Monday, May 30, 2011

Hannah's love

All text & photographs on Dirt Road Heaven © by Darlene Meader Riggs, 2010

So, Hannah and her peeps came to visit this weekend. Sunday morning I was trying to catch a little nap when I kept feeling soft, fuzzy things being placed on me. Wordlessly, Hannah surrounded me with just a few of her friends, making sure my nap was not lonely. Other little girls travel with a bevy of baby dolls. Hannah travels with enough stuffed animals to fill an ark. You gotta love Hannah.

Early Wednesday morning Dave and I will head for Houston, MDA and the last FAC treatment. I am so very excited to say "the last" .. after Wednesday, no more chemo, no more nausea, no more chemo tummy, no more fried taste buds, no more sore head, sore mouth, sore nose, sore NUTHIN! And in case you hadn't heard the news ... my EYEBROWS are making a comeback! And I'm starting to get some HAIR! Baby steps .. but little victories, nonetheless!

If I said the last six months passed by in a flash, I'd by LYING .. it's been a long, hard road but I appreciate all the support along the way, AND Hannah's love.

All text & photographs on Dirt Road Heaven © by Darlene Meader Riggs, 2010

Wednesday, May 25, 2011

I Was A Hot Mess ...

All text & photographs on Dirt Road Heaven © by Darlene Meader Riggs, 2010

Yesterday I felt tired. But I always feel tired. I was cold. But I am often cold when no one else is. Mom said I looked pale .. but I haven't been outside for more than a few minutes in months.

Then, around 9 pm, it was clear I was sick. Dave took my temperature and it was 101.5. Chemo patients are not allowed to have fever. It's totally against all the cancer rules. At 100.5 I'm supposed to run, not walk, to my nearest emergency room. But you know me, right?

Instead I called a dear friend who is an RN. She said I obviously had an infection and needed antibiotics. No problem .. I had some. My last visit to the oncologist, I complained of this constant, dry, annoying cough. It's often associated with Taxol but I stopped Taxol in late March. She thought maybe it was a bug and gave me a prescription. We had it filled but then the cough stopped so I hadn't taken the prescription. And then the cough resumed. So, last night, I started the antibiotics and took two Tylenol.

My friend said if my temperature didn't subside with Tylenol, I should go to the ER. I promised I would. Doctor Dave took my temperature every fifteen minutes for more than an hour when it dropped to below 100.5. We went to sleep but woke at 2 AM to re-check it and take more Tylenol and it was normal. And this morning when I woke up it was normal.

Whew.

So, apart from that little bit of excitement, not much else is going on. My fingernails are funky, some are trying to lift from the nail bed. My feet are numb and that's kind of annoying. My taste buds are getting better and food is starting to taste a little better but I am probably not eating 800 calories a day. I just don't have an appetite. My hair is staring to grow back on my head but I can only feel it -- not see it yet. The eyebrow count is still in single digits. The eyelashes have all flown away ...

One week from today I will have my final FAC chemo.

Last week I watched a news story about a local anchor woman who was diagnosed with BC about the same time I was. There have been several segments on the news since last fall. She's young, adorable and brave. She was having her last chemo treatment and when the final drops of poison dripped thru her IV .. she cried. And I cried. And I know that next Wednesday I will cry again.

Even for me, putting these emotions into words is hard. I feel a sense of accomplishment. I feel profound gratitude that it's almost over. And still I wonder, nervously, if I will regain all I have lost in the process. I know I will never be the same and that's okay -- but I do hope for strength, vitality, stamina ... HAIR!

But we're not done here! The hard part will soon be over but I hope you'll keep me in your prayers as I face surgery, healing and the weeks of daily radiation.

Someday soon we're all going to toast Herschel's vaporization. Meanwhile, there's a bald lady in East Texas who is still kinda gimpy .. so hang in there with me, okay?

Friday, May 13, 2011

As of 05.11.11 We are 3/4 -- DONE with chemo!

All text & photographs on Dirt Road Heaven © by Darlene Meader Riggs, 2010
Talking to my
peeps on FB from the chemo ward!


All text & photographs on Dirt Road Heaven © by Darlene Meader Riggs, 2010
Smilin' for Davey ..
because he won't take "NO" for an answer!

