Still Thriving...

Still Thriving...
Have You Scheduled Your Mammogram??!!

Friday, August 13, 2021

Where Do We Go From Here?

I hardly know how to begin and end this post. 

I suppose I can update you on a brief sequence of events. 

In May I had throat surgery to repair a paralyzed vocal cord. There was a  mishap so I had to go on a very strong anti-biotic, which wreaked havoc on my body. I was throwing up and had bowel issues and all the while trying to swallow as my voice healed. Long story short, my voice is back but I physically have not ever been the same. 

Who's to say what caused what but the biggest issue now is that my liver is failing from the cancer. No, I cannot get a transplant or treat it anymore. I am no longer on any chemo or cancer medication because after exhausting the list of possibilities, nothing seems to be improving. I am still in close contact with my doctors at Sloan Kettering where I've gotten exceptional care. They've been managing my malignant ascites, edema, tremors, and all other cancer related issues. I am, however, primarily under home hospice care. I have nurses visit the house, they get my meds, supplies, etc. Everyone thus far has been very compassionate. 

Today I met with a non-denominational chaplain --I surprised myself--and had a lovely talk. It only occurred to be about a week ago that all of this is permanent. For instance, I recently got a catheter for the ascites and in my mind, once I healed from it, it would be over. But no, it's staying in me. It's drained three times a day by my devoted husband. Not only has my life changed, but his, too. He cares for all of my meds, food, speaking with doctors. He has a new full time job just for me. Instead of planning vacations, we are planning how to get around from pt a to b, will I have the energy, etc. and this makes me feel so anxious and scared. What else is to come that will be permanent? The Chaplain said I am mourning the way my life used to be. She is right. No more beach, dunks in the pool, even a bath. I hope together we can work on my finding a more peaceful place but at night when my thoughts run like crazy, I am not at peace. I am overwhelmed with thoughts of the future. 

I suppose this will be my first writing entry to this new chapter life. Please stay tuned for more and feel free to ask questions. 

Love, 

Elizabeth๐Ÿ’“

Saturday, December 26, 2020

Is 2020 Over Yet?

Hi, All, 

Hope everyone had a nice Thanksgiving even if it had to be celebrated from afar. Christmas was just yesterday and despite a day off from work, in true 2020 fashion, there was a water main break on our block (of the building I manage, not my home) which resulted in the basement being flooded with several inches of water. Thanks to the NYFD and building staff for cleaning up what we hope is the last mess of the year. Monday will be all about insurance claims. Aside from that, we watched "Ma Rainey's Black Bottom" starring Viola Davis and the late Chadwick Boseman who passed away this summer from a four year battle with colon cancer. If you're a fan of August Wilson plays and liked "Fences," you'll like this movie. If you're a blues fan, you too will like it, as Ma Rainey was known as the "Mother of Blues.

The Abraxane (chemo) and Letrozole (estrogen blocker) combination has been very tolerable with the exception of some occasional stomach issues and fatigue. With this treatment it's recommended that one ices her hands and feet 15 minutes prior, during, and after treatment to prevent finger and toe nails from getting crapped up. It's not pleasant but hardly a bother in the grand scheme of things. Plus the nurses are entertained by my wide sock collection. 

 






The treatments would go like this: Arrive at hospital to get blood drawn. At MSK they can get results in minutes and they will determine if my ANC, or, Absolute Neutrophil Count (estimate of body's ability to fight infection) is low. If too low, then can't get treated. Although I regularly fall on the low side of the scale, I've only been low enough to skip one treatment. But for this reason I have to really err on the side of caution during Covid. 

Following the blood test, if I'm treated in NYC, then I go see the doctor. If I'm treated in Basking Ridge, NJ, then there's no doctor visit. Next step is the treatment. The nurses apply the ice while the cocktail is made; it takes about 30 minutes. Then the IV is given and that takes about 30 minutes. Sandy drives me to the NJ treatments and sits patiently in the car as there are strict rules about visitors in hospitals. I usually pass the time listening to music or a podcast or sometimes I partake in a Zoom meeting. 


After several months of treatment, the blood reports were indicating that the tumor markers were steadily increasing. High levels do not always indicate the cancer is getting worse, but you definitely want to do a scan when you see this. So the PET scan scheduled for 12/31 got pushed to this past Tuesday. Unfortunately my insurance company idiotically refused the PET scan because, get this, it couldn't be justified. ๐Ÿ˜ฃ๐Ÿ˜ฃ In lieu of that I got a bone scan and a CAT scan.



It was quite the day. First I went to one MSK building to get a radioactive dye injected; it needs at least two hours to travel through your system. Then I went to another building where I had the CAT scan with contrast done. Then I returned to the first building for the bone scan. First time I ever had one. It was broken up into three sections of the body. It went well with the exception of the first section--a large plate is lowered over your head, just a few inches from my nose. I made the mistake of opening my eyes and going into panic mode. The machine started rumbling and I envisioned myself getting caught in an earthquake thinking how would I escape, etc. I survived it but I did recommend to the tech that maybe people should be informed of this in advance. 

On Thursday the oncologist called us with results. The long and the short of it is, the large tumor on left lung did not decrease from this summer's additional radiation and the chemo, rather, it increased. There are a few new tumors on the liver. The good news is that there were no hot spots (tumors show as "hot" if they react to the dye) on the bone scan, which should indicate that my hip responded well to the radiation done this summer. This report was not yet seen by the bone radiologist, but what the breast oncologist believes to be true.

Sandy and I have great plans for New Year's Eve. We're going to MSK in Basking Ridge for chemotherapy! Not sure if the nurses will mind my swigging a bottle of  my favorite champs, Rose Veuve Cliquot while they give me an infusion. I will start a new drug called CMF , which is supposedly tolerable. It does cause hair thinning so I'll likely remain nearly bald for the next several months. 

Several people have asked if I will get the Covid vaccine. The answer currently is yes, when available. MSK at the moment has no objection to it; it was not tested on cancer patients per se, but it was tested on some immuno-compromised patients. 

