath because of we cannot use general shower.

So, 

Ms. Carole Fraser

Universal Access Coordinator

Division of Operations

NYS DEC

Thanks for attention to my disability needs. Sorry, I will not take your accommodations as you suggest.  There are so many fays around restrooms. People flap doors day and nights. I do have severe headache. You can keep this sites to someone VIP, like Catskills manager. 

From Environmental Conservation Law Part 190 8 (w) No person shall erect, construct, install, maintain, store, discard or abandon any structure or any other property on State lands or subsequently use such structure or property on State lands, except if the structure or property is authorized by the department or is:

(1) a geocache that is labeled with the owner’s name and address and installed in a manner that does not disturb the natural conditions of the site or injure a tree;

(2) a camping structure or equipment that is placed and used legally pursuant to this Part;

Sorry, if someone can see that there is one word how can I use my toilet?  Yes, it is rule how to discharge wast on public land. Still, no one rule addressed that I cannot use my portable toilet. Or Personal Cabin where this toilet sit.

       For every one it is just ugly post to let on Internet and let all globe to know how to discharge own wast on NY State campground. But it is more then just one person and one camp combat. On Catskills I met a lot of problems with staff and campers. I am ill person, almost 400 pounds, hardly able to walk. When I walked into public restroom kid bulled me, and his father stopped by to say that they have to teach children how to behave properly. "Do you forgive him?" - father asked me. I had no idea what to answer.
"Just say, yes',- his father educated me. 400 pounds, I am ugly. Really? This is the matter of personal opinion.

via Ravenvoron

The Danger of Preventing. August 23, 2017

        Diabetes type 2 is one of the leading disease in modern word. According to the medical care publications it is easy can be prevented with right life style: eat right, do not smoke, walk 30 min every day, and so so so on. On the first look it is All Right, and there is no any Bad Medical Care in this highly propagandized right choice. Really, how eating right can be wrong? How losing weight can be wrong for anyone? And how stay fit can be wrong? It is all right, there is nothing wrong to be healthy. Actually it is good. What about those who are not healthy? When we got ill or sick, how we can stay healthy with right meal choice? So American's easy to swallow scam that if they are healthy it is because of they stay active, fit, and they eat right. All other Americans, who happened to be ill do it wrong, and this is why we are ill.
      
         What general population do know about diabetes? That if we keep our body starving we will not have diabetes. So father teach his teen girl she must go camping, take work outs, and eat right. Then this teen girl come to school and .... that's right, her schoolmate girl who happened to be not healthy for any reason widely bulled and abused. Teen girl doing nothing wrong. She actually help fatty teen to stay healthy. The same way how doctor in clinic bulling me that I have to loose weight and it is all what I do need to be diabetes-free. It is interesting, why we go to dentist two times a year to take clinic that if something wrong with our teeth dentist will fix it and we will have healthy looking and good working teeth? Just treat every one with the same Barking Therapy as diabetic treated by society. No. No one even think that teeth pain can be prevented with right food choice. Really, why?
        There are a lot of studies and new discoveries. The new hormone, new food combination, fat tissue studies, and so so so on that if one will try to keep track of all discoveries the question pop-up, why diabetes still have no cure? There are a lot of 'prevention programs' and why they do not work? There are more and more diabetics diagnosed, why? Is this really true that we all eat wrong? Or there is something wrong in all that prevention program. The choice is up to us. It is we who teaching our kids to bulling, not the kids who do this ugly job.
     
         There is another danger of 'preventing'.
Does someone know how many people lost lives in car crash? The question is, do you have car? If you do not have car then you will not die in car crash, right?
How many people lost lives when they got under drunken driver? So, if we sty home then there is not possibility that drunk driver will hit us, right?
And finally, if we are not alive then there is no risk to loose life, right?
      So, there is choice, live as long as one can, as healthy as it is possible, and rely on your Destiny. How much addicts cost to society? No wide spread info about it. How much cost rape? There is even no data how many girls and woman suffer. To stop all this suffering all what society needs just sterilize all men so they do have no interest to sex. Stupid. But why prevention of diabetes taken for granted? Why it is so widely accepted that diabetics type 2 done it for themselves?
      Today it is diabetes type 2 which can be prevented with life style modifications. The heart attacks and strokes also in this category. And tomorrow all what people will need just go to clinic and ask doctor what they have to eat, if they still sick or ill. Easy way to address to any medical problems. Just ask your doctor what to eat. And prevent any complications in own live.

