Missing Her Already

Mom enjoying the beauty in Ouray about a month ago

Mom enjoys the beauty in Ouray from her new wheelchair, jus a month ago

Adam arrived on Tuesday night. It’s good news:  he sleeps irregularly, so he’s often up in the middle of the night — just like Mom. He makes her coffee and breakfast and keeps her company before I’m even up.

On Wednesday morning there is an email from Julio, one of our companions on the Camino de Santiago. He must have read the blog post in the email he is responding to, but he cannot bring himself to mention it. He writes:

Inge , you look nice in the pic, i think last time i saw you, you were looking with less weight …
You still my heroine, my amazon, always struggling to survive and always nice smile. Olé …

She takes Ativan, otherwise known as Lorazepam. The label says it’s for anxiety, but the main benefit is to prevent nausea. The downside? It makes her very sleepy. She is usually sleeping, and when she is awake she is nearly still asleep. Her speech is slower, her cognition slower, her laugh also slowed-down. She is no longer alert. She makes a few jokes, but she isn’t talking about food and cooking, not watching TV, not making much conversation – even the kind that used to annoy me. Our shopping together, even with her in an electric cart, has stopped.

I judge myself for thoughts of missing my mother: am I being sentimental? Maudlin? But the thoughts continue: I miss my mom. She’s still here, but I miss her.

Mom groans and stirs on the couch.

“What is it?” I ask.

“I need something for my lung,” she says, reaching a hand around her right flank.

“It hurts?”

She nods.

Later, she begins hiccuping again. She has done this for a few months now.

“Something you ate?” Adam asks, tenderly.

“No,” she says.

No, I think, something that’s eating her.

And then she sleeps, and sleeps, head back, mouth partially open. Her face has lost its fat, and her skin hangs in some places and is taut in others.

My heart is breaking. My mother is still alive, and yet my heart is already breaking.

In the evening I heat up some drunken noodles, but before eating anything I stop in the doorway of her bedroom and watch her sleep. Her head is back, her mouth open. She reminds me of Oma, at the end. I go into her room and see her eyes open slightly. “Do you want the light off?” I ask. She nods or murmurs and I turn off the light. I bend down and kiss her on the head and hug her and put my head and face against hers. She says something I can’t hear. I tell her goodnight and she repeats herself so I can make it out: she wants me to lie in the bed for a while.

I go around the bed and crawl in. I had wanted to do something like this, but she was usually on her couch when she was awake. Now it doesn’t seem to make any difference if she is sleeping. She turns on her side and I lie next to her with my arm draped lightly over her side. My face is pressed up against the cloth of her pajamas at the neck and her hair. Every now and then, our breathing follows the same rhythm. I smell the scent of her hair and pajamas. She is so frail. My eyes leak water. I feel tears from my right eye drip across the bridge of my nose, down the other side, and around the left side of my mouth. I feel them wet her short, grey hair. I lie there, thinking of stopping time. Of making this moment go on forever.

Will my mother be here in a week?

After perhaps 20 minutes, maybe 30, I am hungry and want to return to my now-cold drunken noodles. I begin to extricate myself but she turns and puts her right arm across my chest and around the right side of my head. The fingers of my right hand clasp her upper arm. “You my sonny boy?” she murmurs. “My sonny boy.”

“Always,” I say, in a fierce whisper.

I try to be present, try to soak it up. Will I remember this? Let me build a memory. I feel her breathing. I feel her hand, lightly clasping mine on her stomach. I see the light coming through her open door from the living room. I can’t believe I am even here. I am so sad, so afraid.

I love her so very much.