Now for the good news...Sandy and I closed on our fabulous new house! We are in the midst of getting quotes for flooring, painting, electric, etc. and hope that work can be done by March so we can move in. It's quite exciting and we look forward to mask-free entertaining in 2021!  ๐Ÿ™ In addition to that, I continue with my Penn State Master Gardening course, which I cannot recommend more if you have a serious interest in gardening. By the way, did you know the "i" in Poinsettia is not silent?!

I wish everyone a year of love, joy, health, peace, prosperity, mask-free dining, less worry, chocolate, and anything else one's heart desires. 

Thanks for reading until the end!

See you in 2021,

eLIZabeth ๐Ÿ‘„

PS I forgot to mention that for no apparent reason I have a paralyzed vocal cord. My voice intermittently gets hoarse and I sound like Peter Brady. ๐Ÿคท๐Ÿป‍♀️ 

Monday, October 12, 2020

Taxol Take 2

Hello One and All, 

Seeing as it's Breast Cancer Awareness Month, I thought I'd share the latest and greatest from New Hope and remind you to schedule your mammogram if you haven't already: 

Since my last post I did three sessions of radiation to my hip socket at Memorial Sloan Kettering (MSK) in Basking Ridge. (Not so flattering pic below.) The treatment itself did not cause any side effects. The greatest pain was caused by lying on the hard, blue mold made to fit my body (getting up from it was a bear and NOT graceful) and keeping my arms perfectly still when I have an impingement in both shoulders. No results yet as I have not had a scan since then (scan date TBD).  



This was in the parking lot when Sandy & I were leaving.
I took it as a good sign that someone's looking over me. :)

A few weeks ago I tried a new chemotherapy called Irinotecan. In a word, it SUCKED. I had only one treatment and it caused nausea, vomiting and diarrhea for the better part of two weeks as well as hair loss. Supposedly it's "well tolerated" with the exception of stomach issues but for some reason I did not respond well. At. All. Twice Sandy had to take me to MSK to get an IV due to dehydration. 


Miserable at MSK getting fluids.

Despite the awful side effects of this drug, I still consider myself lucky. This was only the second time since 2012 that I felt so ill from chemotherapy. Most of the others were pretty tolerable. 

Seeing as my hair started shedding after three weeks --I was shocked it could happen from one treatment--and knowing my next chemo would cause hair loss, I decided to chop it off. I must give a shout out to Thad at Salon Gratitude in New Hope, PA who so graciously and patiently cut my hair and didn't charge me. He brought me to tears. The first time I met Thad years ago was under similar circumstances. My hair was growing back awkwardly and he fixed a buzz cut gone awry that Sandy had attempted at my request. Salon Gratitude has also been donating its services to New Hope's annual Couture for A Cure (breast cancer survivor and thriver) fashion show that I participated in a few times (this year canceled due to Covid). The stylists did the hair of all of the models and made us feel and look special and fabulous. Thank you Thad and Salon Gratitude! 

Last Friday I had my first chemo session with Taxol. Taxol was the second chemo I tried back in 2013 and I benefited from it for several months. Since it's been so long that I've been on it and because it was pretty effective, the oncologists thought it would be ok to try it again; this is not an uncommon practice. The version of Taxol I am on is called Abraxane. Abraxane does not contain a preservative that's in regular Taxol and typically can cause worse side effects. They cannot always administer it because, guess what, it's more expensive and insurance balks at that. I got lucky and thus far with the exception of some mild stomach issues and nausea, I am feeling fine.

And now for some positive non-cancer related news... 


I started a Master Gardener program through Penn State Extension. Classes are held once a week on Zoom and end in March. In addition to the requisite 40 hours of course work, I have to put in 50 hours of volunteer time over the year. There are many ways to volunteer including assisting in the development of a local community garden. Because I have to limit my interaction with people I will likely focus on working on the newsletter and social media. If you are interested in becoming a master gardener, you should know that this program has been around since the 1970's and exists in all 50 states! I originally was just shopping around for a gardening or houseplant class and stumbled upon this amazing course. I will tell you that if you haven't studied in many years like me, studying botany ain't easy! But the volunteer teachers are so kind and helpful and are there to assist with anything.

Last, Sandy & I are in contract to purchase a fabulous house nine minutes from our current address in New Hope. We should close near year end and we are very excited about this development! The house sits on over two acres of land and has many tree species so I look forward to learning about them and sprucing up the landscaping with beautiful plant containers. The house is unusual in that it was shipped from Norway (the best house framers!). There happens to be an electric dog fence so, who knows, maybe there'll be an addition to our little family sometime soon. 

That's the news for now. It's time for me to study Plant Disease. Yup, you read that right.

Be well, keep washing your hands and don't forget to VOTE!! 

Love, 

LB







Thursday, July 30, 2020

Fake News!



Hi, Everyone, 

I gave some incorrect information in my last post. 

The doctor apparently told me we should look into sacituzumab (Trodelvy) but when I spelled out what I thought he said phonetically and then Googled it, it led me to Trastuzumab (Herceptin). Herceptin is NOT in stage 3 trials for ER+ BC like I suggested below and I am NOT going on it. Sacituzumab aka Trodelvy is in stage 3 trials. The doctors are deciding if I will take that or Irinotecan. Whichever one I don't take now I'm sure I'll take down the pike. Following are links to both drugs, which supposedly are well tolerated.



Scheduling for chemo will not occur until the radiation is complete. Monday I go for a mandatory Covid test followed by the Simulation (mapping for radiation). Radiation will take place 7-10 business days from Monday. 

Wash your hands. Wear a mask. Stay positive. 

Love, 

Elizabeth

Sunday, July 26, 2020

It's Been Six Years...

It's been six years since I've posted on Twin Peeks. I had reached a point where I thought nothing was that interesting to share. 

In retrospect, however, I see I may have omitted some important information for other metastatic breast cancer patients who hopelessly search for information on the web. I was one of those people six months ago when I couldn't find any more than two people to "chat" with about their experience with a particular treatment.

So, what follows is a brief summary of my experienced since my last update in 2014. I may be leaving out information simply because I don't remember every detail of my treatment.