       Finally, with this 'prevention' it is easy to drop off responsibility that people get ill and need medical treatment. There is no treatment needed. Medical researchers study how to treat rats if it has diabetes due to fatty diet. How old rat is in human age? Does not matter. If rat got fat and developed diabetes due to life in cage, then there is no need to check up diabetic's pancreas, if this organ healthy to do the job. In modern medical publications there are so many scam how rats stay diabetes-free if they do not eat fatty meal. Still, I did not see any publication, how diabetics pancreas looks like? What really wrong with diabetic's pancreas? What wrong with my pancreas? There is no one test how my pancreas working, if it is healthy, or there are some problem with it, and what problems they are?

       Well, it is out of fanatical needs of doctors to test pancreas to prevent diabetes development. The same as with dental problems it can be easily preventable if doctors will see the problem right in the root of it, and start to treat diabetes as early as it is found. No. With all prevention programs and so high cost of diabetes and so high mortality of human population, level of sugar in blood still not Vital. This is first step to prevent all diabetes complications, and this step never taken.     

via Ravenvoron

Scam from Andrew Ahmann, endocrinologist at Oregon Health & Science University in Portland, Oregon

Ultra-Long-Acting Basal Insulin: Who Benefits? 

http://ift.tt/2v3rYU4

Andrew J. Ahmann, MD, MS

Disclosures

August 17, 2017

In this disclose the saner is, the   author, MD. There is no one who benefit from this publicatiobn but author only. let us take a look at the publication.

I think many clinicians listening to this have recognized barriers to insulin therapy, particularly in patients with type 2 diabetes. We know that there is provider inertia. Many of us are reluctant to move on to insulin, which may be due to the complexity of teaching patients how to use it.

Scam. How provider teach diabetic to take insulin? Really it is nurse who do the job.  What left to provider? Just inertia. With insulin provider at leas have to make face that he count dose of insulin. In reality it is diabetic who do the job. Show me, how provider can count dose of insulin? Based on what criteria? Weight. So, my 400 Lb : 4 = 100 units. 400 pounds is really very big lady. What MD suggested?

With degludec, we can get larger doses. We can get 160 units in our heavy patients who require more insulin. In the future, I suspect that this will be true for the U300 insulin as well.

       So, what really MD is talking about? Just pushing scam. Personally I take 300 units daily. Highest dose was 434 units withing 24 hours. No low sugar. Really my sugar was too high, and only increased dose of insulin curbed the rise in blood sugar level. I take Lantus Solo Star, only this type of insulin.

You really have to think about the barriers and dangers for the patient who has a higher risk for cardiovascular disease in regard to hypoglycemia risk, and for older patients who inherently have higher risk for cardiovascular disease and are more prone to hypoglycemia.      

True? Scam. MD has no one idea diabetes what is it?
       For your education, my dear MD, you have to know that age and low sugar is not connected. So, to pretend that older patients has higher risk to get low sugar is Pure Scam. Low sugar depend from the level of our pancreas destroyed. From this level of development the time diabetic would  still live, or development of complications, such as cardiovascular disease, highly dependable. Diabetics type 2 live for adulthood till our sugar getting to the fatally high level. Then with MD attention we leave this world less then withing ten years. Interesting, why?

 For instance, [blood glucose levels] going down too low at night and still not in control in the morning would be a reason that we might consider going to these longest-acting insulins with the least likelihood of nocturnal hypoglycemia.

   Say me, what MD, endocrinologist, really talking about? If blood sugar going down at night then say me, how it would be controlled in the morning?Just interesting question, how it would be controlled?

This is really I do not like to go to hospitals. At first, they usually stop my insulin therapy.So sugar rush over the sky. All types of complications ready to be developed. They simple discharge my from hospital, and then I have to do my best to stay live.
    MD with fatty face like this one will teach me how to count carbs and do work outs. Why he is so fatty anyway, and has no insulin therapy? Every time I am ib clinic or in ER I told I have to undergo weight los surgery, so I would be diabetes free if I would lose weight. But he is really very very fatty. Why he is not diabetic? Probably it is huge Medical Scam that diabetes is resulted by high body mass. At least with this Scam they are all the time can pretend, they do the job.

I think they (diabetics) would be for patients who insist that if they go on insulin, they want the product with the least hypoglycemia risk. In some cases we can honor this, and in other cases—for financial reasons, for instance—we can't.

