Hi everyone-
We just Rob’s Lambda light chains (myeloma markers) back and they have decreased by 98.96%!! 👏👏👏👏🎉🎉🎉
It is the LOWEST it has been since his multiple myeloma diagnoses!!
We are so happy and wanted to share!
I’ll update this post with M-Spike results when they come in.
Thank you for being here!!❤️❤️❤️❤️
Hi everyone,
We are seeing some improvement!
Thank you for your words of encouragement!!
His appetite is improving. He is still fatigued and very pale. I’ve noticed some breathlessness (like getting winded more easily), but oxygen is normal, thankfully.
We are keeping his doctor in the loop on everything and hoping it was just a hump to get over.
Two of his labs from infusion last week (non-myeloma labs, just regular infusion related labs) were elevated more than normal and marked as high. We’ll get more details on whether those are playing a role in this.
The next myeloma labs will be the week after next. They will also be scheduling scans of his ribs to check on his rib lesions. Finally, they will be scheduling a bone marrow biopsy as well.
Please continue to pray for his energy to return, and the paleness to go away. I feel like we made progress this afternoon and evening, and hope everything else falls back into place.
Thank you for your prayers, support, and love! ❤️
Hi everyone!
Time to celebrate some wins! 🎉🎉🎉
This morning. Rob was able to get some exercise in for the first time in over a month! He waked 1 mile!!👊👊🎉🎉🎉
He also had no rib pain when doing so. This is HUGE!! 🎉🎉🎉🙏🙏
Also, Rob’s myeloma labs came back, and look good. The lambda light chains (myeloma markers) did show an increase, but they are still in the normal range.
We believe fluctuations that remain in the normal range are just –normal. When they begin to spike routinely (like what happened earlier this year) is the sign of myeloma activity. They are re-checking these in 1 month.
Rob has graduated from having treatment weekly at LCI to going every other week, and he continues the chemotherapy at home nightly.
We are thankful not to have to be at LCI every week. We are incredibly grateful for all they are doing at LCI to help Rob Keep Pounding! 🎉🎉🎉🎉🙏❤️
Thank you for all of your words of encouragement and support!! ❤️❤️❤️❤️
First- AMAZING news!! Rob’s lambda light chain markers are NORMAL!!
This is after 5 weeks of treatment, which continues for cycle 2. Since Rob has lambda light chain myeloma (vs kappa light chain myeloma), these markers let us know how the multiple myeloma is responding to treatment.
We are absolutely elated by this!!
He began cycle 2 this week. This will be for 4 weeks in a row. The 3rd cycle will be a bit more spaced out, and I’ll update about that closer to time.
To clarify- this treatment protocol is what he will remain on until the next relapse.
This is what is unique and challenging about multiple myeloma, in that it continues to evolve, becoming resistant to drugs like it did to the last treatment he was on. As a result, he won’t be on this for “just a few more cycles.”
Since it is thankfully working, he will be on it until the next relapse. We are extremely grateful for the number of treatment options available now vs in the past!
Other updates:
They are scheduling a consultation with the radiation oncology team to see about doing radiation on his ribs.
His pain has increased there big time, and is now constant.
An x-ray done this week showed 2 areas of concern, which we think are consistent with multiple myeloma, based on the lab report indicating as such.
1 rib we knew about (rib 2), but the report mentioned rib 11, which is new.
They will be closely monitoring these areas with imaging and testing as Rob continues his treatment.
Another result that came in last night was high protein from the 24-hour urinalysis. It was high last month, and has increased again. This will also be closely watched.
Thankfully, his other labs look amazing!!👏👏👏👏
We want to share the entire picture for those also going through the process, and to keep everyone on the same page. 🙂
There is so much we are learning about being in a clincial trial. We will work on that for a future post to share with anyone else considering a trial.
A HUGE thank you to everyone who has been so incredibly supportive through this!! We are beyond fortunate to have such an incredible Keep Pounding team on our side.
Thank you!!🙏❤️
For anyone else facing challenges, Keep Pounding!!👊👊❤️❤️❤️
Thank you so much, NB family and JS family, for this amazing painting and encouraging words!!❤️❤️❤️
Hi everyone,
It has been a week of adjustments, and Rob continues to Keep Pounding despite the challenges.
He has had 2 treatments at the clinic (the Daratumumab and Dexamethasone, along with pre-meds before) last week and yesterday. He takes the Pomalidomine every night at home.
I’m going to explain the side effects and what we are doing to try and help them.
1. Excessive dry mouth and throat, which has led to trouble talking longer than a few sentences without coughing, sounding hoarse, or having to drink lots of water.
