Showing posts with label cancer. Show all posts
Showing posts with label cancer. Show all posts

Friday, May 27, 2011

Gilda's Club Fashion Show

I will model at the Gilda's Club fashion show next week. I've been active at Gilda's Club Seattle for about eight years and am a Friday yoga regular. Please consider attending or supporting this very worthy cause with a donation. 

DON'T MISS OUT ON THE BEST SHOW IN TOWN!  IT WILL INSPIRE YOU AND TOUCH YOUR HEART.
Fashion Show Invite
Tables of 10 are $1,500... single tickets are $150.  Put a group together for an afternoon to remember!  
  
14th Annual Fashion Show & Luncheon
DATE:June 3, 2011
TIME:11:30am - 1:30pm
LOCATION: The Westin Seattle ::MAP
MORE:Visit our website for more
information or to purchase tickets
  
Featured Models
Magarita Andrijic :: Judi Best :: Kathy Burdick :: Delaney Clark :: Jill Cohen :: Sara Cottrell :: Louisa Cryan :: Stacy Eckert :: Jaymee Espinueva :: Steffanie Fain :: Carol Gaouette :: Doneen Jasman :: Jesse Jones :: Victoria Kemery :: Amy Lanum :: Joanie Mass :: Camari Olson :: Norma Phillips :: Mario Prieto :: Pete & Jill Robertson :: Sherrill Slichter :: Lucho Singh :: Mike Walter :: Reba Weiss :: Jenni Whitney

Boutiques Scheduled to SWS FlowerAppear
Alexandra's :: Barneys New York :: Betty Lin :: Brooks Brothers :: Catherine's Plus Sizes :: Champagne Taste :: Eileen Fisher :: Endless Knot :: Jack Straw :: Karan Dannenberg :: La Belle  Elaine's Bridal :: Mario's :: Opal :: Papillon :: Piazza Sempione :: Ragamoffyn's Road :: Rottles :: Sears :: Tatters :: THE FINERIE :: Via Lago

Thursday, May 26, 2011

Shingles

Believe it or not, this is good news!

I called Dr G this morning about a rash that appeared overnight on my leg and he said to come in before the MRI scheduled for this afternoon. One look, that's all it took -- shingles!

When combined with the kind and spread of pain I'd been complaining about all week, the appearance of red vesicles (rash) enabled him to out all the pieces together. He immediately cancelled the MRI and started me on valacyclovir and gabapentin.

It will take quite a few days for the infection to clear up and perhaps longer for the pain to reduce. Gabapentin will also make me tired and I shouldn't operate machinery (i.e. drive a car) while taking it. I will stay on the fentanyl patches also, since one is supposed to increase the gabapentin slowly to a maximum of three per day.

I had chicken pox as a child and the odds favor that I have carried it around in my body ever since. There's little doubt low immune counts from the chemo caused me to be more susceptible to a flare up. That's also why I couldn't have the shingles vaccination. It's a live virus vaccine and would have put me at risk to develop shingles, which I did anyway.

The Centers for Disease Control and Prevention website says,

Shingles cannot be passed from one person to another. However, the virus that causes shingles, the varicella zoster virus, can be spread from a person with active shingles to a person who has never had chickenpox. In such cases, the person exposed to the virus might develop chickenpox, but they would not develop shingles. The virus is spread through direct contact with fluid from the rash blisters, not through sneezing, coughing or casual contact.
A person with shingles can spread the virus when the rash is in the blister-phase. A person is not infectious before blisters appear. Once the rash has developed crusts, the person is no longer contagious.
Shingles is less contagious than chickenpox and the risk of a person with shingles spreading the virus is low if the rash is covered.

So I will cover my rash, swallow the huge valacyclovir pills (1 gram, the size of my thumb!), and hope the gabapentin controls the pain soonest, plus remember that shingles is NOT MORE CANCER.