       Well, there is no one way that  low blood sugar would be prevented. If treatment work, sugar go up and down. Then higher high level then low it drops.
      Financial reason. My insulin cost $2000 every month.Say me, what MD is ready to Rx it? I can say, even my health plan ready to pay, MD way tooooooo resistant to Rx 300 insulin for one day insulin shot.
It is much better to Rx Metformin, $4 month supply and let my legs and hands and arms be amputated. At least those money $$$$$$$ will drop into MD pocket, and MD has no benefits when one Rx insulin.

Really what MD suggest to me? Do not smoke. LOL
Eat right.
lose weght
be active. take walk at least 30 min a day.
LOLOLOL. No one of this work to reduce severe edema. Legs wrap do the job. It is one wrap for one leg, and I need two of them for a every week, cost $5, $10 for one wrap, (+ unna Boots) + medicine to apply on wounds, and all it every week at least. It is more then $50 every month.

via Ravenvoron

Glucagon Training

A couple of weeks before my daughter went on the five night youth group trip I met with the chaperones to train them in glucagon use, and to talk about diabetes concerns for the trip. These are people I know well, which has a great deal to do with why my daughter went on this trip without a parent in the first place. They were eager to learn how to help my daughter have a successful first trip away, and how to react should an emergency arise.

We gathered at a table.

"Epi pens make me a little nervous," my first chaperone friend said.

"Well, wait until you see this thing," I replied with a wry smile.

He was, indeed, humbled by the sight of the glucagon kit.

"Here's the deal," I said once it was open in front of us on the table, "We've never needed to use this. We've never come close to needing to use this. You guys know her. She's responsible about her diabetes and she's self-aware. She's got the continuous glucose monitor which alarms when her blood sugar goes low. But because diabetes can be unpredictable, there's an infinitesimal chance you'll need this, so it's important to us that you know how to use it. And besides, once you see this, I'm certain you'll listen even more carefully to the rest of the ways I'd like you to look out for her." Cautious smiles had returned.

I walked them through step by step with an expired kit, and then one chaperone physically set up my second expired kit while the other gave verbal directions. They seemed to get the gist, and learned to look for the pictographs inside the packaging for clues. In the end, I reminded them that the first step would be to call 911 and that if they were flummoxed by the kit, the fact that they knew what it was and where it was would be key for the EMS workers.

After striking a healthy fear of glucagon into their hearts, we went over the very simple things a 15 year old kid who's out of her element might need their help with in order to avoid disastrous low blood sugar:

-Someone to hang back with her if she needs to wait out a low.
-Someone to ask her if she's okay if she's spacey or uncharacteristically emotional, which are the primary signs of low blood sugar for her.
-Someone to stand up for her if someone gives her a hard time about stepping aside when she should be doing her volunteer job, or eating when she "shouldn't be," or looking at an electronic device when the kids have been told not to.
-Someone to get up and nudge her if a dexcom alarm is going off in the middle of the night.
-Help getting supplies should she somehow blow through the snacks, juice and glucose tabs we packed.
-Support if (when?) diabetes causes missed opportunities or unpleasant experiences along the way.

In the end they didn't use the glucagon. In the end, it may not have been necessary to show them how to use it at all. But in the end the glucagon training led to a much more important conversation about ways to keep her safe. Which made all of us more comfortable.


via Adventures in Diabetes Parenting

Day-by-Day. August 21, 2017

Rainy day on Limeklin Lake, Adirondack, August 2017.
Today we are home. It is hot in NYC.
110 mg/dl , fasting. I took 147 units of Insulin Lantus Solo Star. Not I take all 300 units in two shots. It is difficult to keep up with more shots. Also, I take meal only two times, so it is just logical to take two shots, right before the meal.
      I do have severe headache. It is usually at night. It is so severe that I even do not wake up, still sleeping. Of cause every one can have a humor, that pain is not so bad if I am able to steel sleeping. Good for them. I afraid, onr day I will stay in this sleep, and would not be able to wake up at all. This is how it works. People think, if we still sleeping then there is no pain, no any danger for us. Good humor. Bad to be subject of it.
      On Saturday we come back from Adirondack, one week vacation. Now the problem I had in the Winter and in Spring returned. It is not on legs, but on hands. What is it? allergy? circulation? or something else. Do not ask doctor. He simple refuse to see me. I do not take surgery as it is option to address to y health problems. I do not take weight loss surgery even my weight is 360 pounds with +. I simple keep going with insulin, and try to hold sugar in blood as close to normal level as I can. It is OK by now. I do have insulin, so I can control level of sugar with daily injections, to add or to decrease dose of insulin in every shot.
 This is how my hand looks like. The yellow liquid drops from tip of fingers. One after another, right now all fingers effected. The problem moving ahead, and now it is spread on the arm, on the body, even inside of me, I can feel it.       My primary and another doctor suggested I take surgery on leg that the problems in the veins. As I see, it does not matter what the problem is, the solution for any problem is surgery, and weight loss surgery is best for doctors. 
     Well, what is good for someone does not mean it is good for me. So, my primary refuses to see me. he canceled my next appointment. He usually do it in the day of appointment or day before. Not he done it in very long advance.
       I try to find solution to my problems as I can. Right now I do returned to wrap my legs, even there is not leak anymore. Also I do wrap my hand as well as I can.  It is not possible to leave hand without wrap. The yellow liquid drop from it all around me.
        This is how my hands looks when it is wrapped. Easy to see, I almost cannot use it. The wrap is homemade from all t-shirts. Yes, it is not sterile. LOL! Where I suppose to take money to buy all supply and medicine I need? I use all what is possible to get, and if it is cheap then it is better. I am American. I do not jhave Medicaid and Medicare how it have most fresh immigrants who never worked in America. They are 'low income' and we are not. We have to pay all medical experiences.