2. Increased heart rate
3. Increase neuropathy pain
To help with this, here is what we are trying thus far:
For the dry mouth and throat/hoarse voice: We are using humidifiers, as I read about this from other cancer patients experiencing similar dry mouth/thorat/hoarseness symtoms. Rob thinks this is helping.
He has a dry mouth spray, and dry mouth rinse he is trying, which I got yesterday after talking with the PA and clincial trial research nurse. He said the spray works for about 45 minutes. We are trying a different spray when it arrives tomorrow.
The ones he has now are small bottles, making it easy to take with him. I’ll update on how that is working soon, in case it can help anyone else as well.
For the increased heart rate, they are monitoring it carefully. Thankfully, today, the day after treatment, his resting heart rate- while still high–is lower than last weeks resting heart rate the day following treatment, which is huge! We hope it continues to improve.
For the neuropathy, we are increasing his visits to acupuncture at the Supportive Oncology department at LCI. This has helped in the past, so they think increasing it will help again.
Along the neuropathy lines, Supportive Oncology recommended a compound cream. We have to run it by the trial nurse (pretty sure it is ok, but when in a trial, you run everything by them).
They said that the pharmacy gives you paperwork to file for insurance for this compound (they don’t file). I’m mentioning this in case anyone else dealing with neuropathy comes across this as an option. I’ll update as we learn more. I have heard great things about compounds for neuropathy from several people, and we hope it helps Rob as well.
If anyone reading has a tip for helping hoarseness/dry mouth and/or neuropathy pain, please reach out to me (Brandii), or leave a comment. Thank you!
Rob is handling these side effects with determination and grace. His attitude, spirit, and drive are simply amazing.
Thank you for your love and support!!
For anyone else facing challenges, Keep Pounding!!❤️❤️❤️
Hi everyone,
First, Rob’s resting at home and is doing good, considering everything he’s going through. I wanted to start with that first, and then give a lengthy update.
Rob completed day 1 of the clinical trial yesterday at LCI. This arm doesn’t require hospitalization, thankfully.
The trial is randomized, and the arm he was selected is Daratumumab, Pomalidomide, and Dexamethasone (DPd). This is also the same treatment he would have been on if he hadn’t entered the trial.
There are no placebos in their clinical trials- you are either in the experimental arm or the standard arm. So Rob is in the standard care of treatment arm.
We were at the clinic from 7:00 am until 8 pm, making for a really long and incredibly anxious day. But, it is over and all is well right now.
Here’s a (lengthy) recap. Excuse typos.
They did labs first thing at 7:15, then appointment at 8. We then had a 2-hour wait (you can’t check into infusion more than 30 minutes before your infusion, understandably). Thankfully, they have a Keep Pounding lounge with comfortable chairs and snacks, which is a good option for waiting in between appointments. They also have plenty of seating outside the infusion suite. – mentioning this as we have some newcomers to the Keep Pounding Rob blog who are also new to LCI. Keep Pounding!!
He checked in to infusion at 10:30, but then got a message while in the waiting room, saying his bilirubin and bilirubin direct labs were high, and this may delay treatment. This was unnerving to hear, to say the least. While they were slightly elevated by .1 from last week, they were up by .1 this week. When they called him back to the infusion suite, we were hopeful and nervous at the same time.
Thankfully, his hematologist oncologist advised him to drink lots of water and retest. He literally “Kept Pounding” many bottles of water they kindly offered, and the second labs met the requirement to proceed.
It is important to note that had it not been for the trial, Rob probably would have been able to go ahead with treatment to begin with, despite the level being slightly elevated (barely high). This was just a trial protocol that had to be met.
If needed for any reason, Rob can withdraw from the trial at any time, as his treatment would remain exactly the same, without the trial protocols in place.
This is something we are keeping a very close eye on as we proceed, and we are so grateful to his AMAZING hematologist oncologist and nurse extrdoinare for doing the same. These two individuals are amazing in their knowledge, help, and advocacy. ❤️❤️❤️
After he got the ok to proceed, he had the premeds (including the Dexamethasone), then had to wait an hour, then they administered the drug Daratumumab.
After receiving the Daratumumab, he had to be observed for 6 hours, due to the possibility of a reaction. Going forward, he won’t have this long of a wait after receiving the med. There will still be observation, but not near as long. Being it was the first time getting this drug, we were thankful to have that observation, just in case something had went wrong.
He will begin taking the oral chemo, Pomalidomide at hone every night.
The Pomalidomine makers advises you shouldn’t operate machinery (like driving) after taking it. We are beyond thankful (once again), for his hematologist oncologist said taking it at night was a good idea with that in mind. It is important to take this medicine at the same time each day.
Rob is feeling tired, as he didn’t sleep well with Dexamethasone from yesterday. He is also coming off of 4 nights of not sleeping due to anxiety. However, he thinks another night of two of getting better sleep will help.
