Thursday, July 31, 2014

I hardly know where to begin…

I’ve been to Bastyr twice now, once with the nutritionist and then we were fortunate to get right in with their naturopath who works primarily with people who have cancer. Her name is Dr. Leanna Standish and Mike has declared her my new best friend. She was a force and she is awesome.

With Kelly the nutritionist, I learned about the chemo and protein and that was very helpful and makes complete sense.She also talked to us about what to do and what precautions to take if my white blood count dips below certain numbers. She was awesome and very helpful. And, she was fairly adamant that we go see Dr. Standish. As it turns out there was a cancellation so we were able to get right in.

Dr. Standish has worked with oncologists around the city and has an ongoing relationship with Fred Hutchison…so, it was great going into it knowing that she works with oncologists and not just doing woo-woo medicine on the side.

Like everyone else we’ve met she couldn’t believe that I have stomach cancer…it is just too weird, as I am otherwise so healthy and had no symptoms. She is the first person to look at me and say “You are going to get through this.” She said it a couple of times in a couple of different ways, and sounded rather convincing. No other medical professional has made this statement. She was easy to talk to, extremely knowledgable, confident and had strategies.

I’ll be taking some supplements for now, ones that actually protect my stomach and work with the chemo to kill the cancer.  Then I go back to see her after my scan in 5 weeks, sooner if there are any issues/side effects I need to see her about. But, she said the real work with her will be after the chemo. At that point she’ll put me on a broth cleanse and then I’ll take herbs and goodies to protect myself from cancer. 

For those who want to know, she has me on turkey tail mushrooms 2x a day and melatonin before bed each night (it not only helps with sleep it is an immune booster …who knew?). She said I can do anything topical (go ahead with the frankincense) but she knows that all of you are telling me crazy remedies and said that I should just say, “Thanks, I’ll ask my doctor about that.”

I am so happy to have Dr. Standish be one of my health care providers. I feel like she and Kelly, the nutritionist will provide answers to all the questions that Dr. Kaplan really does not want to/maybe can't answer. It feels positive and proactive.

Now…the Elwha…it was magical and fantastic!
Last fall, at the beginning of the school year, one of my former students, Owen, brought me a brochure from Olympic National Park about the Elwha River along with a note he had written. I saved it in my: "must go see" pile for a year and finally we went! You can see a picture of his sweet note below. So thoughtful, kids on summer vacation thinking of their former teacher and knowing what I'd be interested in doing and seeing! I love that!

What a beautiful day for a trip to the peninsula! We packed a picnic, hopped on the ferry to Bainbridge and headed on over. We stopped for a  picnic at Sequim Bay State Park and enjoyed plenty of protein; smoked salmon, boiled egg, cheese along with crackers, tomatoes and basil…it was all yum! 

From there we went to Patti (former Pathfinderite) and Paul’s brand new house past and up from Port Angeles. Gorgeous new home, beautiful. It was fun to visit and get a tour. Patti and Paul then drove their car and led us down to the beach where the Elwha spits out. We said our goodbyes, they, headed back home and we went exploring up and down the beach and then back up the trail and through to another part of the river. It was magnificent. This is a powerful river and we’d read a bit about how quickly it is restoring itself to its pre dam beauty and diversity. When the dams were built there was a federal law mandating fish passage, but it did not happen. Already, the salmon are returning and feeding the ecosystems up and down the river. Quite inspiring! 

As we walked down one trail there was a spot filled with damselflies (i think that is what they were). They were fluttering on either side of the trail and leading our way down the trail. We found one golden one. I’m attaching a picture on the blog to show you this beautiful creature. Roz, it was like one of your fairies and I thought of you.

The 2 days prior to this I had been so fatigued and I was worried this day would be no different. But, I was completely energized, and felt great all day.  I shall give mother nature the credit for that. Dee had just given me an article about the power of getting out into nature and in it they said, they don’t call it the great outdoors for nothing…agreed! It was a great day outdoors!

But that’s not all. We left the mouth of the Elwha and the trail that led up river a bit to go find a little more. We passed a road Lower Dam Road I think and Mike said that Paul had mentioned that road, so we turned around and went back. We parked and walked up a fairly short ADA accessible path filled with salmon berries (yum…gotta have my berries!).
We stopped at the oversight there for a bit and noticed another path, less accessible and decided to check it out. We stepped into a magical kingdom of fern and cedar. So gorgeous with that woodland scent that is so rejuvenating. We followed the trail up and down and around and not too far to the end and another lookout. There was an elderly (even more than us) couple with their 2 dogs and we chatted for a bit then they headed out. Mike stepped over to where they had stood to check out the telescope thing and called my attention with a start. Taped to the pole of the telescope was an envelope, on that envelope was written: “Important, Janet Osborn, July 30, 2014.” What the hell! We were dumb struck. We so easily might not have made it down this path, might easily not have noticed that envelope, but there it was. I swear. It was very old-school Pathfinder stuff…you know ancient forest speaking to the kids! Notes from Mary Ann Boren Denny! That kind of thing…so sweet. Our theory is that it had to be Patti…but she has neither confirmed nor denied! Anyway, I’m going to try to post a picture of the letter. It was awesome! Thanks Elwha salmon! It was great to visit you, too!

I continue to feel good and strong even in the face of the daily chemo pills. I feel fortunate to be tolerating them so well. I’m getting exercise in one form or another every day, because I have to. I don’t want to. oh well. I’m eating very healthy, back to a better diet filled with protein. I continue to be blessed with visits and goodies (thanks Maryann and Debbie for the quiche, thanks Brenden for the warm socks) and cards in the mail. The kid cards are starting to arrive and they are so dear! 

So…there we are. Better, way better, than I imagined I’d be one week into chemo, one month since diagnosis. I thank you all for helping me get here.
I'm not planning to write everyday at this point, but I will keep you updated.

Love to you all
Janet



Tuesday, July 29, 2014

What I Learned Today

Chemo kills all fast growing cells. Cancer cannot repair itself, so it dies and is dead. All our other cells regrow and I need protein to help support that cell growth. So…70-80 grams of protein a day to help to good cells regrow.
There is more, but I’m too pooped out today to blog more. Headed to bed and then to the Elwha tomorrow. *Note: spelling correction…it is the Elwha River, not Elwa…


Love to all and good night!

Monday, July 28, 2014

So Many People
Thank you to so many people!
Debbie and Jeff brought dinner Sunday and we had a great visit on the deck in the afternoon. It was so great to have some time with Debbie. This is so ridiculous that it takes cancer to make time to hang out with one of your oldest, best friends in Seattle….humans…or maybe human Americans…we are ridiculous! We do get so wrapped up in our stuff and believe me I know I’m among the best at getting too wrapped up in my stuff to make time for friends! Stupid cancer has an upside!

Thank you Tracy for the delicious dinner…we enjoyed that tonight on the deck and it was perfect for this warm evening. Tracy is a friend/mom of a former student who had pancreatic cancer, just diagnosed last September, and is kicking its ass! Now she is just taking small doses of clean up chemo! So great to talk with you Tracy and so great to see you and hear your good news! You are a picture of health and an inspiration!

I spoke with my first stomach cancer peer late last week. Gaby is a 55 year old, otherwise healthy young woman like me! She is a friend of a friend and former student teacher of mine. She was diagnosed 18 months ago and her tumors are shrinking. She was a wealth of information and inspiration. Thanks Glenda and Eddie for hooking me up with Gaby.

I continue to get cards in the mail and goodies on my porch. You are all so generous and thoughtful. 

Saturday we had the changing of the guard…Michael went home to Portland and Betty came back to Seattle. It is great to have Betty back! It was a long week and a weird time to be away. It was sad to say good bye to Michael…but he’s going to get a few things done back there and be back in a few days. He is kind of spoiling us…Maggie, he has set a precedent for sure!

