Showing posts with label Multible myeloma. Show all posts
Showing posts with label Multible myeloma. Show all posts

Scientists find key to 'turbo-charging' immune system to kill all cancers

FASTER!

jc

http://www.telegraph.co.uk/news/science/science-news/11542544/Scientists-find-key-to-turbo-charging-immune-system-to-kill-all-cancers.html

Scientists find key to 'turbo-charging' immune system to kill all cancers

Imperial College scientists are developing a gene therapy designed to boost immune cells

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A protein which ramps up the immune system has been discovered by scientists at Imperial College London
A protein which ramps up the immune system has been discovered by scientists at Imperial College London Photo: Wellcome Collection
A protein which ‘turbo-charges’ the immune system so that it can fight off any cancer or virus has been discovered by scientists.
In a breakthrough described as a ‘game-changer’ for cancer treatment, researchers at Imperial College found a previously unknown molecule which boosts the body’s ability to fight off chronic illnesses.
Scientists at Imperial College London, who led the study, are now developing a gene therapy based on the protein and hope to begin human trials in three years.
“This is exciting because we have found a completely different way to use the immune system to fight cancer,” said Professor Philip Ashton-Rickardt, from the Section of Immunobiology in the Department of Medicine at Imperial, who led the study.
“It could be a game-changer for treating a number of different cancers and viruses.
“This is a completely unknown protein. Nobody had ever seen it before or was even aware that it existed. It looks and acts like no other protein.”
The protein – named lymphocyte expansion molecule, or LEM, promotes the spread of cancer killing ‘T cells’ by generating large amounts of energy.
Normally when the immune system detects cancer it goes into overdrive trying to fight the disease, flooding the body with T cells. But it quickly runs out of steam.
However the new protein causes a massive energy boost which makes T cells in such great numbers that the cancer cannot fight them off.
It also causes a boost of immune memory cells which are able to recognise tumours and viruses they have encountered previously so there is less chance that they will return.
The team made the discovery while screening mice with genetic mutations. They found one type produced ten times the number of cancer-fighting T cells, suppressing infections and becoming resistant to cancer.
Researchers found that the mice with enhanced immunity produced high levels of the unknown protein which is also found in humans.
They are hoping to produce a gene therapy whereby T cells of cancer patients could be enhanced with the protein and then injected back into the body. It could end the need for harsh chemotherapies as the body itself would be fighting the disease, rather than toxic drugs.
Dr Mike Turner, Head of Infection and Immunobiology at The Wellcome Trust, said: “The discovery of a protein that could boost the immune response to not only cancer, but also to viruses, is a fascinating one.
“Further investigation in animal models is needed before human trials can commence, but there is potential for a new type of treatment that capitalises on the immune system’s innate ability to detect and kill abnormal cells.”
Charities said the protein showed 'great promise' and were eager to see if it could be translated into humans.
Dr Alan Worsley, senior science information officer at Cancer Research UK, said: “This exciting work in mice is still at an early stage and only looked at one type of cancer.
“Cancer often finds a way to suppress the immune system, but drugs that overcome this and allow immune cells to target cancer show great promise. Research into the biology of the immune system could help develop more effective treatments by increasing the number of cancer-killing immune cells.
“The researchers now need to figure out how to develop drugs that target this molecule, and whether doing so would be safe and effective in cancer patients.”
The research was published in the journal Science.

Myeloma patients could soon benefit from targeted therapy |  City of Hope Breakthroughs

Myeloma patients could soon benefit from targeted therapy |  City of Hope Breakthroughs

Many cancer patients have benefited from targeted therapy – medications that can identify cancers by their genetic properties and help eradicate them – but such therapy has been largely a pipe dream for multiple myeloma patients. Until now.
Myeloma
New drugs could provide targeted therapies to patients with multiple myeloma.
Currently, two medications are emerging as especially promising in the treatment of multiple myeloma: daratumumab and SAR650984. Each of the drugs  target different  sites on the same receptor for multiple myeloma.  Each was the subject of research presented at the annual meeting of the American Society of Hematology.
The drugs are offering new hope to patients who have already tried many other therapies with less-than-ideal results.  “The most important thing is that these are targeting the patients who have high-risk disease who have been refractory to the other agents we’ve had standardly available,” said  Amrita Y. Krishnan, M.D. FACP, director of the Multiple Myeloma Program at City of Hope. “To see responses in these very advanced patients is extremely compelling.”
Data supporting the drugs’ effectiveness has been building, and Krishnan expects it to continue to develop in the coming year.
Because the drugs have different targets, if a patient does not respond to one of them, the other may prove beneficial.
“This is going to be a very interesting question as time goes on,” she said. “Right now, I don’t think we have enough to be able to pick out a patient who is going to respond to one compound versus the other.”
Myeloma is a cancer of the plasma cells, which normally produce anitibodies to help fight infections. Ultimately, it can interfere with production of normal blood cells and cause serious complications in bones and kidneys. When these cancerous cells form tumors throughout the body, it is classified as multiple myeloma. One of the treatments for the diseases, beyond chemotherapy and radiation, is stem cell transplantation.
**

