Want to talk about Multiple Myeloma: Anyone else?

It is great to hear a lot of walking opportunities since he walks or bikes almost every day. The doctor made it sound like he has to be with me 24/7!

Jump to this post

My husband is an avid walker/biker too and he was never bored while in Rochester for our 4.5 month stay. The trail system is great along the Zumbro river, Bear Creek, walking through neighborhoods and parks.
It’s a medium sized city with so much geared to the Mayo community. Very easy access off the highway so there’s absolutely no big city-white knuckle driving.

As for being with you 24/7…well, in truth your husband will need to be tethered to you pretty closely, especially the first 2 weeks after your autologous transplant. In my own experience that first month for my allogenic transplant (not using my own cells) I wasn’t (and couldn’t be) on my own very much. But even then, if I was was feeling ok or napping, my husband felt confident in heading out for a good hour or so. Plus, as I’m sure you’ll be, we were linked with cell phones in case I needed him.
This isn’t a walk in the park for you, my dear, so he’s going to need to be a direct part of your transplant journey. This time will pass quickly and you’ll be back home soon enough.

I’m working on a post right now for transplant patients who need to be in Rochester for long term care. It includes lodging ideas, what to bring, how to plan. I’ll post it within the week and let you know. I think it will be very helpful to anyone facing longterm stays at Mayo.
Do you have any specific questions for me right now that I can address in my post??

Jump to this post

My husband is an avid walker/biker too and he was never bored while in Rochester for our 4.5 month stay. The trail system is great along the Zumbro river, Bear Creek, walking through neighborhoods and parks.
It’s a medium sized city with so much geared to the Mayo community. Very easy access off the highway so there’s absolutely no big city-white knuckle driving.

As for being with you 24/7…well, in truth your husband will need to be tethered to you pretty closely, especially the first 2 weeks after your autologous transplant. In my own experience that first month for my allogenic transplant (not using my own cells) I wasn’t (and couldn’t be) on my own very much. But even then, if I was was feeling ok or napping, my husband felt confident in heading out for a good hour or so. Plus, as I’m sure you’ll be, we were linked with cell phones in case I needed him.
This isn’t a walk in the park for you, my dear, so he’s going to need to be a direct part of your transplant journey. This time will pass quickly and you’ll be back home soon enough.

I’m working on a post right now for transplant patients who need to be in Rochester for long term care. It includes lodging ideas, what to bring, how to plan. I’ll post it within the week and let you know. I think it will be very helpful to anyone facing longterm stays at Mayo.
Do you have any specific questions for me right now that I can address in my post??

Jump to this post

Dear Frazer 1 (and any other MM patients, family members, and caregivers),

I am a 58 year old woman who was diagnosed with Multiple Myeloma on June 15th, 2000, only three weeks after graduating with my Master's degree in Counseling (at age 46). I was in the later stages of the disease: I believe Stage B4 would be the correct term? My skull, spine, ribs, upper arms, pelvis, and femurs had tumors. I seriously don't know how I managed to work 20 hours a week and go full-time to graduate school and STILL graduate with a perfect 4.0 (simply bragging here, folks!)

The main point of my reply is the date of my diagnosis....JUNE 15th, 2000... over TWELVE YEARS AGO. And, after having having a double "mini" transplant (my own stem cells and my sister's stem cells) at Fred Hutchinson Cancer Research Center in Seattle, I am STILL IN REMISSION. More good news: last June I went to a reunion weekend at "The Hutch" as we Hutch patients call it, and I met a woman who had had a FULL stem cell donor transplant and SHE was still in remission after FIFTEEN years.

When I was diagnosed in 2000, the blankety-blank hematologist/oncologist (now HE is another other story) informed me I had only eighteen months to two years to live. I wasn't willing to accept that so I started making phone calls to the nearest big medical centers (not being close to the Mayo Clinic). One call led to another and I found out that I had a lot more options than I thought. M.M. wasn't the "terminal" cancer I had been told it was. Yes, there is no specific "cure." But at least I had a chance.

What to expect...it depends...it depends on the specific treatment, on your individual body, and your attitude...and (I can't believe I'm typing this) prayer. Research has shown that patients who were prayed for had statistically significant improvement over patients who weren't prayed for...and these patients were not aware they were receiving organized prayer.

NUMBER ONE: YOU MUST ABSOLUTELY GET ANOTHER OPINION and ADVOCATE FOR YOURSELF. iF you are too ill and/or overwhelmed to do so, assign tasks to your family and friends...doing something for you will aid in their feeling helpless and out-of-control. For example, my brother took care of all the research for me, since "chemo brain" reduced my computer skills to a big fat zero.

NUMBER 2: You need to talk to your oncologist or G.P. about being on blood thinners. It is part of the recommended treatment but one that my blankety blank oncologist didn't bother with and it almost killed me. M.M. patients throw clots. Clots cause pulmonary embolisms. P.E., can kill a person. Watch out for the blood thinner cumadin (warfarin)...I had real problems with it working not enough and then way too much (another near death experience). The "Hutch" put me on daily Lovenox shots, which worked much better with my M.M. body.