Today we saw the geneticist and he has a couple of possible genetics links that might apply to me. It is a little far fetched and not likely, but worth looking into. He said it would not likely change my course of treatment but would inform my relatives. So, they sent blood to Utah and if insurance will cover enough of the costs we’ll find something out in 3 weeks or so.

Following that appointment we saw Dr. Kaplan. It was just a check in and we are going to keep to the course. He says there is no correlation between side effects and how well the chemo is working. He also said the side effect symptoms can be accumulative, so enjoy feeling good now! And so I am!

I continue to feel ok to good. Mostly I am fine. Really my only complaint these days is I’m feeling so tired. I really do not like naps, they drag me down, but I have had to succumb more than once and I’m not sure if I feel better before or after the nap…but I hardly have a choice.
So knowing I feel pretty good now and it might now stay that way we are taking a day trip on Wednesday (first day with no appointments) and I think we’re going to head over to the Elwa River and see where they took the dam damn down. I’m currently reading a novel West of Here, set in the late 1800 and involves the taming of the Elwa River. It’s a good book and I’ve wanted to go check it out ever since the damn came down. So…road trip!The weather is gorgeous and it should be a good day…
Tomorrow the nutritionist…until then…
Good night and love to you all!


PS I can’t help but tell you about our sad bird drama…

We have such a sad drama going on outside the window, on the deck right now. We have a very active productive bird house where many little baby birds have hatched and flown the coop. Currently we have at least the 3rd batch of babies this summer up there chirping away. The typical pattern is all day long the mom and dad come and go bringing food for the babies and each time the adult flies away, the babies hush; as the adult returns they start chirping away again. Today I noticed that the babies just keep crying and it finally dawned on us that no one is feeding them. It’s just awful! They’ll quiet awhile but then another sparrow will come near and they just start up again. This is heartbreaking! I’m still holding out hope that a Mother Theresa sparrow will save the day.



Friday, July 25, 2014

It’s Friday

Physically I'm feeling pretty good today but cancer is making me sad. I don’t want to not go to work. Like I told Jennifer today I want to go to work and complain about how hard my job is! It seems like such a luxury. But we have a good plan with a great sub in the works and I’m feeling great for her and the kids…and I know she’ll let me give her guidance if I’m up for it. And she couldn’t be going into a more supportive environment. Everyone wants her to succeed…so, its good, but it just makes me sad.

The weather has worked perfectly for me this week. After my procedure and first dose of chemo the rainy cold weather for a couple of days was perfect. And today, the sun came out! Mike, Rudy, Gertie and I had a nice walk around the neighborhood. I’m giving myself just a day or two more until I get back downstairs, or outside to get a little more vigorous exercise.

My nausea continues to be mild at most and only once or twice daily. A couple rice crackers, dried apricots, and/or magic broth takes care of it pretty quickly. So, I’m feeling really blessed for that. Mike told me last night I had a good appetite. I told him if he’d said that a month ago I would have smacked him! But now, I get an atta girl for my appetite! The upside of cancer?

The effect of the cold on my hands and feet is becoming less of a problem. I can’t drink cold yet, little pebbles run down my throat if I do, but our instant hot water mixed with tap water is the magic there. I can actually touch things in the kitchen without tingling! We’ll call that progress.

Off and on in my life I’ve been troubled by restless knee syndrome. This has intensified every night and moved to my hips as well. Last night I had some pretty good aches in my bones. I took some tylenol and it helped and it is better today. I imagine, like restless knee, it will creep up when I’m tired…I can manage that.

A little more normalcy for the boys today; Michael went to work all day. Mike went into work and talked to them about medical leave. I cleaned a bit and putzed around paperwork downstairs. Make came home and played with wood while I took a nap. 

Yesterday we had no word from Maggie, she was in a no wifi zone, but today we got a snapchat with Maggie in a darling hat at the beach, I had an email and then the girls showed up on facebook…so adorable and happy…medicine for the momma!

Next week we go to the naturopathic nutritionist and for all of you who have offered to cook for us, I’ll have more information about the foods I should eat and those I should avoid. Thank you all so much for all your offers!
I continue to feel so much and support and love from all of you. You are amazing and a positive force of love.

So, no big news is good right? I’m taking the weekend off from the blog. So I’ll see you next week.

Love to you all
Janet



Thursday, July 24, 2014

so far so good

I know lots of you are having trouble posting on the blog…i get texts and emails everyday. I know some of you have google accounts and still can’t post. If you have a google account…have you registered with this blog? I think that is what you have to do.
If some of you savvy posters want to share tips…go for it. 
I also know some of you want to keep your comments private to me and I am just fine with your texts and emails. And I know you don’t always expect a reply from me, which is great, cause it is a good problem I have…having this much love and support.

Also, when Mike officially asked why can’t people post here is what the tech folk said…maybe you speak this language…my guess is if you can you are already posting!!! Ha!

any he said…
Comments (especially using the embedded form) are sensitive to both cookie and script filters.  You (your readers) may need to enable (stop filtering) "third party cookies", in your (their) browser and on your (their) computer.  That's the most common solution, overall - but you (they) may have to search for other filter(s) that affect your (their) use of Blogger / Google.

You can have a filter:
1. In a native browser feature.
2. In a browser add-on.
3. In a security feature, on the computer.
4. In a network device.
Please, note that any and all filters must be set properly.  If you have more than one filter (cookie or script) affecting access to Blogger, all filters must be set properly, before an improvement will be seen.

Now back to me…
Yesterday we had 2 appointments; Social Worker and Dr. Chen with a second opinion.
The social worker was a very sweet young woman, Lauren. She was kind and dear and is working on getting us some resources around parking vouchers (cause…damn!) and we found out we just get some amount of money because I have stage 4 cancer…who knew!! She is also finding out about some hair/hat things for me and perhaps some resources there for guided meditation.  She offered other kinds of therapy/support any of the 4 of us might need alone or together. It is good to know it is there.

Our second opinion was with Dr. Chen at the Polyclinic. He was so lovely and kind and sweet. He had treated my brother in law who passed away last summer and we were sharing funny Terry stories. When I asked him if I could have a scan, right then and there, because I was quite sure Dr. Kaplan had killed all the cancer the day before, he said I sounded like Terry…always wanting a scan. He was lovely. He agreed completely with Dr. Kaplan, however. As reassuring as that is, it would be nice to also have something new to chew on. He says he absolutely would not start with radiation or surgery, that chemo is how he would have gone as well. He agreed with the 6 week run prior to another scan. So, it is reassuring, but no new ideas…

Last night the lovely Westermans fed and entertained us until they had to go pick up their niece at the airport. Thank you Eddie and Marti for dinner and laughs and thoughtful stories. 

So, I still have my hair…Gillian and Shelly…I should have it another week or two, when it starts coming out I shall have it shaved, somehow, somewhere. I have no plans for tattoos of any kind right now. I’m at my needle maximum! 

I have a good appetite and am eating quite healthily. Good healthy food!
I am not throwing up! My first night home from chemo I felt some nausea and was very toasted. But since then I’ve had only mild waves of nausea that some magic broth has taken care of!
I’ve gone from being ale to say I am taking no medication to not even being able to begin to recite for you my list…no way! Oh well…you do what you have to do!
Mike had to wrap my incisions in cling wrap but I was able to take a shower! Life is good!
so far so good!

My most recently graduated salmon clan has had, all summer long, an open invitation for anyone to show up at EC Hughes park on Thursday evenings. This park happens to be 1/2 block from our house. So this morning, feeling chipper I put it out there that I’d love to visit before I loose my hair and start feeling icky. We had a great turn out and it was lovely to see so many smiling, happy people! That is just what the doctor didn’t, but should have ordered! Love my wee little salmon!

Ok, Mariners are on…Michael made me Bella’s Carrot, Orang, and Fennel Soup using the Magic Mineral Broth…I have a date with my boys.
Over and out and love to you all!