Interesting cancer stuff

http://www.myelomacrowd.org/patient-power-smoldering-orlowski/

Key Answers for Smoldering Myeloma Patients

Patient Power has created a very helpful series of videos to answer important questions posed by myeloma patients. Here are key questions that are critical to smoldering myeloma patients, answered by Dr. Robert Orlowski, MD, PhD of the MD Anderson Cancer Center.
Watching and Waiting for Smoldering Myeloma: What Tests and When?
Can Anything Stop MGUS and Smoldering Myeloma from Progressing to Symptomatic Disease?

What Clinical Trials are Available for Smoldering Myeloma Patients?

Don't care how they do it, just kill it!

http://mag.newsweek.com/2014/03/28/war-against-cancer-alternative-cancer-treatments.html

From his fourth-floor window at Tampa's Moffitt Cancer Center, Robert A. Gatenby can look down to where patients stand waiting for valets to retrieve their cars. They have gone through chemotherapy, biopsies, radiation. They are pale, anxious, resolute. Some will live and some will die: a young woman with short hair, clutching her partner's hand; an older man, alone. Students from the nearby University of South Florida pop out of patients' cars. Peppy and dressed in blue vests, these cheerful valets look as if they could be working at a luxury hotel in the tropics. But nobody here is on vacation.
Gatenby says he sometimes sees patients retching after chemotherapy, which reminds the 62-year-old radiologist that his Integrated Mathematical Oncology Department—the only full-scale outfit of its kind in the nation—does not have the luxury of time. Mathematics is not generally known for urgency. Few lives hinge on proof of the twin prime conjecture, but the mathematicians and oncologists Gatenby has assembled in Tampa are trying to tame the chaos of cancer in part through the same differential equations that have tortured so many generations of calculus students. By mathematically modeling cancer, they hope to solve it, to make its movements as predictable as those of a hurricane. The patients down there, fresh from treatment, need shelter from the storm.
Gatenby's small corner of Moffitt bears little resemblance to a medical center: There are no white-coated doctors frantically rushing to save patients or synthesizing miracle cures deep into the night. You might think you've found yourself in a sleepy academic department where abstract ideas are kicked around like a soccer ball on the college green. Which, come to think of it, is actually a pretty accurate description of what goes on in Gatenby's lab, though not at all a pejorative one. The mathematicians in his employ are convinced that we do not really understand cancer and that, until we do, our finest efforts will be tantamount to swinging swords in utter darkness. As far as these Tampa iconoclasts are concerned, your average cancer doctor is trying to build a jetliner without having grasped aerodynamics: Say, how many wings should we slap on this thing?
A Malicious Green Cloud
We have been fighting the War on Cancer since 1971, when President Richard M. Nixon declared that the "time has come in America when the same kind of concentrated effort that split the atom and took man to the moon should be turned toward conquering this dread disease." Four decades later, 1,665,540 Americans per year hear the dreaded diagnosis, and about 585,720 die annually from some variety of the disease, according to the American Cancer Society. Smallpox and polio have been cured or largely eradicated, but cancer remains the same scourge it was 4,500 years ago, when the Egyptian doctor Imhotep mused, in what may have been civilization's first stab at oncology, about how to treat "bulging masses on [the] breast." Modern oncology makes incremental advances, with a melanoma drug that extends survival by three months passing for a major breakthrough. This is nobody's fault, but everybody's problem.
Gatenby is tired of a fight we keep losing. After 30 years, he has come to the uneasy conclusion that cancer is smarter than we are, and will find ways to evade our finest medical weaponry. The weary warrior wants to make peace with cancer's insurgent cells—though on his own terms, terms that would spare the lives of many more patients. To some within the medical establishment, this might seem preposterous, but Gatenby relishes the role of the outsider.
Gatenby grew up in the Rust Belt town of Erie, Pa., where 12 years of Catholic school instilled in him "an incredible hatred of dogma." At Princeton University, he studied physics with some of the greatest scientific minds of the 20th century. Figuring he wasn't fated to join the physics pantheon, Gatenby turned to medicine. But medical school at the University of Pennsylvania was dismayingly similar "to the rote learning of catechism" he remembered from Saint Luke School. It felt like he was "going backwards."
