
Focus on the Good


Results from yesterday’s blood work is back and I received word that everything looks good. I’m cleared to have my 3rd treatment on Monday. Halfway mark here I come!
Ovarian cancer ranks fifth in cancer deaths among women, accounting for more deaths than any other cancer of the female reproductive system. A woman’s risk of getting ovarian cancer during her lifetime is about 1 in 75. Her lifetime chance of dying from ovarian cancer is about 1 in 100. Of that 1 in 75, and if you are reading this, we personally know one.
Pam was diagnosed with Ovarian Cancer on August 25, 2016, had surgery to remove the mass on September 6, 2016 and began her anti-neoplastic chemotherapy treatment on October 3, 2016. She still has a road ahead of her and has treatments scheduled through January 2017.
You often hear the phrase “money talks” — but it is so hard to actually talk about money. It is even harder to ask for it. This is one reason I chose to pen this letter on Pam’s behalf; because I know her well enough to know she won’t ask.
Pam lost her job in September 2014 and since that time has robbed Peter to pay Paul on her own, and with the help of very close family members. She has never asked for a hand out, or even a hand up. She has done anything she can to make money here and there until she is able to find a role in her profession. These jobs have not paid much, but they have kept the lights on.
As you can imagine, her medical bills are very quickly piling up and are surmounting to a level of unmanageable on top of meeting her “normal needs”. She has tapped into family as much as they have been able to help financially; and that help is leaning out too. This is where you come in. Pam is not planning some grandiose vacation to the Caribbean, or buying a new home or car; but she is at risk of losing the home and car she does have. We are entering winter and the heat and lights need to stay on.
Some of the side effects of cancer and chemo treatment are:
All of these above symptoms limit one’s ability to aggressively seek employment and/or work the job they already have – further causing financial stress and strain.
This is where you come in! Pam needs our help. She will not ask for it – so I am! Many of you have sent thoughtful gifts to keep her head warm, her hands warm and her belly fed when she can eat and she is eternally grateful. But she needs more. Her car note needs to get paid, her mortgage is still due, she has power, water, sewer, trash and phone – the most basic needs – that need to be paid. ANY amount that you can send is the “right amount” and is gratefully accepted. You can help in a few ways:
THANK YOU ALL from the bottom of my heart, Pam’s heart and her Mama’s heart who can’t be here all the time and is home in Alaska nursing her own recent surgery.
Truly,
Jenipher (just a friend who is trying to help, just like you)
*ding*
“go to sleeeeeeeep” admonished my mother from Alaska via Instant Messenger.
*ding*
yawning kitty sticker
I let her know that I had, but I could not stay asleep or fall back to sleep easily after waking up and it sucks.
*ding*
“I’ll tell you a bedtime story.”
oh law.
*ding*
“Once upon a time, there was a princess who was the most beautiful child of the queen”
(suck on that, siblings)
*ding*
“Her mother had bought her queenship when she won the publishers clearing house sweepstakes”
*ding*
“So the princess grew up to bring great joy and happiness to the queen and all that she knew.”
*ding*
“Well, except when she didn’t get her sleep and then she was called Princess Grumpisocks…”
*ding*
“But now she knows that it is far worse to not sleep because the writer of Goldipam and the 3 Bears would tell her totally ridiculous bedtime stories if she didn’t sleep.”
*ding*
“And soon she was enjoying blissful sleep and lived (and slept) happily ever after.”
My mother, everyone, the originator of long distance mothering via text. STILL killing it from Alaska!
don’t worry, I got this…
I should have know when his first degree was in Psychology that it would come back to kick me in the arse one day. Remind me to thank him for that kick, I really needed it.
I got off schedule with my antidepressant and got stuck in a bit of a negative spiral this weekend. Certainly there are a number of things happening at the moment worthy of being depressed and usually I am able to re-frame and re-focus so I can soldier on, but now and again a kick is in order. This was one of those times.

“Change your thoughts and you change your world.”
But he was not done there so he continued with, “Now is especially not the time to be so negative. Lie to yourself if you have to. Negative thoughts can be very damaging to the body, mind, and spirit.”
I responded that I knew that, but DAMN.
That earned me a stern, “nope, no damn” so I called him bossy. Seriously, he’s bossy. He claimed it is only when he needs it…
I railed back that I have been lying to myself about things getting better for so long now while things just keeps getting worse that I no longer believe that particular affirmation.
He suggested, “Find the things that are positive and focus on them.”
A 5 yr old said I was beautiful Saturday; so kids dig me.Dogs dig me.
Yes, so are couples doing happy shit.