Around 2016 I felt so maxed out on chemotherapy. Not one doctor would acknowledge that my symptoms were chemo related. I had a new nagging cough that was so exhausting and at times brought me to tears. I was told I had acid reflux. I had severe stomach cramping, which would occur out of the blue or when I bent over to tie my shoe or just went to the bathroom. Test after test showed nothing, I was told maybe you're constipated. My sense of taste and smell was screwed up. To this day the smell of rubbing alcohol makes me gag. I was tired and for the first time kind of miserable.

Then I received a gift. I asked a contact who sat on the board of Memorial Sloan Kettering (https://www.mskcc.org/) he could tell me the easiest way to reach someone about the possibility of participating in a trial (to date, I still haven't qualified for any). The next day I was confirmed to meet the head of the Breast Cancer department (Take heed: Don't ask, don't get!), Dr. Jose Baselga.

Over a few weeks, it was confirmed that I had definitely gone through menopause (on chemo you might think you have when in fact you haven't) and through extensive gene testing provided by MSK I learned I had no odd gene mutations. This was checked because some mutations can show you're a candidate for a chemo drug that isn't specifically for breast cancer, but you still might respond well to it. It was concluded that I was primed for post-menopausal hormone therapy. I went on Ibrance (a pill, yay!!!) also known as Pablociclib, https://www.ibrance.com/ coupled with Letrozole (another pill, yay!!) and together these drugs gave me a great two year streak with no growth and little to no side effects. Research shows that two years is the average success rate with this cocktail and I was happy to fall into that group. I must mention that all of the symptoms mentioned in the paragraph prior went away after I got off IV chemo. So yes, it IS possible to what I call max out on chemotherapy and if you're doctors say it's not, don't believe them! You know your body best and sometimes, when possible, it just needs a rest!

In the middle of my Ibrance treatment, this sadly happened: 
https://www.propublica.org/article/astrazeneca-hires-dr-jose-baselga
I was stunned and devastated to lose Dr. Baselga especially given the circumstances. He and my Lenox oncologist, Dr. Keith Brunckhorst, were the perfect team for me! Who could fill the shoes of Dr. Baselga?

I was gratefully lead by him to Dr. Sarat Chandarlapaty who still sees me. https://www.mskcc.org/research-areas/labs/sarat-chandarlapaty

After Ibrance, I was put on Fulfestrant, two HUGE shots given in your hip that caused pain, soreness, and numbing for months even after treatment ceased. This drug, more commonly known as  Faslodex  http://chemocare.com/chemotherapy/drug-info/faslodex.aspx bought me a few months. I was then put on a combo of Afinitor https://www.us.afinitor.com/ and an aromatase inhibitor, Examestane and I have no recollection of side effects. https://www.webmd.com/drugs/2/drug-17764/exemestane-oral/details 

Fast forward to April 2019, a scan showed the lung tumors were growing and the cancer metastasized to my liver. It was too soon then to treat the liver with anything outside of using drugs so we decided to just watch it. But we decided, under the care of Dr. Jillian Tsai   https://www.mskcc.org/cancer-care/doctors/c-tsai to do three sessions of radiation to the two largest lung tumors on the left and ride sides. Results were decent with some reduction in size of the lung tumors, but the liver tumors continued to spread.

In February and March of 2020, MSK's interventional radiologist, Dr. Amy Deipolyi, performed Y-90 radiation, a very targeted treatment administered on an out-patient basis while under sedation, through the groin, first to the right then the left lobe of the liver. It was this treatment that lead me to scouring the internet for other people's experiences and eventually writing this post. I had no way to predict for how long I'd be bed-ridden from the side effects that were like none I've ever experienced. https://www.radiologyinfo.org/en/info.cfm?pg=radioembol
There was a lot of nausea the first round but worse, strange, indescribable pain around the abdominal area as a result of the blood supply being cut off to the tumors. I found only two people on Facebook groups that shared they had similar experiences and convinced me the pain would dissipate within about six weeks, which it did. I had much less pain on the left side in March.

Prior to being approved for the Y-90, United Healthcare rejected it three times. They suggested I try a systemic treatment, WHICH I'D BEEN ON SINCE 2012. They said because the liver wasn't my first metastases (the lungs were) it wouldn't work. They said there were less expensive and experimental options out there. It was INFURIATING. Dr. Deipolyi, however, armed with her success stories, persisted and after three appeals re-submitted the request at the beginning of the year and it was approved. Was it a new person reviewing the case or just a new annual budget that got me approved, we'll never know. I urge anyone whose treatments are rejected to PERSIST. Kick and scream. Out the insurance company on social media. Call the pharmaceutical companies. I did all of this. Remember, insurance companies are businesses and like all businesses, they want to make money and they do not have your health in their best interests.

The scan in May following the Y-90 treatment showed excellent results on the right side of the liver--there was little to no activity. The left side didn't fare as well but we thought it had been too soon to make any conclusions. There also was still one pesky lung tumor that was resisting the April 2019 radiation so we proceeded with two double-shot radiation treatments to that one tumor: two days in a row of twice daily radiation. 

A follow up PET scan was done a week ago. It showed that the right side of the liver remained stable with the exception of just a couple of tiny new tumors. Unfortunately, for the most part the left side rejected the treatment and there are a couple of new tumors. There's no explanation for this and Dr. Deipolyi was SHOCKED that one side would respond so drastically different from the other. One reason given is possibly I've been on so many treatments, that the cells aren't kicking butt like they once might have. Lastly, an area on my hip that we've been monitoring closely has been confirmed as cancer. This would be my first, hopefully my last, bone metastasis. 

Next steps: Dr. Tsai is very confident that with three radiation treatments, the tumor in the hip socket can be destroyed. This week I will find out when I will be treated. While this is happening, Dr. Brunckhorst, at the recommendation of Dr. Chandarlapady, is going to see if he can get me approved for "off-label use" of a chemo called Herceptin.  https://www.herceptin.com/  Herceptin has been associated with successfully treating HER2+ BC patients, which I am not. But they are in phase III trials for treating hormone receptive positive breast cancer patients like myself and the median success rate has thus far been eight months. Sounds good to me!