Sunday, March 27, 2011

Yet another death from cancer

A friend from my support group died this weekend. D, a very spiritual person, was a regular at this group for far longer than I. His cancer progressed quickly and his doctor recently told me there were no more treatment options that were likely to be effective. D decided to stop treatment and enjoy his life for as long as he could; the doctors hoped through the end of the year

Sadly, the cancer seemed to progress faster than anyone expected. D began to fail a little more than a week ago and started hospice at that time. He came to group on the 17th looking pale but still giving us suggestions on where to take a walk to enjoy the spring weather. D was looking forward to giving a talk on spirituality last week when we heard that he was failing and slipping in and out of consciousness. I heard this morning that he had died. I imagine that his grown children were able to make it back to Seattle in time for the funeral today, but don't know if they each had a chance to say goodbye. Rik and I will try to make it to a shiva minyan this week (if my health permits after tomorrow's planned fourth dose of Gemzar).

Zichrono l'vracha, may his memory be for a blessing to all who knew him.

Cancer sucks.

Tuesday, March 8, 2011

Effects of Mesothelioma Cancer

A layer made up of specialized cells or membrane called mesothelium covers the most of the internal organs. There are two layers of cells in mesothelium. Organs are surrounded by the first one which is surrounded by the second thick layer. Between these two layer a lubricating fluid is concealed which is produced by the membrane itself. This lubricant allows the organs to move smoothly against adjacent organs and structures (for example the expansion and contraction of lungs, beating of the heart etc…

Mesothelioma has different names according to the different location in the body. One of all those is peritoneum which covers most of the organs in the abdominal cavity. Pleura is the membrane which surrounds the lungs and lines the wall of the chest cavity and tissue called as Pericardium covers and protects the heart.

In a disease known as Mesothelioma or the cancer of the mesothelioma, cells become abnormal and divide enormously and with out any order leading to the development of tumors. The tumors of the mesothelial cells can be non cancerous i.e. benign or cancerous i.e. malignant. As nearly all mesothelial tumors are malignant, cancerous mesothelioma is often just referred to as mesothelioma. They can spread and damage nearby tissues and organs too. Therefore the cancer cells may also metastasize from their parent location to other parts of the body.

The lining or membranes of certain large cavities in the body are get affected by the malignant 2011 Mesothelioma. Some major organs in the body such as heart, lungs, abdomen and others are housed by these cavities, known as the serious cavities.

Malignant mesothelioma undertakes 3 forms.

1) Peritoneal Mesothelioma: It is in the Peritoneum or membrane surrounding the abdomen.
2) Pericardial Mesothelioma: It is in the Pericardium or lining surrounding the heart.
3) Pleural Mesothelioma: This the most common form of malignant mesothelioma which affects the lining of the lung cavity.


The majority cases of malignant mesothelioma are related with an earlier experience of fibrous minerals, of which asbestos is the significant. The mineral which occurs naturally like strong and flexible fibers which can be separated in the form of thin threads and can be woven are called as Asbestos. Asbestos has been commonly used in several industrial products, as well as cement, brake linings, roof shingles, flooring products, textiles, and insulation. Particularly through the manufacturing process, these are simply inhaled or swallowed throughout the manufacturing process as asbestos dust are small particles which hover in the atmosphere.

The time span between developments of mesothelioma from asbestos exposure is 35-40 years. In general people exposed to asbestos for a prolonged period of time can develop mesothelioma, though few individuals with just brief exposure can also developed mesothelioma as seen. Conversely, people heavily exposed are not developing mesothelioma.

In previous decades of the 1970s, huge amounts of asbestos were utilized in industrial construction and shipbuilding. It’s used was restricted by government, by optional materials making available. Regardless of these changes, asbestos was continued in use.

Professions which content with asbestos and usually related with the inception of mesothelioma afterward in life comprise asbestos production, insulation work, heating trades, shipyard work, and construction.

