Monday, December 23, 2013
Heather's knight? NOT! Court jester maybe. 🃏
Sunday, December 8, 2013
Sarcasm isn't just for the smart...
Saturday, November 30, 2013
Last lap!!!
Stay tuned for the final analysis and then it's on to the next race which is a 7 week radiation race commencing sometime in early 2014....date to be determined soon.
Thank you for watching and cheering Heather on. You are our pit crew. Not that you are the pits. Yeah....you know what I mean. 😃
Thursday, November 28, 2013
I Love chemo!?!
Sunday, November 17, 2013
No News Is Good News?
Friday, October 18, 2013
Feeling Loved

Saturday, October 12, 2013
Hi! It's been awhile
We have pretty much on autopilot the last several weeks and keeping our heads above water thanks to the love and support of many, many friends who have helped in so many ways. Visiting, dinners, watching the kids, calling, texting, praying, etc.
Heather will have one final Red Devil treatment next Friday and will start a different regimin for 4 additional treatments that will take us through the end of the year. The Oncologist has been very pleased with Heather's lab work which is so very important to watch during this time. Without going into all of the details her bloodwork has been impressive! This means that the treatments continue on schedule and her immune system is functioning well though we are not taking a lot of extra chances to reduce Heather's exposure to a virus etc.
Heather and I have had some very difficult, important and much needed discussions over the last few weeks and one thing remains clear; we are going to continue to forge ahead optimistically and continue to live our lives so that we look back at this time as a great time with the kids, family, and friends. Oh and Heather had cancer then too.
Heather never ceases to amaze me. Her strength and resilience have been amazing and I love her with all my heart. Thanks for listening. :)
Friday, September 20, 2013
Back in the saddle
Saturday, September 14, 2013
Wednesday, September 11, 2013
Mountains and valleys to traverse
Tuesday, September 10, 2013
Cosmetic Shift
Wednesday, August 28, 2013
I'll have the port please
The port is placed under the skin just below the clavicle in Heather's left shoulder. The surgery went well though she is having significant pain emanating from her shoulder down into her arm. Drugs are wonderful so for now she is sleeping it off. Waking up is not going to be pleasant.
We had a wonderful meal thanks to one of our neighbors and that helped immensly as we arrived just in time to pick the kids up from school and got home about 6:15. Having dinner ready to be passed over the back fence saved us from a cereal dinner! Thanks Penelope!!!
The surgey took place at University Hospital and the same day surgery unit is right across from the surgical intensive care unit (SICU) where our daughter Jackie was working a 12 hour shift! She was able to get away for a few minutes at lunchtime (her lunchtime being 2:45) and came over to the waiting room right when they called me back to see Heather. We all hung out for a few minutes then I got a tour of the SICU (impressive to say the least) and then let Jackie get back to her crazy day which I am unable to begin to describe here. It was wonderful to see her in action and well respected on such an important unit of the hospital. I am very proud of her.
Heather gets "a day off" tomorrow then starts her red devil chemo on Friday. It's almost go time and we are ready to dive in thanks to all of the care, love, and support coming our way. Thank you all from the bottom of Heather's port. (Which is above the heart so that's supposed to be a good thing folks!)
Heather's fashion statement
Tuesday, August 27, 2013
Reality Check!
It probably helps that I come from a long family line of dealing with some very trying and difficult health issues if not out of the ordinary. I have a strong and beautiful warrior cousin who was diagnosed with Myasthenia Gravis at a very young age, I have an adorable niece with Neurofibromatosis (NF), I have an aunt with MS, and so on... So who am I to ask " Why me?"
So that brings me to this week. A very sweet co-worker sent me a book written by a local woman who had breast cancer. It was a quick read and I found some humor and insight in the book but it also got me to start asking questions again. I have admittedly given up googling anything regarding my cancer since the end of June.
I decided to look up some information on the chemo treatment I will be starting this week. The first of my chemo drugs is what they call AC (because the actual names are impossible to say in healthcare we frequently use acronyms). I started by reading a site that was just a forum for women talking about their side effects,etc. Nothing too surprising popped up there.
Then I found a site called Health Central which had some more objective information in it and was actually discussing my full chemo regime which is AC and then Taxol (I won't get too scientific here but will put a little blurb at the end for those who are interested). But I will say that AC is frequently referred to as The Red Devil.
