Viactiv and Myeloma

Okay readers let’s turn up the fire on discussion….

So while eating my lunch from home- spaghetti and turkey meatballs, I popped a chocolate known as Viactiv Calcium Chews-500mg.

Viactiv is a small chocolate supplement for calcium consumption. The popular television commercials had stated just 2 will give you your daily calcium needs, and as myeloma patients (or I hope most of you are aware) we need that Vitamin D and calcium to assist in maintaining stronger bones, as this is one of the dire consequences of myeloma. On my last MRI found small hints of lesions at my pelvis, and since I take Vit. D supplement presently – why not try this as well.

Well during the lunch I mentioned my brief search on internet made me choke on the supplement- when I came upon Medsfacts.com study on Viactiv and multiple myeloma a side effect of Viactiv… I was utterly confused and quite concerned, considering- “Well I have MM, but will this chewable affect me further negatively??” I became so nervous and as any concerned patient would do called my doctor- That’s another story- but my decision after spending $15 for this case of chewables was to cut my lost. Considering I have issues there’s no need to make the situation worst- better yet what is the real deal on this viactiv? I’ve been taking this for about over a month - 1 every other day- not really too consistent. I have noticed some headaches, which is a side effect, but that could be a number of reasons- or could it

Viactiv is defined as VIACTIV® Soft Chews bone-strengthening formula gives you the power of calcium, vitamin D and vitamin K all working together to benefit your bone health.

Anyone else tried this? What have been your experiences? Let’s chat….

Comments

Childrens Book on Multiple Myeloma

I've found I can talk with an adult all day about life with a multiple myeloma diagnosis, some get it, some are still clueless...it is what it is. Multiple Myeloma is relatable for those who are on their own journey, or those who have had a family or friend who was taken from them because of it. The conversation around cancer with young children holds a certain complexity. The question arises, should you say anything about it with small children as opposed to older children? How do you start the conversation? Is it necessary to be so candid with subtlety? After being diagnosed myself at an early age, and found myself in need of my own comfort in bringing on this conversation. Follow my journey as I start promoting my new book...title to be debuted at a later time on my social media page -Instagram @myelomachick . Whether having small children, grandchildren, nieces, or nephews...How have you shared your story with multiple myeloma? Y

Explaining Multiple Myeloma to Children

We always think about how an adult processes the news of cancer; However, what about a child? A young one at that... During Multiple Myeloma Awareness Month , I will launch a children's book titled " Mama's Blood is Purple and Pink" and discuss how to address the elephant in the room, such as cancer. I've written a story of how the conversation can go without it being scary for a child, when it can be, and is a scary experience. Debuting end of March 2026. Preorders available here We're also looking at Guest speakers to join the conversation here Further details will be shared on my Instagram page or website

Still Kicking and Moving All Around

Hey Everyone, I'm doing well on this end. I'm currently in remission, and my follow-up next week will actually reconfirm that. We will also discuss the next steps. A lot has taken place this year and I'm just moving with the flow of things. I've been doing my share of writing via different formats online, so I'm excited about helping those also going through myeloma or any other blood-related cancer. I know this is still a harsh struggle for so many of my fellow MM's. I know in the past few months a few people I follow on social media have had a time with the prognosis of their disease, and one has recently passed away. When I hear stories like this it reminds me, that no matter remission this is still a blunt reality that never leaves you. I will always be on pins and needles, as so many of us living this new life. However, with that said I'm LIVING MY BEST LIFE and doing what I want to do, with a great bunch of friends and family in my corner. Chec...

Another Face..... Of Multiple Myeloma

Search This Blog