Thursday, September 20, 2007

Diabetes and more

I've never blogged about Diabetes (except just after our son, Tomas, was diagnosed) - I try and pretend Tomas is a normal kid that just gets extra medicine (the same way someone with thyroid problems would take a pill). Alas, the time has come that I feel comfortable passing along how it has affected our life.

I do read other diabetes blogs faithfully and they've been fantastic support. I read Mom wants a Diabetes Cure and Sunny Side Up and a few others - I only find the time to read the ones where the parents have a child with diabetes but there are lots of great all-around diabetes blogs around.

When Tomas was first diagnosed this spring - I freaked out. T.G. we had friends in a city where we had previously lived who had a child diagnosed at age 2 with diabetes and they were a huge help in calming me down.

After we'd had 'diabetes in the house' for a few weeks I said "I can handle this. It's only an extra 30 minutes cumulative a day. " But you know what? It's more. It never ends. Ever. And it's not 30 minutes - some days it can be every waking minute wondering why your child has high sugar readings or low sugar readings and how can you make sure they eat their snack when they're at the play date or how do you handle that the other parents don't want them over for a play date because they're afraid something will happen to Tomas (I've prepared a simple hand-out but diabetes is scary and it is a big responsibility). He gets his sugar checked at school at 11:00am and I'm ALWAYS near a phone so I can get it if they call. Yesterday I was at the dentist with my mouth wide open at 11am but I'd told the dentist he'd need to answer the phone if the school phoned.

I try and shelter Tomas from the diabetes work because it will be something he has to deal with EVERY SINGLE DAY FOR THE REST OF HIS LIFE. And it's not like it makes sense everyday. Sometimes Diabetes just goes berserk and you have really high readings all day or really low readings. Or really high THEN really low. It requires constant vigilance. My purse has increased back to diaper bag purse size because of his testing kit, snacks, etc. that I carry everywhere I go. Even if Tomas is not with me - I may get a call and have to go straight to help him.

For those of you wondering - Tomas' diabetes day goes something like this:
7:15am - finger poke
7:30 - needle with NovoRapid insulin mixed with NPH insulin
11:00 - finger poke at school (done by an Education Assistant)
3:00pm - finger poke
5:30 - finger poke
5:30 - needle with NovoRapid insulin
7:30 - finger poke
7:30 - needle with NPH insulin
Middle of the Night - Tomas is checked at least twice a week in the middle of the night - more if his numbers have been off.

PLUS he'll usually have at least one additional finger poke because of odd highs or lows when I'm trying to figure out what the hell is going on.

He eats his meals at 7:30am, 11:30am and 5:30pm
He eats his snacks at 10:00am, 3:00pm and 7:30pm

Tomas' dietitian (who has type 1 diabetes) is excellent. She has helped us ensure that he can still have 'yummy' food (in moderation) but each morsel of food that Tomas eats is measured and the carbohydrates are counted. We record the carbs and insulin amounts in our diabetes record book. And half the time it doesn't make sense. I thought that once you'd been doing this for awhile you'd get it set and just hit 'repeat' for each day. HA HA HA. Every day requires new guesses, measurements and prayers that you've adjusted the food(carbs)/insulin/exercise (uses sugar) to a safe rate that won't damage your child's organs.

[I did just get his A1C levels back and for his first 3 months of diabetes he was 7.6 - we've been told that is very good. For those of you who don't know about A1C levels - that's a discussion for a different email.]

In case anyone is wondering - we've looked at the Insulin Pump but there is no one at the school that is (or can be) trained to help with any insulin adjustments required during school hours (we're lucky to get someone to check his sugar levels). We've also looked at Lantus but there is no one (as above) to give him needles at lunch time. When he is a little older we'll definitely go for the pump.

Mainly I am desperate for child care. We used to have the greatest babysitter in the world. She was a mom, a teacher and was awesome. BUT the big D scared her and she isn't comfortable looking after Tomas anymore.

I'm willing to pay oodles to get someone to look after my kids so my husband and I could at least go for supper or just out for 3 or 4 hours. Never mind getting away for a night or two. I've tried the JDRF, I've tried the local diabetes clinic - the economy is so red hot that no one wants to babysit a kid with diabetes no matter what we'd pay. And quite frankly, at this point I've offered DOUBLE minimum wage. Although I do have a lead on calling the Nursing Department at the local University.

Tomas is the only kid he knows with diabetes. There are no other kids in his school with diabetes. He had another kid in his class this year wearing the medical alert wristband so he thought MAYBE but then he came home and said "Nah, he's just got allergies". He never complains about getting needles, he never complains about finger pokes, he never complains about missing lots of schools when we see all the varying doctors and specialists (well, he does kinda cheer about that).