This is the poem we see many days coming and going through Swedish. I think it is beautiful. It is by Emily Dickinson, in case that print is too small. 




And this is the magic broth before the magic and actually 
before the broth. Lots of yummy veggies and some
mystery items. Then it was stirred by many with love and
simmered for at least 4 hours. It is now doing it's job of
curing what is ailing me!


And look, I added photos to this blog ABMS!
Sharp as a tack!

More later today...
No doctors today!! yipeee!

a

Wednesday, July 23, 2014

Good Morning
It’s so nice to have a morning where we don’t have to run out for fun or doctors…just hanging and getting caught up on things.
I had a PS to add last night, but I was just too spent. So here is an a.m. PS…

Rudy…Rudy is recovering nicely. She clearly is a trooper and since this got so bad without her complaining she certainly has a high threshold for pain, so we are giving her the doggie ibuprofen whether she asks for it or not. Mike called this morning to find out the results and they did not have it yet. 


Michael and Eva…have been awesome! cooking and cooking, cleaning and running errands. Here are some of the things they’ve done, individually or as a team: cleaned Betty’s gutters, cleaned the kitchen (more than onece!) weeded a huge patch in our front yard and then covered it in mulch from our neighbors back yard (thank you Vince and Lizzie), cleaned the deck, watered the gardens, cut down blackberry bushes, fixed the lights in the laundry room, broke down boxes for recycle, cooked and cleaned and went to the grocery store again and again and cooked some more. And most importantly, they both make me laugh, a lot! Such funny kiddos…I thank you both!

Eva had to leave yesterday morning (we miss you Eva) and Michael is staying a few more days, at least till Betty gets back on Saturday.
Such good kids! And, I’m looking forward to Maggie joining the team when she gets back from Europe. We miss her so, but her pictures and messages make me so very happy! I’m so relieved she gets at least 1/2 of her trip.

Magic Mineral Broth is awesome. When my first wave of nausea came over me yesterday evening it was perfect!!!! Warm and soothing and made with love. I had some nut crackers on the side, had to soak them a bit… too crunchy. Michael does not want me to call them nut crackers for some reason…funny boy!!

Side Effects…
The only problem I had last night at bed time, other than generally feeling a little funky, was the site of the port. It just plain hurt. They cut me open in 2 spots put a titanium port inside me and fed a tube down my jugular…hell yes, it hurts! I cannot ice it because of my sensitivity to cold. So I called the doc to get the ok on Tylenol and was able to take some. I think it helped.
But the weirdest thing is the cold, I can hardly touch anything and I need any water warmed up. Cold surfaces (a cup, a plate, the counter, the iPad) just send tingles up my fingers and it spreads across fingers I didn’t even use. So weird. It passes quickly and is not really painful, but I guess if grabbed something out of the freezer it could be pretty bad. Today I thought maybe this is where the superpower “to freeze things” came from!! So many of my girls choose that super power this spring when we were surveying “What super power would you want?” No I don’t want to be invisible, or super strong or fly…really??? I just want to be able to freeze things…thanks Disney!
The other weird thing is food texture. I cannot crunch on my back teeth. It sends weird reverberations through my jaw. So little bites of warm soft food…or tiny bits of other things, seem to be working. I’m drinking lots of tea because water out of the tap is freaky in my throat. But I still have my hair and i’m not feeling nauseous…so that is all good!

Time to get ready for the social worker and then our 2nd opinion at the Polyclinic. Wish us luck!


OK, disclosure…I am finding that I get great pleasure out of writing this blog. I do not expect anyone to read it, at least not all of my babble. You can look at how long an entry is, maybe skim it a bit..yea, she is doing ok and move on to the rest of the cyber or better yet, the real world…this is really for me, it is therapeutic and fun. And I’m happy to share with you!!

Tuesday, July 22, 2014

Mucinex Monsters

This was one long day. We started at 7:30 at the hospital getting my port put in. It was quite a process as they use an antibiotic prophylactically through an IV drip and it takes a bit of time. Then after all the explanations and details the doc was ready and they started the happy juice. It is the same stuff they use for colonoscopies, only not as much. It was awesome…just the right amount. My eyes did not want to open, I was cognizant of what was going on but really could have cared less, was able to hear and respond (probably in grunts). I enjoyed it maybe too much…oh well!

After the port was in it took a while to come out of lala land (and I really did not want to). Then they gave me the boot over to the cancer building. I had a blood draw and thought they’d get it from my brand new shiny titanium port…but no! they had to poke me again…and I didn’t get Billy…oh well.
We headed up from there to Dr. Kaplan. We had a really good visit, we were able to ask him our burning questions and I just had an overall  feeling that this was the right place, and the right doctor. It felt good and I felt very ready to take this on. I had imagined how horrible I would feel walking into my first chemo treatment, but I actually felt empowered…finally 21 days after diagnosis I was ready to go.

Today I played the name game with Dr. Kaplan we talked about Andrea (nurse hero) and folks I know that he has treated. When I left today he said something like: I’ve got to get this right or I’ll be hearing from Ms. Westerman.  Ha! That’s right Hank! Eddie’s got my back!

Shasta was my nurse today and you will not be surprised to hear me say how very dear and sweet and lovely she was. Quite young  but very confident about her job. Perfect. She started with saline, and an anti-nausea drip followed by a steroid. At some point she had to flush the saline and put in a sugar water drip with a fancy name (i called it hummingbird juice) and then came the toughy drugs. The first chemo drug looked like orange kool-aid (and she warned me I would pee orange). She had to stay there for 10 minutes and push it into me. Then another line check and the big guy came out…a 2 hour drip. Let’s do this thing!

This morning during the port procedure I was trying to have these positive thoughts and visualizations of the port opening the gateway for the drugs to come in and heal me, but none of my efforts felt quite right. I did it anyway and changed out my visualizations trying to make it fell right (probably cause I was actually in lala land!!). But when I was upstairs for chemo and the drip started happening, I think it was less than 3 minutes and I saw those creepy Musinex monsters (from the commercial, having a party in your nasal passages), I saw them packing up their party and getting the hell out of Dodge. I did not mean to visualize the Musinex guys, actually didn’t want to, cause yuck! But there they were, they made me laugh and I added them to my more “socially appropriate” visualizations!!

My nurse navigator hero, Deb, came by today and ate lunch with us. She was just as lovely and kind and helpful as she had been on the phone. It was nice to meet her. I had an egg salad provided by my chemo folks and Mike went to get an “unwich”; a lettuce wrap from Jimmy Johns. 

In the blood draw room we ran into a couple of folks we know, Mike grew up with them and we see them now and then at weddings and such. Mom has cancer and one of her daughters was there with her. We chatted for a while and then again upstairs. Later another sister came for the changing of the guard. It’s a small world. Everyone has been affected by cancer.

We read our cancer homework, sent texts, emails and checked facebook. I was not really interested in putting in head phones as I wanted to have all my senses available. The time passed…time to go home.

I felt really good heading home, called my mom and put her mind at ease.
Since then I’ve had a few waves of nausea, not too bad. The side effect that is affecting me most is sensitivity to cold. I can’t touch many things without having tingly fingers. My feet tingled even through my socks. I tried to drink plain tap water but it was way too cold and it felt like I had little pebbles in my throat. But I ate a good healthy, warm dinner. I have blankets and can’t touch a dish (oh that’s so sad! Ha!)  Luckily the keyboard is not too cold. Now I’m done. Time to go to bed.

Again, thank you all for your amazing outpouring of support. I know many of you are unable to post here (even if you have a google account) but I’m hearing from so many in so many ways. 
Thanks, thanks and love to you all.
good night

Janet

Monday, July 21, 2014

Magic Mineral Broth

Wow! I am overwhelmed with the outpouring of love and support that is coming my way. I am so blessed because all of you. Word is spreading; more and more people are learning about this cancer (not “my cancer”, I’m just borrowing it from the universe, I shall annihilate  it and then it shall be gone) and showing up on my phone, in my email, on this blog and I feel so much good energy.

