Weight Lifting

Did you know I was a weight lifter?
I am.

Seriously.

You can stop snickering now…

Yea, yea. I know you’re thinking, “She sure doesn’t look like a weight lifter…

Well.
I don’t lift traditional weights.

Since August 4, 2001, I have been lifting the marriage weight. And man, is that ever tough work!
I juggled the weights of new home ownership and fresh-from-college-now-I-have-a-real-job weights that same year.

Since Carys was born in 2003, and then Cailyn in 2006, I have lifted the weight of motherhood.
Sometimes those little blue-eyed, blond-haired weights are heavier than I could have ever imagined.

As if those weights weren’t enough, I added the diabetic weight in 2006. Phooey!

Then, with Chad’s surprising diagnosis of brain cancer and the discovery of IT in 2007, I have added way more weights that I would like.

The emotional, physical and financial weights of living a life with two young daughters, a husband with a devastating disease, diabetes and all the other stuff….well, it’s almost too much for me to handle at times.

I would look at other people in my life and wonder how they seem to lift similar weights so effortlessly.
I just couldn’t understand how they were able to build a positive emotional workout while I was struggling to lift the daily weights of life and was often out of breath from sheer frustration and exhaustion.

People often ask me how I juggle it all.
And the answer is simple. And it’s no secret.
I do my best. And God handles the rest.

When I sense that I cannot handle one more possible thing in my life, God shows me that I can.
Sometimes, He adds more for me to juggle. And He teaches me that I can handle anything.
I can do it. I can do anything.
And you can, too.

The weights I lift on a daily basis can be tricky; true.
And sometimes I do wonder how easy life would be without such struggles and hardships.
But then I always come to the same conclusion; everyone has weights in their life.
Every single person has something that they struggle to contain or let go of; it’s just the way life is.
And if you think my weights are heavier than anyone else’s…well, that’s not true.
If you have a weight in your life, whether it be illness, unemployment, depression – whatever, you don’t have to lift it alone.

At Chad’s fundraiser, we had the privilege of witnessing a great weight being plucked from our lives.
I’m not sure if I was reaching a breaking point, or if we were just “due” some good news, but a huge weight has been lifted from our family. I can not tell you the immediate calmness and security I have felt since that day. To see all the loving and comforting faces, smiles and tears…it’s taken me some time to process it all.

People are so good to us; and we are so thankful.
We give back whenever we can and we appreciate all of you who did the same.

In the past eleven nights, I have slept more soundly and peacefully than I have in a long, long time.

Thank you.
Thank you.
Thank you.

We have been given an immediate release of stress.
We can breathe again, a little easier at least.
The weight has been lifted, and I thank God that He has allowed us to be a part of such an overwhelming  testimony of what can be provided when you trust Him.

He is the Ultimate Weight Lifter.
And I am so grateful that He carries our load.

104 247

All about my stinkin’ diabetes

I’ve had an insulin pump since May 2008. It took me a while to get used to it; the constant “thing” being attached to me. I even took it off for a while and refused to wear it. Stupid, I know. There was just something mental I had to get past; I didn’t want a constant reminder that my body was failing me.
I still struggle with diabetes. I hate it, in fact. Is it limiting? Not really; at least not in the traditional sense of the word. I can eat what I want to, I just have to be more careful. And for a person that has a severe sweet tooth, that is extremely difficult.

I recently upgraded to the Animas One Touch Ping insulin pump.
My old pump was working just fine, but I felt the urge to take better control of this sugar-fueled life of mine.
If I wanted ultimate control, I would splurge for a Continuous Glucose Monitoring System (CGMS), but insurance doesn’t pay for it — so, I’ll have to wait until they do. If they ever will. THAT (CGMS) would completely help me out. It’s another little device that I would insert into my abdomen every few days that constantly checks my blood sugar FOR me. It tells my pump when I’m low, when I’m high — and makes adjustments or recommendations based on those readings. In order for insurance to pay for it, I have to run severely LOW all the time. And I have the exact opposite problem – I can’t get my numbers low. They are always HIGH.