The Supportive Oncology department (formally known as Palliative Care) gave him the ok to increase his sleep medicine. Hopefully, trying this will help get him back on track for regular sleep soon.
We are grateful for everyone on his team at LCI, and appreciative of their help with this multiple myeloma relapse and treatment, from his doctor and nurse, trial nurses, infusion nurses- everyone. ❤️🌻🌷
We have more to add, but wanted to give a recap of yesterday first.
Thank you for helping Rob Keep Pounding!❤️❤️❤️
Rob is scheduled to begin the clinical trial next week, at least according to the patient portal (pending final trial approval).
However, we have no idea which arm of the trial he is scheduled for, but hope to know that soon. 2 of 3 arms requires hospitalization to monitor side effects, the other two do not.
We are anxious and ready to begin the new treatment.
It’s definitely nice to see treatment appointments scheduled on the patient portal beginning next week. I should have more info soon, and will update as soon as I do.
We are at LCI now for a few extra labs he needed for trial.
Thank you for your love and support!
We learned Rob’s multiple myeloma (the lambda light chains lab result) continued to spike, which we expected.
We also learned that his 24 hour urine test showed the lambda light chains present. We don’t know the significance of this, but when we do, I’ll update here.
Now we are just waiting on the bone marrow biopsy results. No matter what it shows, he will still be going in the clincial trial- I believe they just have to wait on the result before starting. If I am wrong on that I’ll correct that info.
The pics below are screenshots from the patient protal. They provide visuals of Rob’s lambda light chains. These are the light chains that indicate myeloma is back.
It’s important to note that some with multiple myeloma may have kappa light chain myeloma, where they would be more concerned with kappa light chains. Since Rob has lambda light chain multiple myeloma, we are concerned with his lambda light chains.
To help visialize, I’ve added two screen shots from the patient portal, which show what his lambda light chains have done the past few months.
Chart 1: You can see that the middle row, “Free lambda light chains” reads 131.82, far from the normal range of 5.71-26.3.
Chart 2: Starting at the bottom, November 2023, you can see how much and how fast the lamnda light chains have jumped.
We will update you when we have more information to share about the expected start date of the clinical trial (probably within 1-2 weeks). Once we know which arm of the trial he is in, I can provide more information on that.
Thank you so very much for being here! ❤️❤️❤️❤️
Happy Leap Day! 🙂
Today was a long day at Levine Cancer
The first appointment consisted of more paperwork for the trial, and he turned in the 24-hour urine test.
This appointment also answered our questions on the PET scan- if Rob gets cleared for the trial (including labs/bone marrow biopsy results)- he will likely not need a second PET scan since he had one recently.
If for some reason he doesn’t meet the criteria on labs, then he will probably need a second one in the future.
Finally, they did a neurocognitive test, and checked his handwriting by having him write a sentence.
The reason for this is because the drugs can cause neurocognitive difficulties. These tests establish a baseline of what his neurocognitive status and his handwriting is now verses how the meds impacts it once he begins treatment. Thankfully, they said side effects are temporary.
Much more to come on this as we learn which arm of the trial he will be going through, and potential side effects. Ya’ll are learning right alongside us, and we are so appreciative of that!❤️
Next up, we had some time for a picnic lunch in the car, and a brief visit in the Keep Pounding lounge. It provided a much needed quiet place to relax in very comfortable chairs.
Next was labs (22 tubes!), and then we returned to the hematology floor for the bone marrow biopsy. I’ll update our blog as labs and biopsy results come in.
For anyone else facing any challenges, Keep Pounding!!
Thank you so, so much for all of your support and love! ❤️
Hi everyone,
Thank ya’ll for being here!❤️
The pre-screening scheduling for the clinical trial has started, with many tests being ordered.
The patient portal shows 34 upcoming tests, many of which are labs.
In addition to the 34 tests scheduled, he will have pre-screening tests in cardiology, pulmonary, skeletal imaging, and a PET scan. Since he had the PET scan recently, we don’t know if that will be scheduled before or after the first round of the trial.
24 hour urinalysis test will be done next week, along with a bone marrow biopsy, labs, and an appointment with his hematologist oncologist.
The fatigue has been increasingly worse. We are wondering if his platelets are low, or if it is from the multiple myeloma coming back (one of the symptoms), or both. We look forward to labs next week to see if they can pinpoint anything that would be a cause.
This is the hurry up and wait part, as he goes through the clinical trial pre-screening process. I will keep updating along the way, and hopefully, I can begin writing about the next line of treatment soon.
We appreciate your love and support through this so much! Thank you!!
For anyone else facing challenges, whatever those challenges are, we are here for you too-please don’t forget that! 🙏❤️ Keep Pounding!!❤️👊
Keep Pounding Rob! 