How I was diagnosed with Multiple Myeloma: Multiple Myeloma Symptoms & Treatments | Cancer Journey 

Hey girl hey!!! I’m just found out about this, so proud of you for not giving up and being knowledgeable about your sickness! It’s very important and let’s me know you’re still fighting!! Praying for you and supporting you in any way I can!! 🙏🏽💪🏽💐❤️

I just found this Krissy. I have been following your 30 day walking journey. I hope you are ok and you kick cancer's ass! I will be rooting for you! Internet strangers got your back! ❤🙏♥

Thank you for sharing your journey. So happy to hear you’ve continued to be in remission. ❤

Your video appeared in my algorithm today (September 29, 2023). I was diagnosed with multiple myeloma (MM) in July 2021, but for 12 years, my blood was monitored every six months because I had MGUS (monoclonal gammopathy of undetermined significance - a precursor to MM. My initial MM symptoms were excruciating lower back pain and rib fractures. I definitely can relate to your story about the bone marrow biopsy. It is the worse and I had two. The second one came two weeks before last September’s (2022) stem cell transplant and that biopsy was without pain medication because of a shortage at the hospital (The James at Ohio State University). My stem cell transplant was successful so far as no MM was detected in my body so I was deemed in remission. But a couple of months ago, I started having extreme pain in my left femur. I thought I strained a muscle because I walk extensively every day. But this pain is only getting worse. So I will soon have a whole body MM survey. I had not heard of scan anxiety, but I’m definitely feeling a lot of anxiety because my fear is that this pain could be bone cancer. I have a great support system. My husband has been wonderful throughout this whole journey and I have maintained a positive attitude. But the feelings I have right now are different. But I’m hopeful that I will get good news. Hearing about your MM journey is so inspiring. You look great.

OMG I am so sorry for you. But at least you found out. Thank god you kept going. I probably would’ve gave up by then and just lived with it. I hope you stay in remission. I am in remission too from Breast Cancer. God bless and best wishes to you!

Thank you for sharing my aunt diagnosed with multiple myeloma too. I pray you stay in remission ❤

Hi Krissy, I hope all is well. I'm currently going getting ready to do CAR-T. I didn't do the BMT. I have a rare case its only in my blood so I refused the SOC and now that CAR-T is approved going to do this. Hopefully this puts me in a Permanent Remission!!!. Anyhow I drink lots of beef bone broth to help with RBC's not sure if you're doing that,but you may want to ad that to your regimen. Wishing you as well a Permanent Remission. 🙏🏼🙏🏼

Oh this has been so hard for you! Good luck and blessings go with you to your monthly checks.

Grateful for you making it through and thriving. I love you!

❤love and peace for you, Your strong, intelligent and learning a lot. Keep going and praying your outcome is always positive. Be well

Krissy, Thank you for sharing your experience. You are a strong lady! Prayers for remission to continue! ❤

Hugs to you. My brother a friend and uncle had Multiple Myeloma

I am so happy that you are doing better. Bravo on all your research!

Wow what a journey you have been on. My goodness. I am so very very glad you are doing well🎉

So glad you are in remission You are a strong person. Wish you continued success!

Just found your channel hun and will be praying

Well told story! Hoping the remission is long lasting! Thanks for posting your story.

Thank you for sharing your story, you are so articulate and speak with such strength. Sending you thoughts of healing and peace

I am currently going through the same and hoping to have a transplant shortly. Thanks for your input..

Thank you so much for sharing your experience. My mom who is 70 just got diagnosed in april with MM, after breaking 4 vertebrae for no apparent reason. Many years of bone pain. She was sent to an onocologist in 08' and cleared. So we think shes had it for 15 years. She had spinal fusion in april then 5 days radiation, and now on revlimid, valcade, dexamethasone and expected to do stem cell therapy. Also one more detail, the biopsy showed it is in 85-90 % of her marrow. The drs say this is a very treatable cancer and she has a 90 % chance these therapies will work. He was very hopeful it can extend her life by 10 years. 🫶

I am in remission also for multiple myeloma that once a month stuff is crazy

♥️♥️♥️

Hello, I don’t mean to be intrusive but did you have any pain in your elbows as well as hip pain? 😢 Thank you for sharing your story and journey with us all. ❤

just found and subscribed to your channel, healing in Jesus name beautiful lady🙏💐

🙏🏽🙏🏽

Ny husband has multiple myeloma and had 2 bone marrows he said very painful

Can you tell me what clinical trial did you have? My husband has the same problem, he is after chemotherapy bone marrow transplant and naw immunoterapii. I think avery person with this particular cancer type needs to be checked what drugs gonna work for them.❤

How many types are there? My mom was just diognosed

First question: Did you receive any Covid-19 jabs?

Best regards.

What did your blood work look like?

Ugh the misdiagnosis... sounds so familiar.

Hope you got rid of your primacy.