During the pandemic I've been fortunate enough to be able to work from home, which I've been doing in our house in PA since March following the second Y-90 treatment. I do not miss the rat race in NYC and I'm much happier and presumably healthier--mentally anyway--with a garden, fresh air, daily 3-4 mile walks and no Covid crowds to worry about. Yes, I may've jumped ship and abandoned my city to live in a bubble, but I've done so guilt-free. And for anyone reading this who ever said to me, You cannot or will not ever leave NY, you're a true New Yorker, and you'll just be bored, I'm happy to report you were wrong. :)

I plan to provide an update when new results are in. In the meantime, please feel free to ask questions, provide feedback or share this post with anyone who is continually on or looking for new treatments and wants to share their experiences.

Peace. Love. Thanks for reading.

LB

Wednesday, May 14, 2014

Port One, Gemzar 2

Makes me think of the Rain Man. To be said while rocking back and forth: Port One. Gemzar Two. Port One Gemzar Two. Charlie Babbitt made a joke. K-Mart Sucks... I survived my first treatment using the port on Monday. I didn't think it could be done given I still have on bandages but the nurse was able to access Port Authority. She put on a local anesthetic cream called Emla. Great, something else that comes with a warning label. Anyway, it helped to numb the area very quickly. I must say, although I was entirely freaked out by poking a device installed under my skin, it made the treatment go much smoother. We saved at least 15 minutes trying to find a cooperative vein. So that's the good news. 

The not great but bearable news is that I feel like shit from the treatment. I was fine on Monday though extremely tired and irritable to the point of tears. I haven't been sleeping, hence my writing this at 4:00 in the morning. Yesterday I had aches and pains, chills, nausea, and no fever. I was teetering on throwing up every couple of hours but thankfully didn't. I cannot say I'm feeling to great now. This is a typical side effect of the chemo that strangely I didn't experience the first time I had it. Took a bunch of Tylenol Extra Strength, which I'm going to stock up on. By the way, what are you thoughts on the actual name brand vs. say, Walgreens?

Meanwhile, my hair is growing in dark and somewhat thick--still some thinning spots in the back. My insane hairline is back, cowlicks, baby hairs and all. Here's an interesting fact: The word cowlick originates from the domestic bovine's habit of licking its young, which results in a swirling pattern in the hair. I did not know that until I looked up the correct spelling. 



I'm incredibly antsy lying in bed and the bright light of the computer isn't helping. Time to turn on some NPR and attempt to catch more Zzz's...

Thanks again for everyone's supPORT this week. Oh, by the way, my friend Maury came up with a new name: Port CHESTER. How did I not think of that? Good on ya, Maury!

Love to all, 

LB


Saturday, May 10, 2014

Greetings from Port Authority

Hi ya'll... rePORTing back to you to advise that the procedure went OK. Mom and Sandy accompanied me to Lenox Hill. After filling out several forms and a lot of waiting time I was brought into the cold operating room where I was introduced to the staff. I must say one nurse was nicer than the other, the surgeon, or rather, radiology interventionist, did his best to comfort me and I always felt as if I were in good hands. My only question is why are shoes without booties permitted in the operating room? I had to wear a mask during my procedure just so I wouldn't breathe on myself to avoid risk of infection. Everything else is super sterile, but you can wear your shoes and I even did so while I was lying on the table (I only had to undress from waist up). 

The actual procedure started at 11:45AM but I wasn't brought into recovery until about 2PM. I was super groggy, eventually got to eat a sandwich and drink some apple juice and after an hour or two I got to go home. The area hurts or is rather sore but it's not bad enough that I need hard core pain killers. It's black and blue and has medical strips on it that will fall off within seven to ten days; I can only sponge bath for four days. I took off the big bandage this afternoon.

My new device was aptly named Port Authority by my friend Hillary; first because I'm a New Yorker and second because I still have authority over my life! I really couldn't attempt to read about Port Authority until I came home yesterday and checked out the brochure. Here's the most basic information about it:


I have to carry a little card with me to give to nurses any time it's utilized or if it sets off the alarms at the airport. Just think, I may be the reason you miss a flight one day because I held up security. 

Thanks for everyone's supPORT.

Have a wonderful Mother's Day!

Love, 

The Boob Blogger

 

Thursday, May 8, 2014

You're so Vein....You Probably Think This IV is For You...

So, early last week my veins quit on me. They no longer want to be poked and prodded for an IV treatment, so much so that after four attempts I couldn't even get the treatment. Therefore tomorrow I'll be getting a port put in at Lenox Hill. I've been avoiding this because quite frankly the thought of it makes me nauseous. Supposedly it will make my treatments much easier and I'll forever be relieved of all the sticking in my arms (except for blood draws). Some answers to frequently asked questions: 1) No, I will not go off at the airport (but I think I have to carry some sort of card just in case) 2) I cannot infuse vodka in it 3) The procedure only takes about 45 minutes and I'm only under local anesthesia 4) It'll be put in somewhere between my left shoulder and left breast 5) It'll stay in as long as I need chemo which could be for life, who knows, depends on my progress. Any suggestions for names? I hear the word port and it makes me think of Pt. St. Lucie, Port-au-Prince, Port-o-Potty, etc... Suggestions welcome.



 Click below and tune in. Bet you can't get the song out of your head all day... ;)

Enjoy the Spring showers!

Love from, 

The Boob Blogger.........

Wednesday, April 9, 2014

Sometimes Things Don't Go As Planned

I went to the oncologist on Monday to discuss the med(s) that’s been killing my bones and joints. I was all prepared to get my third and last Lupron injection. I understood this to be a necessary evil (evil because of the pain, not evil because it's a means to an end) because if my ovaries aren't entirely shut down from the Lupron, my taking the aromatase inhibitor Letrazol would be a waste of time and have zero effect on treating the cancer; if anything it can get worse. Well, apparently Sandy and I both misunderstood the doctor. What we thought would only be three injections (one a month) was more likely to be for THREE YEARS, at least til I’m 50. I'd take get an injection once a month for three months and THEN start the pills BUT CONTINUE THE INJECTIONS. 