The Xanga!
[or “Why I Think They Should Just Hand You a 1000 Cats With Your Cancer Diagnosis When You Are Single”]
I told him I wanted to write a post about how much it sucks to be single with cancer but I feel like it is just so whiny to cry about all the things that hurt about being single through all of this and would discount all of the great support I have around me. Everyone is always telling me how upbeat and positive while I’m all sad because I’m alone 90-95% of the time and just want someone to cuddle up with me on the couch to watch movies or take me out on a stupid date (or… or… or… the list goes on for a pitifully long time). No one wants to date a sick bald girl who is always tired and weak.
He said, “I think you should write the post.”
I asked him why? To vent my spleen? It just seems so pathetic and I have been single for so long now I suspect everyone just figures that my being single is a personal choice and that I like it being alone as opposed to a “chick can’t land a date if you tied movie tickets and coupons for free steak dinners around her neck” type reality now made all the more difficult by a lack of hair and reproductive organs.
“Just curious if you have tried a dating site.”, he asked, followed closely by, “Also, I think many would not care about reproductive organs.”
Have a tried a dating site? HA! Yes, I’ve tried multiple dating sites.
The most successful outcome is MSEE that I’ve been talking to for years but have only been out on 4(?) actual dates …and none of those recently. He’s not intimidated by my intelligence, loves my sense of humor, and is all kinds of supportive from a comfy introverted distance but that severely lacks a certain something.
The remainder were either older than my father (which is just too weird for me) or more than half my age and applying for my consideration as their sugar momma (in the greatest abuse of the English language I have ever witnessed and I’ve witnessed some major abuse in my day).
“Well, yeah, people are freaks.”
At least the ones who contact me via dating sites!
I told him that perhaps by the time morning hit Zambia my pitiful spleen would vent a post on the blog titled “they should just hand you a 1000 cats if single when diagnosed with cancer.”
“Well, maybe work on the title.”, he suggested.
…don’t worry, I got this, thanks to friends like him (he sayeth so it iseth).
I dropped in on my BamPowChow food truck friends yesterday for lunch (chicken and bacon jam quesadilla for the win!) and after complimenting me on my punk rock stubble Chef Sean gave me some unsolicited but sage advice:
That second one made me laugh because he said it so matter of factly like everyone can hear the razor in their head when shaving. Perhaps that is common for guys, but my legs are a long way from my ears and while I can’t speak for all women, I don’t recall hearing that before.
Now, I have been on the fence about shaving my head with a razor. Before last night, I was thinking I might be able to get away with the closely clipped stubble I’ve been rocking for the last week, BUT there is this weird thing happening with my hair right now and last night it became unbearable. My hair hurt. Every time my head touched the pillow it hurt me so badly I couldn’t sleep. Maria and I have developed a theory that the chemo must kill off the root ball that anchors a shaft of hair in your skin leaving the shaft exposed and able to poke you mercilessly like a tiny needle. Then not long after your hair starts to hurt it starts to fall out in droves. I’ve been using this whole weird series of events as an indicator of when to bring out the clippers. Today I hit the last level of hair to downsize so I hit the showers with razor in hand. Cue the hilarity to ensue!

I wasn’t that far in (and intently listening for the *scritch* *scritch* *scritch* to stop) when I realized this wasn’t going to go as smoothly as I would have hoped. For starters, it was taking a lot of work to get the *scritch* *scritch* *scritch* to stop! I was also getting tired and running out of hot water. I decided to make sure the areas NOT covered by a ball cap were shaved up as best I could and finished up my shower.
After consulting with my authority on all things manish (thanks Brock!) and the rest of the family hive mind (thanks Allison and Sue My Mother!), I arranged with Trish, my Thursday Partner In Crime to pop by Target after my weekly blood letting to pick up a Harry’s razor and some of their Post Shave Balm with aloe vera (which relieves and soothes!). Then, once back home this afternoon I set about finishing this morning’s shower and shave 😉
Take Aways:
Don’t worry, I got this…
I’ve been fine with losing my hair from the beginning, in fact I considered it a silver lining since it would give me a great excuse to do some fun things with my hair since forever. Scott, my hottie hair stylist, and I have had several conversations about what we would be able to do both as it was leaving, while it was gone, and when it was growing back. However, along the way I realized one important thing. I wanted to be in control of it going, not the chemo..controlling the burn as I termed it. It was all fun and games until this last trim when the last of my hair came off.
At my first chemo treatment, where it was evident I was a noob because I had hair, I realized there were actually two important things. The second being that I was okay not having hair as long as it was just me on my own and not identified as a group of sick women. Turns out that the perception of others is something I cannot control. I have known that for years, but I had not made the connection until recently.
My friend, Maria, is a treatment ahead of me and has been preparing me for what to expect based upon her own experiences. She told me that once my hair was gone, I would be hugged and prayed over by strangers, but she did not make as much note about the look.
You know the look, the “oh, you poor thing, how terrible” look. Pity.
I do not need it, I do not want it, and I do not deserve it. My cancer was caught miraculously early, I have been blessed with an amazing doctor, and we are treating whatever cells remaining aggressively. My odds are better than most women who have been diagnosed with ovarian cancer and I know it. Instead, SMILE. Trust me on this one. Look them square in the eyes and SMILE. You might be surprised by the effect it has on the exhausted looking, no hair day having beauty before you.