Monday, March 7, 2011

Mesothelioma New Treatment - Gene Therapy

Gene therapy is a new exciting treatment which has given hope to mesothelioma patients. Gene therapy reads the cause for proteins within particular cells produced them to be resilient to cancer whereas some cells do not. Before that, it was trusted that genes were total upon birth, and so as to they could not influence conditions afflicted throughout life. Yet this, ejected to not be the case. Since that time it has been learned that smoking, sunlight and particular foods may affect our DNA and modify our genetic code. This new approach presented by these conditions let doctors to look at many conditions such as malignant mesothelioma in a new light.

Many factors are there that play a part to mesothelioma. Asbestos exposure is the basic contributing factor, but genetic alteration in persons also make it worse. In mesothelioma gene therapy is a revolutionary treatment as it restores cancer causing genes with genes which are medically constructed to expire while exposed to cancerous growth. These genes called as ‘suicide genes’ are realistic means to reduce and perhaps prevent the quick replication of cancerous cells. Analysis are moreover beginning to start testing with replacement of cancer generating genes with genes vulnerable to particular drugs. It could let the cancer to be removed potentially with some side effects.

Even now the gene therapy is in its initial stages and is still not 100% reliable. Though, this anxious state suffered by mesothelioma victims, occasionally calls fro several experimental treatments. Any aspiration for surviving mesothelioma prevail over no of the risks involved.

Alternative cures to Mesothelioma

Mesothelioma is a malignant cancer and is incurable in general. There have been no permanent cures which have been found for mesothelioma and as a result, most of the available cures for the condition aim to either reduce the pain and the discomfort which is suffered by the patients, or tries to extend the post diagnosis time of the patients from one year to a longer period of time up to five years. Thus there is continuous research going on in the aim of finding more alternative cures for mesothelioma which can be permanently cure mesothelioma for good. There are many alternative cures that are being experimented with today and most of the mesothelioma patients are on at least one alternative mesothelioma cure therapy. Here are some of the most popular alternative mesothelioma cures today.

Firstly, there are Angiogenesis and Anti-angiogenesis drugs. One of the most common treatments for cancer is chemotherapy. Now though it is the most common treatment, it has many side effects too. This is because while doing chemotherapy a lot of healthy cells along with the cancer cells are killed as well, and this causes the subsequent side effects. As a result, some drugs have been developed which allows the doctors to kill juts the cancer cells without affecting any of the healthy ones. These are the drugs which have been mentioned above.

The next form of alternative therapy for mesothelioma is Immunotherapy or what is also known as biological therapy. This form of alternative therapy uses the body;s natural immune system to try and cure the disease. The doctors researching this have realized or rather discovered that the immune system of the body is able to make the very vital difference between the cells which are cancerous and the ones which are healthy. Thus it is able to remove and eradicate those cells which are cancerous and retain and repair those which can still be restored. The substances which are used in Immunotherapy are called biological response modifiers or BRMs. These basically try and change the way the immune system of the body deals with the cancer cells. This modification enhances the ability of the body to fight and remove the disease better than ever. Some of the biological response modifiers are cytokines and antibodies. The function of the biological response modifiers is to enhance the immune system of the body and help it to fight the disease better. Another function is the fact that they can remove some of the cancer cells and repair some of the damage which has been done to the body.

Another alternative therapy is PDT. This is Photodynamic therapy. This school of therapy believes that certain single celled creatures will die if they are treated with some kinds of photosensitive drugs and then, subsequently exposed to a light of a particular frequency.
source: newmesotheliomapatient.com

Sunday, December 19, 2010

Keeping up with Jill

Rik said the funniest thing to my mother the other day. She called when I wasn't home, and when asked where I was, Rik said "She's feeling so good, I can barely keep up with her!"

It's true, I have been feeling exceptionally well. I'm sure most of it is due to being off chemo since October. My return to good health, not to mention hair, has given me even more energy than I expected. And of course, having enough hair to look intentionally short, keeping my reduced weight stable and being again the size I was when I met Rik 16 years ago all contribute to better mental and emotional good health. (The new clothes I had to buy didn't hurt either. Retail therapy can be very helpful.) Even my lymphedema seems to be under better control.