The site is set up as a Q&A type forum and I was reading through finding all kinds of useful information and then I came across a paragraph that knocked the wind out of me.
It talked about how a patient may be put on an accelerated schedule which is referred to as "dose dense" chemo. This is considered a more aggressive way to deliver chemo "when aggressive measures are necessary."
With that last part of the sentence I started to lose my supercharged optimism. I sat on the couch saying over and over that it was just because I'm so young not because its that bad. And then I started to cry. Luckily my brave knight was nearby and could come and hold me and remind me that we can do this, that I can fight this good fight.
Reality is that it isn't great, but it is far from a losing battle. But I have come to realize that it is going to be a lot harder then I have been admitting to myself so far. That I am going to need to rely on my troops even more then ever to help me stay focused and positive. That because it is "dose dense" that I'm probably not going to recover as quickly between treatments as I want to think.
I am worried for my family and how hard this will be on them. I hope that for my kids this will become a blurry memory someday. But the anxiety and exhaustion that is my husband's plight is hard - it's just hard. He is being very strong but its hard for him to hide his true feelings from the one who reads him best. So I worry.
So this is my reality check. And this is my plea to my troops and my guardian angels and my bad ass cancer fighting team. Please forgive me for my excessive need. Please know that I see you and hear you and feel you when you do me a favor, send me a note, or even pray or send your positivity my way. I appreciate every gesture no matter the size and I thank you. There will be many more requests to come - especially around entertaining the kids. So thank you all from the very depths of my heart and soul.
For those that are I interested in the medical details...
AC - is actually two drugs: doxorubicin (Adriamycin), and cyclophosphamide (Cytoxan). I will receive The Red Devil every 14 days for 4 cycles. It is normally given every 21 days. Once that is complete I will be given Paclitaxil (Taxol). This is given to woman who are node positive or have had a recurrence. It follows the same schedule as AC. Radiation details to follow later.
This is a pretty heavy duty cocktail normally so I will be loosing my hair within the first month. So I've tasked Mark with coming up with my cool new bad ass bald chick name. Feel free to offer suggestions he is great with brainstorming.
Tata faux now,
Love you all💕💕
Heather
Monday, August 26, 2013
A little bit of great news!
For those of you who didn't know - they found a spot of cancer in my mother's breast around mid-July. After doing an MRI they found several more spots of concern. There has been a lot of craziness back and forth with biopsies and failed biopsies they narrowed it down to just one new spot of concern. This spot was the difference between a lumpectomy and a mastectomy. They were finally able to get a good biopsy of the spot on Aug 13th. It took until today to get the results.
All I can say is that I am quite relieved that it is just the one little spot. I don't know what the full final treatment recommendations (outside of the lumpectomy) will be but they will be so much less and that is a wonderful thing!
As Mark would say - always keeping you abreast if the situation.
Love to all,
2 Drainz
Thursday, August 22, 2013
Ode to 2 Drainz
Friday, August 16, 2013
Life is Good......but some days really suck!
Starting the week with getting Reilly registered to start school in 2 weeks (what??) - not sure I'm totally ready for that one.
Next up was family counseling - the kids started by telling the lady how mom has "boob cancer" and then they got to throw "feelings" balls at each other and draw rainbows, they loved it.
Thursday was our appointment with the plastic surgeon and after fussing at me about my keeping my street cred as "2 Drainz" she then gave me a couple ounces of boob boost (or as Mark likes to call it IPA).
Our last appointment of the week was the big Oncology appointment we have been anxiously awaiting. Throughout this whole process I have felt pretty positive - realistic but positive. So that is how Mark and I both went into this appointment. We were a bit thrown off our game at this appointment. The basic jist is that the cancer was quite pervasive to the point that they want to do radiation in addition to the chemo.
For those who are interested in more scientific detail please continue otherwise skip this paragraph and go to the next...
They removed an additional 3cm mass which is in addition to the 2.7cm mass they removed which means the mass was >5cm. In addition, they removed 7 lymph nodes 3 of which tested positive. The CT scan came back clear - which means no metastasis (yeah!). So that makes my cancer a T3 N1 M0 or Stage III A. one of the concerns that came up in the pathology was that there were little cancer nodules spread throughout the fatty tissue which leads to concerns about there being cancer in my chest wall. In addition, because my lymph nodes didn't take the blue dye that is supposed to show the path of lymph fluid there is some concern that there may be some sneaky little cancer cells hiding in my lymph nodes that weren't checked. So that is the reason for the radiation.