I can't lie to you. I hate these pictures. I've struggled the last couple of weeks with the further degradation of my appearance. After all .. a year ago this was ME:


All text & photographs on Dirt Road Heaven © by Darlene Meader Riggs, 2010
35th High School Reunion
May 2010


But, even then, I knew something was wrong. I hadn't felt good, energetic or like myself in almost a year. The symptoms were so subtle .. I couldn't even verbalize it. Fatigue, but I was reminded that I WAS 53. And overweight. Still, I wasn't buying it. It would be a short five months till I "felt" literally, what WAS wrong. Herschel made himself known.

So last Wednesday was my third of four FAC treatments after a visit with my oncologist. Have I mentioned how much I adore my MDA team? My nurse, Grace is awesome. My doc, fabulous. I couldn't be happier with my treatment. My port nurses and chemo nurses (all except that ONE) have been attentive and supportive and amazing. I'm so very grateful.

Doc says my blood work indicates I am tolerating the FAC beautifully. She says my tears and emotions are perfectly normal for someone whose body has been bombarded with poisons for five months. She knows I am tired .. but march on we must. My next and FINAL FAC is June 1. Then, I'll get a little bit of a reprieve since my next appointment won't be until June 22. I'll have a final pre-surgical ultrasound (can't wait to see how tiny Herschel is NOW!) and a consult with my breast surgeon. Hopefully, Herschel's eviction will come before the end of June. Can you say PARTAY?

Continued bottomless gratitude for all the love, support, dollars, gifts, CHOCOLATE, cookies, flowers, cards and did I say LOVE? You will never know how much easier this road has been because of all of YOU.

Tuesday, May 10, 2011

Darlene: UNCENSORED

Buckle up. It won't be pretty.

Yesterday I threw my mother's wheelie walker out the front door. It was to prove a point and yes, I did bring it back in.

Dave and I planned to go out for a Mother's day meal on Sunday but I just wasn't up to it, so we postponed for Monday thinking the crowds would be thinner. With my stamina in such short supply, I can't stand in lines or wait for a table. And yesterday I got up, bathed, got my clothes ready and sat down on the bathroom floor to put my make up on. Since I avoid mirrors, I was a little shocked to see my reflection. There's been quite a change in the last couple of weeks. I have four eyebrow hairs on one eye, six on the other. I can no longer connect the dots" to give myself drawn-on ones.

I tried. And then I cried.

Though I didn't count them, I think my eyelashes number about the same. There's just not enough of me to restore my face to any reasonable, recognizable form. So I just laid on the bathroom floor and cried .. which is how Dave found me.

He scooped me up and told me that I didn't have to go anywhere I didn't want to. That if I chose to only go to MDA and back for the next six weeks that was perfectly fine. He gave me permission to hide out .. he understands how devastating this loss of identity is.

So I washed my face and switched out my clothes for pajamas. I came into the kitchen where my mother was to explain that we weren't going out. She immediately launched into a tough love sermon, talking to me like I was a five year old with the IQ of a walnut. Excuse me if I didn't respond positively to that. I told her to "go bite yourself". Yes, I think that might be a combo of "go ___ yourself" and "bite me" but it's the best I could come up with in my depleted state. I removed myself from her presence.

Or so I thought. Here came that damn wheelie walker which parked itself and its driver beside me on the sofa (blocking my view of the TV, I might add.) Her tirade continued with "I didn't raise you to be vain. You get up off that sofa and go fix your face .. blah, blah, blah." I told her she didn't know what she was talking about and eventually she left.

For about ten minutes.

Then she was back, in the recliner, sitting across the room from me, trying to make nice with idle chit chat. I looked her square in the eye and told her that she couldn't talk to me the way she just had and then expect to make nice. That she owed me an apology .. and she disagreed. I won't bore you with the complete dialogue. Suffice it to say that my dear Maggie girl (who can't stand raised voices or conflict) left the room. Dave hid behind his laptop.

The whole exchange aired more than a few of my pent up resentments. My mother, at almost 86, is the last of her siblings and the matriarch of our family. She is much loved. But only Jim and I know what it's like to have her for a mother and it ain't easy.

In my defense, I pointed out that I have been taking chemo since January 5th. That I am tired and sick and sick of being tired. That I am dreading my third FAC, knowing that it's like facing a firing squad of blind men wearing mittens. They won't kill me -- they will just make me wish I was dead.

That even after all the toxins injected into my body in the last five months, I am still cooking meals and doing the laundry and pushing myself when I don't feel good. That I have tried to remain positive for most of this crap and that I have tried to be cheerful for my children. That I have put on my face and my cap and gone out to be in public, ignoring the stares and pretending that I am okay with being bald and painted. That I have tried with all my heart to be graceful, but that I am out of grace. That I can't fake it any more.