NUMBER 3: HYDRATION!!! HYDRATION!!! HYDRATION!!! The Hutch recommended 3 litres of fluids a day (that includes coffee, tea, watermelon, whatever). I couldn't manage to do anywhere near that amount it orally, so for almost two years (due to complications) I had IV. fluids using my central line. I went through 4 months of V.A.D. chemotherapy plus the transplant chemo regimens. Thanks to the fluids, my kidneys are normal! Even though I still need to take meds for other cancer related side-effects (like Addison's Disease) my kidneys are handling all of them! NOTE: My caregiver was a hospital respiratory therapist, very experienced, and she went to war for my fluids. I'll never be able to thank her enough.

#4 Diet: Yes, I tried the super healthy cancer diets and vitamins and naturopathic supplements. They simple made me throw up. And the nutritionist at the Hutch did educate me on good nutrition, but I was just one of those patients who threw up at the blink of an eye. I got very good at it, and could even knit and barf at the same time! Hey, you HAVE to develop a good sense of humor if you don't already have one. The nutritionist finally said, "Eat anything, whatever you can keep down, and don't stress about it."

#5 Exercise: IF YOU DON'T USE IT, YOU'LL USE IT. Even one or two days down can cause muscle wasting (and blood clots). I tried to walk as much as I could...1/2 to one mile almost every day that I wasn't in the hospital, and then I walked the halls if I could summon up even an ounce of energy. I used a walker, which helped support my back. It was an exercise in courage as well, as it was the last thing I wanted to do. The pool was out because of the transplant issues and central lines.

#6 Support: I tried the local women's cancer group, but I was the only one there without breast cancer. No one could even relate. I didn't even get to talk to and MEET anyone else with MM until over a year after my diagnosis, when I started a support group myself after being discharged from the Hutch (The transplant program is out-patient, but you have to be in the area, within half an hour of the clinic and hospital, and my transplants took about 8 or 9 months.)

That being said, finally getting some support, getting some questions answered, and being able to GIVE support to other patients, was so very, very helpful.

I'm not going to kid you. The M.M. journey is long and arduous...that's the truth. There is no pink ribbon for us, no M.M. "month." (M.M's ribbon is burgandy--not a widely known fact.) While I would be happy to tell you more about my personal experience, side effects they didn't tell me about (or I didn't remember or hear), and the length of time the healing process can take, it would only be that...MY experience. Everyone is different. "It depends" is a phrase you will hear again and again. Just know that I am happy to be available to M.M. patients who are just beginning their journey with this weird disease, or who just need another M.M. survivor to talk to. I am grateful for my counseling skills and grief therapy training as they helped me manage my healing process with a positive attitude and a grateful heart (or so I've been told). And, while general cancer support groups have their place, M.M. is a unique experience. Check with the M.M. Foundation and find a support group close to you. Not a support group person? Feeling too ill to make it to a meeting? Online support and informational telephone "conferences" are also available. Thank Heavens for the Internet!!! And if you would like to message me with questions or you just need to vent, I would be happy to offer anyone (patients, caregivers, family members) the support I so dearly wished someone had offered me and mine way back when.

Stay positive, laugh, and learn to knit or meditate (actually knitting has been found to have the same beneficial effects as meditation)!!!

Karen

Jump to this post

I would like to add that if you are on FB, there are numerous Multiple Myeloma Groups. I have learned a great deal from posts on it. It is always good to learn from actual patients/caregivers. Just FYI. It sounds like you have done a wonderful job of taking care of yourself. God bless you.

Jump to this post

I would like to add that if you are on FB, there are numerous Multiple Myeloma Groups. I have learned a great deal from posts on it. It is always good to learn from actual patients/caregivers. Just FYI. It sounds like you have done a wonderful job of taking care of yourself. God bless you.

Jump to this post

<p>I have been diagnosed with MM stage 1. I am considering treatment at Mayo Clinic. <br /> The challenge is that I live in CA. If there are any out of town folks who have been treated at Mayo I would very much like to hear the pros and cons that you experienced and how it worked.</p>

Jump to this post

I am in So Cal too and will get bone biopsy to confirm or reject MM Dx. Multiple doctors ordered PETCT and dozens of Blood tests and are very suspicions of MM. If positive for MM then I wish for Mayo clinic oversight of my local Dr treatment plan and treatment itself. Is this done through staying at Mayo or is remote Telehealth practical? Who are the MM experts at Mayo? Will Original Meficare pay for Mayo and the treatments themselves? What is the on campus housing situation?

Jump to this post

I am in So Cal too and will get bone biopsy to confirm or reject MM Dx. Multiple doctors ordered PETCT and dozens of Blood tests and are very suspicions of MM. If positive for MM then I wish for Mayo clinic oversight of my local Dr treatment plan and treatment itself. Is this done through staying at Mayo or is remote Telehealth practical? Who are the MM experts at Mayo? Will Original Meficare pay for Mayo and the treatments themselves? What is the on campus housing situation?

Jump to this post

It does make one so anxious to be in diagnostic Limbo. When I first heard Multiple Myeloma mentioned as a possibility I consulted with Dr Google while I was waiting to get a hemotology/oncology appointment. Dr Google is big on worst case scenarios, it seems. That increased my anxiety a lot and I felt so lousy. I had trouble sleeping and lost 10 pounds before my first appointment.
I have, thankfully, an excellent HEM/Onc doc who spent lots of time explaining my bloodwork, what was good and what they would watch. I asked lots of questions and he was quite patient with me.
Once I had more balanced information I calmed down and immediately felt better.
Try to relax and do the things you love. I am wishing you the best possible outcome from your diagnostic workup.

Jump to this post