       Before wrap would be placed on hands I wrap every finger with cloth wet by hospital iodine. Every time when I open wrap it looks like that. But it is easy to get rid of wrap, so it works for me.
       Now it is time to take a look at the fingers. Step by step big watered balls strted to decrease in size and with time the wounds started to get dry. Today there is no dripping from the tops of my fingers. They are dry at least. Still I have to keep them wrapped. Very reasonable as I do think.

       Now there is the question, when next area would be opened? On my chest? On my neck?  On my back? Right now the water ball is in the mouth, inside.

      Doctor Rx some sackings. Have no one idea what is it. I did not have the chance to get it. Really, it is so interesting. If doctor Rx some medicine and patient have snake around where this medicine is, how effective this treatment can be? Remember, as diabetic type 2 I have to do work outs. Then more then better. So, one after another I do have Rx to the medicine I cannot buy or I cannot find.  Doctor hate me, I do not follow his order.
       Really it is so simple to ask, do I like doctor? But no one ever asked me, such stupid question. So, before jumping into wagon doctor suggest such as weight loss surgery of surgery on my left leg (really why only left? What about right leg? ) I prefer to wight a little bit longer. So, I canceled appointment with that doctor. Sorry, fish skipped the net.
       Is this good for e? Is this bad for me? I do not know. What I do know, if treatment wrong then there is no reason to expect to have good result.To stay away from wrong treatment is better then to take it. This is my understanding.

via Ravenvoron

Could Big Lifestyle Changes Be Key to Managing Type 2 Diabetes?

Study finds lower blood sugar, reduced need for medication

Source: HealthDay


via Diabetes

Lack of Sleep May Raise Child's Type 2 Diabetes Risk: Study

It found link -- but no proof -- between less slumber and risk factors for blood sugar disease

Source: HealthDay


via Diabetes

Possible Cures In The News (August)

The blog posting is a collection of small updates to existing clinical trials.

The TN20 (Oral Insulin) Phase-II Clinical Trial Completes Enrollment 

TN20 is the name of a specific oral insulin clinical trial, which completed enrollment in March 2017. Since this study will follow people for one year, they should finish collecting data in March 2018.

The following blog post:
http://ift.tt/2vzbwcT
covers oral insulin in detail, describing why people think it might prevent type-1 diabetes, and the other clinical trials (and there are several) currently running.

Clinical Trial Registery: http://ift.tt/2t0XOvE

T-Rex Study Is Half Enrolled

I've previously blogged on the T-Rex study (sometimes under the name "Polyclonal T-Regs"):
http://ift.tt/2vytwUr

It is currently in a phase-II clinical trial, and that trial is now half enrolled (56 people out of 111).

This study is unusual in that it can enroll kids as young as 8, and is recruiting people at over a dozen different sites in the US: http://ift.tt/2wL5aFM

News: http://ift.tt/2tWY5Ei

A quick summary of this treatment is as follows: remove one specific type of T regulator cell (called "CD4(+)CD25(+)CD127(lo)") from a person with type-1 diabetes.  Grow them out so you have about 500 times more, and then put them back in the same person.  Since regulatory T cells naturally regulate the body's immune system, and the patient now has more of them, the hope is that they will prevent the autoimmune attack which causes type-1 diabetes.