My friendly UPS man delivered a ginormous box from the Animas company at the end of January.
And I opened it. I looked at the new shiny pump.
And I returned the old pink one.
And I just let the new one sit in the box for a few weeks.
I did injections while I made up my mind that I was ready for this new journey.
Trust me when I tell you that is stupid. I know that is stupid. I just wasn’t completely ready to dive in and accept this annoying disease….again. It’s easier to ignore it, even though I know I shouldn’t.

I’m ready. I’m taking control. (Again)

Some people have asked me about this new pump – so, here I am – letting you know all about it!

pumping
Every 2-4 days, I insert a new catheter into my abdomen (A). The catheter has a tube that leads to the insulin pump itself (B). From there, I am able to administer insulin before and after meals, before bed…whenever I need it. And gosh, does it seem like I need it ALL the time!
It has a nifty little carb counter that helps me adjust my insulin for meals if I want, or I can gauge how much I need based on what I eat. I also have it programmed to give me basal doses (small doses every 15 minutes) based on my blood sugar history. For example, I always have a higher glucose reading in the morning. Many diabetics do. It’s called dawn phenomenon, and no one really knows why it happens. So, every morning at 2am and 6:30am, while I am fast asleep,  my pump gives me a little extra push of insulin to help me combat the blasted dawn phenomenon. Sometimes it’s enough to help. Other times, it’s not. But it’s a good start.

What’s different about this particular pump (as compared to my last one), is that it has a remote (C). Wearing the pump itself can be a little challenging. I don’t like to wear it on my waistband – I bump things with it and scratch it — which is what happened to my last one. There were so many scratches that I could barely read the screen.
So, I often wear the pump under my clothing, tucked away where it’s out of harm’s way. But that also makes it difficult to give boluses (doses of insulin) when I have to excuse myself to the bathroom or to another room to fish the pump out of my clothing. It was a severe pain!
The remote allows me to wear the pump wherever I choose, and I don’t have to worry about finding a place to excuse myself to give myself insulin.
The remote also has a built-in glucometer, so my glucose readings are fed right into the pump. It knows how much insulin I need based on the glucometer readings. It takes a step out of the process for me – which is less to worry about.
It’s quite nifty!

After some searching, trials & errors, I have finally found an endocrinologist that I LOVE. His office has been very good to me and has helped me get the best possible care for my diabetic life. Is it perfect? No. I have days where the last thing I think about is checking my blood sugar. It happens more often that I care to admit.
I would be lying if I said this diabetes thing was easy. It’s a PAIN. But it’s manageable.

The thing I hate most about the pump is the fact that is so stinkin’ hard to lose weight while you’re pumping. It’s probably not impossible but it feels like it at times. I know a few extra pounds is a fair trade for having fully functioning eyes, kidneys and nerve endings.

Things that happened today

If you follow my ramblings on Facebook, you know that I was busy yesterday. Elbow-deep in paperwork. And frustrated.
And if you don’t follow my ramblings on Facebook, well…I’m telling you now: I was busy yesterday. Elbow-deep in paperwork. And frustrated.

But I did complete Chad’s Social Security paperwork. (Insert audience applause and cue “Eye of the Tiger”)
Not only is it complete, but I actually submitted it, folks!
I had to print eleven copies of medical release forms — because the SSA (Social Security Administration) wants to send them to each doctor, clinic or hospital that has treated Chad in the last two years. Fo’real. Only eleven? It is actually more than that, but I cannot possibly be expected to remember the attending physicians for each ER trip. Or can I? Oh, well. Someone will fill the SSA in, I’m sure.

This morning, after I dropped the girls off, I made my way to SSA local field office.
It was quite an eye-opening experience. Lots of different folks. From lots of different walks of life. All crammed in one very small room.
Thankfully, I made it there before 10am (note to self: NEVER arrive at the SSA after 10am. Unless you like to pretend you’re a sardine packed in a can full of lots of other sardines.) and only had to wait about twenty minutes.

