May 16th Update

Hi everyone,

Rob has been dealing with severe hip pain. Thankfully, he has been able to get some walking back in after not being able to due to the pain. We are hopeful and hoping it is nerve/muscular related vs bone pain caused by multiple myeloma.

His rib pain where the plasmacytoma is has subsided greatly after the radiation! We’ll get this hip pain under control, and he’ll be back to making even more strides again soon. 👊👊👊

Lambda and Kappa Light Chains

I wanted to elaborate on lab results a bit, but didn’t want to include too much in the last post. I’m trying to break up the information so it’s easier to digest.

In multiple myeloma, there is what is known as Kappa light chain myeloma and Lambda light chain myeloma.

Rob has Lambda light chain myeloma. As such, we look for the Lambda light chain results on his myeloma labs to see how the multiple myeloma is responding to treatment.

The past 2 months, while the Lambda light chains have been normal, his tests identified a Kappa protein.

At Rob’s last appointment, we learned that this treatment he is on can cause a Kappa protein to be identified. If this is the cause, it usually stays small and quiet.

They said there is a specific lab test they will do to see if the Kappa protein showing up on the past 2 labs is simply caused by the new treatment, verses caused by the multiple myeloma.

If it is not caused from the new treatment, we’ll discuss what this means with his hematologist oncologist. This Kappa protein is new to us, and we are appreciative of all we are learning from everyone at LCI.

Depending on that result, plus upcoming labs, will help determine next step as far as bone marrow biopsy. For example, if the Kappa light chain is found to be caused by the medication, and his lambda chains remain normal, then we will proceed with a bone marrow biopsy.

The purpose of the bone marrow biopsy is to see how many multiple myeloma cells are still present. More on the bone marrow biopsy and the significance of this test in a future post.

Up Next:

Rob continues oral chemo at home, and is back at LCI next week for treatment. The next labs are in 2 weeks.

Thanks for being here!!🥰❤️

May 8th Update

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!! ❤️❤️❤️❤️

Radiation Complete

Hi everyone,

Rob completed 5 days in a row of radiation yesterday like a champ! 👊👊❤️

It has helped decrease the rib pain. He says he can tie his shoes and brush his teeth without the pain increasing to a 6 or 7. It also does not increase when he walks right now.

The pain still there at the level where it was before it began increasing in the intensity (a “3”), BUT he has noticed a definite improvement.

We are so grateful for the radiation oncologist, radiation techs, nurses, and everyone else in that department who helped him this past week!

Side effects are hiting hard. Rob has pretty bad fatigue. The lotion has helped with the burning. We didn’t ask about the cooling lotion, because the Lubiderm lotion has been doing the trick.

Next week, Rob will have a busy day back at LCI. He’ll have labs, appointment, then we leave LCI to drive just a few blocks over to the CVS Specialty Pharmacy, where he picks up oral chemo. Then, back to LCI for pre-meds, wait an hour, and then he gets the Daratumumab. He’ll begin the next oral chemo that night, for 3 weeks on, one week off.

The next cycle schedule will change a bit, and Rob will be at LCI every other week for treatment instead of weekly- a welcome reprieve.🙏

We will also learn if Rob’s treatment is continuing to work next week, as they are drawing myeloma labs. They are also going to be scheduling a bone marrow biopsy in May.

Thank you for helping us keep pounding, your support, and your tips!

To anyone else facing challenges as well, Keep Pounding!!!❤️❤️❤️