62 Years of Type 1.............CHAPTER 16


In 2002 I was in very good shape physically and mentally. I had my A1c under 6.0 and my blood sugar control was the best I had ever seen. I was enjoying part time teaching and flying twice each year to Atlanta to see my sons, daughter-in-law and grandchildren. I had a temporary setback with prostate cancer in 2003 but recovered nicely after the radiation treatment and two years of side effects. I kept up my exercises as well as possible after radiation treatment and I dieted and counted my carbs and kept very careful charts of my diet and control. In late 2004 I felt great. I had lost 26 pounds and had very good control. Cutting down on my daily carb intake and exercising rigorously on my tread mill enabled me to lose that weight. My A1c’s remained below 6.0. I taught my last class at the college that year. I felt strong and fit and I was like a fish out of water.

I did a lot of work on my house to keep myself occupied. I painted the whole house, inside and out, replaced some interior doors, remodeled the master bedroom and built a home entertainment center in my oldest son’s former bedroom. That is where I sit to type these chapters and post and talk to my friends. By 2006 I had finished my construction work and I was bored again. That is when I started posting on the dLife website. Janis Roszler, the moderator there, is a CDE and a RD and she teaches people all about pumping. She told me, online, that I should consider pumping even though I had good control with injections. Several friends on dLife started encouraging me as well. I liked the idea of only one needle every three days instead of 6-8 daily injections like I was doing then. I liked the freedom and convenience that a pump provides. I wanted to pump so I asked Dr. B. and he said it was not a good idea. He thought it was unnecessary since I already had good control. He told me that several of his diabetic patients had worse control after starting to pump and they had more hypos as well. He would not support me with pumping.

I called an endocrinologist in Poughkeepsie and made an appoitment for Jan. 30, 2007. That was about the time that I had left dLife and joined Diabetes Daily (DD). I made friends there and they too encouraged me to pump and get still better control. The endo approved of my pumping and sent me to get some blood tests required by Medicare. Something about the lab results did not meet the approval of Medicare and they would not finance my pump. I was so disappointed and thought that I would never pump. The pump itself would cost me $6,000+ and the monthly supplies were also too expensive for my budget. The endo’s office phoned me the following week and told me that my secondary insurance would cover the cost of the pump and all of the supplies. I was thrilled! The NY State Empire Plan is my secondary health insurance plan. All employees of the state are eligible to have that insurance. While I was employed the college paid all my premiums and the coverage was for my whole family. After retirement the college pays half of my premiums for as long as I live and we pay the other half. It is a great insurance plan.

The lady from the endo’s office asked me to pick a color for my pump and the order was sent out. I went to the diabetes education center at a hospital in Poughkeepsie and met my trainer and a dietitian. They gave me a kit containing a manual and a CD and told me to become thoroughly familiar with the Minimed 522 pump befor the pump they had ordered arrived at my home. I had also ordered the book “Pumping Insulin” by John Walsh. It was highly recommended by my friends on the DD website. My friends on DD and on Janis Roszler’s site were all cheering me on. The pump arrived in late April and I had one week to have a hands-on experience with it. I started pump training in early May. It went very smoothly but my trainer was old-fashioned and wanted to take it very slowly. She was very sweet and we liked her very much but four different trips for training was not necessary. We made a separate trip to talk with the dietitian about carb counting. The charts I took with me convinced the dietitian that I knew all that I needed to know to start pumping. Another wasted trip. It was all worth it though. I had to cooperate with my endo who insisted on all this training. Her office was in the same building as the diabetes education center. They all work together.

