We've named my cancer Earl

Between Japan (Japan blog to follow soon) and BC we had a great visit with the Rohdes, in town for a wedding.  When ever we are with them it is like putting on an old pair of slippers, comfortable and warm.  We went to dinner at the Heartland in downtown St Paul and then enjoyed the evening together at home.

Lucky for us we got to go to Mayne Island BC to be at our house and with our friends Jan and Irma.  We had a great trip with lots of rest and relaxation as well as:  doing the "Diva" puzzle (we discovered Irma was a closeted puzzle addict), Mayne Island Fall Fair parade, walks, annual general meeting with all the land owners, fun times with Marilyn the dog, dinner with Peter and Gisele at their house and at the Groove with Lynda, Jan and Irma.  The lighthouse at sunset was peaceful and pretty, we enjoyed the community gardens where Nancy walked the seashell labyrinth, ferry rides are always fun even with a delay and we watched lots of the Olympics.  The best part, homemade peach pie and chocolate zucchini cake--thank you Irm!! Nancy's acupuncture and massage were delightful and totally relaxing.  In Vancouver we got to see Jan and Irma's new apartment and have coffee with Sandy and Linda.  Traveling is good but hard, it felt nice to be home.  PS, you might not have recognized any with all that hair!!


Nancy has been struggling with back pain for two months and finally found out she had two ribs out of alignment.  Putting  them back in during a massage helped.  Now Dr Dan thinks the remaining pain  is from the cancer so there have pain pills for that.  We met with him today--increased CEA, pain and increased liver protein all have him thinking now is the time to act.  First step, CT scan to be sure something else is not causing the pain. The Foundation One report finally came back with a mutation found in melanoma so there is a drug I can take to target that--Trametinib. They called my insurance and coverage needs prior authorization--but it is not made for pancreatic cancer so Dr. Dan is skeptical.  The drug company may want to help so they can broaden their claim for effectiveness in other cancers.  If not our next trip budgets all go to pills--$12,000/ month till it no loner works which you don't know for at least 2-3 months.  Scott found a trial in Rhode Island that changes your t-cells (CAR-T) and reinserts them into the liver to create targets out of the tumors and hopefully stimulates the body to attack and shrink the tumors.  Dr. Dan liked that but is concerned that it would be two months before we could get it started.  I will call them tomorrow to iron out a possible timeline. This would involve a month long stay in Providence with a trip or two prior to that for screening and t-cell harvesting. Dr. Dan is also getting more info on a trial that has a center in Seattle.  So there are some possibilities out there.  My MSI, which Mayo asked about, was normal so Mayo trial is not a feasible option right now.

Dr Dan called while we were on the way to the Lynx game (we won!!).  He was checking on my pain and the pain pills but then reported on the CT results.  As he had expected the tumors are active and have grown.  I asked if they had grown a lot or somewhat.  Answer, somewhat.  I like that but also there are new tumors, I don't like that.  The earliest I could begin screening in Rhode Island is October 4, then if I am eligible the very earliest a treatment could start is October 31, after they change and grow the t-cells.  I think Dr Dan is worried about that timeline.  He may consider giving me Trametinib soon which I could stay on as long s it works and then consider the trail, or use it for sa designated time snd switch to the trial.  I would have to be off the medication fir four weeks before t-cell collection.  We will touch base on Tuesday to figure out the best next step and timing.  Needless to say ww were sad and a few tears were shed.  This feels like a big kink in my 5 year plan.  But we continue to believe that we must live each day with joy, dancing, and love, so that is what we are doing.  Do a little dance for both of us whenever the thought comes through your mind.  Thanks

 For fun since we have been home Nancy had lunch with Kim Koeppen prior to Hamline year starting, we celebrated Sue's birthday with dinner with Mary and Co and Jewish theater production--a one woman show that was fantastic, we had lunch with Suzi Hagen, both got massages and Nancy got an extra half hour massage today.  To top it all off we went to see the Dixie Chicks at the State Fair with Kim and Lin.   Parked close by at Steve Jongewaard's house--thank you, went to the creative arts and fine arts buildings then may our way to the grandstand stopping for a london broil with cheese sandwich (nothing on a stick) and Sweet Martha's chocolate chip cookies.

