Saturday, January 31, 2015

BREAST CANCER RESEARCH RIGHT NOW! #29: Dealing With Restless Limb Syndrome…


https://s-media-cache-ak0.pinimg.com/236x/81/e0/17/81e0174e6e01a46b48e0a5fc8ab7a2d9.jpg
From the first moment my wife discovered she had breast cancer, there was a deafening silence from the men I know. Even ones whose wives, mothers or girlfriends had breast cancer seemed to have received a gag order from some Central Cancer Command and did little more than mumble about the experience. Not one to shut up for any known reason, I started this blog…

Every month, I’ll be highlighting breast cancer research that is going on RIGHT NOW! Harvested from different websites, journals and podcasts, I’ll translate them into understandable English and share them with you. Today: http://en.wikipedia.org/wiki/Restless_legs_syndrome

First of course, the definition: “Restless legs syndrome (RLS) also known as Willis-Ekbom disease (WED)[1] or Wittmaack-Ekbom syndrome, is a neurological disorder characterized by an irresistible urge to move one's body to stop uncomfortable or odd sensations. It most commonly affects the legs, but can affect the arms, torso, head, and even phantom limbs. Moving the affected body part modulates the sensations, providing temporary relief.”

Once again, this is something my wife has struggled with. But instead of breast cancer causing it, it has exacerbated it. She’s had RLS her whole life (at least since she was six years old!) Breast cancer – double mastectomy, aggressive tri-weekly chemotherapy (Taxotere + Adriamycin + Cytoxan and the next day, neulasta), followed by five years of anastrazole – just made it...weirder.

I first experienced when we got married. At night, before falling asleep, she would move her legs in order to “short-circuit” the odd sensations. That seemed to work. Then the cancer diagnosis and treatment and as of right now, it has manifested itself by odd sensations in her LEFT arm. This is odd because the removal of sentinel nodes and the resulting lymphedema was in the RIGHT pit and arm (sounds like a medieval British pub, doesn’t it...).

Current research suggests “...exercise, avoiding RLS precipitants (caffeine, alcohol, antidepressants, antihistamines); exercise; counter stimulus to sensory symptoms (hot or cold baths, limb massage, compression stockings, counter-pulsation devices); herbal medicines and acupuncture; and cognitive behavioral therapy.”

Her first “go to” was to up her calcium intake: “Dehydration, prolonged sitting, or not getting enough potassium, calcium or magnesium in your diet can be associated with leg cramps. So can certain medications -- including diuretics, beta blockers and other blood pressure drugs. Sometimes, these cramps also may be related to an underlying metabolic condition, such as an underactive thyroid (hypothyroidism) or a parathyroid condition. Diabetes or other conditions that disrupt your metabolism can also cause muscle cramps.”

The calcium chews she’d been doing were originally to counter the bone debilitation caused by the chemotherapy, so she stopped for a while. The RLS increased and now she uses the calcium chews as well as a hot water bottle to lower the intensity of the sensations.

As I wrote earlier, we’ve also started a regimen of exercise together – alternating strength training (after a visit with the Planet Fitness trainer) and cardio – we usually do a half an hour of stationary biking. The hot water bottle was a “new development” and has been remarkably effective.

I’ll note here something we HAVE NOT tried, but is a recent development: “In 2014, the FDA approved a device that provides electrical stimulation to the legs as a non-medication treatment for restless legs syndrome. Studies suggest this treatment can be quite helpful. Although it is generally well tolerated, it occasionally causes a temporary worsening of symptoms, leg cramps, soreness and motion sickness.” My guess is that this is an outgrowth of the device developed for those who suffer from chronic pain, what’s called Microcurrent Electrical Therapy.

Taken all together, the “therapies” seem to be working for the time being. It’s also light years better than adding ANOTHER pill to her already abundant storehouse!


Saturday, January 24, 2015

ENCORE! #5 – Metastatic Breast Cancer: Brain Cancer




http://www.onlinecancerguide.com/blog/wp-content/uploads/2012/12/Types-of-Brain-Cancer-in-Kids.jpg

From the first moment my wife discovered she had breast cancer, there was a deafening silence from the men I know. Even ones whose wives, mothers or girlfriends had breast cancer seemed to have received a gag order from some Central Cancer Command and did little more than mumble about the experience. Not one to shut up for any known reason, I started this blog…

The first question that comes to mind is, “Is a brain tumor the same as brain cancer?”