Tomas does handle his diabetes like it's part of his life which is great although I noticed he got all defensive the other day when another mother asked how he was doing with his diabetes. He turned red and said "it's fine!" then marched away. He doesn't want to be different but so far he has handled it like a pro. We attended the Walk to Cure Diabetes (which was hard for Tomas to understand because he thought he'd be cured after he walked) but didn't meet any other kids and since it was summer the local diabetes clinic closed down. We're hoping to meet kids at the next diabetes clink "check-in" in November.

Tomas is an awesome kid and I am thankful for everyone around who has supported us and the quest for a cure for Type 1 Diabetes.

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6 Comments:

At September 23, 2007 at 3:53 PM, Blogger Shannon said...

So it wasn't my imagination that you haven't posted about Tomas and the D experience. I was reading through your posts and thought maybe you wrote more about everyday life than D life (sort of like me), LOL.

I read this and placed myself in your shoes. You basically wrote what our life is like as well.

And the only predictable thing about diabetes is that it's unpredictable. We too thought at first that the treatment we did one day would apply to the next. Wrong!

Email me ANYTIME!! if you want to vent, compare notes, ask questions, etc. I'll be that ear you need to chew and the shoulder you need to lean on :)

 
At September 23, 2007 at 7:34 PM, Blogger C.L.W. said...

Thanks Shannon.
I do blog mainly about day to day life. Our family and many friends live elsewhere so I originally started the blog as a way to keep all the relatives and friends in distant places up-to-date.

Alas, today I wanted to tell everyone about diabetes. I'll definitely keep in mind about emailing you.

(p.s. loved your grad dress pic.- I think I burned every picture of mine).

 
At September 24, 2007 at 9:53 AM, Blogger Unknown said...

Hey Carmen - Mom's always do this because they love you. - You are doing a wonderful job dealing with this event (for lack of a better word) in your lives. Tomas is the same great little boy he always was, and you can thank yourselves for that.

The idea of eating at set times is a tough adjustment. You come from a family that was adjustable about meals and snacks. Also, you and I can live on junk food!

Take some time to pat yourself on the back for the great strides you have taken since May.
Mom

 
At September 25, 2007 at 8:20 AM, Blogger foodie suz said...

Carmen - I've known you for almost six (!) years, and watched you grow and blossom as a mom. I think you are simply fabulous.

I'm glad you wrote about the 'D' - it is good for all of us who love you to know what your day to day life is like.

And while you are a very strong capable woman, sometimes it is ok NOT to be strong...and those times know that you have friends and family who love you.

 
At October 3, 2007 at 6:06 AM, Blogger Penny Ratzlaff said...

I came this way via Shannon's blog.

My son, Riley, was diagnosed when he was 3. He is 5 now. His 2 year anniversary date is coming up this Saturday.

Anyway, I just wanted to tell you I can identify with everything you said.

My son started kindergarten last month. It was so hard to turn his care over to someone else. He eats snack and lunch at school. I'm a home health nurse and I carry my cell phone everywhere, but the coverage is spotty in some areas. I always try to arrange my day so that I'm in an area with good coverage at snack and lunch time.

I'm sorry about the pump and the Lantus (sometimes called the "poor man's pump") My son is on a pump now, but was on Lantus for the first five months after diagnosis.

Riley is great when it comes to his D. He handles it much better than me. But, there are days when it gets to him too. Just the other day when I was changing his pump needle he screamed "I hate diabetes!" (sigh)

Riley is lucky because he knew a kid with D before he ever got it. I have an older son who is 16. He has 2 kids in his class with D and Riley just adores them.

Maybe your son can go to diabetes camp this summer and meet some other kids with D?

Sorry this is getting so long. I've been blogging about my son's D for almost 2 years now. And, it's very therapeutic for me. The support I have found from the online community has been wonderful and helps me to not feel so alone sometimes.

Like Shannon, if you ever want to chat or vent feel free to email me. My email address is in my blogger profile.

 
At October 4, 2007 at 10:43 AM, Blogger Kerri. said...

Hi Carmen,

I came your way via Shannon's blog, too. (She's awesome, the best!) I'm not the parent of a kid with diabetes, but I'm the grown-up "kid with diabetes." I was diagnosed 21 years ago and have had diabetes for 3/4 of my life. I'm always curious to read what the parents have to say about diabetes because it gives me such insight into how my own parents may have handled my disease growing up.

People like you, and Shannon and Jamie, and all the other parents of diabetic kids that I've read, are simply the strongest, most remarkable people I've ever known. Thanks for all that you do.

Best,
Kerri.

 

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