Tag Archives: Bone Marrow Transplant (BMT)

Day 32 – Halfway Home?

32 Days Since Bone Marrow Transplant

It’s been 32 days since my “Birthday” (Bone Marrow Transplant) on June 20th, 2019.  I can understand now why they say that each bone marrow transplant patient is different.  We each handle the effects of heavy-dose chemotherapy, irradiation, immunosuppression, multiple transfusions, and all of the side-effects & symptoms differently.  I can say, definitively, that your outlook and determination has a strong bearing on your recovery. I credit my relative youth and persistence to my quick recovery.

How we address ourselves and our mindset has an immense effect on our health and recovery.  In the our daily and hourly thoughts where we grouse to ourselves that “we’re tired, we’re worn out, this is exhausting” the body internalizes our thoughts, our health and personal energy match our mental attitude.  I have to catch myself in such times when I’m quick to complain or be frustrated with my health and recovery.  I change what I tell myself, reminding myself that I love my family and friends, that they are rooting for me, praying for me, supporting me, and that I so badly want to go home to my family, friends, co-workers, and rewarding job again.

People ask me what to expect with a bone marrow transplant.   I routinely ask oncologists and other patients the same questions.  People are still asking me as patients, families, and caregivers struggling with their own journeys.  This is is my attempt at answering those questions.

Chemotherapy is rough.  You WILL lose your hair, it’s not a matter of IF but WHEN.  If your body image has you loving your hair, try to find and do new things to make it easier for when that time comes. Whether it’s sharp and stylish “dew rags”, a jaunty hat, or a fierce shorn look, try to exert control over your situation and assert yourself rather than being unpleasantly surprised and overwhelmed.

My original hair loss due to maxi-dose Cytoxan involved a Stephen King-esque scene where my hair came off in massive clumps as I showered a week after my first chemo.  I felt like I was going to have a heart attack in the shower as I watched my dark hair come off in clumps in my hands.  I immediately screamed for my wife, we calmed each other down, and I shaved my head after that experience.

Immunosuppression and Irradiation are rough.  You will vomit, dry heave, and have diarrhea.  Prepare yourself for the worst.  Prep a “puke bucket” that will be your friend and companion some days and evenings.  Use anti-emetics such as Compazine, Zofran, and Ativan around-the-clock so that your body has a constant protection against nausea in your system.  You will need to “titrate” (slowly scale yourself back) off these drugs once you know you’re over the worst of the effects of NVD (Nausea, Vomiting, Diarrhea).

Expect swelling, dry mouth, rashes, redness, and sores. Brush your teeth and use mouthwash often.  I use Biotin as a toothpaste and mouthwash with a very soft toothbrush after every meal and before bed.  I use Burt’s Bees and Farmacy Honey Butter on my chapped lips.  I sometimes wear athletic compression socks to deal with my swollen ankles and legs.  All of these effects are due to the chemo, irradiation, and immunosuppression your body is under.

And in other news….

My first 30-day Chimerism Analysis was taken last Thursday, June 18th.  I’m eagerly awaiting the results and to discuss it further with my Johns Hopkins oncology team… hard to believe it’s been over a year since I was first diagnosed with Stage 4 Mantle Cell Lymphoma (MCL), but I truly hope and pray this bone marrow transplant puts me into a full recovery and remission.

Allogeneic hematopoietic stem cell transplantation (HSCT) is an effective therapeutic approach for several hematological diseases. Chimerism studies can be helpful to assess donor engraftment, detect early signs of graft rejection, and monitor minimal residual disease. Currently the most common method for monitoring chimerism following HSCT is by PCR amplification of STR loci followed by capillary electrophoresis. Prior to transplantation, multiple STR loci in both the donor and recipient are analyzed in order to identify loci that differentiate the two individuals. Informative loci are selected to calculate the percent donor and recipient present in post-transplant specimens. This is a rapid, sensitive, and cost-effective method for monitoring chimerism in patients following HSCT.

Day T+6: Of Nadirs and Chimerism

Day T+6 at Hopkins

So today is Day T+6, marking 6 days since my bone marrow transplant on Thursday, June 20th, 2019.  All of my blood lab results continue to plummet, with the likely nadir being sometime in the coming week.  Once it bottoms out, the new bone marrow should begin producing blood product and replace my own immune system, with my numbers slowly improving each day, allowing me to overcome my Mantle Cell Lymphoma.

