How Valuable is


How can the value of a site like be quantified? Is it’s value based on the number of members or page hits? How about daily posts or advertising revenue? Cool features, maybe? No, I think the best way to quantify the value of is through a personal story, one that probably reflects the experience of many people.

I lived in a small rural town when I was diagnosed T1 in 1976. I don’t think the family GP had ever even seen a T1, but fortunately he recognized the symptoms enough to send me to a specialists in Seattle (about 3 hours away). I spent 2 weeks with my Mother in Seattle getting educated in Diabetes and set-up on a regime of insulin, urine tests, and carefully measured quantities of food. Then I was sent home, with scheduled quarterly check-ups back in Seattle.

As a 15 year-old, this was completely foreign to me, but I quickly adjusted. I knew that I only had 1 body and abusing it (by skipping insulin or engorging in sugar) simply wasn’t an option. But I was completely alone in the world of Diabetes. There were no support groups in town, no on-line forums where I could interact with other T1’s, no books that explained things at my level of understanding, and as far as I knew not even another T1 (of any age, let alone a peer) within 100 miles. Yes, Diabetes was a life demon that I had to face alone.

None of my friends really understood or could relate to my situation. They knew I couldn’t drink sugared soda or candy (except for certain times, which they never quite understood), but that was about it. I spent my high school years watching others enjoy the freedom of eating and drinking whatever they wanted, while I repeatedly had to decline offers of tantalizing treats.

Don’t get me wrong, life has always been enjoyable to me, but being a T1 without any contact with other T1’s can be a major bummer.

In my first 10 - 12 years as a T1, I’d occasionally be told that so and so knew someone who also had Diabetes. But I suspect many of those “so and so’s” were Type-2’s. I never had any interaction with them anyways, so it doesn’t really matter. The first other T1 I met (other than the strangers I spent 2 weeks with at my initial Diabetes training) was in my late 20’s. She and her husband were casual friends of my wife and I, but nonetheless I actually knew another T1 and she was close to my age. We never had any significant conversations about Diabetes (I suspect because neither of us ever had), but just knowing each other was beneficial. Then I found out a co-workers teen-aged son had T1 and I was able to talk with my co-worker on several occasions about the disease. I think it helped us both.

Over the years, I’ve visited a couple local support group meeting for Diabetics, but in the smaller towns where I’ve resided they’ve always consisted of just a couple much older people with T2 and very different concerns than I had.

As a techy, I’ve used the Internet for years as a research tool and system for business/personal communications. But using it as a resource for my Diabetes is only a recent discovery. Last year I discovered an on-line Diabetes group (which shall remain nameless, so as not to compete with where I could ask questions of other Diabetics. Through that group I became convinced to get an Insulin pump and learned all the cool tricks that no CDE or Endo could possibly teach. Through another group I became convinced to get a CGMS and learned the tricks of that too. Not only is my control significantly better than it was a few years ago, but I now feel like I know and have direct access to numerous other Diabetics. These Diabetics may live more than 100 miles away, but they are only a few seconds away in reality.

Somewhere along the way of asking and answering questions related to
Diabetes on the Internet, I discovered that Diabetes doesn’t have to be a demon we
fight alone. It’s now a shared battle. As Solomon once wrote:

"Though one may be overpowered,
two can defend themselves.
A cord of three strands is not quickly broken."

How valuable is (and other similar forums)? It’s priceless. Thanks Manny.


Well written Ken. This is a very powerful tool (Thank You Manny!!! :)). I think many people can relate to where you came from. I was diagnosed close to 10 years later than you. There still wasn’t any social support, the information and tools were improving from what they were in the 70’s. They were still “lean” though and most other people and doctors didn’t seem to understand anything about T1/IDDM/Juvenile Diabetes (the term that was popular when I was diagnosed). Thank goodness, now when we have concerns we can type them out and know that the people reading them and giving advice back actually understand because they are “there” too.


I second what Alice has already said. I was dx’d 5 years earlier than you and, even though I was in a big city (DC), much of what you said was true for me as well. I remember sitting in a high school biology class (a subject I loved) and listening with horror as the teacher told us that we needed to eat better diets, because it was the sugar we were over-indulging in that caused people to get diabetes. I wanted to disappear, especially since the same teacher had earlier in the year announced to everyone that I was diabetic (she thought that they could “help” me by knowing). I have spent the last 25 years living in communities where T1’s are essentially screened out (military communities overseas), and even the doctors assume I am T2 (they always compliment me on my ability to keep my weight down). TuDiabetes has allowed me to “meet” a wide variety of all types of diabetics and to “hear” other opinions and advice on how to tackle problems that many of us share.

I look forward to you being part of this network!


Well said! I totally agree…this forum is priceless. And BTW, if you are ever in Taiwan again like you mentioned, you should let me know. Perhaps we could meet up. Kaoshiung is not that far from Taipei. Feel free to email me at if you are comin’ this way!