While I don’t usually go to Yahoo Ask for my medical information, I decided today to START there because the answerer is both an MD and clear:

“Interesting that you bring this up. Primary brain malignancies have always been called brain ‘tumors’ rather than ‘cancer of the brain’. Yet many are clearly cancerous, locally invasive, progressing malignancies. Strange the way people perceive words. If you tell patients they have a ‘tumor, it does not seem as ominous to them as saying they have ‘cancer’…there is confusion that many people have in regard to this topic. A person with lung carcinoma that has spread to the brain has lung cancer in the brain. It is not a brain cancer. It is still lung cancer that is growing in the brain area. A person with a glioblastoma multiforme has a brain tumor - but these are usually aggressive cancers. As for cures - that depends on the primary brain cancer/tumor type and the stage.

Interesting question regarding the semantics of this.”

Source(s): MD medical oncologist - cancer specialist doctor Spreedog, 2010 http://answers.yahoo.com/question/index?qid=20091114024633AADSsIx

This is in concordance with what I’ve already found out about bone cancer and lung cancer – when you have had breast cancer and is spreads (which is what Metastatic Breast Cancer is), you have breast cancer cells growing wild in the bones, liver, lungs, brain and various  other places.

So what happens? This seems to me to be a truly horrible kind of MBC because the brain is the seat of Human consciousness.

The writer here expresses this terror: “It was because of a few unusual symptoms, that several months ago I requested a brain scan. By the time the date arrived for the scan, the symptoms, along with my fears, had disappeared. Imagine my surprise when the next day my oncologist called to say that they had found 2 tiny spots on my brain. The news was devastating. While breast cancer is every woman’s nightmare, and metastasis is the nightmare of everyone who has breast cancer, brain metastasis is the nightmare of everyone who has metastatic disease. It was so frightening that I couldn’t speak to anyone about it. I could barely allow myself to think about it. None of this is news to you. You wonder how many tears you can actually shed. You wonder if you will ever feel like your old self again and if your friends and family will ever think of you in the same way. You wonder if you will lose the person you are. It is the most terrifying diagnosis anyone can have, even those of us who are used to bad news.”

What are the symptoms? Please keep in mind that the symptoms are DIFFERENT depending on where the cancer attacks first. Also, OTHER things can cause these symptoms. My wife works as a classroom aide with kindergartners – she gets headaches sometimes, as anyone would who tries to work with a room full of five-year-olds!

Symptoms include: “changes in the ability to think, understand and use words correctly; emotional changes; weakness; dizziness; seeing lights, seeing double, or narrowing of vision; problems with balance; seizures; nausea and vomiting; changes in smelling, taste, hearing. If any of these symptoms persist (that is, stick around for a while) like a headache that is worse in the morning, lasts for days, or recurs every day, then you’ll want to talk to your health care authority.

Once you report to the cancer care center or your doctor and there appears to be reason to suspect MBC-brain cancer, an MRI (magnetic resonance imaging) is the most effective technology for diagnosing breast cancer brain metastases. It does a better job in distinguishing a single metastasis from multiple metastases, which is an important factor in determining what kind of treatment a patient needs.

Unfortunately, treatment for MBC-brain cancer is problematic still. In m0st cases, whole brain radiation (which is exactly what it sounds like) is the first line of offense. There is good evidence that this treatment is effective almost half of the time in completely reversing the effects of the cancer. In MOST cases, it reduces the symptoms significantly. It is also a shorter-term treatment than the original chemotherapy with radiation doses given daily for 5-10 days (though this is sometimes spread over a longer period to lessen the side-effects.

At other times, the radiation is aimed from multiple directions at specific metastases. This has the advantage of fewer side-effects, but there is no clear EVIDENCE yet that this is as effective as whole brain radiation treatment.

Other, less common treatments include brain surgery (physical removal of the cancer), chemotherapy (not effective usually because the chemo can’t break through the barrier into the brain through the blood (called the blood-brain barrier); and a combination of the above.

Finally: “‘So much depends on the aggressiveness of your individual cancer, the time to recurrence from original diagnosis, any other metastases, and overall health—and, the number, location and size of the brain mets (metastases), and whether they are symptomatic or not,’  Patty observed. ‘I was so sure that I would die within 18 months of my first diagnosis with brain mets.  I readied for the time of my death. Now, I’ve had to revise things a few times.  I wonder if I hold some kind of record for brain MRI’s, having had them on average every two months for five years—that would be around thirty, with bad veins! I’ve had brain mets for five years and have been living with eight lesions for two and a half years.’”