Starting the Camino de Santiago, September 2011

Mom and I starting the Camino de Santiago, September 2011, with Don Julio Redondo of Bilbao, left

True History of the Camino de Santiago

Mom’s new favorite book, featuring Mom and Julio

Messages to My Mother

Listening to all the letters and Facebook posts we’ve been reading to her, my mother has had a

Mom, early September 2014

Mom, left, and sister Christa, early September 2014

hard time believing how people really see her.  She seems truly bewildered that she inspires people so much with her signature combination of passion and gratitude. With her passion for cooking and teaching kids to cook, she’s inspired an extraordinary proportion of her pupils to go into the culinary business.  She inspired many people with her walk on the Camino de Santiago, and with the blog she wrote of her journey with cancer before, during, and after the Camino.  On Facebook, and especially in the Teal Warriors group of women with ovarian cancer and their caregivers, she is known as an eternally positive, encouraging presence, and readers are clearly inspired by her perspective, like her gratitude for nature’s beauty even in the midst of life’s great challenges.

Here’s what I’m talking about.  Herewith, a letter from Grace, whom I met in Washington, D.C. several years ago, and, below that, a number of Facebook posts from my mother’s Teal Warriors, a wonderful Facebook group consisting of women with ovarian cancer and their caregivers:

Dear Inge,

We have never met, and yet, you have influenced my life immensely. I write these words to you today with so much love and gratitude.

Many years ago, I decided that someday I would walk the Camino de Santiago.

Last year, when the funds were (finally) there for me and the trip became a real possibility, I began my research and planning.

Your blog, Camino not Chemo, appeared on my Google search.

I read the entire story in one evening. I remember so clearly curling up on the couch, laptop there with me, ignoring my phone as it rang, literally blocking out the world… reading long into the night. “Just one more entry…and then I’ll go to sleep…”

But I couldn’t stop reading. Hours went by. Quickly!

Reading all about your journey, the physical one and the spiritual one, was a godsend to me. I know the words were sometimes yours, sometimes Cameron’s, but what shined through always was your strength. Your infallible spirit. Your determination. Your bravery. You are, quite frankly, one of the strongest women I “know”.

I was truly overcome with emotion when I saw the pictures of you there, outside the Cathedral in Santiago. A beautiful, joyful face. Healthy in body and soul.

And then, upon your return to America, I continued to follow your journey…

This battle that you have faced with such dignity and courage.

Many months later, when I began my own pilgrimage across Spain, you were with me. I thought of you as I followed your footsteps across the Pyrenees, when I knelt at the base of the Cruz de Ferro, when I swam in the lake at Molinaseca, and when I embraced my friends when we arrived in Santiago. I thought of you as I continued on to Fisterra, when I jumped in the ocean there at the “end of the world”; for me a pagan baptism, of sorts.

And I think of you now. Everyday! With so much love and gratitude.

Thank you Inge. Thank you for sharing your journey. Thank you for sharing your life. Thank you for educating so many of us, your faithful readers, on healthy living.

Your story has inspired me. In many ways, you have changed my life. My journey would not have been the same without your words. And I will think of you as I continue to walk my life’s journey.

I am eternally grateful.

Your friend,

Grace Santarelli

The notes below are a sampling from the comments from members of Mom’s Facebook group, Teal Warriors:

‪Denise:  Please tell Inge I’m thinking of her from the UK. Her posts, her pictures helped me through my toughest times with my late ‘Little Mum’.

‪Pam: There are no words to describe my feelings and I am sure those of many others. ‪Inge Cheatham‬ – you are an amazing warrior. As Kerie said, you have set a very high bar. I too was drawn in by the beautiful pictures and inspiring comments you posted each day. I miss them but mainly because they reflect you. Even through all of what I just read about, you were posting encouraging positive comments when you could. I am pleased that you are receiving such wonderful support. We will have tea together in a beautiful flower garden someday… Praying for a miracle. Also comfort, peace, and some joy in each day. I love you my friend!

‪Susan:  Please Let dear ‪Inge Cheatham‬ how very much she is loved by us all. We are keeping you all in our thoughts and prayers. She has warmed all of our hearts at one time or another.. God Bless

‪Linda: ‬ This flower is for you Inge… Protea – the flower of strength. Love and Prayers to you sweet Inge. Thinking of you now and always.