Seeing as I cannot tolerate the pain from the two injections I had (I still ache from an injection given to me three weeks ago), I opted out for a third and thereby opted out for the Letrazol. What does this mean? I have to go back on IV chemo (there are no more oral alternatives). It's likely I will be getting Gemzar. Gemzar is administered once a week for three weeks and then I'm off for one week. Rinse. Repeat. So it's back to the weekly blood draws one day and IV the next day. Typical side effects are flu-like symptoms the day of the treatment (achy, nauseas, fever), flush face day of or even three days later, and swollen feet and ankles. Chances of hair loss are minimal on this drug although it may thin. 

Next step? I'm waiting for the authorization for another cat scan (chest only) next week. If the results are the same as last time (or better) I will immediately start the Gemzar. 

I cannot say I was happy about this. I've accepted a lot thus far and I think I've been dealing with it well, but somehow this felt like a step back. I cried. A little. I wasn't angry, but I was really disappointed. Deflated. I thought I'd have the easy task of taking a pill once a day. But if I don't have the strength to open a bottle of water, which is now the case, that's an issue. My treatment is all about maintaining a good quality of life and in order to do this, I have to weigh my options.  This definitely reinforced that my fighting this cancer will be a lifelong endeavor until someone comes up with a cure.  But just the fact that I can tips the scale in my favor and I must remember that. 

In the immortal words of Mick Jagger....
                  
             You can't always get what you want....

                    https://www.youtube.com/watch?v=OagFIQMs1tw

                                         Th-th-that's all folks....

                                                 The Boob Blogger



Saturday, March 29, 2014

It Hurts to Laugh

Hello one and all!!

I have been MIA but not for lack of stuff to write about. I sometimes get paralyzed by the thought of all the things I want to share and then this turns into avoidance, which turns into self-criticism, which turns into my own little pity party, then a pep rally and then some force takes over me and I finally sit down to write. There's been a force. But before I delve into that, I'll catch you up on the status of my health. For if not for that, there'd be no Boob Blog!

On January 29th, yes nearly two months ago (trust me, there was a lot of self-criticism!), I had my last Paclitaxel IV treatment.


It was a great day, what I remember of it anyway, because quite frankly, I'D HAD IT. My veins were no longer cooperating, I'd blown one a couple weeks prior (I still have no sensation in the injection site), and I was tired of being constipated, bleary eyed and nauseas. Plus I knew, I JUST KNEW, the following week's scan was going to be good, at the very least status quo. For those tuning into the Boob Blog for the first time, the two prior scans showed the metastatic breast cancer tumors in my lungs were shrinking so I was hopeful. 

On Monday, Feb 3, just one day after Punxsutawney Phil warned us there'd be another 2000 feet of snow, AND, I'd won my first ever Super Bowl pool (Cha-ching, $250 big ones!), I'd dragged my sorry butt outta bed at 6:30AM, imbibed two bottles of banana chalk flavored barium sulfate (aka Fartbag Cocktail) and got a CT scan of my lungs and abdominal area. One day later the results came in and sure enough they were good. The tumors did not shrink, but they didn't get larger (with the exception of one that possibly could've been misinterpreted on the scan). The tumors didn't decrease in number, but there were no additional tumors. Everything was status quo. BAM!!




The following Monday, February 10th, my loving beau escorted me to Dr. Brunckhorst for the first of three painless injections of Lupron in my butt.  Although it appears by my symptoms that the past year of chemo has put me into menopause, to be certain, since my cancer is estrogen receptor positive, this drug is administered to shut down the production of estrogen in my ovaries. In addition to these shenanigans I began taking an aromatase inhibitor (AI) called letrozole, brand name, Femara. In addition to the ovaries, estrogen is produced in the adrenal glands. The letrozole inhibits the enzyme in the adrenals (aromatase) from producing more estrogen (or, the sex hormone androgen).  Less sex hormones = menopause. The most common side effects of these drugs are hot flashes (check), hair loss (too late!), (excruciating) pain of the joints, muscles and bones (check, check, check!), tiredness, excessive sweating, nausea, dizziness, and trouble sleeping. Waiter, CHECK PLEASE!

After two weeks of being on the letrozole, I could barely get out of bed and stand straight. Of course I did but the joint pain (arthralgia) was so awful and the last thing I wanted was to get hooked on pain killers. For the record, my limited research shows that the lives of others in my boat was compromised such that several became non-compliant and just stopped taking the drug way before the recommended five year period. I don't want to do that because my only other alternative is to go back on chemotherapy. My doc gave me permission to go off of them for a few weeks to see if the pain subsided. It has only somewhat leading me to believe that the pain was a side effect of both the pills and the injections. I go for my third and last injection next week so I'm hoping once the lupron leaves my system I will only have to deal with the pain from the pills, which I have not yet resumed taking. There are two alternative AI's however anastozole (brand name Arimidex) doesn't target the estrogen as much as letrozole and the the other, extemestane (brand name Aromasin), is a steroidal drug that can create resistance to the anti-estrogenic effect. Now, it is possible, that when I start taking the letrozole again it won't bother me as much as it initially did; the doc said this can happen. The proof'll be in the puddin. 

Another negative side effect of all of these drugs is bone loss so I must be monitored for that. I'm guessing in another month I'll have another CT scan to check on the status of the tumors and probably I'll have a bone scan. (I don't  know how else bone loss is monitored. There's a whole other education that awaits.) In the meantime I'm taking calcium, magnesium, fish oil, vitamin D, hot baths in sea salts and the occasional ibuprofen. I've been going once a week for acupuncture with Dr. Yamaguchi who I really like and respect, but I've no idea if it's helping (perhaps I'd feel worse if I didn't go to him?).  At a $110 a visit I go in thinking that I'm being healed and if anything I take a quality nap. There is research that shows acupuncture helps so I'm not pulling this out of thin air. As for weight bearing exercising to help strengthen my bones, I can barely lift a three pound weight without my wrists and fingers screaming for relief. 

Ahhhh, good times. 