I’ll admit it. It was hard. Sitting in a room full of people who are all there for different reasons….but I knew what my reason was. I caught myself getting teary-eyed a few times, but I reminded myself that this is best for Chad. This is best for the girls. This is best for all of us, as a family. Moving forward is the only way to move.

A woman called “Number eighteen to desk two!” over the speaker, and I made my way there. I attempted to explain the situation in as few sentences as possible. (It’s hard to do!) The clerk then had to get her manager….who then came to ask more questions. But he was polite, and assured me that he was going to submit my paperwork to Raleigh by this afternoon as the latest.
He also told me, given Chad’s ultimate prognosis, that we should expect to hear a response (approval or denial) within three months. I was relieved; that’s hardly the amount of time I was warned it could take. He proceeded to tell me that if we were denied, to contact him directly and he would handle our appeal.
The word appeal makes my stomach ulcers revolt – so I am not thinking about it for now.

***

Chad got up around 3pm today.
By the time I got home at 4:15, he couldn’t remember if he had eaten anything yet. He did take his meds, though.
And he took a shower last night without me bugging him to do so.

Tonight, he says he’s feeling a bit better. He says his headache is not as bad this evening, but is anticipating it coming back as soon as NC State loses tonight. He didn’t say that — but I suspect that’s when the headache will come back….of course, I’m kidding.

***

I ordered my new insulin pump today. I hope it will make things easier for me because I have had a hard time managing diabetes with all of the stress lately. I also have an appointment at the Diabetes Center this week — so I’m hoping I can get the upper hand with my glucose again very, very soon.

***

I started working outside the house again today. I’ve been doing inside sales for the same company for a little over 2 years – 4042.com -  and now I’ll be adding outside sales as well. I saw a few people today and it was good to talk to someone over the ages of 3 and 6.

***

I also got my dress fitted for Holly’s wedding on the 23rd. And I bought shoes. And I successfully tired out my 3-year-old by lugging her to about 13 different shoe stores before my 3:00 dress fitting. Oh, her mood was ugly by the time we were done…and yes, I know it was all my fault!

***

Anything else?
I don’t think so — but I’ll be back tomorrow.
And I hope to have some new pictures soon. I haven’t taken many lately, but I will soon! I get to test out a new fancy lens next week prior to Holly’s wedding, so I bet you’ll see my little divas posing about this time next week. And maybe even Chad. And maybe even me.

***

Happy Tuesday night!

My Diabetic Journey, Part II

November 2006

I will never forget the day I discovered I was no longer safe from diabetes.
I was standing at the stove, preparing dinner. It was kielbasa with peppers, and broccoli.
I remember it so vividly, the way the kitchen smelled. Salty and earthy.
I felt a little jittery and had a headache that wouldn’t stop. I just didn’t feel like myself.
A little voice told me to check my blood sugar.
I resisted. I didn’t want to. I was done with diabetes. I was done.

Cailyn was about six months old.
Carys was almost three.
And I was delaying the inevitable.

I checked my blood sugar.
I looked at the number and panicked.
It could not be true.
I checked it again.
And then a third time, just to be sure.

It was 586.
A normal person’s blood sugar is typically below 130.
My glucometer shuts off at 599, which I’ve found out the hard way a few times since then.

Suddenly, it all made sense.
I was nursing Cailyn, and hadn’t thought much about the weight loss I had been experiencing.
I had welcomed it. I loved it. I felt like I was getting my body back.
I was insanely thirsty and I visited the bathroom more times than I could count.
I really didn’t think much of it.
I was nursing; I was burning calories, resulting in weight loss.
I was nursing; I was thirsty. Extremely thirsty.
I was nursing; I used the bathroom a lot. Because I drank a lot. Because I was nursing.
This was all because I was nursing.
And because I had a busy, full life chasing two kids around.

It was not because I had an issue with my blood sugar.
It couldn’t be.
I was happy. I was healthy.
I had a new baby, and a big baby.
I was able to stay home with my girls, which was a dream come true.
I was fine. Absolutely fine.