‪Andrea:  All the beautiful words and photos you have given us Inge here is one for you [with a photo]

Colleen:  Thank-you for letting us know ,your Mom has helped so many of us please let her know we are sending her positive healing thoughts.

‪Betty: ‬ Inge, my dear teal warrior sister, never have I known a more compassionate and loving lady that understands the sad part of our illnesses yet always finds joy in everyday. I love you, Inge. Please find peace and comfort in your coming days. God bless you, my special friend.‪

Valerie:  Inge….you are an inspiration to a lot of us,,,you are very courageous and beautiful. Prayers to you my dear.

Victoria: Cameron! Thank you very much for updating us. I am thinking about your Mom every day, and she is in my prayers. Even when i am not feeling good and can not write my post, i am looking if there an update from Inge. She is Amasing. Sending my prayers, energy and healing hugs to her. God bless your family!

Karen:  When I check Facebook, I usually start by looking for Inge’s post. The beautiful pictures and encouraging words are a great start to my day. Even when she is going through a rough time, she remains optimistic and informing. I have been going through a rough patch and had not checked for Inge so this news is hitting hard. Please let her know what an inspiration she is to us and what pleasure she gives us. You, Cameron, are such a loving and caring son. I’m sorry for all you’ve gone through but you have given so much to your mom and her pride in you comes through in all her posts. My heart is breaking but thank you for keeping us informed.

‪Ruth:  Please tell Inge all the messages she is getting, she has helped so many of us. She inspired me to get on with life. Cancer does not define us, it’s a part of us. She has helped so many of us to stop and see the beauty in nature around us. She is the rock on our teal warriors. (((((((((((((((Biggest hug ever))))))))))))

Susanna:  Thank you for letting us know Cameron , I think about you Inge every day , you are my backbone , you giving all of us hope and strength , and a lot of useful advice, a kick in the butt sometimes, you made us cry, and you made us laugh, you are an absolute angel. Lots of hugs prayers for you and your loved ones.

Sharon:  Prayers for you ‪Inge Cheatham‬, you have given so many of your teal sisters inspiration to keep going. Love and hugs to you.

Beth:‬ ‪Inge Cheatham‬ has been a beacon to me. She is the light of love and caring. Always striving for just a bit more of life’s beauty.

Want to see what they all mean?  Then enjoy this!

True History of the Camino de Santiago

Mom’s new favorite book, featuring Mom and Julio

After Chemo..

The cancer ward at St. Mary’s is a depressing place. Not one little, ol’ plant. No nice, soothing colors. Nothing to feast the eye on. There’s a row of Lazy-Boy chairs against the walls and that’s it. Nurse’s station in front. When I remarked on the bleakness of it, one Nurse said, that as soon as it’s nice, one could go outside. (What to do in winter months?)

Once we came home, I rested since it was somewhat tiring. I was a bit apprehensive waiting for the second day ‘boom’. I was on tenderhooks to see if this awful nausea would appear. I was given prescription and instructions how to take them. Compazine at bed time and Zofran in the morning. In between I would take some Marijuana as I’m always worried about side effects from pills. I only felt a small ‘tinge’ of nausea which disappeared later on.

It went pretty well, I must say. NOTHING like the first time, when they threw the whole chemo truck at me.

Friends came with soups and flowers and warm hugs. Took me for walks to get things moving. That is the challenge now. This awful constipation caused by chemo. By the time it’s finally working, then it’s time for the next chemo. I thought a bit ahead and took a softener and small laxative on the day of the 2nd chemo. I figured by the time it would shut down, I would be a little ahead. As well as eating Prunes. My Oncologist advised that I should drink warm prune juice, first thing in the morning. Well! I don’t think so. That is truly a horrible thing to do. My gag reflexes work very well on that one.