In the last week of May I was pumping saline solution just for practice. That solution put too much salt into my body and I had a lot of water retention. I already took water pills for water retrention. I called my trainer and she said to stop pumping saline. I went in on June 19 to be hooked up with my pump. The endo looked at my charts and read off numbers for my trainer to put into my pump. My basal rates, carb ratios, targets, insulin sensetivity factor, and all the rest. I went home full of enthusiasm and was really looking forward to the next few days. Later that day my blood sugar was over 200 and climbing. My endo did not want me to change anything without her approval. I called her that evening at her home. She had given me several phone numbers. She did not seem to know what to tell me. She had me change a couple of things but it did not help. I decided to take over my own control. Before doing so I disconnected the pump and resumed injections for a few days until good control was reestablished. With my math and statistical background, my 61 years of injections and the good control I already had I should be able to do this by myself. I completely changed all the numbers in my program. After a few days I had much better control. Everything was going much better but I started having trouble with the needles in my Quick sets pulling out of my body. Putting my clothes on and off, rolling over in bed and other such things seemed to cause this problem. I started having very high blood sugar whenever this happened. I tested for Keytones every time my test was 250 or higher. I used injections to get myself back under control before reattaching the pump.

I told my friends on DD my problem and I learned about the Sure-T infusion set. It is made very differently and the needle is very unlikely to pull out of my body. I ordered a new supply of the Sure -T’s and have been using them ever since. They are great! My control was much improved and my analysis of my testing from mid July to late August showed control equal to the control I had before pumping. The lab visit I had in the third week of August was only 10 weeks after I had started pumping. I expected the A1c to be very high because of all the high blood sugar I had had during the beginning stages of pumping. I had an A1c of 5.6 before pumping. When I went to Dr. B’s office in late August my Aic was 5.7. I was so surprised. The A1c covers the three month period preceeding the lab date. I had poor control with very high numbers during the last 11 days of June and the first 10 days of July but my control was quite good for the rest of July and all of August. The numbers for the first month of the three month period covered by the A1c are not so influential in the A1c result, the numbers during the second month have a greater influence but it is the numbers during the third month that have by far the greatest influence on the A1c result. My numbers were very good for the last 6 weeks of the period covered by my A1c test and that overshadowed the bad numbers preceeding that 6 week period. That is why my A1c was so good.

I was very happy with pumping at that point. I was able to sleep late in the mornings. I could delay meals. I could vary my eating schedules and eat very different types of meals without affecting my blood sugar. Counting the carbs ever so carefully and pumping the insulin that my pump indicated to be the correct amount was working very well. The very rigid schedule that was necessary while still on injections was no longer necessary. I was unnchained and free to live like a more normal person. I had a machine that worked very much like a pancreas and I was ver proud of my pumping experience.

dear richard, even thou i’m type 2 would i in the future be using the pump. i haven’t heard anyone with type 2 mention about using the pump. i was just wondering, have a great day. patti

Patti, if the combination of shots and meds no longer give you good control at some time in the future then a pump may be recommended. There are many Type 2’s in the USA and elsewhere who pump for this reason. Lloyd, a member of this site, is a prime example. He is Type 2 and has been pumping since March, 2007. Send Lloyd a private message if you want to ask him questions. He is a good friend of mine and he probably has better control than any other diabetic I know.


Hi this is mary ann jacob I am a type 1 diabetic for about 38 yearss now I was diagnosed at age 15 I am currently on5 shots of insulin daily one being Lantus,once in the AM and once in PM and the Humalog pen before meals. Most of my life I have had good control and have no complications just a little problems in my digestive system nerves so God has blessed me with this However, for about a year now I have been exxperiencing hypoglycemic unawareness and it is quite scary and dangerous for me. I am a home daycare provider of 7 children and this hits me out of the blue My Endo and I are working on it but still is the same any advice? what happened? Also Any info n SSA disability for diabetics? I was denied bt social security they say diabetes is not a disability which in part is true but I feel that me along with millins of ther type 1 diabetics should be given at least temp-disability until we get our health problems under control . I am the only adult in the house with the children my husband is always checking on me but sometimes I can not even answer the phone any ideas on getting some help from disability from anyome out there? My husband does not make enough to take care of the family alone so it is necessary there be 2 incomes

Mary Ann, you should enter this post in the Type 1 forum instead of making it a reply to my story. Very few people will see it here. I have no suggestions for you at this time, I am not familiar with the SSA’s policies here. I hope you will find better responses in the main forum. Good luck!