It didn’t dawn on Vicky and I until today that my blood’s DNA is changing.  Johns Hopkins will perform DNA tests of my blood on Day T+30 and Day T+60.  The DNA should reflect the fading away of my own DNA and the replacement of my donor’s DNA in my bone marrow.  The results of the DNA tests should be fascinating, effectively making me a chimera?!


NATURE: How and when should we monitor chimerism after allogeneic stem cell transplantation?

Chimerism analysis has become an important tool for the peri-transplant surveillance of engraftment. It offers the possibility to realize impending graft rejection and can serve as an indicator for the recurrence of the underlying malignant or nonmalignant disease. Most recently, these investigations have become the basis for treatment intervention, for example, to avoid graft rejection, to maintain engraftment and to treat imminent relapse by pre-emptive immunotherapy. This invited review focuses on the clinical implications of characterization of hematopoietic chimerism in stem cell transplantation.

“Happy Birthday!” (Day of Bone Marrow Transplant)

“Happy Birthday!” (Bone Marrow Transplant)

At 8:04 PM on Thursday, June 20th, 2019, I began the transfusion of an extraordinary gift from a donor I never met. Thanks to his or her loving generosity, I have an excellent chance to beat Mantle Cell Lymphoma.

I am so very thankful to our family, friends, and medical teams at Johns Hopkins and Kaiser-Permanente for making this possible! 💕✌🏻

“Happy Birthday!” (Bone Marrow Transplant)
“Happy Birthday!” (Bone Marrow Transplant)
“Happy Birthday!” (Bone Marrow Transplant)

Last Week Before Hopkins

Sunrise over Sterling, VA

This week was overwhelming.  It began with a bone biopsy and many more blood tests, followed by near-daily visits to Johns Hopkins in Baltimore for a battery of tests, classes, and paperwork.  Yesterday we met with our Hopkins oncologist again, to sign the consent forms for the study, blood products, and to acknowledge the myriad risks throughout a bone marrow transplant and its recovery.

While chemotherapy and radiation therapy make sense to me as two protocols intended to kill fast-growing cancer cells at a faster rate than slower-growing normal cells, much of bone marrow transplants still reminds me of trepanning in how it’s performed, how it works, and all of the side effects and risks a patient need be concerned about.  As the oncologist explained the process, risks, recovery, and possible life-long side-effects, I’m reminded of the analogy of “trying to swat a fly with a Buick.”  Except maybe this is a swarm of flies, and the flies will most certainly kill you.

Being away from home, from family, and friends, is as heart-wrenching and overwhelming as any other part of this process.  I truly hope that I’m able to keep my mental acuity and strength through all of this, and to push myself for a quicker recovery and return home.  Having gone through the last 16 months of chemo, with some of it being very strong and having dramatic side-effects, I think I have a reasonable idea of what to expect when the oncologist and team explained all of the drugs, risks, and side-effects.  I hope I’m able to look back on this in a month and find it true.

I don’t know what I can say.  This week had a lot to take it, and the visuals as I toured the oncology floor and patient rooms didn’t dissuade me or put my mind at ease.

 

Open Discussion with other Mantle Cell Lymphoma and Bone Marrow Transplant Survivors

Ken Foreman, Cancer Combant/Survivor

(Originally posted to Bone Marrow Transplant Survivors as a means of meeting others and discussing Bone Marrow Transplants)

Hi.

I was diagnosed with Stage 4 Mantle Cell Lymphoma (MCL), which is a Non-Hodgkins Lymphoma in February 2018.

I immediately did 6 cycles of R-CHOP (Nordic Protocol) in accordance with Kaiser-Permanente, Johns Hopkins, and NIH. I was briefly in remission for a little over 2 months while doing Rituxan as a maintenance chemo (I declined BMT in favor of Rituxan).

Doing several cycles of Imbruvica-Venclexta showed no response, so I was moved to R2 (Revlimid-Rituxan) which showed progress by its 4th cycle.

Now after 16 months of chemotherapy and postponing my BMT twice, I’m to be admitted to Johns Hopkins Baltimore for chemotherapy and total body irradiation starting June 14th with the transplant on June 20th, 2019.

At 47 years old with Mantle Cell Lymphoma (MCL), it’s been a scary ride this past year. Having read so much about MCL and Bone Marrow Transplants, my wife and I are remarkably anxious about what we suspect to be an ordeal ahead.

Are there there other MCL patients in this group? Any advice you’d give to someone about to undergo an Allo (Non-Related Donor) bone marrow stem cell transplant in 3 weeks’ time?