When Tuesday came for 2nd chemo, Cameron drove me to Grand Junction. Blood draw and waiting for Lab results before going in to be attached. This time, there were quite a few people there, a lot of them, men. Older and younger.

Cameron and I worked on the ‘Camino Book’ until I fell asleep. (He had ghost written a book with his ex-wife, which is now on Sale everywhere. ‘The Cat Whisperer’ by Mieshelle Nagelschneider. A truly fantastic book for any and all cat problems. Without Cameron though, this would have never taken place. Even though he was barely mentioned, we know of his contribution and efforts. )

Two days after chemo, there were the first  signs of ‘side effects’. Almost nauseous. No appetite and tired. Joint pains and Neuropathy on my foot soles. Those are like electric currents of shooting pains. I am going to have treatments for that. There are pills and good creams but who can afford it? Medicare does not pay for that.

My dearest friend, since childhood (now, over 60 years of great friendship) called and told me she was coming to visit. I am soo happy. There’s nothing like a good, ol’ friend who knows you inside out and still likes you.

Friends ask me, what can I do for you? I am so very lucky and blessed by so many wonderful people in my life. My neighbor, Rob who comes to my aid, no matter what it would be. Small repairs and taking care of the garbage to the curb. My favorite Mike, who comes and checks on me, texts funny stuff and repairs bigger things but also giving me his friendship along with that of his wife and son. Then, a aprade of wonderful friends. My Bonnie, who comes like clock work each Tuesday, either to take me out or brings food and good cheer in.

Yesterday, my friend Monika came with good soup and a few grocery items, instead of flowers. (Thank you.)

When people are sick, there are a few things which would really perk them up. These are my suggestions and thoughts. A gift certificate for a pedicure, massage or Accupuncture. A few could get together and pitch in, that way it’s not so costly for one person. As I look around the house, even though it’s fairly clean, there are things left behind. Just don’t have the energy or I am near nausea and have to keep still so as not to invite it in. A gift certificate for house cleaning would be awesome. My friend Inge B. showed up yesterday with a Orchid plant, fresh, organic strawberries and a British movie.

This is a very expensive illness. Even with GOOD Insurance, which I don’t have. I am constantly stuggeling to make ends meet.

My friend Berle made an awesome Ginger veggie soup with chicken ‘meat balls’. My friend Lynne came with a very good carrot-ginger soup. My little buddy comes, just to be near and we watch companiable T.V. So far, so good. I have now 3 good days before next chemo and then I have 1 week off. I going to ask how many chemo’s my Onc has in mind. I would agree to six or eight but NOT 20!! It’s too soon to test the effectiveness, so I don’t know what the numbers are.

(I try to write with minimal mistakes/typos. But, I did notice that when ‘chemo brain’ happens, things get fuzzy and sometimes, I cannot recall a word or know how to spell it, whereas before, there was no problem. So, for those mistakes I appologize.)

I aslo want to thank the people who send uplifting e-mails and comments. Most of them, I have never met but you must know how much this is helping.

 

 

 

Days on the Camino, What I Miss (Part II), and a Secret to Happiness

I was married, briefly.  The nature channels tell me there are penguins with longer relationships.

El Acebo to Ponferrada: More Jamón and What I Miss

Supporting

DSC_0395 (1)
” Inge’s most loving embrace. Reuniting with a fellow pilgrim “

Supporting Treatment

Inge is a fighter. She beat cancer after grueling surgeries and chemotherapy 11 years ago, and she walked nearly 500 miles across Spain, in late 2011, in part because she hoped the returning cancer might just go away on its own. But the Emperor of All Maladies, as it’s been called, is still with her.

She’s been sent to test after test, and there are probably more tests, and treatments, to come.  We’ve been asked for an easier way for her friends and supporters to help out with the expenses, so here we invite anyone who has been touched by her or her story either to (1) buy the amazing book True History of the Camino de Santiago, written by Inge’s son, Cameron, or (2) donate any amount you choose toward her treatment. Subscribe with your email, above right, to watch Inge’s progress.