Ok, for some good news... My breathing had gotten really bad for a while despite my lungs sounding clear as a bell. It wasn't until a couple of days ago that I realized I haven't been getting short of breath like I used to.  I attribute this to the chemo leaving my system. A few months ago I met a woman who told me that six weeks from her last chemo treatment her hair starting growing in. Sure enough, at six weeks, the patches of hair that would not grow at the rate the rest of my hair would, started filling in. I actually have my hairline back and I've been busting out the mascara for my lashes!  It seems like six weeks is the "magic number". If you know others going through chemo, I would share this six week marker with them just as I would the three week marker of one's hair falling out. When you have cancer you constantly want to know next steps and what to expect; it gives you some sense of control. This little bit of info might help. 

There's been a lot in the news lately, and by news I really mean by way of social media, about body image. Finally people are grasping that the images seen on the covers of the glossies are unobtainable simply because they are not real. Even the "prettiest" (in quotes because it's a subjective term) models' photos are Photoshopped because really, are you going to reach for the magazine that shows you how to encourage cellulite, split ends and skin damage rather than eradicate it? There are funds being raised for the production of an average size Barbie-like doll called Lammily. There are ad campaigns (e.g. Dove) featuring "real" women. And lest I forget to mention Lena Dunham and all she's done for re-shaping women's body images? (I love Lena's work, her perseverance, her attitude, her gumption and even her new haircut. I just dislike her stylist assuming she even has one.) I was always told looks only matter so much but in spite of my mother always telling me I'm beautiful and Gloria Steinem paving the way for women, I always found myself comparing myself to others on some superficial level. Someone was skinnier, prettier, and had nicer clothes and if I had what "she had" I'd be happy. Or so I thought. The truth is, even in a  society that rewards better looking people with higher salaries, more attention, etc, if  you have and show your confidence, that's what puts you ahead of the rest.  But it took years, and I mean YEARS for me to get it emotionally vs intellectually. In my dirty 30's it started to "click." Then it really clicked in my naughty 40's probably because at 40 I was diagnosed with cancer and my breasts were regularly poked, prodded, smashed and a topic of discussion. I couldn't hide behind my examination gown. I was OUT THERE. Where am I going with all of this? 

I turned 47 this year. It wasn't too tough a number for me --I find the 9's to be the worst...29, 39...I am a happy woman in her mid-40s. For a dig, my boyfriend would say, Liz, it's your late 40s. OK. I'm in my mid to late 40s. One expects things to change with her body at this age especially if she doesn't work out too regularly and follow a regimented diet and takes drugs that wreak havoc on just about everything. I can deal with some change. But I swear, and I think I've said this in other posts, I feel like I've stepped into the skin of another human. I recently on Facebook morned the closing of Loehmann's. Loehmann's has a special place in my heart, not just because it had great discount shopping, but because back in the day when the discounts were far greater for quality designer clothes, I'm talking Halston, Calvin Klein, YSL and the like, I was shopping with my mom at the store in Hewlett, L.I.  At about ten years old she'd point out the great designers, how to recognize good quality from bad and how having a good seamstress is essential to your clothes fitting best. We'd take piles of garments into the fitting room and sometimes she'd send me out with an article of clothing to find a match. Elizabeth, go find me a few pairs sof navy blue pants in a size 6 that will match this top. It was great fun to go on these missions (today a mom would fear her kid being abducted) and see the look of satisfaction on my mom's face if I came back with "a winner."  The Loehmann's open fitting room culture was eye opening to me.  Not only was there a variety in women's tastes in clothes, there were myriad body shapes and sizes, too. Tall, short, wide, pear shaped, apple-shaped,  there was bra-fat, pre-Spanks big underwear, girdles, cellulite, varicose veins and so on, non of which applied to my mom who always maintained a great figure and literally looked amazing in everything she wore. Now? Now I am one of those women I used to stare at in the Loehmann's fitting room with bewilderment. 

There's only one breast cancer "chat site" I look at somewhat regularly. It's called Team Inspire and I look at it only to search to see if women are experiencing similar side effects as me; the rest quite frankly is depressing. One day a woman posed the question, Am I Vain? She wrote, "I am having a bit of a struggle with the changes to my appearance from chemo. I know that my biggest concern should be the cancer itself, but I no longer recognize myself in the mirror, and it is getting to me.There were hundreds of (supportive) responses to this and it seemed everyone felt the same discouragement with their physical changes and was eager to share their beauty secrets (e.g. how to re-create eye brows). I tried my hardest to convince the group it's ok to forego a wig and wear a great pair of earrings and red lipstick, but I don't know how well this translates in Petticoat Junction, USA. What I really struggle with the most is growing (read: busting) out of almost everything in my closet. I grab one of my favorite tops and when I hold it up it looks like it would fit an infant. Did I once fit in this? Did someone accidentally boil this in hot water and dry it on high heat for an hour?  I get annoyed with myself for getting fatter and mushier (vs. voluptuous and Rubenesque) and when someone says my face looks full thinking that's a good thing to say to a cancer patient, I. Want. To. Wring. Her. Neck. And then something happens. I FINALLY find a top I'm comfortable in, I slap on some makeup and jewelry and I go outside and realize, today's going to be a good day. No one really gives a shit if I am heavier, those who care are just happy I'm doing well. And then I am happy I am doing well. 

A few weeks ago I really did get down about what I'm sharing. Sandy and I were going out for dinner and I simply could not get dressed. Everything I put on was a disaster (in my eyes), tight and ill-fitting and I was embarrassed to walk out the door. I'd reverted to being a teenager. I didn't cancel our dinner plans because that would be wrong to the others (and make me a loser), but I really wanted to. I wanted to roll up in a ball on my couch and feel sorry for myself. The next morning at about 4:00AM I couldn't sleep. I was looking for something on the internet and I came across http://www.jenniferpastiloff.com I knew nothing about her but apparently her inspirational yoga classes and retreats sell out regularly and she was coming to NYC. Having only taken about three yoga classes in my life, I decided to sign up for this one because the requirements were to show up with a pad and pencil and a sense of humor. My friend Dana indulged me and she signed up, too. We went to Pure Yoga on Friday night at 7:00PM, both of  us tired and achy (Dana has a bad hip), teetering on canceling and tossing $30 out the window. But we went. And were we happy. 