There have been quite a few folks wanting to visit and there is not enough time in my day so yesterday I invited a few folks over to visit. Prior to that Mike and I had made a run to PCC to load up on healthy foods and thanks to Emily’s awesome book: The Cancer Fighting Kitchen, I whipped up a batch of Magic Mineral Broth. I asked all who came to visit to give it a stir and add some healing wishes to the broth. Now, tomorrow, after my first chemo, I’ll come home to my magic broth. It is mostly veggies with some kombu (some form of seaweed) and whole allspice thrown in for good measure. It’s actually quite yummy. It was a lovely day of “sit and visits” with good positive energy stirred in! 

The down side of yesterday was our little Rudy (miniature schnauzer) needed to go to the emergency hospital (it was Sunday of course). Turns out she had a tumor surrounding 3 back teeth. The teeth and the tumor needed to be removed. We found a great emergency vet…the people were so kind…and they were able to the whole thing yesterday and she came home at 5:00. I’m calling it a sympathy tumor and really praying it is benign, cause damn...

I have tricky veins. They are not easy to find so drawing blood can be a challenge to some of those who do that for a living. Today I had to get my blood drawn…again. Well, as soon as Billy came out and called my name I recognized him. For the last few years I have been involved in an ovarian cancer research project at the Swedish Marsha Rivken Center and every 6 months I have to get my blood drawn. One time the young woman just couldn’t find my vein and she said, let’s go see Billy. We walked through the maze that is Swedish Medical Center and she requested Billy. She told me he was the master and told him she wanted to know his tricks. He said, “you feel the vein, you don’t see it” and “you wait for the vein to come to you.” Ever since, when someone has had a tricky time finding my vein I think of Billy…and there he was today.

He took one look at my left arm where an IV had left a bruise and said “Who did that to you? I won’t let that happen.” I told him how I remembered him and what he said and he laughed and said how he has a reputation and people all over know him and request him. He was so sweet and adorable and had totally corny yet funny comics up in his little cubicle and told me a couple jokes suitable even for me to share in my job. He is my hero of the day! He told me I can request him when I need blood drawn. I love Billy!

We proceeded from Billy to another part of Swedish for an echocardiogram. It was kind of cool to watch my heart beat and see the ventricles and valves and such. It looked like a strong heart to me, and I have really awesome blood pressure! 

Mike and I met David (my principal) for lunch. It’s so hard to see people who I care about and who care about me for the first time. Everyone just wants to make this go away or at least say and do the right thing. And right now I am so healthy that the whole thing does not make sense. We had a nice lunch and were able to catch up and have some laughs. We agreed to the plan that Jennifer, Genya and Lisa and I came up with for my classroom for the fall.

Then Mike dropped me at school for a couple of hours. I just needed to go through and throw out a few things and pack up a few things to bring home. I did not do nearly as much as really NEEDS to be done…but it is something. I have been teaching at Pathfinder for 19 years… this would be 20. One tends to accumulate a bit of “stuff” when one teaches in one spot for so long. I feel for my sub, there is a lot of “stuff” for you to weed through.  Luckily most of it is awesome stuff…some of it, well, they are treasures to me. 

I was not alone at school. While I weeded through the room Lisa D and Andy had a picnic on my floor and Jennifer pulled pages out of old planners to be able to recycle the paper and toss the covers. It was great to see them and so good to visit. Again, it’s hard to see people who really just want to be able to make this go away. Everyone feels so powerless. But you are not, because I’m getting so much power from you all.

Early on Saturday we took Maggie to the airport  for 2 1/2 weeks in Europe (she is currently romping in Paris with her college roommates) and then we took Betty to the airport to spend a week in KC (so glad she gets to visit my momma). Michael is staying here all week holding down the fort and supporting me and his daddy while everyone else is gone. Eva is here, too, supporting us all and making me laugh. She has to head back tomorrow.

So, we are plenty supported and plenty loved! During chemo tomorrow I’ll be taking Roz’s suggestion and I will visualize my body accepting chemo and healing the cancer.

I’ll let you know how it goes. 
Lots of love and good night to you all.
Janet

Friday, July 18, 2014

Thank Yous
Thank you Kathy and Dan for letting us take your boat out today…in spite of our difficulties we had a great time! And the way I look at it  I was “stuck” in a small space with my children longer than I would have been if not for our engine troubles. All’s well that ends well, for us,  and I hope there are no major issues with the boat. As I sit here typing my body is still rocking back and forth a bit.

Thank you Emily for the FU cancer voodoo doll! Love it Love it! And your note, not unlike all the notes you’ve ever written me made me cry.

Thank you Andrea for going to bat for me with the doctors office.

Thank you Maria for making me laugh with a random text this morning.

Thank you Roz for the visualization.

Thank you Jenni for the reminder about all the things cancer cannot touch.

I hesitate to start thanking you by name as I don't want to leave anyone out…but you know, for sure, I thank you all. Thank you for being there for us.

And to my daily readers, I want you to know ahead of time I’m taking the weekend off. I feel good, I have good energy, I'm going to be ready on Monday to begin the fight and I'm taking all of you with me!
good night
Janet



Thursday, July 17, 2014

Success and Accomplishments
I played ping pong today calling back and forth between my doctor and my insurance co. The doctor insisting that they were waiting to hear back from the insurance and the insurance insisting they told the doctor that no prior authorization was needed. A little frustrating, to say the least. Finally, Dixie, my shero, from KPS heard my plea. She called the doctors office for me, straightened them out, called me back and told me they would be calling me and moving the appointment up. I asked Dixie for her cell phone number. She chuckled, I said I was kidding, but I wasn’t.

Not long after that Sharon from the doctors office called and let me know my appointments were moved from Wednesday and Thursday to Monday and Tuesday. It is only 2 days difference…not really a big deal, but it feels monumental! And it feels like a success and an accomplishment, my first of many on this road.

But, the highlight of the day was eating with Mike, Maggie and Eva at the taco truck on Fauntleroy, binoculars in hand, watching Michael inspect the tower crane behind Trader Joe’s. It was so cool. We were sitting at their table on stools, applauding and cheering at each up and down and turn he made. It reminded us of watching him play ball for so many years…”Go Michael!” “Woo Hoo!” Part of his job involves crane inspections, and it just so happened he had one to inspect in West Seattle. We wanted to tell the people in the taco truck and everyone else walking by (“Hey, that’s my son up there inspecting that tower crane!” “That’s my baby boy!”) We resisted the urge, but enjoyed ourselves quite a bit.

For the next three days I think I get to relax a bit. My appointments are set, my treatments are authorized. I’m hoping to talk to the social worker to get a few extra supports lined up, but mostly, I’m going to enjoy these last 3 days before I start my new job.

So, again, thank you all. Many of you, I know are having trouble leaving comments, no worries. I know you are out there and I appreciate all your positive thoughts, energy and prayers.

Love and good night to you all.
Janet



Wednesday, July 16, 2014

Lessons and Pizza on the Grill

I spent a good deal of the morning on the phone and the computer trying to figure out what to schedule, who to talk to and other bits about our new world. It is time consuming, frustrating and no fun. My first call was to my docs office, they were to set me up with an echocardiogram one day followed by an appointment to get my port installed and have chemo on the next day. I'm ready to go...echocardiogram tomorrow?? Oh no, they insist on having a week to get preauthorization from the insurance company for such things. So, she set me up with appointments for next Wednesday and next Thursday. That seems too long. Carrie was here, she agrees with me...that's too long. 
So, I contacted Deb...is that right, wait a whole week? Yes, they are picky about preauthorizations. Deb also set me up with a social worker to help coordinate some other services; meditation, visualization, etc.  