Results from the previous phase-I trial found that this treatment preserved beta cells.  C-peptide levels remained constant in the treated group.  Since C-peptide levels drop during the honeymoon period, these treated people did better than untreated people would be expected to do.  The previous phase-I study did not have a control group, but the current phase-II study does.

Results of Phase-I Clinical Trial of REMD-477 for T1D

I probably will not cover this moving forward, because it is more treatment than cure. REMD-477 is a  Glucagon Receptor Antibody.  The hope is that giving this to people with type-1 will cause them to produce less glucagon and therefore use less insulin.   This was a 21 person trial, where half the people got the treatment and half did not.  The people spend a few days in a hospital, and then were followed for a few weeks "in the wild".

They found that glucagon levels did go down (20-30%), insulin requirements did go down (about 10%), and people did spend more time in their target BG range (about 15%), for a few weeks after treatment.

Slides: http://ift.tt/2wLbRHY
Several Press Releases: http://ift.tt/2vz8bdB
Clinical Trial Registry: http://ift.tt/2vz5Tv8

They have started a follow up study, which will enroll 75 people and last 24 weeks.  They hope to finish it in Sept-2018: http://ift.tt/2wL5bcO

I suspect that any treatment which lowers glucagon levels is going to have some impact on people who play sports, and anyone who has an unexpected low (especially if they need a Glucagon injection, but even if not).  This study did not address either of those issues, but I suspect that follow on studies will need to, if they want FDA approval for this as a treatment for type-1 diabetes.

Diamyd Unsuccessful in Phase-II Clinical Trial on Presymptomatics 

This study is another testament to the optimism of researchers.  Diamyd ("GAD Vaccine") has been tested for over 10 years.  None of these trials has been particularly successful.  They culminated in an unsuccessful Phase-III trial years ago.  You can read my previous blogging on Diamyd here:
http://ift.tt/2klYwzs

However, researchers are natural optimists.  And it is important that they are.  Society needs optimistic researchers so that they will repeatedly attack problems, and not give up, even in the face of adversity.  Previous Diamyd trials had been done on honeymooners, so this trial was done on presymptomatics. Unfortunately it failed.

News Coverage: http://ift.tt/2vz6oW6
Press Release: http://ift.tt/2rMAMb0
Clinical Trial Registry: http://ift.tt/2vpJI90

Discussion

This trial reminded me that, in the world of type-1 diabetes, if the headline reads "new treatment shown safe" that really means "new treatment is not effective".  Almost all clinical trials aimed at type-1 diabetes measure both safety and effectiveness. This is especially true of phase-II trials, like this one, and phase-III trials. Since effectiveness data is obviously more news worthy than safety data, if the headline talks about safety, that means the treatment was ineffective.

The headline for the press release above is classic that way "Autoantigen GAD-Vaccine is Safe for Children at High Risk for Developing Type 1 Diabetes", while the headline for the news coverage is much more accurate "ADA: Alum-GAD (Diamyd) Vaccine Fails to Prevent Type 1 Diabetes".

Joshua Levy
http://ift.tt/29DuN3o
publicjoshualevy at gmail dot com
All the views expressed here are those of Joshua Levy, and nothing here is official JDRF or JDCA news, views, policies or opinions. My daughter has type-1 diabetes and participates in clinical trials, which might be discussed here. My blog contains a more complete non-conflict of interest statement. Thanks to everyone who helps with the blog.


via Cure Research

Diabetes Makes Me Do That Thing Where I'm Always Checking

So..... checking as it relates to diabetes - does it drive you batty and please tell me I'm not the only one!

Do you have any tips? 

If so, please feel free to share - diabetesalicious minds want know!

Also, I apologize in advance for the ridiculous amount of times I use the words "checking," and "check." 

########

Diabetes makes me do that thing where I’m always checking. 

Checking to see if I have enough insulin and other meds; checking to see if I have my pump attached to my person before I walk out the door, and now checking to see if I have my PDM because I’m currently podding. 

Checking to see if I have enough test strips on my person and in my stash. 

Checking to see if I have enough pump supplies. 

Checking to see if I have enough juice; juice boxes, glucose tabs, and regular food in my house. 

Checking to make sure I have glucose tabs, or other low treats in my car.

Checking out the latest diabetes related studies, news, and the likes there of. 

Checking for little signs of diabetes burnout before they become big signs.

Then there’s the paper work required for all of the above, checking to see if my insurance not only covers certain med/supply, etc.,making sure RXs are up to date, doctors appointments are scheduled. 

