Skip to main content

I know the plans I have for you

There's a verse in Jeremiah 29:11 of the Bible that gives me great comfort. It says, " For I know the plans I have for you,” declares the Lord, “plans to prosper you and not to harm you, plans to give you hope and a future." I was thinking a lot about this verse today, in fact, when I woke up this morning, I was thinking about it. I'm a planner and I find security in knowing the plan. It's so much easier when there is a plan and I know exactly what's about to happen. Since I was diagnosed with breast cancer, all my plans have gone out the window. I've had to learn to be flexible. Instead of having a solid plan A, I've had to learn to be willing to move from plan A to plan B or even plan C, D, or E. It hasn't been easy, especially since I'm a type A personality. I like to be in control of things. I need to understand the plan.

I've never liked change. I like things to remain the same unless I get the urge to change them. Little changes don't bother me too much but big changes do. And it seems God has some big changes in store for us in the near future. 

My husband and I have been feeling a stirring in our hearts. It seems God is getting ready to move us. We don't know exactly when or exactly where but we know it's coming. Even if we don't know the details, we know God does. He knows the plan. We've been doing a lot of praying lately and asking God to give us the details, but He hasn't yet. This has been difficult. I like knowing the plan! I don't like waiting and I don't like wondering. My husband is more patient than I am. He doesn't mind waiting. I admire that quality in him but sometimes I wonder how he can be so calm and collected when we have no idea what the future holds. 

I guess God's continuing to teach me to trust Him completely. That's one area He's been working on in my life for some time now. I hate to admit it, but it's easier for me to trust when I know the plan! Maybe that's why He hasn't revealed it to me yet. He wants me to learn patience. 

So....as we wait, I'm trying my best to be patient. I'm trying to trust completely. I feel like a child sitting in the backseat of the car while my parents get ready to pull out of the driveway. I keep asking a zillion times where we're going and all they'll tell me is, "It's a surprise!" I feel eager and excited but also frustrated and confused. I sit in the middle of the back seat fidgeting. I want so badly to know where we're headed but all I can do is look out the window, watch, and wait. 

The destination looms far ahead of me. I can't see it. I am so curious it makes me crazy but I have to wait. I know God's timing is always perfect. I know the plans He has for me are good plans, plans that will be beneficial for my future. I know God loves me and wants the best for me. Knowing all these things help me stay put...but it's really, really hard. 

I can't wait to see what God does in the days ahead. I'm going to be watching and waiting for His revelation to come. Until then, I'm going to try super hard not to bite my fingernails down to the quick...I know the wait will be worth it. So, I wait.

Comments

Popular posts from this blog

Sometimes I just want to pull my hair out

Sometimes I just want to pull my hair out, especially when I read a friend's blog post and I just can't wrap my head around it. This morning, I was reading a post from a fellow breast cancer survivor. She said her cancer has returned and is growing in her spine. As soon as I read the words, I burst into tears. I just didn't understand! We'd been diagnosed with the same type of cancer in the same year. How could it be that her cancer had returned and mine had not? And what made it even more difficult to understand and accept was the fact that she'd chosen to go the traditional treatment route. I'd opted not to do that. She'd endured chemotherapy, radiation, and the anti-hormone therapy afterward. I'd refused chemo, had done 28 rounds of radiation, and had only taken the anti-hormone drugs for a couple of months. It just didn't compute and it certainly didn't seem fair. But that's what sucks about cancer. It doesn't follow the rules.

Cancer the gift that keeps on giving - the high cost of cancer

There's a basket of bills sitting in the corner of my bedroom. I try not to look at it as I enter the room but I know it's there. Its contents spill out onto the floor whenever my husband stuffs another bill into the basket. Usually, when the mail comes, he gets it first so he can filter what I see and what I don't see. Since he's the only one working, he takes care of our financial responsibilities and while I'm thankful for that, I'm not ignorant about our mounting bills. Cancer is expensive. Even if you've reached maintenance phase, it's costly. There are always tests to be run, blood to be taken, doctors to see. It never ends. Just knowing this will be a continual process for the rest of my life frustrates me and the alternative, death, will be my only way out. It would be nice to know that cancer could be a once and done kind of thing but that's only wishful thinking. Everyone knows cancer is a long and very involved illness. I had no id

Annual checkup yields good news!

Yesterday I went to the Cancer Treatment Centers of America for my annual check up. For those unfamiliar with the cancer treatment center, it's an integrative facility that provides services for the body, mind, and spirit. My day began in the survivorship department. While there, I met with the doctor and was asked about how I'd been feeling both physically and emotionally. We talked for about half an hour. The doctor and I had a few laughs and it was probably the most pleasant visit I've ever had. Instead of making me feel that she was the doctor and I was the patient, I felt like we were old friends just having a good chat. It was refreshing and I left her office feeling very optimistic. Next was the port lab where I have my blood drawn. It's always a challenge there because I always have to explain about my lymphedema and why it's necessary to have blood drawn from my hand instead of my arm. You'd think, after 4 years of being a patient there, they'