Arrived in time to see the second opening act--Vintage Trouble--which was very good, upbeat and entertaining.  It was a beautiful night and the Dixie were great fun   Musically talented, full of energy and entertaining as well.  You may have noticed my cancer is now named Earl--one of their songs is called Goodbye Earl with a line "Earl has to die". We think that is true of Nancy's cancer so now we can sing Goodbye Earl. The night ended with fireworks-who doesn't love fireworks.

We got the Escher puzzle set up again to give it another try....it is a tough one.

Mayo Clinic

Scott and I went down to Mayo last night to easily make my 7:00 checkin time at Mayo.  Sue stayed home as we decided Scott would ask better questions and listen better and had lots of information about trials.  We had a low key night walking a bit to get the lay of the land, eating at Chester's and then walking along the river.  7:20 blood test and 8:00 CT test.  Process slowed as they tried to figure out if they could use my port for the CT.  Turns out the card I carry did not have enough info and eventually we went with an IV.  I was a wreck since my last IV experience was awful but I decided it was Mayo and they should be good at it.  Chelsea was great, both in trying to figure out the info they needed for the port so I will have it in the future and in putting in the IV.  After that I was only a little nervous about the dye going in but Jason was great and all went well.  We were hungry by the time we got to breakfast in the small Eisenberg building cafeteria   Bought sandwiches and cookies (we are related) for lunch and went back to  the room to rest.

Walk and picnic lunch before 1:20 oncologist appt.  Dodged the rain and arrived early.  Met with a physicians assistant first who said the doc would be in to talk about the diagnosis and treatment.  Treatment sounded good.  Turned out he had three options-trials rather than treatment.  An immunology trial for which I have to have a positive MSI to participate.  Hopefully the Foundation one test Dr Dan has ordered includes this so I could know soon.  The other is an agent added to gemcitibine which I did with Dr Dan first.  Third option wait and see.  The CT did not show any radiological growth, a good thing but is active bio-chemically as shown by the CEA.  This matches Dr Dan's "the cancer is active, we just don't know in what ways."  CT showed that.  Mayo Dr Yoon was patient, forthcoming, protective when Scott's questions were too direct--making sure I was comfortable and wanted the answer before continuing.  He thinks immunology is the way too go, there just are not a lot of pancreatic cancer trials with that.  He also cautioned about using two agents as some of the second agents have severe side effects.  He is cautious about quality of life, and trials that are far away with difficult regime timetables.  He is much like Dr Dan in thinking about what is important and where we are now, different words and manner but re-affirming what Dr Dan has been saying.  At this point success in trials is measured by adding three months lifespan.  Some immunology trials for 2-15% can add more but they don't know who, why or when,  and he could not point to any.  His best hope is the MSI trial if I am eligible, then if foundation one turns up anything interesting.  I think he was at a draw between the other and waiting/watching.  No silver bullet, no secret that Dan does not know about but glad I went.  He said, as everyone does, that I look great and am otherwise healthy.  I keep holding on to that and in spite of reality I told him I wanted to live 5-10 years, just not sure how to do that!

Next Dan appointment is Monday the 15th.  Next trip--Vancouver and Mayne Island Tuesday the 16th!

Cancer Update

Hi there. Thought we would give you a little update. The blog posted before our Japan trip gave you a the status on where we were with Nancy’s cancer. Numbers up and re use of same treatment pretty well eliminated.
So we are at the what is next place. 

We returned a week ago today from Japan. A nice little trip. Right before we left we decided that now would be a good time to see what was cooking at Mayo Clinic. We had talked with Dr Dan about this some time ago and we all had decided to hold it in our back pocket for later. We think later is now so we called and talked to them before we left. We left them with info and headed off on the trip. Just before coming home we got a message from Mayo Clinic in Rochester saying to call as they would accept Nancy for a consult. We did that and have an appointment for August 9. Have no idea where this will take us but here we go. Nancy’s brother Scott is going with her as he is such a great question asker and listener. Sue’s idea. She will impatiently wait for a report when they return
Dr Dan is looking for alternative treatments or trials and we hope to hear something from him this week.
Most likely if alternatives are found they will be elsewhere and we will have to go there for treatment. He also sent a sample of her tumor off to a group that is looking at it for what types of cancer cells are in her tumor in hopes that it might give some clues as to next treatment types that would be recommended.

So thats where we are right now. Kinda limbo. Nancy handles it with grace and Sue hates limbo!!!!!!!

