UnDomestic

Writings of a teachermom, choosing to stay home with her kids, while loathing all domestic responsibilities! In late Aug. 2008, I was diagnosed with Triple Negative breast cancer. After surgery, chemo and radiation, I was given theall clear. However, in the late summer of 2008, I was diagnosed with a brain tumor, which metasticized to other areas.

Friday, October 10, 2008

No more info really

Not really much to report here. I continue with the brain radiation, and yesterday I started the spine radiation. The treatment is all short and painless, but still an everyday (minus weekends) affair.

I guess the spine radiation can cause nausea and diahrea. But I have drugs for that if I need it. I am experiencing a lot of pain down my left leg, which is causing me to limp if not on pain meds. Motrin or something stronger usually helps.

My husband was out of town this week, but is coming back early tonight. So this weekend I'll learn more details about what has happened, and what is to come.

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Tuesday, August 19, 2008

Details can be too much

The brain mapping was done this morning. It's sorta scary to think about the fact that they can map out my brain by simply having me tap my fingers over and over again, point out when I recognize a word and just stare at a red dot while black and white squares move up and down a screen. That's what they did for about an hour today. That's how they'll know where to cut and not cut when removing the tumor. Scary.

In the afternoon I had cranial teaching and prep. Basically they took a few vials of blood and had me answer a bunch of medical questions that I've answered a million times already. Then this wonderful nurse went over everything they were going to do from presurgery to post-op. They're actually going to drill holes in my head, lift up part of my skull, and get at the tumor. I can't even grasp my mind around this. The nurse kept asking if I had any questions, but in actuality, I just don't. The only thing I can think of is...do what you gotta do. Get it out. I'll be here. Just do whatever. I feel quite distanced from the whole ordeal right now. It's the only way I can deal with it. It's just not something I want to think about really.

The actual surgery could last six hours. My brain could be exposed for six hours! See why I can't even think about this! Whenever I try to even begin to write about it, I go blank, and I don't want to write about anything else anymore.

I think I'll use the Olympics to distract me right now.

Trust in the Lord with all thine heart; and lean not to thine own under standing. In all thy ways acknowledge him, and he shall direct thy paths.” Proverbs 3:5-6

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Monday, August 18, 2008

Maybe they just lost my brain


Tomorrow they are mapping out my brain.

Does that not sound funny or what?

I mean really. It's supposed to be some test that takes a few hours, but I don't think it should take that long. I can't help but giggle that there's not much to map out. I mean come on...do you know how often I forget things, can't pinpoint things or just plain blank out on information? It's comical really...and this was BEFORE I was diagnosed with any kind of tumor.

I told my dad the test won't take long. He told me otherwise. He said you'd be surprised what they might find in my brain. Possibly we're thinking there's no tumors there after all. Maybe, just maybe, there's a bunch of little brains smashed up in my head causing all this ruckus!

Can't wait to see these results!

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Sunday, August 17, 2008

Just a brief list

I want to document my experience better.

I want to write all about the wonderful people at church and at a local restaurant (Khoury's) who embraced me with their love and prayers today.

I want to tell everyone how grateful I am that my parents are here to support me.

I want to tell everyone how Cameron reacted, sad because he doesn't want me to have cancer again.

I want to thank all my friends and neighbors for just everything.

I want to write about my frustration about getting numbers all mixed up, and my inability to recognize my "normal" confusion with my tumor confusion.

I want to write all about how incredibly grateful I am to my husband for all the phone calls he's making and appointments he's setting up and just his patience with me.

But my head hurts...bad. Sometimes it's better than other times, but mostly it just feels like someone took a baseball bat and smashed me in the back of my head.....not that anyone has ever done that...but it's how I imagine it must feel.

I want to continue to be honest.

So I'll keep writing...but it might be limited.


Deuteronomy 31
31:8 The Lord himself goes before you and will be with you; he will never leave you nor forsake you. Do not be afraid; do not be discouraged."

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Saturday, August 16, 2008

Which pill do I want today?

I hate taking drugs. Well, unless you're about to have a baby, then I say BRING THEM ON! But other than that, I usually try to do without taking extra pain killers, cold medicines or other medical and natural remedies.

But today I have taken the following:

Zoloft...for obvious reasons.

Decadron...this is the steroid that is supposed to be reducing the swelling around my tumor, which is causing all the pain. It doesn't seem to be working very well. It keeps me up and wired, but the pain is still there.

Tylenol...right now I'm taking some extra strength stuff, but it's not working. I might be switching to some Vicodin or something stronger tonight, but I really don't want to be all drugged out.

Keppra...this is anti-seizure medicine. There is concern that until the tumor is out and all has settled back in, I could have convulsions or something. This is actually the same medicine that was prescribed to Cameron last year when he had that lone seizure. I'm so glad we decided to take him off the meds, because this Keppra is some strong stuff. On the good side, it seems to have counteracted the jitteriness of the steroids, but on the flip side, it makes me lightheaded and a bit dizzy. No driving for me obviously.

At least I can seem to relax abit now with the Keppra added. I so just want to be fine for my kids. Right now I have shuffled them off to a friends' house for a few hours, but really, I don't want to keep doing that. Melvin and I still need to talk about what we're going to tell the kids, as they have no clue yet what's going on. We have quite a few appointments next week as well, doing testing for surgery, and also looking at other options down at the Mayo Clinic in Rochester, just to get a 2nd opinion and to cover all our bases.

But I feel the Lord getting things in place for us, and I know he will not abandon us.