Whether in the lab, the classroom or the clinic, Western medicine relies on cautious experimentation, its zeal for breakthroughs tempered by the Hippocratic injunction to do no harm. But that can foster a frustrating incrementalism that is itself injurious. David B. Agus, one of the nation's most prominent oncologists and a professor at the University of Southern California, explains that "you are not rewarded, in general, for taking risk. It's very scary to do something radically new."
Gatenby specialized in radiology and, after receiving his medical degree in 1977 and completing a residency, went to work in 1981 for the Fox Chase Cancer Center in Philadelphia. Fox Chase is to cancer research what the Boston Garden was to professional basketball. It was home to David A. Hungerford, one of two researchers responsible for discovering the Philadelphia Chromosome, a major clue to cancer's birth within the human genome. Among its current Ã©minences grises is Alfred G. Knudson Jr., whose "two-hit" hypothesis holds that cancer is triggered by an unfortunate accumulation of errant genes, harmful outside events (too much sun, too much red meat) or a combination of the two.
The study of genes did not interest Gatenby back then, nor does it interest him now, even though much of medicine is now in the thrall of genomics. Gatenby wanted to discover cancer's "first principles," the basic ideas behind the seemingly sudden explosion of cells that want to kill the very body that nourishes them. Sure, you could know the BRCA1 gene better than you know your own mother, but unless you had some insight into why it caused a furiously impervious breast cancer, you were trying to find your way out of a forest by studying the bark of a single tree. Gatenby sought to understand cancer with the same totality that Newton had understood gravity.
As with Newton's famous laws of motion, mathematics seemed to hold the key. Math had been used to model the weather and financial markets, which like the human body are fickle and incredibly sensitive to outside forces (a run on Greek banks; a low-pressure system moving down from Canada). Gatenby saw no reason the same could not hold true for cancer. He spent a year reading math, which puzzled his colleagues. Then, while visiting the Cloisters museum in upper Manhattan with his family, he took a sheet of stationery and started scratching down equations he thought could get him closer to cancer's fundamental truths.
"To say they hated it would not do justice," Gatenby says of the response of his Fox Chase colleagues. Other oncologists told him that "math modeling is for people too lazy to do the experiment" and that "cancer is too complicated to model." The latter is a refrain that, 30 years later, still dogs Gatenby and his staff at the Integrated Mathematical Oncology Department, which includes five mathematicians with no formal experience in medicine.
Among those five is Sandy Anderson, a young Scotsman who dresses as if he were on the way to a Beck concert. There is a bottle of single malt on his desk. "Of course cancer is complex," Anderson tells me, brogue rising. "But how can you say it's too complex? That complexity should be viewed as a challenge that we have to try and tackle. And just because there's complexity doesn't mean there aren't simple rules underlying it.
"What we'd love to do is have everybody's own little hurricane model for their cancer," he explains. This is less a metaphor than you may imagine. Anderson shows me computer models of a breast cancer's growth, the cells spreading like a malicious green cloud across the screen. Different versions of the model show what happens when different treatments are applied: Sometimes the cancer slows, but sometimes it explodes. This seems like an intuitively rational approach to the disease, predicting how it responds to a variety of treatments. But it isn't common. There are about a dozen drugs for breast cancer approved by the Food and Drug Administration. Depending on which form of the disease is diagnosed and at what stage it's discovered, there's a maddening number of viable drug combinations. Best practices exist, but these can be anecdotal, doctors simply doing what they think works. The War on Cancer is fought by competing bands with their own weapons, cancer's chaos exacerbated by our own dismaying disorder. Anderson would like to provide the onco-soldiers with battlefield maps.

All OK!


Well, those lesions that showed up on the full body x-ray ended up being... something else.

What?  I dunno - and neither does Dr. Lee.

But what is known is that the bone density scan, full body x-ray, blood tests, and bone marrow biopsy all concluded that there is no cancer present, presently.

I have to admit, I was more than a bit worried that it was back.