Nancy was a trooper in Japan. Long days and hot and humid but she held up very well. The group we traveled with was very nice and supportive. They could not believe what she was doing and how well. Me too!!! We will do a blog posting but wanted this to get out so you are not wondering what is happening.

So the plan was to travel to Mayne Island in BC to our home  in late August. As of last night we still do not know if we will . Our focus needs to be on whats next and getting it going. So lets say we are still thinking about it and if it works that we can, we will. 
Terri (our niece) and her daughter Lauren and friend are here from Milwaukee. Lauren is grown up. They drove her car (we bought it for her) up to show us and to do a visit to the University of Minnesota as a possible school for Lauren.
And then there was the all day shopping to the mall. Terri and Nancy and I went to an art fair and home.

So Japan blog and pics soon. 

Detour

I've was pretty apprehensive about the CT this time around and the results of the tests--Finally calmed my nerves by realizing they would tell me I have pancreatic cancer.  Seems silly but that helped and anything else is just part of that.  I expected to find out the results on Wednesday but Dr Dan called Tuesday tonight so I could get a good night sleep.   At that time, he considered the disease to be stable due to slight but negligible growth in the liver tumors with no new spots.   The story changed in the morning once be saw the tumor marker numbers--I am not getting to 45 just yet as we are now up to 225 (from 60 something).  He said the number is not important just the direction and the direction indicates cells that the chemo did not destroy so the tumors could be growing.  But we do not know how fast or aggressively they will grow. Another CT is in order after Japan.  For now Dr Dan is exploring trials so that we can have a plan when we need it.  He is also sending a tumor sample in for genetic testing to see if I have any mutated genes that are common to other cancers so that a trial for a different cancer might be useful to consider.  We had hoped that the chemo I just finished could be used again but since the numbers increased so quickly he does to think it would be effective a second time.  So we are keeping our fingers crossed for a good option when we decide I need it--that answer will come sometime after Japan--hopefully later rather than sooner.

It has a been a full and fun two weeks.  We enjoyed a morning walk at the Stone Arch Art Festival--it was warm but we had not been in a few years so enjoyed the collections of artists.  Bought earrings and a little fairie house.  We saw the Calendar Girls with Linda Kelsey playing the oldest member of the group.  She is so good as was the entire cast.  We all laughed over and over again throughout the night.  Nancy got new glasses that arrive this week--light purple!  Our friend's grandson, Aidan, is in the midst of planning for choosing a college, we enjoyed a conversation with them.  He is a math and music guy, I can't wait to see how and if he ends of combining these passions.

Listened to Lynx at Seattle, we improved our record to 12-0 record, then watched online against LA,  and our record 13-0 start to the season.  Then we went to the game here against LA, we lost. What a fun team to watch, even when they lose. Went to the game Wednesday night--lost again, three in a row.  Ugh.

Our trip to Harbor Springs to see Cindy Rohde was perfect.   Non stop flight and Cindy met us at the airport.  On the agenda: walk around town, walk along the lake (Michigan), work on a puzzle, nap, eat, tell stories and hang out.  We had a nice dinner at Bill's Aunt Pat's house and enjoyed both the food and company, drove out to a farm for lunch, made our own pizzas one night and had deli sandwiches by the lake one afternoon.  All in all a great time.

Scott and Debbie came the day after we got home from Michigan.  We finally got the pool up and running so we all found some time to swim.  We went to the Lynx game and on the hottest day of the summer Scott and Debbie decided to weed that back patio area outside our office.  We made them stop eventually but they were at it again the next day.  We have a beautiful spot now with our outside ornamentation well planned instead of growing haphazardly each time we got a new piece.  Scott helped me make progress on the Esher puzzle I am trying to do.  There is still a long way to go.  They left Monday.

Tuesday was CT and a massage, Wednesday, Dr Dan and a visit to see cousin Nancy and the Lynx game.  Today was a massage for Sue, shots for our trip, acupuncture for Nancy to help with hand and foot neuropathy and then our friends from Calgary arrived:  Leonorah, Eddie and their four month old son Tanaka. They are on their way home from Boston and Vermont where their 9 year old son is going to camp for a month--the same group of camps I worked at in Vermont.  He should have a good month!  And so it goes, we are all tired and headed for bed early.  I will add pictures tomorrow and send out the blog then....Love to you all, I hold you in my heart and spirit every day.