See what the True History of the Camino de Santiago book is all about: www.TrueHistoryCaminodeSantiago.com.

Donate:

 

Below are two little movies we made of Inge on the Camino de Santiago. We think they show her passionate, fighting spirit quite well.

Watch Inge Symbolically Leaving Her Cancer at the Iron Cross

In Santiago at Last: How She’ll Look Once She Beats the Emperor Again!

You can donate any amount you wish. Buen Camino!

The Verdict: Cancer. Again.

A few days ago, Mom must have been having thoughts of mortality again, because she arranged for me to have power of attorney over some funds she has in an account in Germany “in case anything happens to me”.  She also mailed me her “UBC [USB] stick”, which has her notes on her life story, illness, and, not least, recipes.

Today she Facebooked this:

Dr. just called with Pathology report. Yes. It was cancer but he’ll send it off to Mayo clinic as he disagrees with pathologist [who erred in one of his key premises, that Mom’s lung cancer was her “primary” cancer, when her primary is the one from ten years ago:  ovarian]. It was “clean” without any others in there.

And she sent me a message from there too:

Just got report and it’s what I knew. Will now start the ‘Gerson method’ for sure. Need a different juicer. Mine’s crushing and not expelling the juice.– Will you start checking on flight cost? Where are we starting? French side? It’s the prettiest. :-)

In other words, she’s as determined as ever.  So here’s where things stand:

1.  We expect a report on the actual kind of cancer, and type of cells, from the Mayo Clinic within several days’ time.

2.  She’s throwing herself into the Gerson Method.  We’re looking into juicers that actually facilitate the whole point of juicing – at costs of around $1000 on eBay, but stay tuned to see who – we humble deserving sorts or the faceless eBay masses — wins the next auction (I’ll even take bets on who wins the betting).  Pricey, but we think it’s worth it.  Penny-wise, pound-foolish – and Mom’s pounds, so to speak, make up some very precious cargo!

3.  Mom is now clear that she wants to spend six weeks in Europe, walking as much of the Camino as she’s able, and then – and this thrilled me to hear it, Alp-lover that I am – reward herself with a few days in some Alpine spa, a la the old-fashioned “rest cures” popularized in Nobelist Thomas Mann’s The Magic Mountain.*

4.  I’m researching online and asking Don Julio, our Man on the Ground, what city to fly into, where to begin, what to bring, what it should weigh (a critical consideration), and so on.  As I do that, I’ll build our Resources page . . .

 

* Except that, if I recall correctly, Mann’s hero, Hans Castorp, a symbol of [pre-WWI Germany? European bourgeois society?] was sort of in love with being sick and dying. Though he visited the Swiss sanatorium of the title (based on the famous Waldsanatorium in Davos, Switzerland) only to see his tubercular cousin, his health got mysteriously worse and worse, so that he spent seven years there before being called up for World War I and, presumably, his end.  Mom is the anti-Hans.

“It wasn’t a minimally-invasive procedure after all”

Mom called me today, having just gotten out of the hospital.  My first reaction to her voice was concern:  she sounded . . . sad.  Or emotional.  Turned out she was, in fact, in “a lot of pain.”  One of the first things she said was that the procedure “wasn’t minimally invasive, I can tell you that.”

“I don’t know why I thought it was going to be a simpler procedure,” she said, in that slightly higher, sleepier tone.  “But I guess I’m glad I didn’t know what it was going to be.”

“You probably would have just worried more, to no effect,” I agreed.

“I just wanted you to know I’m going to be out of commission for a while.  Julie” – a close friend of Mom’s who is around my age – “is here and she’s helping me.  I have to go now, though.  I need to lie down and just rest.  The pain is really terrible.”

“Okay,” I said.  “I’ll talk to you later.  I love you.  And have someone read you my blog article!”

She said she would.  And off she went, probably to sleep.