I will see my orthopedist this week and get his take on why I have pain in my knee. Then all the docs will "talk" and hopefully Dr G will recommend that I stay on the high dose Faslodex.

In the meantime, I enjoy feeling good!

Friday, December 10, 2010

Branding and charities

Check out this article in the Wall Street Journal. Can you believe Komen wants to own the phrase "for the cure?" And they're not the only ones....

Charity Brawl: Nonprofits Aren't So Generous When a Name's at Stake

Friday, November 26, 2010

Travel tips for breast cancer survivors

My online friend Chemobabe posted a notice on Facebook from the Komen Foundation, warning breast cancer survivors on how to travel by air during the holidays.

If you’re a breast cancer survivor traveling by air during the holidays…

…you may be concerned about what to expect from the Transportation Security Administration (TSA) screening guidelines at U.S. airports beginning this week.

TSA is now using full-body scanners at 68 U.S. airports that can detect surgical clips, prostheses and implants. If these devices are detected, breast cancer survivors may be subjected to a more thorough and personal secondary screening by TSA agents.

The secondary screening has been controversial: One breast cancer survivor says she was told to remove her prosthesis; another told us that she was in pain for days from pressure to her chemo port, and others say they felt invaded and distressed.

Susan G. Komen for the Cure® has written to Homeland Security Secretary Janet Napolitano to offer Komen for the Cure’s expertise into the special issues around the nation’s 2.5 million breast cancer survivors. We’re not national security experts, of course. But we can do our part to ensure that survivors are treated with respect and dignity.

As we do so, here are some steps you can take as you head to the airport this holiday season:

• Komen is recommending that breast cancer survivors arrive earlier than usual at the airport, with ample time to go through the new secondary screening if necessary
• If you are concerned about going through the body scanner for any reason, you may request a private pat-down screening
• If you choose, or are selected for, a pat-down screening, you may request a private screening away from public areas
• You should advise the TSA agents of any chemotherapy ports or other medical devices.
• You should not be asked to remove your prosthetic device
• Most airlines strongly recommend that customers use carry-ons, rather than checked luggage, to carry medicines or prosthetic devices

Here is more information from TSA’s website that may be helpful as you plan your travel: http://www.tsa.gov/travelers/airtravel/specialneeds/editorial_1374.shtm#1 
We don’t at this point have reliable data on the potential impact of these new screening procedures on breast cancer survivors. We want to hear from our survivors about their experience at the airport – good or bad. Please send an e-mail to news@komen.org.

Please know that we are watching this situation as it develops, and are more than happy to work with TSA to ensure that the issues of breast cancer survivors are heard.

Thursday, November 11, 2010

Miss Manners And the Big C

Christopher Hitchens wrote this great article in the December 2010 issue of Vanity Fair magazine. Newly diagnosed with stage IV esophageal cancer, he comments on people's etiquette (or lack thereof) when speaking with someone who has cancer.

If you don't have cancer, I recommend you read it. And if you do (and if so, I am sorry to hear it), you may find yourself sympathetically nodding along.

Wednesday, October 27, 2010

On recent deaths

In the past week I have attended two funerals and two shiva minyanim for three different people. One was a man who died at age 89 after escaping Nazi Germany in his late teens, arriving penniless in Seattle, rebuilding his life here, and becoming a leader in our community. The second was a Russian woman, age 79, whose four daughters, and eventually she and her husband, fled the USSR in the 90s for Israel and Seattle. The third death was a woman, age 68, whose ovarian cancer returned earlier this year.

The first two, that's the way it's supposed to be. You live a long, fruitful life; have the opportunity to tell the ones you love how much they love you and hear it from them in return; and move on to the stage of being. The third, who died from cancer -- that's NOT the way it's supposed to be.

What struck me most was how three different people all said the same thing about two of these deaths: how they left things unsaid and wished that they had written that card, made that phone call, before it was too late. One woman said as much in a eulogy she gave.