Saturday, January 17, 2015

GUY’S GOTTA TALK ABOUT #11…Life TOGETHER!


From the first moment my wife discovered she had breast cancer, there was a deafening silence from the men I know. Even ones whose wives, mothers or girlfriends had breast cancer seemed to have received a gag order from some Central Cancer Command and did little more than mumble about the experience. Not one to shut up for any known reason, I started this blog…

We joined Planet Fitness during the Christmas holidays!

I know, I know...EVERYONE joins The Club after the holidays because they’ve got their New Year’s Resolutions to fulfill. And The Clubs offer Special Deals!!!! Like PF offers a “No Commitment” Deal of $10 a month and no commitment!

My observation is that not only are they being...sarcastic, they’re being realistic. Sarcastic because how can you commit to a new lifestyle if you don’t have to commit to it? They’re being realistic because I’m sure that every New Year ushers in a rush of people who are Going To Get Fit This Year.

 My wife and I have BEEN those people more than once in our lives, but This Time It’s Different! (I’m sure you’ve all heard that before...) The thing is, is that this time it is different. Why?

First of all, my wife is now an almost-four-year breast cancer survivor. The initial surgeries are healed, the IV chemo is done, the breast reconstruction is done, and she’s as healed on the outside as she’s going to get.

Second: I had treatment for skin cancer in November and December. This brought the concept of invasive disease more close to home than it has ever been. It made me think. It made me shudder. It finally made me act with an attitude SO cavalier that I doubt anyone knows how horrified I was.

Third: We have grandchildren. It has been my avowed intent to be there for the weddings of my son and daughter-in-law's kids; and any that my daughter and whomever she pairs with has. My wife joins me in that.

Fourth: We are AGING (gasp!) Things are harder to do because the joints and muscles ain’t what they used to be. The benefits of even a MILD exercise regimen are documented (http://www.livescience.com/42820-light-exercise-benefits.html) and now that the nest is basically empty, two futures present themselves: we can watch whatever TV we want to, go to whatever restaurants we want to, stay at home and not have to interact with the world as much as we want to; or we can start going to a non-threatening, and moderately inexpensive gym, learn muscle-building and cardio workouts TAILORED to us and our age and condition (with the Trainer who comes with The Club’s standard package and who actually knows what she’s doing in general if not specifically when dealing with breast cancer survivors). One will end in a matched set of couch potatoes. The other will end in a matched set of sore, tired AFTER mild exercise, couch sweet potatoes (which are better for you than regular potatoes, but not by much.)

Fifth and final: As long as we’re going to grow old together, we might as well make sure that we’re doing things...together. Exercise is new for us and instead of joining different exercise groups and clubs and exclusive organizations, we’re going to do this...together. I love my wife and we’ve raised two kids, advanced our careers with education and experience, traveled together, worked together, and done everything else together. Now we’re going to get as healthy as we can be together. I’m certainly not going to win the Mr. Universe Pageant (http://www.thatslife.com.au/Article/Real-Life/Real-Life-Stories/Im-Mr-Universe-and-Im-60), but together, me and my wife CAN be healthier. Exercise. Better diet. Lots of talk. Classes. It all goes together.

And it’s what we’re going to do – TOGETHER!

Saturday, January 10, 2015

ENCORE! # 4 -- "The Doctor Gave Me A Pill And I Grew A New Kidney!"


I haven’t talked about STAR TREK yet, which isn’t like me at all!

ST was my favorite TV show growing up, as an adult and now as an “old guy”. During the opening week of the STAR TREK 2009 reboot, my dad (who introduced me to STAR TREK), me (a total ST fan) and my son (who grew up with ST and at whom the new movie was targeted) – went to see it. None of the wonder was gone and I love the NEW as much as all of the old.

At any rate, it got me to thinking about a scene from STAR TREK IV: The Voyage Home in which an elderly woman is laying on a hospital cot waiting to go in for dialysis:

McCoy: [McCoy, masked and in surgical garb, passes an elderly woman groaning on a gurney in the hallway] What's the matter with you?
Elderly patient: [weakly] Kidney [pause] dialysis.

McCoy: [geniunely surprised] Dialysis?[musing to himself] What is this, the Dark Ages? [He turns back to the patient and hands her a large white pill] Here, [pause] you swallow that, and if you have any more problems, just call me! [He pats her cheek and leaves]

…a few moments later…

 Elderly patient: [the dialysis patient is being wheeled down the hall after being given the pill by McCoy] [joyfully] The doctor gave me a pill, and I grew a new kidney!