That the next six weeks will likely be the worst six weeks and that I am just going to do my best to endure it. Here. At home. On the sofa. And that she has no right to judge or criticize me or shame me.

It was bad. For most of my life I have accepted her opinions, her will, her dominion over me. Those days are long gone. And she doesn't quite know what to do with me. There is a reason 54 year old women don't live with their mothers.

I'm not proud of what happened but I feel justified in everything I said to her. My delivery might have been a little harsh but lack of sleep and five months of debiliating fatigue will make you cranky. At some point mothers need to recognize that the relationship with your children should change from one of disciplinarian to one of friendship and companionship. That, as a grandmother myself, I don't need her permission to do anything.

She finally asked me what she should have said to me instead of what she did say. I told her that, right now, her understanding of my experience would be a whole lot more loving that her condemnation. That, without having walked in my shoes, she has no right to judge me.

I'm not trying to garner sympathy. I've shared this whole experience for two reasons only. That in writing about having breast cancer, I am better able to accept this as my new reality and so that I could, perhaps, provide information for others facing this as their new reality.

Cancer doesn't affect just the patient. It affects the family. And the family needs to understand that the loss of eyebrows and eyelashes is just symbolic of the loss of so much more.

Yes, it's temporary.

Yes, it means the medicine is working.

But, day to day, the battle is a long and uphill struggle. The last thing anyone needs is to be reprimanded. Understanding and acceptance might be a more loving choice given the opportunity.


All text & photographs on Dirt Road Heaven © by Darlene Meader Riggs, 2010

Wednesday, May 4, 2011

Two down, Two to go ...



The rumors of my demise have been greatly exaggerated. But it was touch and go there for a while. The second FAC treatment was supposed to have been "easier" than the first but that was hardly my experience. Now I am dreading the third and fourth but take pleasure in the fact that I am halfway through the process of this more toxic chemo.

There are no photos of this chemo session since I slept through most of it. Besides .. how many pictures of me lying in bed hooked up to bags and bags of Herschel-reducing chemicals do you really need to see? I just thought I'd spare you.

Instead, I am posting a video of photos Dave and I took one day last week when I thought I was strong enough to get outside and enjoy the wild roses, yucca and cactus flowers. Dave saved me from falling into the roses when I lost my balance and almost went face first into the brambles. It hurt my pride to think I was so weak I couldn't even bend over to enjoy a rose but I was grateful for Dave's attention.

Moments later, back on our property, I squatted down in the meadow to take some close ups of the beautiful, waxy cactus blooms that were just glowing in the sunshine! My joy and wonder over the flowers soon turned to tears and frustration when I realized I couldn't get up. There was just no strength in my legs and Dave, yet again, had to come to my wobbly rescue. It just broke my heart and I cried for awhile grieving for the loss of all the things chemo has taken from me.

In fact, the tears have flown pretty freely the past couple of weeks. What little hair I had (ugly, granted!) flew away within a week after the second treatment. My eyebrows consist of a few hairs now and look more like two scraggly spiders there above my hollow eyes.

I no longer recognize anything about the person who looks back from my mirror. She looks like those sick ladies at MDA. There's no sparkle, no life in those eyes. They aren't mine. I've tried to tell Dave that it's not just a matter of vanity. I've accepted, grudgingly, that I am vain. But this is a disconnect between who I think I am and the identity of that sick person staring back at me from the mirror. And the fear that that sick person in the mirror might be the one I am stuck with .. and the strong, brown, healthy, happy girl I used to be lost forever.

I know that everything happens for a reason. That God is in charge and that there is a plan. I've walked through fire before and come out tempered and strong on the other side. If this is just another test to show me what I am made of then so be it. On this day, I know that I can make it to the end of my chemo sessions. And after that, surgery and radiation will seem like a walk in the park.

Cancer has not been at all like I thought it might be. It's shown me a lot of things about myself that aren't all that appealing. It's made me realize that I am mortal and sometimes fragile. It's humbled me. It's broken my heart and withered my spunk but's not gotten the best of me. And it won't. I know that this time next year I will be cancer free with renewed strength and hair and eyelashes and eyebrows and the face I see in the mirror will again be mine. All the things that cancer has taken will be replaced with healthy new vigor and all the things that cancer gave me, the boundless love of family and friends, the knowledge that my God watches over me and cared for me, will remain.

In the end, cancer will have given me far more than it has taken. And I
can live with that.