Showing posts with label insulin pump. Show all posts
Showing posts with label insulin pump. Show all posts

Thursday, November 14, 2013

World Diabetes Day


It is very very hard to imagine, knowing that your child (relative or friend, adult or child) has Type 1 diabetes and that there is nothing you can do to help save their life because you cannot afford insulin, test strips, a glucometer, let alone the advances of modern technology which we see in the insulin pump, and the soon to arrive, artificial pancreas. They would most certainly die. The cost, even with insurance is costly. Just recently, Edward was presented (yet again) with the idea of the CGM, or the Continuous Glucose Monitor, which sends information to the insulin pump, all in the quest for tighter control of blood sugars. The cost for the new equipment with insurance ( I drive this point home), ran in the thousands of dollars. Would we have signed on? Yes, absolutely, but Edward maintains that he does not want to stick yet another device into his body. The pump requires an infusion site which needs to be changed every 3-4 days, and sometimes it really hurts when he puts it in the side of his body. It is his choice to wear the pump rather than taking multiple shots during the day. The point is, he has a choice. I remember so clearly seeing footage after Katrina hit New Orleans, of a young girl passing out as she slipped away, not having any insulin, and a nurse hollering frantically for some 'Regular Insulin'. They were able to save her life. It can happen quickly. So, all this to say, we acknowledge World Diabetes Day, for all the people, young and old who simply cannot afford or have access to life saving medical supplies. I think now of the Philippines and the many people who are not only suffering because of a natural disaster, but those who may perish because they have no insulin.

We continue to pray for a cure, in whatever shape that takes. Be it the artificial pancreas (another high tech device), one shot of insulin every 6 months or a year, a vaccine, a pill...we'll take it.

I am a diabetes Mom.

Sunday, March 18, 2012

10 Years Ago Today...

Test strips, lancets, glucometer, insulin, Sure-T infusion...diabetic paraphernalia
The butter section of the fridg, holding the latest supply of insulin...
The insulin pump, the Paradigm from Medtronic...a wonder of modern technology...

Edward was diagnosed with Type 1 diabetes. We were in New York visiting Mom and that Sunday morning Edward woke up w/ what we thought was a stomach bug. His breath was 'fruity' and he seemed really uncomfortable. We decided to high tail it out of the City and get back to Providence quickly. He was curled up in the back seat the entire way. The next morning, it was snowing. He still didn't feel well and went to take a shower. It was then that we realized that w/in those 24 hours something terrible had happened. He was literally skeletal (as he said, 'I looked like a Holocaust survivor') and after his shower just curled back up. We called his pediatrician and raced him over there. Jimmy had to carry him. He was still just a little boy, only 12 1/2 and in 7th grade. Within 5 minutes of his visit w/ his doctor, he came in and told us, 'Edward has diabetes'. (Little did we know at the time, that his son also had Type 1). Our first thought was 'Well, it's not cancer, we can deal with this'. He was rushed over to Hasbro Children's Hospital, just a few minutes away. He was seen almost immediately, as he was in a crisis situation known as ketoacidosis. 'Ketoacidosis (key-toe-ass-i-DOE-sis) is a serious condition that can lead to diabetic coma (passing out for a long time) or even death. Ketones are acids that build up in the blood and appear in the urine when your body doesn't have enough insulin. They are a warning sign that your diabetes is out of control or that you are getting sick. High levels of ketones can poison the body.' His blood glucose levels were off the charts high. As soon as they got an I.V. in him and started giving him insulin, he looked better. But, he wound up in intensive care for the next 24 hours and spent the rest of the week in the hospital. Diabetes 101 had just begun and life had officially changed on a dime.

We never, in a million years, could have imagined exactly how Edward's life would change, and as parents, ours as well. Over the past 10 years he has taken thousands of shots of insulin, he has been in intensive care twice with a stomach virus, which left him terribly dehydrated, he has been to Camp Joslin for diabetes, as a camper and then as a counselor. Eighth grade was a total loss, as we were all still learning about these disease. Very difficult! He has gone through high school and 4 years of college, he has made the switch over to the insulin pump. He has dealt with 'feeling different', having to go to the school nurse every day before lunch in high school to test and record his blood sugars, and he has dealt with taking care of himself for the 4 years he was away at college. His friends were very protective...(you know who you are!!) As parents, bringing him home from Hasbro was like having a new born. We had to start over. We had to count carbs, begin really reading labels on food, and monitor every piece of food which went in his mouth (at least as far as we could). We had to keep records (books upon books upon books) of how much insulin he was taking everyday, 4 or 5 times a day, there were formulas and ratios which had to be calculated. When he made the switch over to the insulin pump, he was 16. Thankfully, he was able to become more independent. Someone once said something I will never forget. When a diabetic is taking injections, the whole family has diabetes, when he or she goes on the pump, they re-gain their independence. The pump is a wonder of modern technology and he is very blessed, if you will, to be living in such a time as this. He is a young man now, no longer a little boy.

Jimmy and I have met the most wonderful and dedicated families through our involvement with JDRF and have joined with them in their fund raising and advocacy efforts for research to find a cure. I have written about this numerous times on my blog. But, today is 10 years, a decade, since our little boy was diagnosed with this disease. So, Jimmy and I honor him. We think he is extraordinary and courageous and we love him so much.
Here's to you, Edward!!

Post Script: I have received wonderful e-mails and comments from this post, however, I was especially touched when I received an e-mail from Nurse Norman, the nurse @ Edward's high school. I don't know what we would have done w/out her support and friendship for the 4 years Edward was there. Priceless.