Still, the odds are that something will pop up, at some point.


Here is to later, as opposed to sooner...

I need a nap.

jc

Doctor update

Well, the unending stream of good news has stopped.  Perhaps just a pause...



The bone survey showed three lesions  - right arm, left arm, and the top of my skull.

Kidney function was still "ok" but pretty close to the upper edge of normal.

So - still waiting on the IGD blood test to come through, and I have a bone marrow biopsy in July.

Scheduled a bone density test for later this month also.

The cancer shows up in the bones first - so yes - I am sweating it.

Now I have to go to COSTCO and prepare for an audit/EPA action/OSHA inspection/NSA anal probe...

jc

Cool! Thanks for the views

Considering I never advertise, it is nice that I get hits.

This is basically a place for me to rant and leave my thoughts for the moment.  It is also a time capsule of progress on my cancer  - the first motivator on starting this blog.


I just thought that this was cool...

Thanks!

jc

Update: Trip to see Dr. Lee

Had an appointment with Dr.Thomas Chung-Kiang Lee, Hematology Oncologist to the Stars.

So far, things look OK.  Some tests have not come back yet, but that is due to the holiday.

I asked about my new found ability to profusely perspire seemingly on command, and we both agreed that it may only be a problem when the weather turns cooler.

And how did I celebrate that AND loosing 5 pounds since the last visit?

Yep:  Breakfast Burrito at Nick's Super Burger!

I need a nap...

jc

Yep - cancer causes cell phones


Love Xkcd.com, and I do think that the stats are totally out of sort on this.

Just another bad research project working on headlines, not science.

jc

Hubris - I feel thy sting...

Well, what can I say.

My battle with Multiple Myeloma and the after affects, has brought up my first big scare.

Yesterday, I went to the ER with a 103 fever and labored breathing. If it weren't for some pesky women insisting that I go to the ER (and not wait for an appointment) it could have been much worse.

Kaiser got me in, took blood and x-rays right away. Then they put a bag of fluids in me, as well as an initial dose of anti-biotics.

I am taking DOXYCYCLINE for the pneumonia, and I am feeling MUCH better today.

This is a setback, as I was getting fairly good stamina from the gym. Not that I can't get it back, but it will take even longer to get back to my pre-cancer levels of stamina.

And we are having such lovely weather outside, I am a bit pissed that I can't go out and enjoy it.

jc

Medical Update

Checked in with Dr. Lee today. Despite a small snafu with the blood draw (it expired, I forgot to get it done), all is well on the cancer front.

I came away with a few instructions from the good doctor, some of which may sound familiar:
  • Keep up with the Calcium, to REbuild my bones
  • Loose weight to relive my compression fractured back of any stress
  • Remain aware of the peripheral neuropathy in my fingers and (especially) toes
So, I am happy that I remain, the same.

I asked if my long term prognosis improves with time. For example, if you survived breast cancer five years ago, you are pretty much in the clear. Not so with Multiple Myeloma. Every day you play the lottery, and every day you loose (not get that 1:1,000,000,000 prize) you win.

Constantly hovering over my head is this inescapable fact: There is no cure.

At this moment, I am happy to be living in a cease-fire instant between my life and death battle with this monster.

And so, good news is: I am in pretty good shape -- but pear shape isn't what I should be.

Bad news is: As with all things, this is a fleeting moment that could vaporize with a bad result coming out of one of the eight vials of blood they took today.

Other than that, I had a nice day, sat outside with Mom and killed some time, had a Philly Cheese steak for lunch (hey - it has calcium rich cheese), and enjoyed a remarkable warm, sunny day.

G'nite
jc

Health update

I have been busy with appointments this week -- three and it is only Wednesday!

First was with Dr. Lee. My white blood count is still low -- OK considering that I don't have fully functioning bone marrow and am taking Thalomid. Still, the new (lower) strength Thalomid should help. We discussed the Aredia infusions, and decided that we should get a bone density scan done. Other than that it was "eat less carbs, more veggies, loose weight, bla bla bla". Yea, I am still quite overweight, but the meds will either make me gain weight or go anorexic. Got the fat side of that coin toss.

The bone density scan was scheduled for later that day at the new facility on La Palma, next to Fry's. Pretty simple procedure. Just that holding still on a slab of ice cold steel threw my back into spazams of muscular revolt. Give me five minutes to settle down, and I can do it, but it takes a lot of effort to relax the back and get "Zen". When he wanted to scan the hips, I had to point my toes inward and hold it for two minutes. That was NOT going to happen, as my toes never have pointed anywhere other that 11 and 2 o'clock. So we scanned one thigh at a time.