We took some time this afternoon to escape to Lincoln Park. A nice, hot walk and the kids, Michael, Maggie, Eva and Lillie took a swim.  Mike and I headed to PCC because all of a sudden a spontaneous pizza on the grill night was starting to form. 

On the way home I picked up the phone to call Andrea...I'm still not settled with waiting a week. As I grabbed my phone Andrea called  me...weird! Andrea gave me permission to take matters in my own hand (something I usually don't wait for permission to do...weird...cancer is weird!) and lots of other good advice. So after our conversation I called the insurance company. The nice lady there told me I do not need prior authorization for an echocardiogram!! It was 4:30 by now. I called Dr. Kaplan's office and talked to a different person. She tried to tell me that a week was ok, even not needing prior authorization.  I begged to differ, with this diagnosis, a week is a year! She heard me. I'm hoping tomorrow morning I get the whole thing moved up. We've been patient and waiting long enough. 

So that was my lesson...sometimes, even with all these good folks around, I just need to take matters into my own hands!

Now onto the pizza...we had 13 adults and 2kids on the deck for delicious pizza on the grill! Yum, the best! It was a fabulous evening!

Good night, more lessons tomorrow, I'm quite sure!

Thank you all for your loving kindness and support. I feel well loved.

Tuesday, July 15, 2014

It’s the bad kind
I’m sorry to say, really sorry to say, I do not have better news to report tonight. We are all kind of numb here, tonight.
Bottom line, it’s bad. Stage 4 stomach cancer spread to my liver through my blood. I can’t believe I’m saying this about myself. I am perfectly healthy (other than this little detail). I have my appetite, I am sleeping well, I’m having a great time with my family. Really my planter fascists is bothering me more than my stomach. It is really hard to believe. But it is real, so…
Next step: later this week I’ll have a heart test that will test the strength of my heart, which I know is really strong.
Then, I’ll be scheduled to put in a port and that same day I’ll start chemo.
The doc is not sure this chemo will work, but we have to wait 6 weeks to take the next scan to find that out. I will have 2 IV chemo treatments, 3 weeks apart and take daily chemo pills. So for six weeks we’ll be praying for that miracle. If that does not work, we’ll try a different kind of chemo. I’m counting on it working, because it might and it can, so it will.
So I will take all those positive thoughts and prayers of any kind. However you put that good stuff out, send some my way. 

Thanks to all of you for your kind thoughts, words and prayers.

Monday, July 14, 2014

Happy Cheese Day!
Monday, July 14
Today I had to be on a special diet to prep for my PET CT tomorrow. High protein, high fat, no sugar, no carbs. Eggs, meat, cheese, greens…yum!

Today I talked with Deb, my nurse navigator, a couple of times and got several emails. She made an appointment for me to see a naturopath/nutritionist who works with oncology patients at Bastyr University. She made another appointment for me to see a genetics counselor at Swedish. Both of these appointments are next week.

Tomorrow we may find out the real deal on the liver and frankly I’m not looking forward to it. I was trying to “see” the doctor telling me that it is not cancer. But, I said to Mike, it’s science. It is cancer or it’s not. There is nothing I can do right now to change that outcome. It’s not that I don’t believe in miracles, I think I do. I also believe in the positive energy of the universe and I’m working on putting out as much positive energy and thinking as I can, it's my way of praying. But as for my liver, tomorrow, I think it is or it is not.

Maggie is coming up from her overnight in Portland right now, Michael and Eva are coming up tomorrow, so we’ll be all together tomorrow night for better or worse…



Sunday, July 13, 2014

The First Week of Summer 
June 24, 2014
On Tuesday and Wednesday I laughed, danced, acted, sang, drew and colored my way through two days of Arts Impact classes with my friend Jennifer at the Seattle Art Museum. Each day I took the water taxi downtown and walked up to class. It was a fabulous professional development with the emphasis on infusing the arts in classrooms as a way to teach to the common core but also as a way to allow children to show what they know. Jennifer and I had a blast playing together in this geeky teacher way and it was actually a great start to the summer.

Thursday my day was spent at home, nose to the grindstone, cleaning my house for my sister, Kathy, and packing for Ireland. I was in control and crossing things off my list. Thursday night I went to pilates and Megan gave us a kick-ass workout. Part way through I got giddy with excitement thinking about our upcoming trip.

Friday morning I continued with my packing and cleaning. About 10:00 I was hit with a wave of nausea and dizziness. I had to lie down and each time I tried to get up, I realized it just wasn’t gonna happen. I had a heaviness in my arms, like my blood was rushing there (though in hindsight I think the blood had left my arms, for I had very little blood). It took me a good hour and a half I think to completely get over this. I had many theories, most of them involved hormones.

I rallied in the afternoon, for I was on a mission to complete my tasks! I made it to PT for my foot and ankle, I had a pedicure, and then went to acupuncture. I told Jim and Kerry all about my symptoms and Jim thought I might have a flu. He treated me gently and gave me herbs. By the time I got home I was just tired and grumpy. I really did think I might have the flu and started taking my remedies. 

So much for being in control…
I got up a few times through the night and was ok.
In the 6 o’clock hour Saturday morning things really got rocking.
I sat up and immediately felt dizzy. I headed down the hall to the bathroom and had the most serious case of vertigo I’d ever had (not sure I’ve ever had it, but this was intense). I had to crouch down and hold the wall. The room was rocking and pushing me off balance. I made it to the bathroom and had to hold on to the counter to sit on the pot. I was as white as a sheet. Here is the gross part…I pooped what I call the black poop of death (BPOD). It was horrible, disgusting. Then I could only make it to the bathroom floor. And I had to lie still. I know I got up a couple of times to the pot but then immediately back to the floor. Mike came in maybe 15 minutes later. It was too early for urgent care, so he called Dr. Dagg’s office. The on call physician said what Mike had tried to do from the start but I wouldn’t let him; call 911.
Michael was home and had awakened to our noise. When he heard 911 he jumped up out of bed and came in. I think I had crawled to the kitchen by then as the bathroom floor was too cold. Right away, Michael grabbed a pillow for my head and a blanket to warm me up. 
When I heard that 911 was on the way a burst of adrenalin helped me make it to the bedroom to change into yoga pants and a T-shirt. I lay in bed and they came in there to take blood pressure, check my pulse and generally assess my health. They knew what all the health care professionals knew automatically after hearing about the BPOD and the dizziness; I was bleeding internally.

They called for an ambulance as I was stable. As we chatted we talked about Carrie being a medic. One of the firefighters could not say enough good  about Carrie (which is true for all of us). They canceled the ambulance, and 2 firefighters transported me to Swedish First Hill in a medic unit. They were so sweet and kind. The driver would alert me to upcoming hills or turns. The guy in the back with me was kind and comforting. Mike sat in the front and Michael followed behind in his car.

I was taken directly into a room (NO WAITING! WOO HOO!) and they started, very gently and kindly, mind you, putting me into hospital attire, poking me with needles, asking me all kinds of questions etc. I cannot say enough good about the people I encountered at Swedish. My first nurse Carly, was so sweet and caring. My admitting doctor/hospitalist, Dr. Connolly, I just loved. Both of them gave us the right combination of hope for our trip to happen and the realization that it just might not. As it turns out Dr. Connolly has dual citizenship in Ireland and the US. She has 2 men cousins that never married, live in a tiny village near Galway, wear those caps, tweed vests and mostly speak Gaelic. I promised to find them and tell them about her and lift a pint for her. Our nurse that replaced Carly was named Erin but spelt Eirann. She had visited Ireland and promised that we would see her name everywhere, even on the money! She loved Ireland. We took all this to be a good omen that the trip would happen. Mike and Michael stayed by my side and Betty showed up when she could get there.