Preparing for the Long Stay at Johns Hopkins

IV Chemotherapy via Mediport

IV Chemotherapy is difficult: physically demanding, exhausting, and with a list of side-effects depending on your mediport, oncology hygiene, and the effects of the chemotherapy drugs on your body.  Rituximab, Cyclophosphamide, Doxorubicin, Vincristine, Prednisolone, and Cytarabine were all prescribed to me over 6 cycles from February 2018 through June 2018.  They were each administered through a mediport placed in my chest, which I would receive in both in the oncology lab and at home using a portable IV pump.

Prior to my chemo, my wife and I took a couple of seminars on chemotherapy and intravenous (IV) line care.  My wife (Vicky) is already a licensed and registered nurse with multiple certifications in critical care, advanced life support services, and drug administration, but we still attended the courses to see what we’d learn about cancer care and chemotherapy administration.  I’d recommend all of the classes and seminars available to you if you’re about to go through the same.  I can’t say I’m looking forward to Hickman Catheter Care next, but it’s necessary for my stay at Johns Hopkins.  While I attended several classes and seminars on intravenous and intramuscular hypodermic needle injections, I still cannot self-administer but need my wife to do such things for me while I look away.

Since Vicky and I will be staying at Johns Hopkins for a while during the chemotherapy, radiation therapy, bone marrow transplant, and months of recovery, we’ve begun preparing ourselves for the long stay.  We’re both bringing our laptops and tablets to keep us occupied for the months of hospitalization.  I’ll be bringing my Kindle Oasis and Nintendo Switch in addition to my 17″ Razer Blade Pro 4K.  While I won’t be able to play or practice on a piano keyboard, I can still use and play with FL Studio on my Razer Blade Pro.  Vicky will be using her MacBook Pro heavily and reading on her iPad.

My oncologist and transplant coordinator tell me that for 2-3 months I’ll mostly be “out of it” and in little condition (or with little desire) to work remotely or do anything much.  I really can’t imagine being that mentally and physically incapacitated for that long, even if with pain management and medications.  Much of what you see on Facebook, on this blog, and on my wiki, are my efforts to prepare myself for keeping busy while away-from-home and stuck in a bed.  I am truly hoping to keep myself mentally stimulated, engaged, and making the most of my downtime by reading, engineering, gaming, and learning mindful meditation.

Vicky and I have begun organizing, inventorying, and packing 3-months of supplies into bins with heavy-duty handcarts to move them.  Once we’re done preparing, I’ll take pictures and post them along with our inventories and checklists.  Maybe other cancer patients or caregivers might be able to make use of our lists and preparation?  If nothing else, I’m impressed with how prepared and methodic we’re approaching this.

Of all that is going on, it is our two Shetland Sheepdogs, Kiyomi (清美) and Tōshirō (俊郎) that we’re going to miss the most.  Our two beloved pups will be staying with close friends while we’re away from home.  Thankfully Chris and Brad also have a loving family of Shelties, and our two will feel at home among their family.  It is truly going to be difficult for Vicky and I to be away from our little family together with our two “fur-children.”

And so it goes… I hope to emerge on the other side of this healthier, wiser, and in complete remission.  I hope this ersatz cancer journal and my rambling thoughts on how I dealt with and survived cancer will be use or hope to others?

Gallery (click any thumbnail to enlarge)

Administer IV Chemotherapy via Mediport

Home IV Chemotherapy via Mediport and Portable IV Pump

IV Chemotherapy via Mediport

 

Adventures in Cancer and Chemo

Kiyomi, Toshiro, and Korg KROME-88
Managing chemo pain with Kiyomi and Toshiro
Adventures in Cancer
Adventures in Cancer

 

“We have a date for transplant for you: 3/11. Chemo prep will begin on 3/6. Your line will be placed on 3/5. We will begin evaluation tests with Kaiser first starting the week of 2/11. I am requesting that a PET be done first. I am planning for you to be come to Hopkins on 2/15 to begin evaluation tests with us.

Monday February 11, 2019 at Capitol Hill
8:00 AM – Full-Body PET Scan

Wednesday February 13, 2019 at Tysons Corner
8:30 AM – Echocardiogram in Cardiology
9:30 AM – Pulmonary Function Test in Pulmonary 
10:30 AM – Sinus CT in Radiology
11:30 AM – EKG with nurse in Internal Medicine
– Extensive Lab Work
– Pick up Hickman Care Kit from Pharmacy

Friday February 15, 2019 at Baltimore
9:00 AM – Bone marrow aspirate and biopsy with sedation

…and so it begins? I am excited and terrified.

#cancer