Just to be sure, I checked my ketones.
I had been given a ketone test kit when I was pregnant with Cailyn to test my urine randomly.
The doctors wanted to make sure I wasn’t spilling ketones; a vital test to make sure I was controlling diabetes well.
Ketones are produced when the body burns fat for energy or fuel. They are also produced when you lose weight or if there is not enough insulin to help your body use sugar for energy. Without enough insulin, glucose builds up in the blood. Since the body is unable to use glucose for energy, it breaks down fat instead. When this occurs, ketones form in the blood and spill into the urine. These ketones can make you very sick.

The test showed that I was spilling ketones alright. And a lot of them.
The test strip container has a comparison chart, to tell much (or little) ketones you’re producing. The colors range from light pink to dark mauve-purple; few ketones to large ketones respectively.
My strip was nearly black.

I did the responsible thing and called my endocrinologist.
It was a Wednesday evening, and I got the nurse’s voicemail.
I left a brief message that I was about 6-month post-partum after a bout with gestational diabetes. I told her I had a high glucose reading, and I was spilling ketones.

About twenty minutes later, she called back.
She asked me a few questions and said she’d call back after she talked with my doctor.

About ten minutes after that, the phone rang.
The caller id displayed the endocrinologist’s office was calling.
When I answered, I was a bit shocked it was actually my doctor, and not the nurse.
I knew it was serious. Why would he take time to call me personally?

He: I hear you’re spilling ketones and have a high blood sugar reading?
Me: Yes, I am. I do.
He: I want you to go to the nearest emergency room or urgent care. Right Now.
Me: Really? Because I feel okay. Really, I do.
He: No. Go. Now. I’m putting you on my schedule for Friday evening. I don’t have an appointment, but I will not leave the office until I see you Friday afternoon.

I was scared to death.
The ER? Really? Because I feel fine. It’s just a headache.
I was freaking out.

I went to urgent care, and told them what was going on.
The PA there was wonderful, and got me through the office quickly.
I left with a prescription for insulin and syringes.
Again.

I was devastated.

Friday afternoon came.
Chad & I made our way to my endocrinologist’s office, a little worried about what we’d be told.
True to his word, Dr. Becker saw me around 6:00 that evening. We talked a lot, he listened. I listened.
And it was determined that I would need more blood work.
Great. Just what I always wanted.
Oh, and by the way, he also found my thyroid to be out of whack.
More blood work.

He went through the obligatory statements about women with gestational diabetes having a greater chance of developing Type 2 diabetes later in life. In my case, it was sooner than later.
We all agreed that I could handle my “old” regimen of insulin injections and carb counting.
And I would start a different medication for the thyroid issue.
Things would be okay, he said.

And they were.
For a little while.

My Diabetic Journey, Part I

I often stick my foot in my mouth.
Often.
Did I mention I do it, often? Stick my foot in my mouth?
Yea, well, I do.
Sometimes it comes back to bite me. So I just shut up as often as I can now.

2003 was a year of great change. Chad and I had been married a little under two years. We had just bought our first home, and I was struggling to find the balance between being a young, married, post-college girl and a career-oriented wife with a home and real responsibilities.
In April of that year, I discovered we were expecting our first child. Having a baby on the way kind of lit a fire under my butt to move a little quicker than I’d planned on the career front. When I was 13 weeks pregnant, I switched jobs.  None of my friends were in the baby-making business yet, so I felt a little alone in the adventure. Excited, but alone.

At my new job, there was another preggo, Sue. She was a few weeks ahead of me in her pregnancy, and was in great shape. It calmed me down to have a fellow first-timer around; we commiserated about swollen ankles, late-night bathroom breaks, extreme hunger, increasing belly sizes and the little feet that seemed to be perpetually lodged beneath our respective rib cages. We compared doctor’s visits and talked excitedly (and a bit nervously) about the tiny diapers, bibs, pacifiers and thing-a-ma-bobs that were starting to take over our spare-bedrooms-turned-nurserys.