It made me wonder for two reasons. The first was that while today breast cancer survival rates are as high as 98% (for early detection and treatment), at one time tumors could only be detected when they could actually be felt – and then the ONLY treatment was radical mastectomy which, in the late 19th Century removed not only breast tissue but muscles and all lymph nodes as well. If a woman survived that, she was profoundly weakened and handicapped for the rest of her life.

The introduction of modified mastectomies (1950s), mammogram advances (starting in 1967), ultrasound (late 1970s), followed by MRIs, digital mammography, 3D mammography and increasingly refined chemotherapy (introduced in the 1940s), radiation (early 20th Century) and lumpectomies combined with radiation therapy (1970s) and most recently, hormonal treatment and genetic testing improved treatment – and subsequently survival rates.

I’m going to delve into the history of breast cancer later, but for now, let me just say that while it still terrifies me even now; I do have a daughter and hold VERY high hopes that either her or her daughter will someday be able to pop a pill and cry out, “The doctor gave me a pill and I’m cured of breast cancer!”
Image: http://content6.flixster.com/photo/11/05/69/11056948_gal.jpg

Saturday, January 3, 2015

BREAST CANCER RESEARCH RIGHT NOW! #28: Implant Pressure…



From the first moment my wife discovered she had breast cancer, there was a deafening silence from the men I know. Even ones whose wives, mothers or girlfriends had breast cancer seemed to have received a gag order from some Central Cancer Command and did little more than mumble about the experience. Not one to shut up for any known reason, I started this blog…

Every month, I’ll be highlighting breast cancer research that is going on RIGHT NOW! Harvested from different websites, journals and podcasts, I’ll translate them into understandable English and share them with you.

My wife wanted  me to find out the answer to this question: “Why do the implants make it feel like I’m in a C-clamp all the time?”

I found out that she’s not alone. In addition to covering other issues with breast reconstruction, the BREASTCANCER.ORG website has this to say: “Some women feel pain or discomfort from the tissue expander, the implant, or scar tissue putting pressure on a nerve or other sensitive area.”; also “A breast reconstructed with an implant may move in unnatural ways as you flex your chest muscle (pectoralis muscle).

In both cases, the solutions while not “simple”, suggest that exercise and massage may help alleviate the discomfort. Some suggested exercises are: shoulder “shrugs”; should rolls; shoulder raise; arm swings; body turns; lifting your arms above your head (while laying down!); “walking your fingers up the wall”; same as the previous one, but “sideways”; “beach pose”; and finally, the chest stretch.

The Breast Cancer UK site article “Exercises after breast reconstruction surgery using implants” will give you specific details and directions of how to do each one I mentioned as well as a time frame. They start with immediately after the surgery and proceed to weeks and months later.

This doesn’t completely answer however, the concerns of Roseanne Valletti (54) “...she is uncomfortable. All the time. ‘It feels like I’m wrapped up in duct tape,’ [she] said of the persistent tightness in her chest that many women describe after breast reconstruction.”

It appears that this kind of feeling is both common and unavoidable: “...it is major surgery. Even with the best plastic surgeon, breast reconstruction carries the risks of infection, bleeding, anesthesia complications, scarring and persistent pain in the back and shoulder.”
“A syndrome called upper quarter dysfunction — its symptoms include pain, restricted immobility and impaired sensation and strength — has been reported in over half of breast cancer survivors and may be more frequent in those who undergo breast reconstruction, according to a 2012 study in the journal Cancer.” As usual, when you’re talking about pain, there are a million voices all clamoring for your attention. This site written by a chiropractor makes the startling claim that everything from butt pain to deafness can be cured by breaking up something he calls “fascial adhesions” with some sort of bruising method...he does, of course, rail against the medical establishment because they don’t acknowledge his methodology as effective. (http://www.doctorschierling.com/fascia.html)There are claims that shots work (usual hydrocortisone) as well as surgical removal of scar tissue all the way up to and including the removal of the implants altogether.

What works will likely be what you decide works. All of these methods are available and you will find a physician somewhere who will agree to treat you with whatever method you find online or through conversing with doctors.
I myself don’t know WHAT to think.
Resources: http://www.breastcancer.org/treatment/surgery/reconstruction/types/implants/risks, http://www.cancerresearchuk.org/about-cancer/type/breast-cancer/treatment/surgery/reconstruction/exercises-after-breast-reconstruction-using-simple-implant, http://well.blogs.nytimes.com/2013/05/20/no-easy-choices-on-breast-reconstruction/?_r=0