I know most people don't want to acknowledge that death is a part of life, that we should always maintain hope. But too many of us let our fears get in the way of telling people how much they mean to us. The woman who died of cancer? I believe she would have been overjoyed to get those cards and notes from the people who couldn't bring themselves to write. The young man who wanted to record his grandmother's stories admitted that he let small, unimportant things eat up his time.

Why can't we all tell those we love what they mean to us, as frequently as possible? There is no dress rehearsal for life, and when we let our fears or our busy-ness get in the way, we miss out on the authentic experience of loving and being loved. Isn't this what life is all about?

Friday, October 22, 2010

Another article

A few months ago I was interviewed for an article on lingering effects on life after (or in my case, with) cancer for Health To You magazine (h2u). h2u is a membership organization providing "benefits and resources that support your health and well-being." The article came out recently and I received a copy of the magazine from the author.


The article is called "A lifelong journey: How cancer survivors pick up the pieces." Although I was not featured on the cover, the table of contents on page two shows a picture of Bobka and I (he's nosing my face) as the draw for the article on page six. There is also a cute photo of me with both dogs at my section of the article. In this one, Pumpkin is licking my face.


The article itself features four people: a man with advanced melanoma that has spread into his bones and liver; a woman with advanced, squamous cell carcinoma on her tongue; a woman who developed lymphedema after her breast cancer surgery; and me. The man and I are the only people interviewed who have metastatic disease -- cancer that has spread outside the original area of diagnosis.


I was happy to talk with the author and she did a great job of listening to me and telling part of my story in this article. 

Thursday, August 19, 2010

Bone scan saga

Bone scans have been a regular part of my cancer experience since the day I broke my leg in 2002. I don't remember that one (I was sedated) but usually they go something like this:

1) Have port accessed by specially trained nurses at Swedish Cherry Hill Ambulatory Infusion Center
2) Go to bone scan location in hospital basement and receive injection of radioactive dye
3) Head back upstairs to have port de-accessed
4) Drink lots of water, get a snack and amuse myself for a couple of hours
5) Return to bone scan location
6) Use the toilet and
7) Lie on scanner bed, get strapped in and covered with warm blankie for bone scan (duration about 60 minutes)

Luckily, they always let me listen to music during the bone scan. Before the days of iPods I brought CDs; now I just set the iPod to "shuffle" and enjoy random music for the duration.

Yesterday's bone scan was at Seattle Nuclear Medicine, not at Swedish's Cherry Hill location. SNM has some fancy, new machine that can read your bone scan after less than an hour's wait.

People who don't have ports must have an intravenous line started by a technician. I wanted to use my port but never heard back from the doctor's office to see if they had arranged for the Swedish Cancer Institute (in the building next door) to access it. As I sat down in the chair for the tech to start a line, my cell phone rang: yes, I could get my port accessed.

Well, I was already at the bone scan building, and I will let anyone try to start an IV line once, so I asked to lie down for the experience. Sure enough, my vein collapsed as the tech was trying to start the IV. That was it, I told him to stop and that I wanted to have my port accessed. He was a good technician; he listened to me. I walked over to the Cancer Institute.

After a 30 minute wait, a nurse was available to access my port. She did, I headed back to SNM, and received my radioactive contrast injection. Come back in 45 minutes.

I walked back to the Cancer Institute, which was extremely busy. I suggested to the receptionist that I could return after my bone scan. I went out on the street, found a new crepe place that had been open only three days, and had a freshly-made crepe with bananas, strawberries, Nutella and (sadly) fake whipped cream. I drank a huge glass of water.

Back to SNM. I went straight back to the bone scan room, used the toilet, took off my glasses and shoes and tried to get comfy on the narrow scanner bed. I wear an eye mask for these scans, so I can't see how close my nose is to the scanner ceiling. This scanner was in the shape of a CT machine, like a donut with a hole in the center, so less claustrophobic than others.

I put in my earphones and set my iPod to shuffle. The tech strapped my arms to my sides, covered me with a warm blanket and started the scan.

