So I was diagnosed. Dr. W put me on a low dose gluecophage. I was instruct to take one pill at breakfast along with my fasting blood sugar (BG) and one at dinner along with my BG two hours after I eat. I was surprised to find that the feeling in my arm came back after a day or so. But I was still tired, still fatigued, and still thirsty. I was hoping for overnight success. To be cured by a single a pill was my hope. But that wasn't the case. Dr. W told me that if my sugars ever get over 500 that I need to call her right away. Since being diagnosed my sugars always ran between 300-400. From what I have read and from what people told me I should try and eat between 30-35 carbs. I found that easy. But I was always hungry! Cardboard even seems appealing to me. I thought that eating carbs or eating food would drive my sugar up and I didn't want it to get any higher. I was eating like a bird and my numbers were going up.
One day I drove down state to my co-workers house (about 2 hours from where I lived) and when my son and I got to her house I wasn't feeling good. Soon as I got there I thought I should check my sugar just to see where I am at. It was 579! That was one hour after I ate a grilled chicken sandwich with extra lettuce minus half the bun. My son had a happy meal and I was chugging down the water. I just wanted to cry. I thought I ate healthy and I am doing everything right...why is my sugar still going up. So I called my family to let know where I was and what was going on. Cue my mom who started bawling and my very frequent phone calls from my dad. I promised that Iwould not drive home with my son until my sugars where much lower.
In the meantime I talked my dr's PA. She instructed me to take two pills with dinner and to eat all protein that night. Thank goodness for my co-worker Missy who also happens to be diabetic. That night we went for Chinese and she told me the secret to eating out is to fill up on salad first and then to get your meal. Frankly after my salad I was full....but I did have to get my protein in. 2 hours after dinner my sugar was in the upper 200s! I was feeling better...not so shaky...but man was I tired.
A few days letter I met with the PA. Her name was Charlotte and she was so wonderful! I was a crying buffoon. I don't cry at home, or when I talk to my family about my situation, or when I talk to my co-workers. But the moment I step into a drs office I turn into the hoover dam and the flood gates just open and the flood starts. She said I was doing everything that I was suppose to but my body needed more help and she started me on 16 units of Lantus Solo Star. I didn't want to be on insulin cause I didn't want to poke myself with needles for the rest of my life. However, feeling the way I was I wanted to get back to normal. I was instructed that every three days I need to get my fasting average. If that average is above 100 then I need to increase my two units. Then my poopaphage was changed to something more stronger. I started taking 2000mg of Metformin.
The first two days I felt better. The shots were a breeze. I found it less painful and much easier than pricking my finger. That job beloved to my son. He loved being the one, "to poke momma's sugar". He is such a good boy. He knows mommy can't eat sugar and he begs me all the time to let him poke me. Hahhaha. Feeling better only lasted over the weekend. It didn't seem to touch my BG numbers. I met with Charlotte again two weeks later and at that time I was up to 24 units of insulin and I was still feeling tired. Charlotte upped me to 34 units of insulin and had the diabetes clinic at my hospital get in touch with me to start classes.
Fast forward to that following weekend. I had just arrived to work (at 6:30pm) and I felt that awful feeling I felt when I was Missy's house. So I took my BG and it was 525. I had the hospital operator page Dr. N for me and she instructed me to go right to ER since I was already there. Nothing was really done other than the fact that Dr. N told my ER dr to up my Lantus to 40 units for the next day. I was discharged and punched back into work. That was the worst weekend that I have ever worked. I was tired, had a massive headache, and my muscles were so weak I had tremendous difficulty lifting and moving my patients.
That week I started my orientation for my classes. The women at the center were great. They were comforting, supportive, and shocked at my BG numbers. I learned that I wasn't eating enough carbs. I was told that I need to keep my carbs between 40-50 carbs at each meal. I learned more about the diabetic exchange and lets not forget that the hoover dam exploded again. It is so humiliating when I loose control of my emotions in front of people I just met. Why does this always happen at dr appointments?
That night I increased my carbs and I was skeptical. No matter what I put in my mouth my levels always shot up. How could eating more lower my numbers? Surprisingly they knew what they were talking about! My numbers didn't go down but they didn't go sky high like they normally did. Few days later I went back to Dr. N for a check up and she decided that I am insulin resistant and thinks that I am a type 1 diabetic and not a type 2 diabetic. Dr. N then increased my insulin to 50 units and gave me novolog to take at each meal. New rules for my units: If my fasting average is above 100 then every three days I need to increase my Lantus by 8 units. My novolog units range from 10-6 units depending what my sugars are like before I eat.
I have been on novolog for almost a week now and at first I was feeling amazing! My energy levels went up, my headaches got smaller, my muscles feel stronger and my appetite got better. However there still isn't much impact on my BG numbers. I am still in the high 200's-300's. I have just had some labs done to see what my GAD is. I have an appointment with an endocrinologist and there is talk between my dr, PA, and councilors that I may be looking at going on the insulin pump.
Let me just say that the unknown terrifies me. To me the pump seems like a desperate attempt to control my BG levels. I feel like a failure. I feel like I am doing everything I am told to do and nothing is in my control. I DO NOT want diabetes to control my life...I want to be in control of my diabetes. I have made a promise to myself that I will do everything I can to get healthy and maintain that health. I want to set a good example for my son and my husband. I do not want the complications of this disease. Perhaps that is why I cry like a baby in the drs office cause I am scared of what COULD happen if my levels are not controlled. I am angry and frustrated and scared. No matter what I read and what people tell me I still feel like I brought this on myself.
I want to meet other people who are just like me. I know there are people out there. I want to get involved with the local diabetes center and do any kind of activity they offer. I wanna educate myself better and those around me. I know I have a LONG journey ahead of me and everyone says that it will take a while for things to get normal. I want a fast result and I know that won't happen. So it is all one day at time.