Wednesday came and went

We are enjoying the current break.  I can't figure out how we had time for chemo and the down days after, we seem to be very busy these days. It is still hard feel like taking a break is a good thing when it comes to fighting this cancer so I try to do my three jobs: eat, maybe a little better these days, drink lots of water and exercise.  Trying to walk more since that is something I can control.  I lost some of my routine so have to think hard to call on my minions to continue their work and do my guided imagery. Every so often I look in the mirror and let my fuzzy head (not to mention my neuropathy) remind me that I still have cancer and need to rally mind, body and spirit in defense of my body.Your support continues to buoy my spirit.  Next update after CT scan and visit to Dr Dan Wednesday June 29th.

We helped Sue's cousin Nancy unpack after her June 1 move to Hudson.  We were pooped.  She is settled in now.  She is still trying to figure out where we put things and is waiting for pictures to be put on the walls.  She seems happy and all her relatives are happy that she lives closer to us.

Mary McDougall's niece and niece's husband are comedic/physical theater performers who did a show at the Ordway during the Flint Hills Children's Festival.  Called "Air play" they worked with fans and body comedy to create a show with balloons, umbrellas, kites, confetti and fabrics as air sculptures that was entertaining for big and little kids.  Not sure whether is was more fun to watch the show or her parent's and the children in the audience whose faces lit up over and over again.

Other things to keep us busy:  Two Lynx home games and now 11 straight wins to open the season, a WNBA record.  Diary of a Wimpy Kid at the Children's Theater was lots of fun.  We met up with Carolyn Levy and Sheldon Berkowitz, Kim Koeppen, Mark Olson, Jeff and Lisa Post, Toni Holweger and Kae Lovaas for a variety of meals--breakfasts lunches and dinner.  We met Jeff and Lisa at the St Croix casino in Turtle Lake and 10 minutes at the penny slots netted Nancy $100.  Not bad for a $3.00 investment.  We had fun at Kelly Keil's graduation party (with photo booth) but are sad that the Keils are moving to Georgia.  We look forward to seeing them when they are back in town for visits.

Marjorie and Franck were here from France for two days on their way to Seattle.  Marjorie is Nancy's cousin and Franck is her husband.  His daughter, Emma,  spent a year with Scott and Debbie for her final year of high school.  We had a delightful visit.

Throw in a few massages, walks and work on trying to get the pool up and running for one last summer and we find ourselves busy and tired.  It is all good, and I am grateful to be busy and tired because we are doing things instead of tired from chemo.  Here's hoping for a long break.

Minnesota stands with Orlando

Yosemite and chemo break

So as we drove to chemo today I said, "I really don't want to do this today."  Sue says, "be careful what you wish for."  Dr Dan says, "I think we should take a break."  So there you have it, no chemo today.  I hit 63 so the number has hit a plateau.  And I finally developed side effects that he does not want to increase in intensity by continuing the chemo.  So I am healing from chemo for how ever long I can hold the disease at bay and then we will try the next thing, which could be this chemo again.  My job is to exercise.  For now I can get stronger, lose my numbness in my feet and hands, the new side effect, get my taste buds back to normal,and maybe eat ice cream soon as the cold sensitivity completely wears off.  The next CT and blood work  are in a month, Japan is in 6 weeks.    Here is what I wrote a couple of weeks ago....A little nervous about what is next.  Eventually in two weeks or 6 I will stop chemo and let my body rest and recoup,  It is hard to imagine not continuing the chemo fight. I will have to rely on my three jobs, eat, drink, exercise and the guided imagery, yoga, healing touch and support of friends and family to keep the positive momentum going.

I have been nervous about stopping at 10 or 12.  Once Dr Dan figured out I was nervous about stopping at all vs when I stopped he went full speed ahead with stopping now.  He is very comfortable with how well the chemo has worked and that a break will be a good thing for being able to tolerate the next step.  With the extra week after the last chemo I have already gained some energy.  Looking forward to a trip to MI, and visits from Peter and Gisele, my cousin Marjorie and husband Franck and Scott and Debbie, all before Japan.  

Last weeks trip to Yosemite....

Yosemite. We made it. We are traveling!!!

Up early with great anticipation for this first trip in many months (7).  We were greeted in our driveway by the fawn many of you saw on our face book page. She came to see us and mom eventually looked for her and saw us and ran down the hill. We moved to the bottom of the driveway to wait for Deb and Jim to pick us up. We did see mom again but trust she circled back to find her baby. She was so young that her legs were wobbly.  What a treat. 