I actually fell asleep for the first 20 minutes. But after what felt like an hour, I really had to pee again, my back hurt from lying on the scanner bed and I was beginning to get really uncomfortable. I called out "How much longer?" and was told three more minutes.

Those last three minutes felt like another thirty. I had to pee. I wanted to move, or at least wiggle. My back ached. I had to pee! I asked again, how much longer, and heard back "only a minute and 30 seconds." Believe me, I sweated out those last 30 seconds.

The tech released me and I ran into the bathroom. I got dressed and headed back to the Cancer Institute, where all was quiet and a nurse de-accessed my port immediately.

Of course, I got stuck in rush hour traffic on the way home. Total elapsed time, door to door? Four and a half hours. Total aggravation? Extreme. From my doctor's office not calling to tell me he had written orders to get my port accessed, to the collapsed vein, the walking back and forth between buildings and the hour-plus scan duration, this was an afternoon from hell. I was so exhausted I fell asleep for an hour on the sofa.

This is one day in my life in Cancer Land.

Tuesday, July 20, 2010

Visiting a friend

This morning I was fortunate to spent some time visiting with my friend Josh who recently entered hospice care for his advanced epitheliod sarcoma. You may remember his film, My Left Hand, and of course his blog.

A week ago everyone was sure he was dying, and soon. When I arrived today he was sitting in a chair eating breakfast. He was able to take a cell phone call. The human body's ability to hang onto quality of life and the human spirit's need to connect with loved ones never cease to amaze me.

Josh was surrounded by family and beloved friends last week. That's a good way for all of us to live, basking in the care of those we love and who love us.

Monday, June 28, 2010

First Doxil

Today I received my first treatment of Doxil (doxorubicin). First they gave me a new anti-nausea drug called Emend (given by IV), then i took Decadron (a steroid) and Ativan (for anxiety) orally. Then they finally set up the Doxil. Two chemo nurses sat with me to monitor how well I reacted and to make sure there were no problems. They gave it very slowly at first, then began increasing the speed. It took about 90 minutes - two hours for the whole infusion.

Doxil is a bright peach color, or as one nurse put it, exactly the shade of peach Jello. I don't eat too much Jello but I liked her softer imagery.

I felt quite chatty, especially compared with my morose behavior of the past few days. Either the Zoloft (anti-depressant( is kicking in quickly, or the steroids gave me just enough lift. D and C came to visit and I was able to have good interactive conversations with them both. D called me "perky." Either way, I rose to the occasion and provided the nurses with information they needed.

One bit was about the interaction of lymphedema with hand-foot syndrome. Evidently, if you get this, it comes on for a few days immediately after treatment and then eases. You can help prevent it by taking tepid showers; not using knives or tools; not kneeling or leaning on your arms. So far none of the providers recalls treating anyone with hand-foot syndrome who also has lymphedema. I have left a message with my physical therapist asking about her experience and I'm sure she will call back if she has a solution to offer.

Meanwhile we have decided that for these first three or so days post-Doxil, I will cease all lymphedema management to avoid putting undue pressure on my palms, and then return to night-time bandaging more loosely (if I can do this). At least I have a plan.

We came home with two prescriptions: Emend is given via IV on treatment day, and then via oral pill on each of the next two days. I have oral Zofran to manage additional nausea, should I experience any. And despite his not wanting to order me additional Ativan last week, Dr G wrote a new scrip for Ativan today, so I am covered for both anxiety and nausea.

It all went very smoothly. I was surprised that my counts were high enough to permit starting this treatment, but Dr G thinks it's best to start asap and he's the boss of my cancer. And last Thursday he said in plain words, "Your cancer is going to get better."

Tuesday, June 15, 2010

Drop Everything and Fight Cancers Below the Belt

As taken off their website ...

Join Alberta Cancer Foundation’s Underwear Affair® presented by Mark’s Work Wearhouse and help uncover the cure for underfunded below-the-waist cancers like prostate, ovarian, and colorectal. On June 19, 2010, run the competitive 10K or walk the fun 5K and show Edmonton that there’s absolutely no shame in bringing a little awareness to down there-ness.