What does this all mean going forward. ..
I will get a port installed next week to make blood draws and chemo treatments easier. I will get my drains removed by August 22. Then I will start chemotherapy treatments on August 30th (To my BABC -I still plan on being there!) My chemo treatment will be a high dose treatment which means that I will have a chemo cycle every 14 days. Once the chemo is complete then I will move on to radiation therapy. I still need to meet with a radiation oncologist to find out that plan but that is a ways down the road - so I will not think about it too much yet.
How am I doing?
Right now I'm worn out. I'm sad and disappointed and pretty ticked off! I'm hanging on to the ticked off piece and trying to let the rest go. I know I will get through this. I know it will be a hard fought battle but it is worth every ounce of pain and energy I have to be here for/with my family - both blood and chosen. My spirit is a little wounded for the moment but I know by tomorrow it will be refreshed and renewed with the hope and optimism that has carried me thus far.
Love to you all.
2 Drainz
Thursday, August 8, 2013
Heather's new street name
Wednesday, August 7, 2013
For us...and the kids
Sunday, August 4, 2013
Holding pattern
We have had an incredible amount of support from family and friends alike and we are very appreciative for the dinners, visits, cards, and help site/blog/Facebook comments and well wishes.
Tuesday, July 30, 2013
A self serving post
In the last few days I have come to realize that while I am still feeling positive that the double mastectomy was the right choice and that moving forward with chemo as the next salvo in eradicating this cancer is essential I have underlying feelings that are really confusing me.
Despite knowing all of the things that lead us to believe that the outcome for Heather will be a good one I have been experiencing some situational anxiety and, yes I will add, depression. I just don't feel right. This is not normal for me and I hate it.
I am worried about Heather and the pain she is in. I worry about the coming chemo course and how that will affect Heather physically. I worry about the kids; not that they aren't well cared for by Heather and I and all of the helping hands but that they too are worried about their Mom and don't really know how to express it. I worry about the big kids too because I know they are worried. I worry that some day Heather may miss her breasts. I'm scared too. Scared about all of the things I'm worried about. Heather and I are supposed to have a long and happy life together and we fecking better.
For years as a Social Worker I was always on the other side of this. Discussing life and death issues with my patients and their families. Young people with bright futures that suffered devastating spinal cord injuries, head injuries, or both. Older individuals who had become dependent on ventilators or lost limbs or suffered multiple trauma. All these things lead to major life changes for all involved and I was charged with helping them explore their feelings and provide them with the tools to become as functional as possible in their new realities.
Thankfully I have been talking to Heather about this and she so wisely reminds me that it is ok to be upset, fearful, afraid. Good...because I am. I am working on allowing myself the opportunity to feel these things, experience them, and talk about them as a mechanism to bring into balance my ability to look forward positively and accept the fact that there is a scary side to all of this and it is ok to acknowledge it.
So if you ask me how I am doing you may not get the quick and easy answer you might have hoped for! I feel better. Thanks for listening now and in the future. Keeping you abreast of my feelings.....Mark
Saturday, July 27, 2013
Staying Positive
Friday, July 26, 2013
Chemo it is
Another positive is that the left breast which was also removed showed no evidence of cancer.
It's all good. Thank you for your ongoing prayers and support. Heather & Mark
Thursday, July 25, 2013
Good morning!
Wednesday, July 24, 2013
Thanks for the mammaries!
T minus 2 hours
Heather with Merida....my brave girls! We are all ready to go. Eager to get this over with and on to the next phase!
Sunday, July 21, 2013
Lose the Tatas, Save the girl...
I AM the browned haired girl with cameleon eyes - blue/green/gray with golden stars, and more importantly the girl with her mother's smile. My definition includes a mother, a wife, a daughter, a sister, and a friend. I am an information gatherer and provider. I am a caretaker. I am not my boobs - although I can certainly act like one at times.
