I commend that badrirag wants to have tight control, and not be on medications any more. It is a BIG goal to set for oneself, as a diabetic that many of us have struggled greatly to achieve, at all odds, and against the “better judgment” of our doctors offering us medications and diets much higher in carbohydrates. A life of tight control is a desirable life, eliminating likelihood of complications, and extending our lives.
Now, there are many reasons why it is important that we understand that “tight control” is not a cure, and it is not merely semantics. One of those reasons is that the media seldom talks about how type 2 diabetes, is indeed, a progressive illness. How fast, and how degenerative it is, is a very individual and genetic thing… (not a mental thing). It IS a degenerative illness. What does that mean, exactly? It basically means that the cells within our pancreas that produce insulin (beta cells) are slowly dying. All we do with a lowered carbohydrate diet, meditation, and exercise, is slow down this dying progress. However, there comes a time when that deterioration is enough that we no longer can do “tight control” by ourselves, and we all will need medications or insulin. It is a fact of a diabetic life. It is unavoidable.
Calling “tight control” a cure causes many problems:
- It creates a sense of failure for the patient who was told all he had to do was eat right, and exercise, and control their stress levels (or even meditate), when they can no longer control their own bodies and they have to get on medications or on insulin;
- It creates an unsupportive, uneducated public who does not understand that this is not the patient’s fault. Often, persons who do not understand that this is a life long, chronic illness, lay a lot of blame on the patient, bullying the patient about their diet, weight, exercise, etc… and suggesting if the patient “did enough things,” they would be cured, but they are not because they don’t wan’t to. This, as before, creates a sense of depression and failure, for the patient;
- It damages our ability to raise funds to research better treatments and a true cure, whatever those are. (And believe me, scientists are not just researching pills, and chemicals. They are researching everything there is, from injecting insulin into lettuce leaves, to transplanting new beta cells into mice, to transplanting fecal matter from patients.) When the general public does not understand and know that diabetes has no cure, because they believe people could just diet and exercise and meditate into a cure, then they do not donate money to our campaigns, and sometimes huge fund raising dollars go unearned because of these myths. Laws from Congress do not get enacted because no one truly understands the magnitude of this problem, and leave the responsibility just up to the patient.
Right now, the only cure for diabetes is an informed patient. A patient who knows and understands to do all they can to remain with as non-diabetic blood sugar numbers as possible, but who also understands that when that is not physically possible to manage on their own, that it is NOT a failure to take medications or insulin; a patient who understands that one day, we all want a cure, and not a cure just so that we can eat junk… but a cure so that we can enjoy eating the things that we love again, like any person without Diabetes. A cure so that we don’t have to suffer the consequences of complications, which many times are NOT dependent on one’s tight control or blood sugar levels, and are often times genetically pre-disposed. There are many reasons why the understanding of a true cure is important, and not just “tight control.” We do the world a disservice by allowing them to believe that the two are one and the same. No one in this forum is not wanting to have tight control… We ALL fight hard, and sacrifice a lot, for tight control. You can learn much from many of us. What we do not want is to call those things a cure. Diet, Exercise, and Meditation (with no medications) is no more a cure for Diabetes than injecting insulin. We desire for our community to know and understand the difference, and to be empowered about their condition.