May

Tonight MM is at the cancer hotel in Tampa. In the morning he'll get his labs drawn, early. Then an 8:15 appointment with The Weber. He has promised to tell him about the recent respiratory illness with fever and the cough that still won't go away. Also the episodes of leaving the stove top on and leaving the house. Those were three weeks ago and it hasn't happened since. It was a week filled with forgetting. His brain is so mysterious these days. We enter periods of scheduling mishaps, forgetting appointments, forgetting entire conversations. Then we have a clear patch when everything seems to be firing correctly. Then a patch of chills every night and fever, shortness of breath induced by the exertion of putting on socks, coughing all night, oxygen saturation a of 85-87. A few days later no more chills, no fever, oxygen saturation holding at 90. Through it all he is emailing, making phone calls, taking ibuprofen and showing up to volunteer at the library book sale, or to run the Boy Scout meeting. Then home to collapse and have me try to patch him back together. No, he doesn't want to see his internist. He wants to wait to see The Weber.

We attend to the activities of daily life such as groceries, homework, swim team for Butter, Karate for iMac. On Saurday we squeeze in a trip to the UPS store to have a power of attorney notarized giving each of us control over all the accounts just in case the other should die.

This morning I dump the three baskets of clean laundry onto my bed in order to trick myself into putting it away tonight. It worked. There are clean sorted clothes which we all be able to find in the morning.

Tonight

On the way home I stopped to do an errand. Waiting in line I heard the voice of a toddler speaking Russian to her Mama. Instant happiness. I was transported back 10 years to a time in my life when I was the foreigner, listening to the locals speaking Russian and Azeri. Standing in line tonight for those few moments I was with Liana, Farhad, Sabina, Erika, Fiona, Tshai, Jena, Basia, Nancie Jo, Krassi, Natalya. It made me smile. 

The Visitors

They came from Atherton California, Reno, Nevada,  Phoenix Arizona, Birmingham Alabama, Baltimore Maryland, Washington DC, Westfield New Jersey, Reston Virginia, Westbury Connecticut,  Boston Massachussetts, and Portland Oregon. Ostensibly they came to row, an annual rowing reunion of the class of '71, of which Melanoma Man is a member. The one thing I had in common with them was Melanoma Man.

The rowing reunions started in 2002 after Steve's funeral. Many hadn't seen each other in the 31 years between college graduation and Steve's death. So it was decided then and there that they would meet annually. Due to raising children and working I had not attended the rowing reunions previously, but Melanoma Man was quite faithful in his attendance.

This year they came to us in Florida. They tried to come last year, but Melanoma Man discouraged them saying, "you are just choosing Florida BECAUSE OF THE CANCER." Seems a good enough reason to me. This year he acquiesced and it was good. I was intimidated by the idea of it all, by the idea of the wives, by the idea of how my life and specifically my living room might measure up to theirs. Me and my leaky roofed rental house, complete with tarp and sandbags to keep the rain from coming in. Growing up I was the behind the scenes support team for many events hosted by my Mom and Dad. They were great entertainers, so that backdrop loomed in my head as well. Enough is what it all comes down to with me. Am I enough. On my own the answer I usually come up with is No.

MM spent Monday through Thursday shopping and cooking. I tried to catch up on the hopeless task that is housekeeping, without being grumpy, angry or perfectionistic. I got home from work Thursday night, entering our house as I always do through our ping pong, pantry garage, laundry room. The front door has been broken for three years, so the only way in the front of the house is via "le garage." I glanced into our living and saw the IV pole, still up from Melanoma Man's infusion earlier in the day.

In the kitchen nine people plus my three people greeted me. I had met Kathy & Mike, John & CJ, Bruce, Don 13 years ago. Skip, Linda, Karen were new. I chattered nervously, pushing worry away, trying to remaining open and awake to all the people. I had seen a post on Pinterest earlier in the week that said simply, " Let's just be who we really are." Sounds simple, but still hard for this hostess with an IV pole in her living room. Gwen and Ron arrived around 7:30, straight from the airport.

Mike and Kathy had taken charge of renting two beach houses. Mac had cooked Thursday night's dinner. Karen cooked Friday night's dinner. Oz and Vicki had dinner catered Saturday at one of the beach houses. Friday Karl & Terry, Rob & Nancy, Bob and Jay arrived. Saturday Vicki and Oz arrived. 

 On Saturday night Oz presented a toast to me and Melanoma Man with wishes that we'll get to go around the board again and again. Vicki presented us with a corresponding Monopoly themed mug. I knew that they understood how hard this journey has been and will continue to be. They did not avert their eyes but took us just as we imperfectly are. I didn't know most of them at the start of the weekend.  I came to feel like these are my people by the end. That sense of community and love surrounded us. 

Things that Blew Me Away Last week and This

Every weekday morning I get up at 5, turn on the coffee maker, which has been preloaded with coffee grounds and water the night before by Melanoma Man. I spend an hour watching the weather channel, checking Facebook, reading the Skimm. At 5:45 I hit my fast forward button and spend the next hour getting myself, one kid and three lunches ready. The other kid gets ready after I leave for work.