Then there are things I shouldn't even have to check for, but must -  because someone else didn't do their job. Case in point - making sure my insurance company covers the right copay. 

Since I switched up my plan on March 1, my insurance company has charged me my old 60/40 co-pay for two different prescriptions instead of my current 80/20 co-pay. 

That's a big damn difference.

Guess who was the one to figure it out? 

Guess who was the one who spent two hours on the phone trying to fix it the first time and hour on the phone the second time making sure it was fixed? 

But back to checking. 

Checking blood sugars, checking for ketones, checking to make sure I have extra everything before I go out the door and start my day. 

.

Most days it doesn’t bother me because the checking has become second nature and I've figured a way to streamline my prep check. 

I have a cool looking (and slightly bigger than my 6+ iPhone when in it’s otterbox,)size brightly colored/insulated bag I use for my diabetes.

I keep my PDM; meter (which I don’t bring now, because I can check my blood sugar via the PDM,) test strips, pump/pod supplies, K-Tape, insulin, backup batteries. 

But even with streamlining, there are still some days when diabetes and checking throws me for a loop - like if my blood sugars are wonky, or if I’ve run out of test strips, or left something D related on the counter.... at home....or at the restaurant I've just left. 

When that happens, I feel like I also forgot to check for my sanity before I left the house, because I clearly feel like it's missing. 

And on those days when I feel as if I’ve checked for my sanity a million times and can’t locate it to save my life - I’m glad I have the Diabetes Online Community, DSMA, and my diabetes peeps.

“Checking out,” and taking a few minutes to read a blog post, chat on twitter, or text with a D friend - that makes all the difference. 

That right there is the best medicine - and I thank you guys for it.   

via Diabetesaliciousness

Day-by-Day. August 9, 2017

Depression. I watch one video after another, do nothing more, just sit and look at the monitor. There are no one reason to be sad or unhappy. All is good, at least not so bad. But I am Blue and in very bad mood day after day.
    Not the same problem which bring me to ED in March 2017 started to spread over my left hand. I do not know what medicine to use to find the cure. My middle finger getting darker and darker with every day, and it is in pain. Two other fingers also effected, and infection spreads all over the hand.
     I do not see to what doctor to go. My primary does not want to give any appointment to me. He is never for me. He will Rx all Junk, but never medicine which will work, at least possible to work. Now I really very doubt if he is really able to be a doctor any type but money machine only. With so high resistance to do the job he finally simple not able to do what he was trained to do.
      Well, I can take another doctor, right? Say me, which one? I read all medical publications which widely published in medical e-journals. I also do have very good medical library. What the cure or treatment suggested to any one of us when we visit medical clinic? That's right, life style modifications, diets, work outs. And I lot of Junk medicine which kill heart and finally every one of us. Say me, how Invokana can cure diabetes type 2? Very simple. There is no definition of diabetes type 2, no diagnostic what is it and what mark of this condition. Take a looks at the definition, diabetes type 2, what is it? It is wide middle area. It is Metabolic Syndrome. It is high blood sugar level. It is high cholesterol. And so so on. I am really sick of all those crap.
      But I cannot stay out of this industry. I was born diabetic. Not type 1, nether type 2, just diabetic, person with unhealthy pancreas. Regardless of any size of middle area, pancreas does not became healthy. It is still getting worse with age and time. But no one see or even take a look at the problem. If I am ill or sick, it is all my fault. Period. Regardless the size of my body, or the ability of my brain to work out, I still abused and accused in wrong doing.
      Why really I do not even try to get another doctor? I cannot. I bounded to my primary. At least in this faculty I still have Rx to Insulin, so I can live. I live in pain, but I cannot take painkillers. Now I am allergic to many medicine. In hospital there was band on my arm, allergy on diuretics and metformin. So, my primary stopped insulin and Rx Diuretic and Metformin to me.
      It is also very interesting point. Every time diabetics type 1 pretend that if they skip even one dose of insulin they can possible die. True? False. Scam. Crap. Show me one diabetic who died when one skipped insulin injection. Also say me how many diabetics type 1 or type 2 who take insulin injections skipped injections? Every one. Not once, but many times. Simple, every one can forget to inject insulin on time, have to place to take injection, or simple has no insulin to inject.
       There is another point about insulin injection. It is dose of insulin. There is nothing about amount of shots, but all about dose of injected insulin. So, the claim that diabetic type 1 can die when he skipped insulin injection simple crap, scam.
      There are almost 100 yeas after insulin discovery. What now new in diabetes treatment?  Life style modifications. Diet as it was 100 years ago when only one option was available tot to safe life but prolong it. Today diabetics can live practically as most non diabetics with insulin injections. Many would be able to recovery. With time diabetes would be no longer danger and fatal. But it is only possible when diabetics would be treated not according to Medical Care Greed, but with proper medicine, respect, and recognition.
     Sorry, this time will come, I strongly believe in the future. But it is not for many of us. Our  time would be cut short. We live in corrupted society, under pressure of money which can buy all, Death including. Not even think, I posted it wrong that money can buy life. Not for us. Money paid for our Deaths. This is the problem for every one of us under slope of High Everest.