There were about 25 women 90% of which, including Jennifer, were wearing tight LuLu Lemon outfits and looked like they do yoga and take spin five times a week. I was in a 25 year old MS Walk T-shirt, a tired sports bra and worn out sweatpants trying to mask my new improved muffin top. I positioned myself next to a wall because I knew I'd have to hold on to it in order to even attempt half of the exercises. When asked to kick our leg high in the air, mine was about six inches off the ground. When asked to do a plank for 30 seconds, I lasted about ten. Half the time I was in child's pose, my favorite position since all you have to do is lie there and stretch.  One of the writing exercises was to write down on a Post-It what we were manifesting that evening, then stick the Post-It anywhere in the room. A few minutes later you had to take a Post-It other than your own and for the rest of the night, you had to hold that Post-It close to your heart and manifest for some stranger in the room, what she wanted (secret: I purposely took Dana's). The idea was to share of yourself and take for your self. Give and receive. It's so simplistic and I have to say it really works. We did some Karaoke yoga (Phil Collin's In The Air Tonight), which literally brought me to tears as we were belting out the chorus and at the end of the evening we did some major sharing. We had to write down what we would do if fear didn't hold us back. No one expected that our thoughts would be read aloud. One of my shares was that I'd be doing what Jennifer does--going on tour (don't ask me where) inspiring people to stay positive despite given a diagnosis of stage four cancer. (My new slogan: You have breast cancer. There is no death in that sentence). In Jennifer's case, she recovered from years of battling anorexia and striving for perfectionism. Jen's slogan? It's OK to fall as long as you laugh. It was a Friday night in New York City and two dozen of the most beautiful, powerful women were in the same room sharing their fears. Some cried, some hugged, some laughed. It was a very touching experience and Dana and I both left exhilarated. No matter what our size, hairstyle, athletic ability, we were all rock stars. 

And for the next week I couldn't stop thinking of this class and what it means to hold your head high, give in order to receive, and constantly reach for the stars. I was in so much pain from the exercises that I had to tell Sandy, Stop making jokes. It hurts too much to laugh.

And that, my friends, was the force that finally got me to write today. 

Love and hot dogs (Hey, why not?!),

LizB. 

With Kelly Turner at her book launch / signing  of 
RADICAL REMISSION: Surviving Cancer Against All Odds
http://www.radicalremission.com

It just made the NY Times April 6th Best Seller List!





Monday, January 13, 2014

Pass The Chemo to The Left Hand Side...

Hello New York,

I've been surprised at the number of people I've spoken to who are unaware of the progress NY State has made in getting marijuana legalized for medical reasons. I for one am not the most learned, I'm pretty ignorant about most world news and I'm the last person with whom you'll want to discuss politics because I abhor them. But this to me is a topic of great interest to me.  Read: Cuomo and Marijuana in NYS .

I did bring up the topic with my rather conservative oncology nurse today and I was only slightly surprised by her reaction: "I don't know what's going on with our world. It's all turning to pot!" (Hrmpf.)  Before I could snicker she realized what she'd said and turned to me with wide eyes and said, "Literally!" and stomped away.  I dunno. Alcohol can kill you and it's legal. Cigarettes can kill you and they're legal. Chances are marijuana on its own will not kill you and might even help you!! One week I was so sick from my (first) chemo that I thought I'd never feel human again. I wanted to shut out the world for what I thought would be the rest of my life. Each minute that passed seemed like an eternity and no amount of anti-nausea medication, ginger tea, or crackers was going to help me. I hadn't thought about it at the time, but just maybe, if Mary Jane had made a house call, perhaps I could've have gotten that week of my life back. The nurse today said the patients she knew who "used"pot while undergoing chemo, reported that they got sick from it, only adding fuel to her argument. I asked her, Had they every smoked before? How old were they? Is it possible they just smoked too much? Did they eat it? Did they get it from a reliable source? She had no answers. I can attest that in a serious time of need, not quite the level of nausea I mentioned above, but definitely feeling extremely queasy, a little bit of "medical" chocolate or cookie is what the proverbial doctor ordered. I was mellow, the queasiness ceased and the last thing on my mind was cancer. That, dear reader, is what I call relief.

I say east, say west, say north and south (on the left hand side) 
This is gonna make us jump and shout (on the left hand side)
                                        --Musical  Youth



He're...

Love,


The Boob Blogger

Tuesday, January 7, 2014

Happy New Year From The Boob Blogger!

Hello everyone,

Reporting from my couch in cozy sweats under an equally cozy pink fuzzy blanket because with the wind chill factor, it feels like it's 400 #@$$%^ degrees below zero outside! Have I told you I never, never, never exaggerate? OK, it's super freezing out but I got to and from work in a taxi and my office is as hot as hades, I came home to a hot meal (read: I warmed up left overs in a toaster oven), and I don't plan on doing much more than reading and watching TV tonight. So who am I to complain? 

2014 began on a really positive note, literally and figuratively. My amazing beau got us floor seats to the Billy Joel concert at the Barclays Center. For those of you who haven't been, the walk from the subway is less than a minute so it's very convenient. I didn't form any real opinion about the aesthetics; let's just say it's a bit cold. We enjoyed a very good buffet at the 40/40 Club where we waited 40 hours and 40 minutes for our complimentary drink. So our waitress brought us three. (Several of the waitstaff and bartenders thought it was a great idea to call out on the busiest night of the year.) The couple next to us were dear friends of Mr. Joel's sax player so they had a few good stories to share. Most important though, the venue was awesome, Billy still puts on an amazing show (he might consider retiring his rock n' roll microphone bit before he dislocates a hip) and Sandy and I spent our third New Year's Eve together. 





There's a new member in the Boob Blogger's household. Hold on, hold on, don't get too excited. It's a rabbit. Like I SAID, don't get too excited, it's not THAT rabbit. It's a Rabbit AIR PURIFIER. http://www.rabbitair.com It's supposedly the best one for my needs, which are, detox my dusty-no-matter-how-much-you-clean-it-NYC-apartment. I went to an allergist hoping to get some clues as to why I was choking to death--my oncologist would just kill me if he heard me use such language--and all I learned was that I'm allergic to dust and dust mites. Like, who isn't? So I invested in this thing for my lungs and I like to believe it's helping me. For the record, I still choke when I cough but my cough subsided substantially, pre-Rabbit, whilst sea bathing in Turks and Caicos. My friend Whitney said that was very late 18th century of me.
You can purchase different artwork for your Rabbit and hang it, too.
I selected the Japanese inspired cherry blossoms.