No long lines at the airport and were at the gate when they announced discounted first class upgrades. We liked that idea. The trip out was gently turbulent but nice to be in first class. Nancy slept but woke up for the fresh baked warm chocolate chip cookies. Hooray for Sun Country.  Picked up our high off the groundToyota 4runner. It did not come with an included step stool so this group of four shorter folks comments every time we get in and out. Sue falls out, no graceful exit or entry. Jim has been driving, we are grateful.  We stayed outside the park and had a good dinner at the brew pub---yea Mac and cheese!!!  Breakfast at the local spot Pete's and we were off to Yosemite. No plans so we just kept driving. 

Today (Tuesday) was alternately sunny, cloudy, drizzly and foggy. We managed to capture the mood and the view of this gorgeous park. We did the valley loop stopping often to marvel at the scenery.  Unfortunately Mariposa grove is closed for the season to build boardwalks to protect the shallow root systems of the redwoods, apparently our collective enthusiasm for visiting this area comes with consequences. The glacier point road is closed for weather, snow and ice and an incoming storm. We are hopeful it will be open before we go on Friday. So we have seen Yosemite falls, Bridal Veil falls, El Capitan and Half Dome. We stopped in the valley village for requisite shopping and lunch. A wrong turn took us to Yosemite lodge so we explored there-- quite the beautiful old hotel--we love national park lodges. This one is full of Native American artifacts and beautiful Native design stain glass windows. One room has two fireplaces each the size of a small room.

We finished and headed back to our Big Trees Lodge to check in and collapse. On the way we stopped to take one last photo where ansel Adams took his first brownie camera shot of the valley. 

Our hotel is the oldest hotel in the park, we were warned to take everything out of the car to avoid vandalism by the local bears...

Wednesday and the sun is shining.  We head off to the valley again to explore Bridal Veil and Yosemite falls and other pull off short walks.  We arrived early so the crowds were at a minimum, unlike yesterday afternoon when the parking lots were packed.  We hiked up to the Bridal Veil falls and got appropriately wet and cold from the mist. Quite lovely.  Then off to Swinging Bridge (which does not swing) where we walked out to have a new perspective on the valley--views were stunning in the bright sunshine.  Next stop Yosemite falls. Walked into the lower falls and then upper falls.  Deb and Nancy spotted a sunny bench for our picnic lunch which we were smart enough to buy earlier in the morning when the deli lines were short.  Our plan was to drive out to a sequoia grove but discovered that Glacier Point road was open--off we went.  Up the twisty, turny road with snow on the side of the road.  Stopped at one overlook and enjoyed the view with clouds rolling in.  We made it up to the point and hiked out to sounds of thunder--didn't stop us or anyone else.  Great view, though we liked the first look out a bit more.  Back to the car, and headed down the hill as the rains came in. Back to the hotel for a late afternoon rest. 
Then up into the Valley (Nancy driving) thru the longest tunnel in California to watch the sunset on El Capitan and Half Dome. It was fun to see the fog  roll into the valley and the shadows on the mountains.  Stopped on the way home to see more sunset and look for the ghost bear which Nancy thought she had spotted. Log or Rock bear. Shoot!

Thursday we headed outside Yosemite Park to see Sierra National Forest see a stand of Sequoia trees. We  had debated driving to Sequoia National Park but the 3 1/2 hour drive one way just was too much.The forest road  took us up into the mountains and was much closer. We noticed a few wild flowers on the roadside but kept heading up. Then off the paved road into the forest we went. We found the interpretive center at a camp ground where we set off on a hike to see the last standing Sequoia that was 2700 years old, 247.31 ft high and 84 ft around. 



Then on to another trail. Here we saw lots of Sequoias. Hike was up hill and our necks got tired from looking up.
What a great hike. Then down we came to make a drive into town to repeat mac and cheese. But with the morning sun all the wild flowers  popped open so the drive was lovely. We kept seeing new orange flowers but none near pull outs so no pics. We did get pics of many others.

Back to our place to relax and pack for Friday's departure.

Up early again today to have a nice breakfast with a sweet wait person from the Dominican Republic.
She charmed us all. Check out and hit the road to exit the park. It is a new adventure because we had entered in the South Gate and we are now leaving the West Gate. Oh, It is Nancy's birthday. Her birthday wish was to stop and buy a National Parks Senior Pass. The world's greatest bargain. But alas before we can do that we must see gorgeous scenery, wild flowers and waterfalls. Ho Hum, another gorgeous day in the Yosemite neighborhood. 