"Nay in all things we are more than conquerors through Him that loved us." Rom 8:37

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Friday, August 15, 2008

Just the facts.

Disclaimer: Please allow me to preface this with a reminder...except for being married to a doctor, I have NO medical background. So my information will be vague, probably quite elementary sounding, and hopefully at least somewhat correct!

Praise the Lord my husband is doctor. Which sometimes can be a pain...when they know too much...but mostly it's such an incredible blessing. Without his level-headeness, knowledge, patience and calmness, I would never be able to decipher all the information being thrown at me.
My husband and I went see Dr. Jerone Kennedy today, a well-recommended neurosurgeon. Looking at all my scans, he said the tumor is too big to remain and it will need to be removed. Fortunately, it looks like they can resect it (resect is my new medical word of the day) because of its location, and because it appears to just be a solid mass.

Until they actually take it out, they won't know what it is. Very best case scenerio, the miracle one, when I have all my tests done next week, the tumor will have miraculously disappeared. Next best case scenario, it's just some benign tumor that will just be removed and all will be well. Most medically likely, it's breast cancer mestasticised to the brain. Or it could be a completely separate tumor, which could actually be worst, depending on what it is. So those are the scenarios we're looking at here.

The surgeon doesn't feel that getting the tumor out will be a problem. They'll actually be doing all these crazy tests next week where they'll map out different parts of my brain so that they make sure they don't cut out the important fuctions of my mind. I could possibly have some vision and math function issues as a reult of the surgery.

The earliest the surgery could be is next Friday, but most likely the following week. I'll be in ICU for a couple days and then in the hospital for a week.

Those are just the facts. Obviously, there's so much more going on...even a lot that I'm finding quite amusing, but I just need to TRY and get some rest, and not be long winded here.

As usual, thanks so much for all the well wishes and prayers. They're so needed. I'll be posting some of the verses people have been sending me. They're such a comfort.

I will both lie down in peace, and sleep; for You along, O Lord, make me dwell in safety.Psalm 4:8

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Thursday, August 14, 2008

Of course I have a headache!

Needless to say, it has been an emotional day for me. From being quite content, completely relaxed, unbelievably tired, completely frustrated, quite confused, very irritable, overly anxious and completely at peace.

But isn't that everyday for everyone, especially when you have young kids?

On a good note, I had my PET scan today, and like my earlier scan, it came back clean. Nothing new has popped up. So the only cancer they need to look at and confirm now is in the brain. It's quite possible that the cancer was always there, we just didn't know it. It just started showing its symptoms recently. I'm not sure if that really matters or not now. It is what it is.

We meet with the neurologist tomorrow. I'm eager to get this appointment over with so we know where and how to proceed from here. Not knowing what the hell is going on is what's really affecting me negatively right now. Will I need surgery? Can they even do the surgery? Will they just biopsy it? How will this tumor affect me mentally? Physically? When do I start radiation? What about chemo? Should I go elsewhere for treatment? So much to think about...but nothing I can really deal with until I have this initial appointment.

Thank you to everyone who has sent e-mails, blog comments, phone calls, and given offers of help. I appreciate you all and thank the Lord for placing such amazing people in my life.

I'll continue to update.

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Wednesday, August 13, 2008

Not what I expected.

(See Update Below)

For the past month I've been having headaches. I didn't think too much of them until a bad migraine last week and then just continued headaches throughout the week. Yesterday it was bad. I felt that my head was going to explode! A couple times I could feel my head throbbing.

So I finally called the doctor, and the nurse said that although it's probably just my body adjusting to all my running and exercise, we'd do an MRI of my brain just to make sure and put myself at ease.

Well, it's not something I can just brush off. The doctor who read the scan (it was late at night so it wasn't my regular oncologist), told me that there's a 1 1/2 inch spot on my brain. That's what's causing all the pain. They gave me steroids to relieve the pressure. It feels better. But I was up all night last night.

I will probably have the lesion biopsyed or removed entirely.

I know nothing else, except that if it's the triple negative variety breast cancer mestasticized to my brain, then that's not really good. If it's a totally separate kind of cancer, that's actually better news apparently. Or maybe it's just some cute little adorable dot just decorating my brain...I heard that's the latest style!

I'll update when I have more info.

Update

So here's the deal. After my oncologist and general surgeon looked at the report, they said it's most likely cancer.

You're probably wondering how that can happen if I just had a scan that said I was all free and clear....well, what I thought was a full body scan, was only a scan in the breast and chest area. They only do the whole body if there are other symptoms. I didn't know that obviously. With my cancer being Triple Negative breast cancer, and being so aggressive, I'm surprised that they didn't do an entire scan. Needless to say, I'm not happy about that, but oh well.

I will have a PET scan tomorrow, that will scan me from my knees to my neck (they don't need to do my brain since the more precise MRI was completed yesterday). I sure hope no cancer in my tippy toes appears, since apparently that area will be bypassed.

Then on Friday I will meet with a neurosurgeon. He'll read the scans and then we'll decide a plan of action from there. If the tumor can be removed, then that will be the plan, along with radiation. If not, I will just have radiation.

I have no idea when I'll have the surgery, or where I'll even have it. How do you know who the best doctor is? We have the renowned Mayo Clinic nearby, but is that really the best place to go for my situation?

So we obviously need some serious prayer.

On a good note, the steroids are sill working and my head doesn't hurt. On a bad note, they keep me up....I can't sleep. But on a good note again...with my new found steroid induced energy, I'm being very productive!

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