Running; usually I enjoy it, occasionally I wonder why bother… but most of the times I can get myself off the couch and into the great wide open. Since before I had diabetes I already participated in track and field team, and ever since I’ve spent more years running than doing other sports. However the last two years before the insulin allergy treatment were tough. I would often want to go running yet often my sugars would be so inconsistent I either wouldn’t go or would need somebody to accompany me. My dad has been my coach for years and my mom my biggest fan. They were there when I would be soaked from the mud after a cross country run, would accompany me if my sugars were bad, cheer me on if I lacked motivation and picked me up if I couldn’t finish my run.
Continue reading Running with diabetes
14 November 2015: my one year anniversary being insulin-allergy free, World Diabetes Day and the day after the terrorist attacks in Paris. How then, to write a blog post?
Continue reading Blue – White – Red
World diabetes day (November 14th) is the day that diabetes is the center of attention worldwide. It is also the first day of my ‘new’ life with diabetes. Do I feel different? To be honest, not really… yet I know that I will look back at this day for the rest of my life. I can remember the things I did the first couple of days after my diagnosis with diabetes. This day feels a little less drastic then after my diagnosis, but it is still the first day of the rest of my life.
Continue reading World Diabetes Day
Today I was ready for my last vial as I had put in so much effort and time the last two days. However, usually something happens which changes everything again but I was still hoping on getting out today, or at least not to have dinner in the hospital!
Continue reading Hospital day 3
I ended up falling into a restless sleep. The boyfriends alarm went off at 06.00 and for some strange reason I couldn’t sleep anymore. I ended up watching some series in bed.
I wasn’t very nervous, there was still a chance I wouldn’t get to start the treatment. If my temperature would be too high I wouldn’t be allowed to start and there could always be an emergent situation causing my bed to be needed by someone else. The wing my bed was on doesn’t have specific beds for the desensitization so if anything would happen my bed would be given up. This is also the reason it takes so long before patients can be treated. The chance that I would get the treatment and it wouldn’t work is also an option. But then at least you can continue, you don’t have to wait on something which may or may not work. For now I am taking a step forward, regardless if it will work or not…
Continue reading Hospital day 1
Last week I have been very busy with forms to request study delay due to medical reasons and trying to figure out how I can improve my situation. The student doctor gave me the advice to call the insurance company and to try and email the doctor which made my allergy diagnosis. Thursday I received a confirmation my email was sent to the doctor.
Continue reading It’s time!
Last Wednesday was October 1st, the date was circled in my agenda. After October 1st I was allowed to call the hospital to ask where I was on the waiting list to get treated for the insulin allergy. This was as exams were coming up and I wanted to know if precautions needed to be taken, and mostly to not drive myself insane by deciding every day if I should call or not.
Continue reading The phone call
Unbelievable, no idea that it was possible but apparently it is… As a person with diabetes you can be allergic to insulin… I am allergic to the adjuvant in long-acting insulin and on top of that I am allergic to humane insulin which is in all types of short-acting insulin. Huh, come again? How is this possible? And how can I be alive, insulin is my lifeline after all!
Continue reading Insulin allergy