Author: Beth

I was diagnosed with MM in January of 2003. I underwent various treatments, including thalidomide/dex, revlimid/dex, dex alone, a clinical trial of CNTO 328, and Velcade, Doxil and dex until late August, 2007, when I had an autologous stem cell transplant after high dose melphalan. I experienced what's known as a very good partial response (VGPR). Since then, my myeloma has been stable.


If you’re reading this and don’t have cancer, I recommend the AFLAC cancer policy. I don’t know what possessed me to get this for myself, but I’m glad I did. AFLAC pays money to help cover costs by sending checks for chemo and trips you might make to get a second opinion. So far, they have covered my bone marrow biopsy, each month of Zometa/Aredia, Thalomid and dex. It doesn’t pay for everything, but is intended to provide supplemental coverage. It’s paid directly to you, not the healthcare provider. For example, each month I have received a check for $300 for my Thalomid rxes. I have also received $300 for each of my Zometa infusions. Whatever I paid in was well worth it. I hope I don’t ever need it, but I also bought the long term care policy (AKA nursing home insurance).

My AFLAC rep’s sister has MM.

AFLAC’s web site

Water tested

I sent my water off to a national testing lab for a complete analysis (bacterial, mineral, etc). The results came back, and the only abnormality detected was low pH. I’ll be getting a water treatment system to resolve that. I’ll also get a countertop distiller to use for cooking and washing vegetables. I drink bottled water, but may use the distilled water for drinking too. It’ll save some money on water delivery.

Waterwise Distillation Products

Buying time

All along I’ve thought that I need to hang in here for a few years until researchers find a way to manage MM as a chronic disease or there’s a cure. Bob Meyer just posted something on the MM list that is encouraging. There are many of us who have the same optimism and are doing what we can to keep our disease under control with as little damage to ourselves as possible. Bob’s email to the list follows.

—– Original Message —–
From: “Robert H Meyer”
Sent: Saturday, May 24, 2003 9:21 PM
Subject: [MM] A note of serious hope

Hi All,

Having, like so many of us, taken on the very depressing task of mentally
acknowledging the passing of “Aussie Pat” and Violet Kimball’s husband,
Stanley, and then having sent painful and upset emails to both Chris and
Violet, I decided it was well past time to once again prowl about the
internet to see how things are progressing on MM research.

What I found is extremely hopeful and actually goes well beyond what I had
expected to find. Much of the primary mechanism that “makes MM go” has been
unraveled and moves are well underway to develop methods to disrupt the
vicious cycle of MM cell growth and bone resorption that characterizes most
MM. I won’t go into technical details at this point as I want to keep this
post short and to the point. In any event I have posted some of them
several years ago when they were first suspected. The main thing is that
much has been verified and fleshed out in the last three years so now there
is near certainty about much of the way MM escapes natural controls.

If anyone cares about the technical details, I will post a review (hopefully
in nearly plain English) of what is now known and what is being done. If
anyone wants to see the abstracts for themselves, one good way is to use the
PubMed search engine with the key search directives “OPG AND myeloma” and
“RANK-Fc AND myeloma”. What you will find is extremely uplifting (assuming
you can digest the highly technical terminology).

My main message is that what I am getting from the abstracts is the very
definite impression that some of those on this list who can manage to beat
back their MM for just another few years may quite possibly (I want to say
“likely” but am trying hard to be cautious) outlive their disease. Yes,
there can always be some unexpectedly nasty side effects to the treatment
ideas now being pursued and that could of course lead to disappointments and
some delays as treatment details are further refined – but barring all that
I think the medical community is extremely close to being able to halt the
MM growth cycle in most cases. They don’t yet know what triggers MM, I
think, but they do know an awful lot about how it maintains itself once it
gets started.

Just my personal opinion of what I’m reading in the research abstracts, of
course. I try hard not to be a prophet of false hope but I really am very
impressed at what the medical researchers have managed to figure out about
MM and the way the body loses control over MM cell growth. I certainly
believe that we will very shortly be seeing another new generation of very
promising anti-MM drugs entering the clinical trial gates.

Best wishes all,

Bob Meyer in San Diego county
NO formal medical training but former caregiver to wife (Patricia) dx’d rare
extremely aggressive IgG kappa MM with plasmablastomas and M-spike of 1100
in 4/98, died 11/98 at age 52; prev. MS history; also hepatitis, severe mono

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ePocrates for PDA

If you have a Palm Pilot, you can download a free version of ePocrates, which can be quite handy. It’s like a mini PDR, containing all the pertinent information about drugs. You can select all the drugs you’re taking, and it will display the drug interaction precautions as well. Another nice feature is the insurance formularies. When installing, you select your insurance company, and you’ll be able to tell if the drug is covered by them.

UNC Appointment

I called the University of North Carolina (UNC) for an appointment with Dr. Robert Orlowski and left a voicemail message, but nobody ever called me back. In today’s mail was an appointment card! I’m curious about how they got my address. All I did when I called was leave my name and telephone number. (The phone number is listed under my company name.)

I am hoping Dr. Orlowski will be my local oncologist, since he has a lot of experience with MM. Chapel Hill is about an hour from here. I’ll feel more secure if I can have a doctor who is up on the latest research in MM. I do want to continue to have Aredia at the local hospital though. As far as I know, there’s a standing order for it, and changing doctors shouldn’t nullify that. I’ll have to ask though.

Wouldn’t you know it, the appointment is for the day I’ll be leaving to drive up to Boston for my appointment with Dr. Richardson at the Dana-Farber?

Good news!

I just had my first serum immonufixation and protein electropheresis done since I started dex and thal on April 4th. The results are encouraging. My local onc says much improved and we’ll stay with current rx.

I have the lab report posted at LABS. You can compare the January test to the May test to see how much of an improvement there’s been!

Dex day, oh yay!

Monday was my dex day. I got mad at my kitchen utensils and put them all in the dishwasher, washed the dividers and cleaned out the drawers. One of the utensils was too long, hitting the top rack of the dishwasher, so I was wishing I had a saw. Good thing I don’t.

So now it’s 2:00 am, the next day. I’m still up, and don’t want to be. Luckily, I have nothing scheduled. I can sleep in!