When the tech looked at my back, he could only find 4 vertebra. I have had one whole spinal vertebra disappear! Man, that realy messed with his brain. I have 1, 2, mushyblob, 5.

Yea, I can feel it, too.

Today I went up to the City of Hope for my follow up study on chemo brain. Man, that place is humming with construction! After being beat between the ears (yes, it is rough on the grey matter), I went and had a Tommy's Burger (sorry Dr. Lee). I had forgotten how good the chili was, and how meh the hamburger is.

Oh, and I get a bone marrow biopsy next week. Joy.

Well, it is now tomorrow, I better get into bed...

jc

Update from Dr. Lee's office

I had an appointment with Dr. Lee yesterday, and while I am still "OK", there are some trends that need to be reversed.

First, I am turning into a very large spud, weighing in at 275. True, a vacation followed by a week of preparations for a major party on the 4th didn't help, but still, I need to figure out how to loose weight. I have never voluntarily lost weight. Only twice have I lost weight, once when I had pneumonia, and then when I was having radiation. I need a third way.

Second, my IGD number is creeping up and up. Still within the normal range, but it went up from zero. Steadily.

The neuropathy in my feet and fingers are ever present. Typing -- being a touch typist -- can yeald surprising results. Walking and standing with little feeling in the feet can be a challenge too. I find that I don't lift my feet up, and snag stuff, causing a trip response. Since I don't have control over those micro adjustments that everyone uses to stay upright, I tend to stumble.

Memory, names, and descriptions can still escape me. Instead of caulk, I blurt out "white stuff in a tube that you squirt out to fill gaps in the trim before you paint stuff".

Bottom line, I am a fat stumbling, chemo brained idiot.

Eeesh, I need a nap.

jc

Health update

Generally, pretty good, but could be better.

On April 30th, I went to the City of Hope BMT reunion. This was my second one (celebrating 1 3/4 years). It is a very upbeat party on the lawn of the hospital grounds. I went by myself this time (girls were in school) and had a very nice time.

I come away with deeply turbulent feelings on these things. First, everyone there is a cancer survivor. That in itself is a reason to be happy. You can also see what damage has been done to the body, scarred faces, missing limbs, unstable gaits. But they survived. When you sit down to eat, you always chat with the people around you. I sat with two ladies that had cancer -- one even had the same doctors as I did! The second lady was your stereotypical older lady with loud clothes and super bright personality that you see at art openings. She survived (her first year), but the toll on her body was enormous. Didn't seem to effect her spirit, though.

Walking around, comparing yourself to other survivors (yes, that is what you do -- and you know it), I seem to have come out pretty good.

That is untill you see the kids with the BMT buttons.

This is what always disturbs me the most. The little kids with a button that says that they had a BMT x number of years ago, but they look only half that age. The toll on their bodies is telling, and obvious, at this early stage of what should be a long life. It can't be easy explaining to everyone that they are not able to (fill in the blank) because their body was attacked by cancer, radiated, chemoed, rebuilt from stem cells harvested from them (or someone else), and somehow they survived -- albet in a much weaker form.

I am blessed that the girls are healthy and strong.

I also like to wander the campus and look at all the plaques placed around their. While interesting, it is also a reminder that these people didn't survive. Hope only goes so far.

The statistics are irrefutable. For me, I have 5 years from initial diagnosis. While I may be cancer free now, there is a 70% chance that it will return. The doctors know the numbers, and while they are quite positive about my long term health, the stats don't change just for me.

That puts a different spin on career track guidelines.

+++++++++++++++++++++++++++++++

As far as how I am doing physically, not bad.

I am fat as a cow, can't feel my toes, can't feel my finger tips, off ballance ( because I can't feel my toes and I am fat), can't remember names worth a crap, get cramps at weird times on weird muscle groups, and can't see well in bright light unless I have my cool new sunglasses.

While I did sign up for the YMCA, I have yet to get into a groove. Excuses, trips, projects, and hey -- is that something shinny? Hopefully, I can get the girls to take me there so they can swim.

My eyes have healed nicely, according to Dr. Rice. I can see 20/20, with some help from reading glasses. While it is nice to "wake up and see the clock", my brain still hasn't been wowed by that. I have to remember to look up to see the clock. It is nice, though.

