This patient support community is for questions related to juvenile diabetes including celiac disease, depression, diabetic complications, hyperglycemia / diabetic keto-acidosis, hypoglycemia, islet cell transplantation, nutritional issues, parenting a diabetic child, pregnancy, pump therapy, school issues, and teens with diabetes.
Please post again and let us know how you're doing. I will be praying for you.
While I'm complaining why I'm so unfortunate, I should think that I'm already better than most of the patients with the same disease as I have a relatively late onset (I'm 22 now) I'm also cared by almost the best endocrinologists in Hong Kong who are working in a teaching hospital. But I would say that being a type 1 patient in the US should be easier as the endocrinologists have more experience.
I guess all of you have your medical expenses covered by insurance companies? In Hong Kong people seldom buy medical insurance as most of the services are provided by the public system, but this is going to change and the patients will eventually need to pay for the services themselves. I don't know what will happen to me in the future, as I didn't buy any insurance, but there are too many things to worry anyway.
I always think that it's harder for me to accept the diagnosis than lay people as I know too much about the complications. Take retinopathy as an example, a lay person will only get concerned if the vision is affected, but the doctor (or I myself) will get concerned if there're early sings of retinopathy (like background, non-proliferative etc. if it involves the macula it's called maculopathy). And the figures tell me that 100% of type 1 patients will get retinopathy within 20 years after diagnosis of DM (but doesn't count the years before puberty), sometimes retinopathy can be quite independent of glucose control, there are still people who have been controlling well but still have severe retinopathy. Doctors won't tell lay people about these, as this is too discouraging. Being a patient and a patient only has the advantage that you can only hear what you need to hear and what is encouraging, but I'm different, I need to hear facts for the doctors as well (which are not for patients as they are too bad for that)
Perhaps it's because of the lack of exposure to type 1 diabetic patients, that you haven't seen the odds beaten time and time again. Yes, we are not medical professionals, but we have heard hundreds of personal stories from people who have lived with diabetes and not experienced the side effects that you are so afraid of. Yes, it is a very frightening disease to have, but once you get your blood sugars within a normal range, you may see things more clearly and realize that you too can avoid them with good blood glucose control. If you are running low all the time, you might not be thinking clearly. Being a medical professional, you know all you need to know about the best way to prevent the side effects of this disease. Take this knowledge and use it to take the very best care of yourself that you can. Don't be frozen in your fear, take your knowledge and do something positive with it, for yourself and others.
At first, it's so very difficult to accept diabetes into your life, but in time, you will feel differently. You need to face the emotional side of diabetes. It may be more difficult in your culture than in ours to do this, so please, come back to our site to let us know how you are doing and feel free to ask any question or comment you may have. We are here for you!
God Bless You!
But - you read too much into it as well. The complications you speak of, normally are associated with people who don't take care of themselves or are too lazy to take care of themselves - pure and simple. And many of those people are Type 2s.
I gave up blaming God a long time ago - if there is one. Neither God nor Allah have anything to do with this. And if they are there - it looks like they are not too interested in lending a hand because there are so many of us and our numbers only grow with each passing year.
I would highly suggest you get an Insulin Pump as quickly as possible. There are people who will tell you to wait until your honeymoon period is over - forget them. At least with a pump, it may be possible to give your Pancreas a break and not burn out the remaining insulin producing cells you still have. It'll mean lower basal doses of insulin and give you more freedom that you'll never get with just needle injections.
However - the pump has its own set of issues the pump makers don't advertise because people wouldn't want to use the pumps then. But - it does make life easier somewhat. And injecting an infusion set once every 3 days sure beats having to stick yourself with a needle before every meal or hoping someone doesn't bump your chair while you inject yourself.
I wouldn't hold my breath for beta cell transplants or