And now I am a warrior - ready to head into battle and do what it takes to succeed. For my children, my husband, my parents, my siblings, and my friends because they are, what matters most. So forget the Tatas - let's save the girl with the chameleon eyes and her mother's smile.
Saturday, July 20, 2013
Wow!!!
Monday, July 15, 2013
Is Mercury in Retrograde?!?!
Reminder to self - everything is going to be fine! Just a bump in the road (or mt. Trashmore).
She doesn't have full pathology yet but they are saying stage 0 or maybe 1 and its a slow grower (stage 1).
So I guess my fam could use a few extra prayers and such....
Saturday, July 13, 2013
Caring for Yourself: Advice for Cancer Caregivers
Caring for Yourself: Advice for Cancer Caregivers
Posted on July 12, 2013, 6:30 AM

By Paul H. Brenner, M.D., Ph.D.
There are few harder tasks than being a caregiver for a loved one going through the journey of cancer. Caregivers are patient advocates. They take notes during office visits, remind those they love to ask specific questions about symptoms they are experiencing, and prepare their own lists of questions for both physicians and nurses.
As a family member or friend taking on a new role, caregiving can take individuals completely out of themselves, their routine, and their life in unconditional service to another. Since patient care can be overwhelming, it is essential for the caregivers to take care of themselves, set goals, exercise, and most importantly, be honest about their feelings of helplessness, frustration, exhaustion and often anger.
There are many potential sources of negative feelings for caregivers. Seeing a loved one suffer a serious disease is painful for everyone, and can be exacerbated by worries about finances and the future. Additionally, the individuals who have cancer tend to feel disempowered by those who are dedicated to helping them. So, ironically what you perceive as a loving act can be interpreted by the patient as disempowerment. In my experience as a psychosocial oncologist, the anger that most caregivers feel is directed toward medicine for its failure to alleviate the pain and suffering of their loved ones. The caregivers often find themselves desperately glued to the Internet researching the latest treatments, procedures, and natural therapies, getting overwhelmed by it all.
It’s important to find healthy ways of taking care of yourself as a caregiver. Start by acknowledging, rather than denying, your feelings. You don’t have to pretend to be cheerful, even when you are feeling overwhelmed. It’s okay to cry. Don’t be afraid of making mistakes. And don’t expect to be perfect – no one is.
There are simple things you can do to make your life easier. Much of the caregiver’s frustration can be resolved by staying away from the Internet, which is filled with anecdotal tails of cures and complications. Medicine is not a pure science and cannot, as a result, offer absolutes solutions for all problems. But today’s medicine is the best we have presently, and is closer to cancer cures then ever before.
Rather than trying to tackle everything, focus on tasks you can control. It could be scheduling doctor visits, helping with meals and errands, and so on. Don’t be afraid to ask for help. Many of us feel that we need to “do it all.” Ask friends and family to help with chores, appointments, and so on. You may need assistance with the emotional challenges of caregiving, too. Try talking with your inner circle of support: loved ones, faith groups, or social circles. Or go beyond your inner circle to join a caregiver support group, or speak with a counselor, social worker, psychologist or other mental health professional. Each of these people may be able to help you talk about things that you don’t feel you can talk about with your loved ones.
So dear caregiver, be kind to yourself and treat yourself as lovingly as those you love. Find time and space for yourself. This allows the person who is ill to feel better and less guilty for consuming your life and for the suffering they feel they have caused you. To paraphrase the Serenity Prayer, change those things in life that you can, and have the wisdom to accept those things you cannot. Caregiving is a love beyond love that has no beginning or end, so cherish yourself with the identical love that your have for your beloved.
Paul Brenner M.D., PhD. was a gynecological oncologist who practiced obstetrics and gynecology, and also holds a Doctorate in Counseling Psychology. His journey through the healing arts has been in search of those unseen processes that play into chronic illness. He presently is the Psychosocial Oncologist at the UCSD Health Systems San Diego Cancer Center. Also, he is a Research Fellow at The San Diego Cancer Research Institute. He is involved in studying the impact of Trans-Generational Emotional Patterns on Health and Illness. He is the author of “Seeing your Life Through New Eyes” and “Buddha in the Waiting Room.” He also has lectured throughout the world.
Wednesday, July 10, 2013
1 in 8
Or maybe I'm just foolin' myself!