The thyroid keeps me warm, and I have to keep myself super hydrated or else I start having weird cramps and spasms. I still am learning to listen to my body, something that I really neglected to do in the past.

We will see if I do better over the summer.

I probably should go exercise now (but ice cream sounds soooo tempting).

jc

Cancer update

Last week I had three trips to Kaiser -- one infusion and two doctor appointments.

Infusion went well, as usual. This time, though, the aridia really hit me afterwards. I never experienced the fatigue before, so it was new.

Dr. Sahebi (Kaiser BMT specialist) was pleased with my progress, and took me off another pill. I still have to take the Thalomid, but that's OK. Now it's just vitamins and supplements.

Dr. Lee (Kaiser Oncology) was pleased with my progress too, but was concerned with my white blood count. I get another CBC next week to check on that. He also wants me to take B-12 for my blood. Perhaps I will just eat more steaks.

Toes still tingle, fingers still a bit numb, but that comes with the nerve damage and Thalomid. Balance is a challenge when you can't feel your toes to make the billions of micro corrections you make when balancing.

Cramps are still there, and I can feel it when my feet get cold... it gets painful when you are standing still and your feet cramp up. Looks real bad when one falls over with foot cramps and bad equilibrium.

Well, I need to get dinner started...

jc

A new blood draw record!

One.

Yes, I was shocked too.

I will probably have more later this week, as it is a busy week. Thursday up to Kaiser Sunset for an appointment with the BMT folks, then Kaiser Lakeview on Friday for my regular oncologist.

Damn, that means I have to loose 10 pounds by Friday.

Well, I better sleep on that one.

jc

Health update

Well, I saw Dr. Lee yesterday, and all seems to be going well.

The bone marrow biopsy came back as generally OK. He noted some elevated numbers in my IGD, but nothing else -- which seems like an anomaly and not much for concern. Yet.

He gave me the surgical pathology report, and while I am not a doctor (or even play on on TV) I can read this:
NO EVIDENCE OF MONOCLONALITY IN B-CELL POPULATION
I take that as something good.

My visits to the chemo lab for AREDIA are to be cut in half, and I don't see Dr. Lee until next January.

Generally good, eh?

My back still has its days, and my bone marrow is only at 50% or so. If I get sick (something I don't do very often) it will take me much longer to get better. I really notice that I notice faces, but absolutely blank out with names (very awkward, socially). I am quite stiff when it comes to movement, except when standing still: my back does an involuntary wiggle that seems like it is under/over correcting itself. My stamina is OK for a while, but it takes me much longer to recover. I seem to be just barely stable -- my balance is just not as balanced as before. If I do get off balance, I don't have the quick (or even automatic) muscle response to correct it in time. Not good when dodging beagle pups.

All told, I think I am doing quite well. Considering that in March of 2008 I could only walk with a walker, and could not get out of a bed without horrific pains in the back, I think that I am doing VERY well. Just wish these 100 little things would hurry up and stop making me feel older than I am.

Gotta go clean up puppy stuff --
jc

Quick medical update

Well, I went to see Dr. Lee, and things are cruising along.

Yes, I have some Peripheral neuropathy that makes my toes feel weird. Something of a concern, if I stub my toe. I also detect a bit of it in my fingers, but nothing to get concerned about -- yet.

I will deal with it.

My back isn't 100%, but I try to stretch it out and keep it flexible, eat some calcium, and that keeps it in check. Related to that is the almost constant cramps I have in either my toes, legs, lower back, middle back, abs, and hands.

I will deal with it.

My blood counts are low-ish, but that is expected with the Thalidomide. Seems that it also is responsible for the cramps. Problem is, if I stop, the cancer can come back, bigger and badder than ever. This is keeping it in check for the moment. I quit, that is the last I can use this drug -- forcing me into a different chemo regimen that may or may not be as effective.

I will deal with it.

Slightly more challenging is the thyroid. Still have days of "manic-ness", and I recently refilled my RX. Well, I wasn't supposed to eat my calcium or multivitamin right after the 1 hour time limit is up. My pill regimen is getting complicated again.

I will deal with it.

Tomorrow, I have an appointment at the City of Hope for my "brain test", where they test my chemo brain functioning. Long, hot haul up, and a hotter haul home. It will be interesting to see if they finished that building they started when I was there a year ago.

Well, I gotta go get a kid out of school...

jc