Hi Everyone,
It’s been awhile since I’ve posted, as everything is generally stable with me. After watching my mother and friends her age suffer with shingles, I asked my oncologist when it would be appropriate to get the first dose of the Shingrix vaccine, as it is very effective and I definitely don’t want shingles on top of MBC and Type I Diabetes! Anyway, I got my first Shingrix on Tuesday this week. I just started my first week of the monthly cycle of Ibrance, so the oncologist said my counts were great and to go for it. I got a whopper of an immune response, with aches, pain and redness at the injection site, severe fatigue that began about 11 hours post injection and stopped at about 28 hours post injection. I was happy about this, as it means I have a robust immune system! It made the Pfizer mRNA booster reaction seem like a dish of ice cream by comparison. I felt good after about 30 hours, then noticed that I have what looks like evidence of some chicken pox, 4-5 marks on each inner elbow crease, and a few spots on my knees—both on the vaxxed arm and the unvaxxed sides. I don’t have skin problems, generally. I am 50 now and I remember having Chicken Pox when I was 6 years old.
My oncologist said to stop Ibrance until the marks subside and the injection site calms down (it’s still red and itchy—while pox marks are not itchy nor painful at all). The Shingrix literature says that this reaction can happen among 1/10,000 people…but, not much other info is provided.
My question is, has anyone had the Shingrix vaccine while being treated for MBC? What was your experience? If so, how was your second injection and when did you receive it? I’m really trying to understand if this reaction with the ‘rash’ is common among MBC community members, or if it’s just another doorway into my very bizarre immune response. Another learning opportunity?
As always, you all are amazing and I appreciate any experiences you may have.
Many Blessings to you All!
JeniMcC