via Ravenvoron

Diabetes And Changing Things Up~

I’m a go with the flow kind of gal, except of course when I’m not. 

I love new experiences, meeting new people, and exploring new places. 

But I’m not great with big life changes - even when they're good - and I know that about myself - It’s one of the things I struggle with and I know it holds me back. 

I have no idea why I struggle with life changes so much - but I’m pissed that I do and I’m actively working on fixing this issue - and some others. 

I liken how I embrace life changes to my love of swimming in the ocean - Seriously, it’s like one of my favorite things in the world to do! I love swimming, surfing, body surfing waves, and embracing my inner dolphin.

 I’ve been going out over my head since I was a kid  - jumping off a boat and learning to swam towards Lucy the Elephant at the age of 4. I bought my first surfboard at 25, There was a time I'd take a wave runner out on a 40 mile ocean jaunt no problem - and to this day I swim in the ocean until I start to turn blue. 

But as I grew up, I want from diving in the ocean without thinking... to easing my way in, jumping and dodging waves through the shallow water, cursing the cold waves as they hit my body and splashed my face - until I was finally ready to dive in and take the plunge. 

FTR, I knew in my heart and head that if I would just take the plunge and dunk my head under the waves, the water would immediately feel warmer - but I still don't. 

I ease my way in - It takes me a good 5 minutes to dive under my first wave  - and then I’m home free, feeling groovy, and riding waves until I'm too tired to continue. 

Which brings me diabetes - after years of wearing an insulin pump with an expired warranty and using the same brand glucose meter for most of the time, I knew it was well past time to make some changes in my diabetes tech management. 

It’s not like I didn’t want to - I totally did. But my old insurance deductible was super high (and my co-pay, not what I would call generous,) and don’t even get me started on commitment issues re: warranties. 

But enough was enough, I was well overdue and I knew I needed updated diabetes technology in order to not only stay healthy, but to utilize the elixir of life we call insulin. And I was THIS CLOSE to meeting my deductible - it was the perfect time to switch things up. 

Sidebar: I’ve been dealing with abdomen scar tissue issues for quite some time - problematic on all fronts - not only absorption issues, but I was literally having to change my infusion site every 24 to 34 hours, instead of every three days because of absorption issues - and that gets freaking expensive. 

I tried my legs and that would work slightly longer, but I could never navigate my arms (tubing issues,) or my back (contortion issues). 

I spent an inordinate amount of time on the phone battling my insurance company to pay for extra boxes on infusion sites, my daily 24 hour insulin insulin consumption kept creeping up, as did my frustration levels. 

I seriously considered taking an extended pump vacation, but after having a heart-to-heart with my fabulous Endo Dr. J, and we both felt that Insulet's OmniPod would most likely be the best solution for me. 

I could give my abdomen a much needed and extended break from infusion sites, while trying out other sites on my body. Plus, I'd have 45 days to see if the switch was working for me

After talking with the some folks at the Insulet/Omnipod booth at the Children With Diabetes, Friends For Life Conference, the paper work was set in motion, my insurance company approved my switch from 15 years on Medtronic, to Omnipod (and paid for a nice portion of it,) and from LifeScan test strips to FreeStyle - no problem. 

Two big diabetes changes for me in a relatively short time.

Beginning with a convo at my Endo's office on June 5th, followed by a convo in Orlando this past July at CWD,FFL, and officially kicking-off on July 31st, at 3 pm, eastern standard time - when I inserted my first OmniPod. 

How's going?? 

My next post is all about my first 10 full days podding - stay tuned!!

via Diabetesaliciousness

Heart Health Ignored by Many With Type 2 Diabetes, Really? August 9, 2017

Taking steps to prevent heart disease is crucial for people with type 2 diabetes. But most diabetic adults in the United States aren't meeting recommended guidelines, health officials say.
 http://ift.tt/2uoqi7n

Well, to see if this is true let us take a look at the recommendations, how to prevent heart disease if one is diabetic type 2.