I ended up waiting 6 hours in the emergency room waiting for a bed upstairs. During that time I began to think that I had been admitted to a tiny UN. Everyone that came in was from somewhere else in the world. And everyone was lovely. When my time finally came to go upstairs Eirann  was on the phone to the nurse who would take over for her. In the midst of her phone conversation she put her head in the door and asked, “Are you a teacher?” “Yes.” “This is Andrea, Gracie Peterson’s mom!” I just won the nurse lottery! Andrea is a firecracker and I’ve now learned what I always assumed, she is an awesome nurse. She had Eirann ask me if I was comfortable with her as my nurse. Absolutely!

Andrea welcomed me to the IICU (intermediate intensive care unit) with open arms and a fervor. She was not going to let Gracie’s kindergarten teacher down. I’ve always liked Andrea. She is hilarious and energetic and not afraid to speak her mind. What a great combination for my first trip (hopefully last) to the IICU. I had a huge room which was needed for all the monitors they hooked up to me. Andrea was like a mother wolf, protecting me and making sure I had everything I needed. She was a rock star. I can't remember all that went on up there in those first hours, but I was so sad when Andrea had to go home that evening. 

In the middle of all this Kathy and Mickey were coming in to vacation in our home while we headed to Ireland. They flew in Saturday and came up to the hospital after checking into their hotel. 

On Saturday afternoon I had an endoscopy and they found a bleeding ulcer, as expected, but it did not look typical. It looked like something was pushing the stomach lining in from the outside rather than the ulcer originating in the stomach lining. They ordered a CT scan to get a better picture and threw in a chest X-ray and a EKG. I got 3 bags of O+ blood (explains why I could not get up off the floor! thank you blood donors). The CT scan showed things (spots? tumors? lesions? things?) on the outside of my stomach, my pancreas and my liver. Not good news, to say the least. We had to wait another day to get an ultrasound and another endoscopy with a biopsy and internal ultrasound before we would know anything. 

Hello Ambian and good night world.

Sunday was a waiting game. I did get moved to a less intensive care unit as they determined after many many draws of blood that I had stopped bleeding. Bill, my Jamaican transportologist showed up to take me up stairs. He grew too weary of waiting for the nurses to have me ready so he “went to see a man about a dog.” Another character in this play was EB. He was one of the night nurses. He has an energetic, bright 5 year old son and he is from Gambia, so we had lots to chat about. He was lovely. I had a wonderful nurse from Iran who just oozed love and caring. She took great care of me. I had another nurse from India and many others who came and went were from all over the world.

I had many visitors. Lindy, Carrie and Lisa all showed up and spent the better part of the day at the hospital. Kathy and Mickey came and went a couple of times. I felt very supported and loved. I found out at some point the endoscopy I needed was a Monday-Friday kind of thing, so I had to wait for that. I did get an ultrasound which is so easy! No drugs, no pain. Unfortunately it did not tell them anything they did not already know.

By Sunday mid-day it became quite clear we would not catch our afternoon flight on Monday. But we still held out hope of putting it off a few days. Mike and Michael were able to Skype with Maggie and tell her the news. I don’t envy them that duty. It was not pleasant. After I’d found out they had Skyped I texted Maggie but could hardly do that through my tears. There was no way I could Skype at that point.

As an aside, I was on a “nothing by mouth” diet almost this entire time. Sunday night I was allowed to order from the clear liquid menu and enjoyed some cherry jello, green tea, black tea and gummy bears. After everyone left I ordered a second round! All my peeps left early on Sunday because Mike and Gillian generously, super generously, offered to let Kathy and Mickey stay all night at their house while they vacationed in Yellowstone. So they all went to dinner there so everyone could meet and Kathy and Mickey could get the lay of the land. I watched Waking Ned Devine and cried thinking about the distinct possibility of missing our trip entirely. After their dinner and my movie Mike and Michael came back to entertain me until it was ambian o’clock.

I was able to start Monday with a Skype session with Maggie. It was great to be able to see her and talk to her. We did a good job of keeping it together and we had a good conversation. Then I spent the better part of the day waiting. I was waiting for the endoscopy that would include an interior ultrasound, a biopsy of the stomach ulcer and spot on the pancreas. The doctor had a busy schedule and they had to try to squeeze me in where they could. I finally found out that I had a 3:00 appointment. Good to know. Prior to that I had more fabulous visitors. Jennifer came with her sister Allison and her two kids Gideon and Kincaid. Anyone of them on their own would be very entertaining, but altogether, they are hilarious! I highly recommend them as hospital visitors, anytime. Next came our neighbor Lizzie and her 9 month old June. These are our next door neighbors and we just love that June Bug! She is adorable and she gave me just the baby therapy I needed. Betty had to work but walked up from there to spend some time. Kathy and Mickey were there again, of course, enjoying a different kind of vacation than they had planned. 

At 2:00 they fetched me for my 3:00 appointment. Mike and Michael stayed with me for that hour while we waited in the holding area for the procedure. Finally I was rolled into the procedure room and 2 assistants entertained me while we waited for the doctor. Dr. Schembre is a highly regarded doctor. Andrea gave him the seal of approval and we looked him up on line. I knew I was in good hands. He was a lovely man and had a good bedside manner. He told me what I needed to hear and then away I went to la-la land.

Unfortunately I think I could have used a little more sedation. I remember trying to grab at my chest and I remember hearing them say “Not yet, Janet.” My visual image is that I had shipping containers being moved around my chest. They happened to be yellow-orange if you want to know, just a little detail. When I woke up I had a feeling they left a shipping container inside me. 

Monday evening after the procedure, I was rocky at best. I have faded memories of being up in the room with my people; Mike, Michael, Betty, Carrie, and Lillie, Dr. Connolly and Dr. Schembre. They were all talking but I was fading in and out. How about some more ambian, people? OK, good night.

Each morning I woke early and with a headache. Tylenol helped, but who wants to be up by 4:30 am in the hospital. Oh well. Tuesday morning was no different. I did get some black tea and saltines followed by a few bites of yogurt. I had a good Skype session with Maggie. We are still holding out hope, Maggie, but it is looking less and less likely. I watched The Book Thief and was able to escape reality for a while.

Dr. Connolly came in on the early side of the morning and refreshed my memory from the night before. I had really not been cognizant while they were all up in the room after my procedure. I am very fond of Dr. Connolly. She helped put all the pieces in place for me to get some clarity around what was going on and questions that I had…very helpful. She was kind and generous with her time. She said they would probably not know the results until Thursday and the trip looked less likely because of that. I think I was still putting the trip off just a few more days in my mind…at home we were all packed and ready to go, we just needed new tickets. But then she said the magic words…I could go home!! No aspirin, ibuprofen or the like. No alcohol. Anything else was ok.  Pantoprazole; one tablet twice a day. She said she did not think Dr. Schembre would make it up this morning but to expect a call today.

Mike and Michael were already on their way, so it would not be long. I did what I could with tubes still in my veins, to prepare for departure. Mike and Michael showed up and helped and the nurse showed up to give directions and remove tubes. During this time Dr. Schembre came in with his assistant. I had the clarity I needed, finally, to ask the direct and necessary questions. 
Do you know yet if it is cancer?
No.
So, the biopsies will show us if it is cancer or not?
Yes, and if it is cancer, what kind of cancer.
So, if it is not cancer can I travel?
No, too many unknowns.

Ok, now I’ve got my marching orders…take one pill twice a day, cancel your vacation and unpack your bags. 
It was great to get out of the hospital. We stopped by the pharmacy on our way out to  pick up my prescription and Michael went to get the car. Mike and I stepped out into the sunshine to wait for Michael and I could hear, in my head, a soundtrack. I said to Mike I felt like I was in a movie…a sad movie…I would really love this movie, but I don’t want it to be about me!