My chemo continues and I have only three more sessions before my next scan. I've been experiencing nausea the last few times so I've been hitting the Odansetron and just trying to eat whatever my body craves. My taste for food is what I imagine it would be if I were pregnant. One minute I want herring, another minute salad, and another, my new fave, a toasted bialy with olive oil and rosemary (thank you, Lory D.!). Sometimes the thought of food is repulsive and all I want is cold seltzer and other times I'm ravenous. My doctor doesn't really know how to address this. He just sees me putting on pounds and thinks it's kind of funny when I complain about it (thank you, menopause). The truth is, he's just happy I'm otherwise tolerating the treatment ok and I'm not a vomiting bag of bones. 

The nausea with this chemo is rather strange. Until I wake up the next day after treatment, it's as if I drank a bottle of acetone. I don't really know what acetone tastes like, but I don't know what a liquified roll of aluminum foil tastes like either and I had to choose something strong and metallic. (Side note: Did you know Billy Joel once tried to kill himself by drinking furniture polish?). And if you can picture a clear soda bottle, say, an old fashioned bottle of Coke, and you fill it to the near top with water knowing that one more drop will make it overflow, that's what the chemo feels like inside me. It's as if I'm filled almost to the brim with clear toxic liquid and if I take one more sip, it'll start pouring out of my throat. Not too good on the psyche. I get very heady, my eyes blur a little, I'm queazy, a bit depressed and slightly agitated. Once home (I go to work from treatment), I look forward to the clock striking 11:00PM because it's a good time to retire without waking up too early in the middle of the night. I tell myself there's only X number of sessions left, but the reality is, I can stay on this for several months more if it's still, thankfully, helping the tumors shrink. 

You may notice from pictures that I'm sporting a bit of a 5 o' clock shadow on my head. This chemo is weird inasmuch as even in the midst of treatment, what hair you lost can come back. Just not all of it. My eye lashes started to come back--Sandy says they look like insect legs--and so did part of my eye brows. The hair on my head grows in dark, some grays, too, but there are patches that are much thinner than others. You get my drift. It's been suggested I go for a comb-over a la American Hustle (of all the characters in that movie to emulate...).





I'd like to end this blog with a lovely meditation that my cousin Jennifer shared with me for the New Year:

May I be at peace
May my heart remain open
May I realize the beauty of my own true nature
May I be healed
May I be a source of healing in this world

May you be at peace
May your heart remain open
May you realize the beauty of your own true nature
May you be healed
May you be a source of healing for this world

May you be happy as I wish to be happy
May you know peace as I wish to know peace
May you be safe from inner and outer harm as I wish to be safe
May you be free from suffering as I wish to be free


From my couch to yours, I wish every one of you a peaceful, healing, safe and happy 2014. 

Thanks for tuning in. 

With an abundance of love,

Liz B.
New York City's Boob Blogger

Thursday, December 26, 2013

My Cancer Gave To Me............

Christmas Eve 2013…the anniversary of my taking my first oral chemo, Xeloda. I've officially been toxic for a year. Since September 2012, the five year anniversary of my first breast cancer surgery, the following has occurred:

To be poorly sung to the tune of the chorus of "On The First Day of Christmas My Cancer Gave to Meeeeee"

On the first day of Christmas my cancer gave to meeee:
1 needle biopsy  
1 Thoracic surgery  
20 golden chest x-rays
1 super fun Pet scan
5 boring cat scans
4 months of oral chemo (which didn’t work)
31 Paclitaxel IV’s
48 weekly blood draws
10 chiropractic adjustments
Oooonnnneee EMmm Rrrr IIIIIIIIIII  ....
1 tooth pulled
2 bone graftings
2 epidurals
4 nasal probes
Cheeeeeemo-induuuced menopaaauuuseeee....
Put on 10 pounds
Lost my hair and eye lashes
2 wigs were made (and never worn)
A-aaannnnd ooonneee sha-ving accident (behind my ear).

Now the other version of this song goes something like this:
On the first day of Christmas my cancer gave to meeee:
Several amazing doctors
Three terrific phlebotomists
Several shrunken tumors
Lots of well wishes
A trip to the Caribbean
Summer in the Hamptons
Friends getting married
Some even pregnant
Wonder Woman gear
Amazing blasts from the past
One fu-u-u-nd-rais-errrr (thanks, Amy!)
To-o-ns of love and support
One great razor
Aaannnd the courage to face all of life's challenges (knowing every one of you friends, family and readers are in my life!)

Take a breath.................

Happy Holidays, Everyone! 

Love! Joy! Thanks! Peace! and Health in 2014!!!!

Jingle Bels


Exec. Producer Paul Faulhaber with Trish Goddard cheering me on!
Thanks, Annie!




Looking back from the start...
When it all began, thoracic surgery at Lenox Hill, November 2012. It sucked.

46th b'day party after recovering from oral chemo (Xeloda) hell, 1/12/13

First IV treatment, May 2013. F-U-Cancer!
Chopping hair off  on the 1st day hair fell out,
exactly three weeks to the day of 1st treatment.


Chemo chic a la Janet Wadell!

On a mission with Sandy to cover new bald spots.


This chemo chicK's got super powers. 


Warren Haynes and Boston Pops cover the Grateful Dead 
at Tanglewood on our 2 year dating anniversary. 


2nd time (probably last) since I'm 15 on a horse.


At the best farm wedding in Hudson, NY

Growing hair in the all the wrong places with Lady G.


Flying High (not really)


With Kid Rocks!

Gettin' fat at Sammy's Romanian


Chilly in Philly

Halloween W69th St.


Flying high. Really. First time parasailing. 

Turks and Caicos sunset cruise.

Beautiful sculpture, "Infinity" dedicated to me 
by my sister-in-law Harumi Osawa


Momma Me-a on Christmas Day!!

Healing. Always.