The fun continues even after you cross the Finish Line with the EXPOsed After Party! Grab a well deserved drink, strut your stuff in the legendary costume contest, and dance the night away with your fellow participants!

It’s time to hit below-the waist cancers where it hurts. Register today!


Friday, June 11, 2010

A new cancer dream

Last night (or probably very early this morning) I dreamt that I was somewhere with people I knew. But they didn't resemble themselves and they were chasing me. One was spreading all sorts of nasty rumors about me. Another was trying to drown me. I fought back with a broom, screaming and shouting for them to stop. And I didn't drown but clung to a railing and pulled myself out of the water.

After I woke up it became clear that this was another cancer dream. The unrecognizable people were my metastases, and they were trying to kill me. My broom weapon was the Abraxane. And pulling myself out of water too deep for me? That represented my body's ability to heal itself.

I've had these cancer dreams before. I think this one means that I am worried the cancer will get the upper hand, but that I feel strong enough to fight it back into submission. In this household, I am the alpha dog!

Sunday, June 6, 2010

National Cancer Survivors Day

I read this yesterday on Facebook, as posted by ChemoBabe, am reprinting with her permission:

If you ever had a cancer diagnosis and you are reading this, you are a survivor. Happy National Survivors Day. I look forward to the day when everybody with a cancer diagnosis survives. And then the day when nobody gets cancer.

Support research. It saves lives
.


I couldn't agree more!

Wednesday, May 19, 2010

Remembering Charisse

I always think of my dear friend, Rabbi Charisse Kranes z"l, on the eve of Shavu'ot. I remember that evening in 1989 too clearly. My roommate and I had just finished a delicious dinner when the phone rang. It was a friend of Charisse's from California, calling to say that she had died that afternoon. (Of course, it was three hours later back east due to the time zone difference.)

Charisse had been diagnosed with cancer four years earlier. Despite her advanced cancer, she continued to live life to the fullest. She started her first job as a congregational rabbi and was the first female rabbi on a pulpit here in Seattle. She married her grad school sweetie and they moved to California. When she could no longer work full time, she led services for the high holidays at various locations and later took on a part-time position.

We grew up together in the Zionist youth movement Young Judaea. In high school Charisse flirted off and on with increased religious observance. She used to bring a plastic toy Jeep to regional YJ conventions. During one particular weekend, she took the wheels off the Jeep so that we couldn't "drive" it and thus violate Shabbat while we played with it on Saturday afternoon.

Zichrona livracha: may her memory be a blessing.

Wednesday, May 5, 2010

An update from the oncologist

I saw Dr. G, Seattle's best oncologist, yesterday and we agreed on the following --
Chemo will be three weeks on, one week off (yay! a plan!)

Although they test my blood before every chemo to see if I am healthy enough to be treated (i.e. not anemic), I will also have a test of my tumor marker CA 27.29 in a few weeks to see how effective the abraxane is.

I told him about the burping and he prescribed an OTC chewable medicine called Gas-X which gave me immediate relief last night after dinner. I am to take one after every meal and before bed (maximum four times a day) if I find myself burping. I could call the naturopath also and get his advice, but I'm pretty sure he'll tell me to take more of the digestive enzymes which I can't stand and don't think work very well.

We think we have resolved the confusion over orders placed in the electronic system. The Swedish Cancer Institute is still getting used to this way of doing things, and they were not expecting electronic orders from Dr. G. Hopefully all will go smoothly next Monday.

In the meantime I am feeling well this morning and have plans to see yet a third wig provider and have lunch with a friend later today.

There is a 90% chance I will lose my hair to the abraxane. But that means 10% of people don't, and I know someone who falls into that category. So I thought of another addition to my chemo mantra: I hope to keep my hair, but if I do lose it to the chemo, I am prepared. Because (say it with me) this chemo is well-tolerated, very effective, with minimal side effects.