So we walk into a house full of mostly packed bags and lists of things to remember to pack at the last minute. Talk about rubbing salt into a wound. Damn. After a break I spent a good deal of time working on canceling our plans. How much quicker that was than making the plans. Maggie cancelled all our plans on the West Coast of Ireland (I now have many B&B hosts praying for me…good Irish Catholic prayers!). I cancelled everything from Dublin on including our flight to England and our Matilda tickets (so bummed). We were able to take care of it all pretty quickly and heard back from everyone in a timely way. Oh well…maybe next time.
We also made a decision to bring Maggie home on Friday, the fourth of July with the help of her Aunt Carrie and send her back to pick up in Paris for her month in Europe with her college room mates mid July (fingers crossed).

Coming Home
Tuesday as soon as I had finished with canceling plans, talking with Maggie and settling just a bit I texted Kathy and said we were home, settled and they could come over any time they liked. They headed over immediately with lots of good food and energy. It was a beautiful day, actually, quite hot, but that worked for me. We sat on the deck all afternoon and I think everyone was back and forth talking on the phone and catching people up to date. Betty was there but Michael had headed back to Portland. It was a waiting game, now and we might not hear anything until Thursday.
We did not have to wait that long. Dr. Schembre called about 7:30 that evening to give us the news.
Mike and I sat in Michael’s room to talk on the phone. Bad news…cancer. Good news…NOT originating from the pancreas, but from the stomach. Stomach cancer. The cancer started on or in the wall of the stomach lining. What is on the pancreas are the same kind of cells and most likely that is what is on the liver as well, they just can’t say it definitively as they did not get a biopsy. He gave me names of possible oncologists. He said I’d most likely start with chemo and then depending on shrinkage I may or may not need surgery. He gave me the name of a surgeon to be thinking about. There you go…here we go.

We headed out to the deck and I had to say it for the first time. It’s cancer. We all cried and cursed. But what are you going to do…you just have to do it, right? Kathy and Mickey have been in our shoes and it was so good to have them there. Betty is Betty and will always be here for us. We spent the evening talking to each other and lots of time talking on the phone. I talked to my sad momma, that was so difficult to do. I talked to my brother, Paul. Finally I hit the wall and we ended the evening.

We spent a good deal of time Wednesday morning looking up the potential oncologists and surgeons on line. Mike and I talked to Andrea as she gave us her number and told us to keep her posted and she could give us her opinion when we wanted it. She had lots of information and opinions on the oncologists. So helpful! Mike talked to Carrie and of course she is right on this, gathering all kinds of information and being so helpful and supportive. I got a phone call from Debra, my nurse navigator, from The Swedish Cancer Institute. What a treasure! She is the person who, if I stick with Swedish, will make all my appointments and help us navigate this new world. She is very upbeat and knowledgable. She knows the ins and outs as a professional but in addition she was diagnosed with stage 4 colon cancer a number of years ago, so she, unfortunately has an inside view as well. I told her my doctor preference and of course our calendar is completely open as we were expecting to be roaming the hills of Ireland this month. She said she would make the appointments and call me back today. Waiting, again. Later in the day we talked. We have 2 appointments scheduled for next Thursday, July 10, one with the oncologist, Dr. Kaplan and one with the surgeon, Dr. Ong. We are going to get to see the oncologist who is top on our list…fabulous! And we are going to see the latest addition to the surgery department, a young and very smart surgeon recently recruited from Arizona. 

In addition, Carrie has talked to the oncologist she knows; Dr. Chen from the Polyclinic. He has given his seal of approval to Dr. Kaplan and we have an appointment scheduled with Dr. Chen later in the month for a second opinion.

We have a whole week to wait. Andrea had said to me “cancer is an emotional emergency, not a medical emergency.” She said we had time to take things step by step and be thoughtful and pragmatic. Thank goodness for Carrie and Andrea! We have 2 insider advocates and navigators, they have our back, for sure! We understand these doctors are worth waiting for, so in the meantime…


Let’s Make Lemonade
Let’s have a picnic! My dear Michael had made a Bakery Nouveau run for me yesterday and brought back 4 pieces of quiche (I had a distinct and strong hankering for quiche while in the hospital). We packed up some quiche, cherries, nectarines and grabbed Rudy and headed for the beach. Beautiful day! Right as we parked and got out of the car Andrea and a friend walked by…what a coincidence! Big hugs and laughter. I told her about Debbie and our appointment with Dr. Kaplan and she told us she was having surgery next week but she is always available to us. How generous! Love her! Mike and I had a nice picnic on the bench and took a stroll down the beach. Lovely.

Carrie came over when we got home and we all spent time talking cancer and doctors. Carrie’s advice: eat lots of good food while I can! Starting now: we’d stopped for organic coffee ice cream on the way home from our picnic!  I spent time talking to Jennifer and telling her the bad news. They have had so many medical issues in her family,  she is already a great friend and I know she’ll be a great support. 

Then we had to Skype Maggie. She was not thinking we would have a diagnosis yet and came on the screen with Daragh and Rian and her friend Kelly. We had a great chat then she took the computer downstairs so we could say goodbye to Cody and Lisa. She headed upstairs ready to sign off but we told her we had the news. It was no easy task telling Maggie and I know it was even harder for her. She just wanted to have some magic that would bring her right home, through the screen. We’d have to wait.

Thursday following Carrie’s advice I went to eat good food! Mike and I went to pick up Kathy and Mickey (so weird to go to Mike and Gillian’s to pick up Kathy and Mickey!). Mike dropped me and Kathy off at the water taxi and the boys went to try and walk on the golf course. Kathy and I walked right on to the ferry and cruised over to downtown. We went past the gum wall into the Post Alley Theatre and met Bridget our Pike Place Market Food Tour guide. We had a fabulous time, along with 14 or so others, following Bridget around the market, through the crowds to sample delicious foods and hear entertaining stories about the market, the people, the history and the food. Smoked salmon, Market spiced tea, cherries and peaches, meat from BB Ranch,  Beecher’s  cheese and mac and cheese, Pike Place Chowder and bisque, gourmet sandwich, Jon Boy caramels, Etta’s crab cakes and I know I’ve missed a few. Kathy and I are cut from the same cloth; it is more difficult for us to inhibit our quippy little thoughts than just blurt them out. We had a great time. After the tour we retraced our steps and bought yummies for dinner. We high-tailed it back to the ferry and the guys were on the other side waiting for us. By the time we got home Michael was waiting, Betty joined us and we had a lovely dinner on the deck! YUM! Eating good food while I can!

Happy Fourth of July
I have never had a 4th of July that has so little to do with the 4th of July. We did chores (I could not take these floors one more minute!!). I went to PCC and TJ all by myself. I was worried about who I ran into, but it was fine. I saw Maria Cheha and she already knew so I got a big hug and it was lovely. However, I had not been warned about one of my side effects:  “the first trip to the grocery store after being diagnosed with cancer and having to miss your vacation you’ve been planning on for 9 months and then feeling entitled to any thing you want!” Let’s just say I love sunflowers and zinnias and now I have some. Oh and pickled beets, too. Oh and Beecher’s cheese and lots of cherries! I’ll stop there! It was kinda fun!

At home I cleaned Maggie’s room, a quick dusting. I felt like the British shows when they come back to their homes after the holiday away and have to dust everything off. I had to get Maggie’s room back up and ready.

6:30, about 20 minutes early, a mighty tearful and heartfelt reunion! Maggie is home!
Freedom from the sadness and longing of missing Maggie! Happy 4th!

More Lemonade
Saturday was let’s just hang out and be a family; Micael and Maggie were both home! We watched Felix pitch an epic long game that we finally won. We went to the park and everyone else played frisbee, I took pictures, we watched Cloudy with a Chance of Meatballs which made me laugh out loud!
Great day!

On  Sunday, Kathy and Mickey came over for an early Sunday dinner: salmon, roast veggies, salad, sautéed garlic spears. Kathy brought dessert; coconut milk ice cream with fruit compote. Yum-O!