 Drugs such as cholesterol-lowering statins, aspirin and blood sugar-lowering medications plus lifestyle approaches should be considered for all type 2 diabetes patients, according to the Aug. 7 report in the Journal of the American College of Cardiology.

       Interesting point. One is diagnosed with  diabetes type 2, and now what? Blood sugar lowering medication the first step to address to diabetes type 2, or any other types of diabetes. So, one does not have medicine to control blood sugar? Or there is another problem, medicine such as SU, Metformin, Invokana, and all other Junk Medicine still do not control blood sugar level, right? If so then say me, how diabetics type 2 adult in America can prevent heart disease? With time pancreas getting weaker, secret less insulin, so more and more complications of diabetes type 2 developed by diabetic type 2.
      As I posted before, diabetes type 2 is not high blood sugar but it is disease of pancreas. If this problem would be addressed and pancreas would be under treatment which is effective and appropriate, then sugar level in blood would go under control without any medicine to lower it. The same as it is with any infection, or many other health conditions. But instead to treat disease our medical industry treat people with abuse that we are ill because of we do not live in healthy way.
      Say me, why it is important to take aspirin? Because of aspirin make blood more fluid. Otherwise diabetic's type 2 blood clotting. 75 mg of aspirin can work for a while, but not for long. The dose going up and up. This is why there is no Rx for aspirin. WE have to buy it, because of no one MD will Rx blood thinners to diabetic type 2 when we do have high A1c. We left outside of medical care. Of cause we can have Rx and visits to clinic, why not. What we never do have is treatment we need. In this condition any treatment can be complicated. We are just too far away from healthy path.
       Really, time to change Life-style to Afterlife-style.

Suggested lifestyle approaches include exercise, good nutrition and weight management.

       Sure, why not. Just do not forget how many of us lost legs at this time.  Do remember, please, that before MI and stroke happened we already do have heart disease. Also do remember, at the time we get into Strip Department to donate our organs, we already did have many silent strokes and heart attacks, usually never in our records. Just trust me, it is not possible to take Marathon training without legs and heart disease.

About one-third of Americans may have type 2 diabetes by 2050, the U.S. Centers for Disease Control and Prevention predicts. This means diabetic patients will make up a growing segment of heart disease patients.      

        If so then why today it is so important to 'prevent' heart disease or diabetes type 2, but there is no any guidance how to diagnose diabetes type 2 and how to treat it? As I just said, diabetes type 2 must not be diagnosed according to the level of sugar in blood. It is the same as no one will diagnose pneumonia according to body temperature. No one test treatment effectiveness according to the body temperature. But diabetes type 2 is only about blood sugar lowering medicine, why?
      High Profit!!!!!!!!!!!!!!!!!!!!
       There is nothing more important in America then high profit. So, why do not keep it as it is and let every one out of three Americans carry on diabetes type 2 and provide highly profitable industry to effect our lives. All supported work already done. Today every one do know very well that diabetes type 2 can be prevented with life style modifications. Also it is in high progress and now every one American out of ten is diabetic type 2. We carry on in our sweet blood millions to amputate our legs and arms due to poor circulation; blood sugar lowering Junk Medicine to keep life stock in high amount; painkillers are in high demand, and it is diabetics type 2 who need them in great amounts; and so so on. Also it take about ten years to collect money. Pretty good for any business to have customer so loyal to industry.
       The question is, does this publication is really 'true'? Not at all.
     Go to Amazon, how many books on sale to teach population how to prevent diabetes type 2 in Natural Way? Countless.
     What Dr. Oz suggest? How to reverse diabetes type 2 just withing 11 days.
      What about professor Taylor? He is celebrity who developed Diabetes type 2 Cure, according to American Diabetes Association. He 'cured' 11 diabetics type 2, how he present, but there is no one evidence how do they doing now. "But they still eating!" - professor Taylor cry out so disappointing! Good for them. At least they are alive.
     So, say me, is this really true that people do nothing to 'prevent' diabetes type 2 or heart disease? Is so then no one would pay for this scam, go to Dr.Oz show, or buy shakes professor Taylor present as "Cure".

Heart Health Ignored by Many With Type 2 Diabetes

New evidence review reconfirms patient guidelines

By Robert Preidt

Tuesday, August 8, 2017 
 http://ift.tt/2uoqi7n

via Ravenvoron