A stop and Nancy had her pass and a Yosemite birthday t shirt. HOORAY!

On the way to the airport. A misadventure trying to find lunch. No lunch and we better head off. Birthday cupcakes with a iPhone candle. Wishes work just the same.
Easy pass thru security, lunch and an on time flight. Home to find beautiful birthday flowers from Mel, Jacques and Eva in Brussels.  Off to bed by 1AM.
Nancy was exhausted but loved every minute of it. Walked an average of 4 miles a day. Sue 
is also exhausted and she does not have cancer!!!!!!!!!!
Thank you for the new puzzles, Peg and Edie and the shirt, Jill.

 

Just so you know we weren't slacking before Yosemite--We went to two retirement parties--Jenny Keil from Hamline and Mary Margaret Smith from St Catherine's.  Congratulations to both and we enjoyed both parties.  We had fun at a Minnesota Jewish Theater  Company benefit with a pirate theme.  The speaker is a salvager who discovered a pirate ship off Cape Cod.  Fascinating story.  We got a Lynx game which was fun.  And we spent three days in Madison helping Sue's cousin Nancy pack for her move to Hudson. Also met an old friend there for breakfast. We will go to Hudson this afternoon to help Nancy unpack.....Had to head home early from Madison to attend a funeral for Ralph Jewell, our good friend Kae Lovaas's husband.  He was the sweetest man and will be missed by many.

Yosemite wildflowers......

 

The elusive 45

My two week chemo cycle starts on Tuesday with a blood test.  That is when we find out about the all important CEA.  No one is worried, me, Dr. Dan and Sue but the CEA went up from 60 to 66.  It could be a blip or a plateau.  We did chemo today, Wednesday, and will see what the CEA does in two weeks.  Dr Dan says this happens and if the number goes down next week we will continue, if not we will decide what to do.  There is no reason to continue if the chemo has done what it can.  Then we wait to see what happens, hopefully a period of non-progression-partial remission.

Thinking this morning about things I did not do before cancer--wear a hat to bed, nap almost daily at 3, eat mac and cheese and hot chocolate for breakfast, drink hot water at restaurants and warm tap water at home, do salt water rinses every night and now in the morning as well, carry around a ball of chemo for two days and nights every two weeks, moan and groan and sigh as often as not, slept with a stuffed polar bear and a heating pad with continued use of the hot water bottle, write a cancer blog, carry around a hand warmer, see my brother every month, stay home, do chemo, give myself shots, say thank you more often, had private yoga lessons and healing touch sessions, use guided imagery which can take me to all the places we have traveled, pictured minions running around in my body disrupting the cancer system dn planning flowers in my pancreas and liver, wake up every morning glad for the next three days and hopeful for the next three years, have a family reunion in MN, been all the more grateful and aware of good friends and their support.

Bouncing back from chemo was slow again this week.  Tired and weepy but that did not stop us very much. Scott and Emma (second cousin from France) were here for the weekend.  We had a great visit.  Turns out Emma loves puzzles too.  We did one and then Emma was keen to start another.  Unfortunately they left that to me to finish.  We all, saw Harvey at the Guthrie with Phyllis and Mary Margaret.  Toured around the cities a bit and met Mary and Colleen for dinner at a Thai restaurant we all enjoyed. Scott and I patched the pool leak and we put chlorine and algaecide in so now we can see the bottom of the pool.  Waiting for some warm weather to vacuum.  We went to Hastings to walk to the locks and did the requisite Mall of America visit and enjoyed Mexican food there.  Emma expanded our restaurant trials, with good results.  She also made a a beautiful pot which will find a special place on a wall.













We enjoyed night at the MN Orchestra to hear/see Pink Martini, thanks to Lisa Anderson and Diane Young.  Steve and Sally Klingel stopped by for lunch.  They live in Florida so we enjoyed catching up with them.  It was a delightful visit.  A healing touch session, lunch with Suzi Hagen and Jan Frisch, and Jenny Keil's retirement open house and a bike fitting rounded out the highlights of the two weeks.

Next chemo is three weeks away, I am anxious to see how the extra week will make me feel, usually I am getting in good shape the weekend before chemo, it will be nice to have a healthy extra week.  We are headed to Madison next week to help Sue's cousin pack for her move to Hudson.  And then Yosemite the next week.