Michael had to head back to Portland at 5. Mike took Michael to the train, Kathy and Mickey headed “home” and I got a text from Genya that they were home. She called and I started crying so she came on over. It was not easy telling Genya about cancer because she is my teaching partner and I am to be her son’s teacher in the fall. But, Genya has been through plenty herself. She is so practical and pragmatic and would not let me think at all about the impact on her and Ian. Of course she wouldn’t. But it was good to let her know, and hear that from her, it was a relief.

On Monday I tried to connect with David, my principal,  in person but I couldn’t make it happen. I ended up having to tell him over the phone. He was gentle and kind and said all the right things. Now I’m done with my absolute want to tell you in person list and I am just going to let it all out there. Anyone can tell anyone and I’m fine with that.


At some point talking to my mom this weekend she informed me that my great grandpa, her mom’s dad, Louis Heinz, at the age of 85 in the 1950’s had stomach cancer. They treated it surgically, he survived a few more years and died of a heart attack while working in his garden. Mom also thinks one of his sons had stomach cancer, but she may have just made that part up.

Talking to my mom is hard. It is hard for her to believe that I am feeling as well as I feel, but I do feel good, physically, right now. If it had not been for that bleeding I would not have known about all this happening inside me at all.


So my list was: college, college, kitchen, computer camera, Ireland, lathe and then more…A cautionary tale: do not wish for a long list of things that start with the “k” sound. Cancer snuck in right after camera, before I could change to another beginning sound.

Tuesday July 8
I continue my “eat what I want” food plan. When we were doing the Abascal food plan she talks about how to be on “maintenance” the Abascal way and she prescribes a “day off.” On that day you can eat and drink whatever you want. I always said that dream day would be Bakery Nouveau, followed by Zippy’s, followed by pizza (at one of a few spots). Today I am 2/3 of the way through that dream food day and I absolutely plan to finish it off with 3 for 3 at Delancy’s with Kathy and Mickey and Maggie and Mike. 

Delancy’s was closed…but there is more than one spot to get a wood fired pizza! Our neighbor Vince suggested Humble Pie. Yum! We had delicious pizza in a very “Portland-esque” setting. We finished this food day with a trip to Full-Tilt ice cream. 

Wednesday July 9
Mike, Maggie, Betty and I packed up early and headed to Mt. Rainier. A glorious day! We ended up on a nice hike starting at Ohanapecosh and hiking up just over a mile to Silver Falls. Betty and Maggie did an extra couple of miles to hike at the Grove of the Patriarchs but Mike and I skipped the extra miles, headed down in a slow meandering way, catering to my low volume of blood in my system and taking time to learn our new camera a bit better. 
It was a beautiful day.


Thursday July 10
That was a lovely bubble week. I really only worried about how unworried I was. It’s not in my nature not to worry and in hindsight I realize everyone else was doing that for me. I was building a fantasy that the oncologist would chuckle and say, “Oh, a few chemo sessions will take care of this!” And my fantasy continued with everyone saying, “Well that was a lot of hassle for no big deal.”

Thursday my bubble was burst. This is no little thing. This is going to be quite a fight.
We saw Dr. Ong the new head of the surgical/oncology department, at 11:30. We spent an hour with him as he drew pictures, made lists, wrote big words, drew arrows on his white board. He was quite informative and clearly very smart. He explained what was known and what was left to find out. He took the wind right out of our sails. We were punched in the gut. This was happening to us.

We spent the next several hours in a daze on Broadway (not the only people in a daze up there…I’m just saying!). We found places to just sit. Had lunch, had coffee, sat some more. A daze, unreal, out of body.

At 4:00, we met with the well regarded oncologist Hank Kaplan. He was just as kind and lovely as we expected. Such a good manner but I am here to say this man is not afraid to call it like it is, and it’s not pretty.

Here is what we learned on Thursday from the docs. This is unusual. There are 200,000 cases of colon cancer a year in this country. There are only 5-6,000 cases of stomach cancer, and it has been on the decline. So, it is really weird that I got stomach cancer.
There are different ways that cancer spreads. When it just keeps moving along to it’s neighbor it is “invasive”. So my stomach cancer invaded my pancreas, and that too is unusual. Most likely these will be treated with chemo.

What is on the liver has not been proven definitively to be the same, however both doctors think that it is the same stomach cancer. What is unusual here is that usually cancer moves through our bodies through the lymph system. My lymphs are clear and that means it has moved through my blood. But…there is a chance, still, that what is on my liver is not cancer. Until they have all the information they cannot determine the course of treatment. More waiting…I keep remembering Andrea’s words that now is the time to go step by step and be pragmatic.

I am scheduled for a PET scan on Tuesday July 15. This may or may not give us the definitive information regarding my liver. If it does, then they can, hopefully decide on a course of treatment and we can start fighting this cancer. If not, I’ll need a liver biopsy.

Kathy and Mickey came over for dinner. Betty had gone to the store and had a nice salad bar started for us. Mike and I relayed the new information, not pleasant, but we had a nice evening before Kathy and Mickey moved out of West Seattle to their new digs in Lynnwood for the rest of their time in Seattle.

More Lemonade, Anyone?
I love riding my bike! Friday was a hot one so we got an early start, Mike, Maggie and I, and loaded up a picnic and our bikes. We drove to the Green River Trail and had a lovely/flatish/shaddyish bike ride along the trail. We went off the trail and found a little park in Renton, then headed back. We stopped for our picnic at Starfire and then finished up before the heat of the day. It was perfect!

Mike and Gillian and Conor had returned from their trip on Thursday so they came over Friday evening. We had not seen them since all of this started. Maggie took Conor down to the park for some fun so we could talk frankly with Mike and Gillian. They ended up staying for our dinner of leftovers and we had a great evening.

Girl Time
Saturday I convinced Mike to go to his wood session up in Lynnwood. I reminded him there would be times he wouldn’t be able to go and I was fine! I had already invited Jennifer over for the day and I knew Roz might come by so we were gearing up for a girl day.
Baby June came over about 9 for a visit while Lizzie and Vince were busy around the house. Jennifer got there about 9:30 and we played with the babe for a while. Maggie was there, too. It was a nice morning. We sent Maggie to the store and set out lots of fruit and salad fixings to fix a nice lunch.

Roz texted me, she came over, followed by Lisa Gluckman and Kathy Ludwick. We all sat around the table snacking on yummy fruit and drinking tea and lemonade. Betty joined us when she got back from her chores. It was quite lovely. Mike came home and saw I was in good hands and disappeared down to the workshop and into wooden bowl land. After Roz, Lisa and Kathy had all left, Maggie’s Lisa and her brother Peter showed up. We had a nice visit with them, too.
Jennifer stayed for the duration. It was great to have her here all day. We fixed dinner and I called Lisa Clayton to see if she could come over. She did and we sat on the deck and I told my story once again. So sad to think about not starting kindergarten in the fall, but I have to be real so I can find a good sub and get things as set up as I can for them. I don’t like to think about that part. This impacts so many people.




No Exercise…OK!
Starting today, Sunday,  to get ready for my PET scan I can engage in no vigorous exercise (you know how sad that makes me, ha!). Tomorrow I have to eliminate all sugars including fruits, all grains and white potatoes. I can eat a high fat/high protein diet including: eggs, cheese, meat, fish, nuts. I can do that! On Tuesday I can only have water, as much as I want though, all day. We have a 12:30 appointment for the scan. They will shoot me with radioactive dye and I have to lie quietly during the scan and for a while afterward. I should be out by 3:30. The doctor will get the results by 5 and we have an appointment to meet with him at 5:30. Hopefully it will give him definitive results. If not, I’ll have to have a liver biopsy.

Today we are meeting up with Kathy and Mickey to say good-by. We’ll have lunch at Dukes and then take them to the airport. They are cutting their vacation short and heading back to Boulder. It has been so good to have Kathy here. I know it has made mom feel so much better knowing she was here. It was good to spend time with them and have some fun in the midst of this cancer fog.