MM had been feeling "under the weather" over the weekend, very short of breath, chills, aching all over, no fever yet, but getting a little cranky. I am friends with many of MM's cousins on FB, since MM won't use FB, it's how we keep up with some of the family and they with us. Cousin Ella had posted Lennon and Maisy singing "That's What's Up." I liked it so much I downloaded it onto my phone and listened to it on my way to work. It came in handy all week long. MM would be cranky with me for helping or he would be cranky about forgetting something or someone. I would sing a line from the song, many of which I now know by heart from the extensive car singing rehearsals I have been conducting. It was a tiring week, which culminated in nothing in particular being wrong. Let's call it a Dabrafenib storm. He has had them before as a result of this miracle drug and he will have them again. The trouble is they look an awful lot like coming down with something dreadful. I don't sleep well on storm weeks. I wake up, and eyes closed listen to his breathing, assessing the sound and whether it just requires monitoring or requires eyes open and action. He reads books, lots of books and plays solitaire on the computer, and does puzzles during the storms. He does not ask for help, or shop or cook. He doesn't want me to shop or cook either because it makes him aware that something is happening and we don't know what yet.  He thinks, maybe tomorrow he'll bounce back, but they usually last 5-10 days, not one. I make helpful suggestions like, " maybe you should give Dr. Array a call?"  I send him helpful emails that recap his symptoms, hoping he'll send them on to one of his health care providers. Honestly I can't tell. Does this the shortness of breath look like a pulmonary embolism, pneumonia, plain ole worsening alpha 1 disease, or is it pneumonitis from the drugs. Since I can't tell, have no lab in my living room, no X-ray or Ct scan or radiologist for that matter. I always wish he would consult the pros earlier than later. It is hard and tiring work being married and being nice, but Lennon and Maisy helped me to be nice. Then yesterday work colleague KW showed me this: Blind Devotion. She said I would need tissues. She was right. Last night I showed it to MM. We sat on the edge of the bed, tissues in hand watching it on my iPad, tears streaming down. Then he said this: Thank you.

The long and the short of it

The elation of no NEW brain Tumors wore off pretty quickly this time. Dr. Etame noted that the left temporal lobe tumor is still present, appears stable in size. He went through the images one by one with Melanoma Man on Wednesday, with a caution that the official reading by the radiologist is still pending. Separately today MM and I checked the electronic record, still no radiology report.

I found a new acupuncturist, since my last one moved to Colorado in December. As usual I tried to tough it out, but have not been entirely successful. The days are mostly fine, but nights are filled with bad dreams and nightmares. 

Last week the nightmare was me trying to find my eldest son in the children's hospital. In the dream my eldest also had melanoma, and had just undergone surgery. I was not allowed entry into the hospital unless I took all my clothes off and left them in security. I was the only lost naked person wandering the hospital halls. Let's just say that even in my dreams I am no Cindy Crawford. The only thing we have in common is that we are both 48. There was one person in the dream who would acknowledge me and help me find my son, TW. TW is one of my real life colleagues and is also kind and helpful in real life.

Last night's nightmare involved Melanoma Man fixing something on our roof. He had the brilliant idea to get to the roof by holding on to the garage door, pressing the garage door opener and riding the door to the top. In the dream things didn't go well with the garage door. MM made it to the top and was then catapulted to the pavement. We were in West Virginia for some reason. I knew to call 911, but couldn't remember where we lived. Of course I couldn't remember where we lived, because we have never lived in West Virginia! 

So in the morning I will walk on he beach with my Stephen minister. I'll say my prayers. I'll try out a new acupuncturist. Sweet dreams to all.

More time

Brain MRI is clean. We got more time. We can go around the board again!

Nobody Bothers Me or Why I am addicted to The Americans

I am madly in love with both Downton Abbey and The Americans. Downton Abbey is a wonderful escape into another world, for me almost like visiting a museum. It is full of clever quips, such as Mrs. Patmore's "Sympathy buttered no parsnips." The boys and I enjoy inserting little Downtonisms into our current day conversation. It's a weekly challenge. Usually it is Cousin Violet, played by Maggie Smith, who provides our phrase of the week.

I shared my love of Downton Abbey with my work colleague,TW. She, in turn, offered me The Americans. I watched seasons one and two in January so I could get up to speed in time for season three. I am utterly and entirely hooked, in large part because I was born in the 60s, grew up outside Washington DC in the 70's and 80's, when there were five television stations. The Americans has managed to work in all the appropriate cultural features of the place and time, including this advertisement which was routinely featured on WTTG when I was growing up. You will also notice the soundtrack, cars and clothes in the Americans are just so, Most familiar is that feeling perfectly captured of living two lives, one the day to day routine, the other a desperate battle.

On the surface the main characters Elizabeth and Phillip are small business owners, trying to raise a family. They do a lot of laundry, another reason I love the show. Their other story as KGB agents secretly living as Americans, puts them in constant peril.

Today I am the working Mom, taking a day off, at home on early release day, so I can pick up Butter from swim practice and iMac from band, bake Apple Pie Breakfast cake, make dinner in the crockpot, do an extra load of laundry. I am waiting for Melanoma Man's report from Tampa, after today's brain MRI and neurosurgeon visit. Everything is fine right now. I try to be in the right now.I can't remember what I had planned today besides laundry and dinner. I don't know what to have for breakfast or lunch. The phone rings. It is Butter, not feeling up to swim practice today. Then rings again, it is Melanoma Man. MRI is running behind. It is 1:20 pm and his 11:45 am. MRI has not occurred yet. They send him away to go get lunch. Back from lunch they give him an estimated MRI time of 3 p.m. His appointment to review the MRI with neurosurgeon, Dr. Etame, is at 2:45. Looks like this is going to turn into an overnight trip possibly. He hasn't taken any of his medications with him. I am warding off a headache and trying not to throw up in anticipation of news good or bad which may or may not come today. Telling myself I can do this, good or bad, together or alone. I can do this.