Around the 24-week mark, Sue had the dreaded glucose tolerance test I’d read about in the What to Expect book. She came back a bit upset, and told me that she had to stay away from sugar and eat a low carb diet. She didn’t have gestational diabetes, but she was borderline. She was playing it safe.
I think I replied by stuffing the rest of a Krispy Kreme crueller in my face.
A few weeks later, we were at an office birthday fiesta in the break room. There was a beautiful, glorious cake. And I couldn’t wait to have some. I planned my day of sales calls around the 3pm cake call, actually.
And poor, poor Sue. She didn’t have any. I felt a bid bad for her. But I also felt a bit bad that people might think I was feeding a starving Ethiopian village under my shirt with extra slices of cake.
Here’s where I stuck my big fat foot in my mouth…I flippantly said, “No cake? That sucks. I hope I don’t have to deal with that.” What a stupid, insensitive thing to say. I immediately regretted it, but it was already out there. Stoopid.
I can still taste the faint bitterness of red toe nail polish…and none of the cake.

A few weeks after I finished cleaning the foot-funk from my mouth, I had my very own dreaded glucose tolerance test. The test itself wasn’t bad. I had to drink a bit of sweet orange fluid, much like flat Sunkist orange soda. SO many people had told me how terrible it was, and that I would need crackers or something afterward to help me from getting sick form the high amount of sugar.
Nah. I didn’t need any of that. I tolerated it well.
The results weren’t great and I had to complete a 3-hour test the following week.
The results of that test were also high.
I cried when I got the results. I was scared to death I was going to unintentionally hurt my growing baby.
I was sent to a nutritionist, who taught me more than I ever cared to know about carbohydrate counting. I felt confident I could make some small changes and make a big difference with my glucose levels.
With a controlled diet and strict glucose monitoring, I was able to keep my blood sugar at normal levels.
I delivered a beautiful 8 pound, 7 ounce baby girl a few days before my scheduled induction.
She was perfectly healthy. And I was perfectly thankful.
Immediately after delivery, my blood sugar returned to normal. I was given permission to resume a normal diet.
I was warned that I would be at an increased risk for Type 2 diabetes later in my life, and should be careful of what I eat and keep my weight in check. I joined Weight Watchers and after a lot of effort and frustration, got my weight down to a normal number.

pregwcailynThen I got pregnant with Cailyn in late 2005.
Almost immediately, I began to feel strange. Shaky if I didn’t eat at certain times, nervous and jittery if I ate to much.
I was nervous when I went in for my first prenatal visit. I told the OB I was feeling strange, and I thought it was blood-sugar related. She didn’t seem concerned and told me I’d be checked a little earlier in my pregnancy, since I had a history of gestational diabetes.
During a routine obstetric visit, a nurse tested my urine and blood. They found a large amount of glucose in both.
I was immediately given the 3-hour glucose tolerance test, and the results stunk. I was around 13 weeks pregnant.
I was sent to an endocrinologist and started insulin. Immediately. There was no “let’s try a diet restriction” approach, it was straight to medication. I was devastated. I felt that I had failed myself, and was failing my baby.
I was on a mission to be as healthy as possible and make sure the baby’s health was not compromised.
I checked my glucose religiously. I took insulin injections at least four times a day.
And I cried.
A lot.
I threw myself a pity party almost every day the first few months.
And I fervently hoped that I wouldn’t have to continue the nightmare after Cailyn was born.

I continued to be strict with my regimen, hoping to keep Cailyn growing safely in my body.
I went to the OB two times a week for a fetal stress test, to make sure Cai wasn’t under any strain from my bout with gestational diabetes.

In June of 2006, she was born, two weeks early, at a whopping 9 pounds, 11 ounces.
She was perfectly healthy. And again, I was perfectly thankful — especially that she came early. Can you imagine what she would have weighed had she stayed on my sugar-fueled diet for two more weeks? Yikes!

My glucose levels seemed to return to normal immediately following delivery. I was thrilled to be back to “normal”. I ditched the insulin syringes and said “Adios!” to my endocrinologist. My OB told me that the best cure for gestational diabetes was delivery, and that’s all I needed to hear. I was so done with being a pin cushion with routine finger pricks and insulin injections.

Yet, it was not over.
It was just beginning.