Multiple Myeloma Life Expectancy
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- เผยแพร่เมื่อ 20 ต.ค. 2024
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I have this cancer, and since my diagnosis it's been 5 years. I have done no treatment and live by looking forward to my ten year run. I do have pain. trouble walking and loss of energy, but I get up every day and enjoy the world as God put it here for us and try to explain to people what a cancer patient and their family goes through. I have your mom in my prayers and you.
There are ways to get help for those side effects. You don’t have to live life in pain, unable to walk and not feeling as energetic as you can. That’s the effects of myeloma on you bc you’re not being treated. Please don’t accept this as it bc of God or something. Life can be made better with medicine bro.
I also have Multiple Myeloma. I was diagnosed when i was only 39 years old in May 2020 right as the pandemic was starting to kick in. I had a stem cell transplant in may 2021 and i have many other chronic illnesses and medical issues (diabetes, heart attack, psoriasis, Psoriatic arthritis, osteoarthritis and a couple other things.) I have hopes that i can survive but i also have no idea what is in store for me in my future. Its not easy living with Multiple Myeloma but i will always keep fighting. I have too much to live for ❤
Wow so sorry to hear this, if yiu dont mind me asking what were your initial symptoms, my legs hurt here and there and fingers hurt, sometimes below rib cage and center of chest hurts when i move. Back doesnt hurt tho. Only reason i feel i might have is because my esr levels were a bit high when they did a blood test.
Healthy keto (low carb) and intermittent fasting can help with many general diseases.
I am very poor and my mother is in final stage i dont know what to do
I had my Stem Cell Transplant in 2020. Unfortunately, the cancer attacked my kidneys, which is how they discovered i had Multiple Myeloma, rare form called Heavy Chain Deposition Disease. So in 2020 had the massive dose of chemo followed by a Stem Cell Transplant. I was on dialysis for a year. Thankfully, my kidney function increased enough that i was able to stop dialysis. My kidney function now is a GFR of 40. Im coming upon that 5 year mark in another year. I hope to pass that and continue on maintenance chemo and remission. My doctor at UNC said some patients go 10 years and he even had 2 patients go 20 years before releasing.
He’s not lying… I was diagnosed in 2018. My Dr was running a trial. Fast forward to 2021. I started the newly approved regiment he was working on. Thank you science and meds.
How r u right now. Feels good
Great content
Thanks! You can share this video on linked in or facebook to bring awareness to myeloma!
WHAT ABOUT ZERO stem cell transplant? My Mom has been experiencing this... I have seen the serious side effects of the ‘treatment medications’... Mom is 76; most recent medication causes cognitive dysfunction and memory effects, dizziness
My mother is taking temreatment she has taken 6 doses of wekaly injection of bortezomib nd dexa she is feeling wekness nd less appetite is she can be normal with medicine we would not go for bone marrow transplant as her age is 64 we dnt ant to see my mother suffer pls advice 🙏🏻
@@mahipanchal2650n i talk with ypu?
@@mahipanchal2650brother searching for the same ans....please tell me if you have got the ans
Not if you're James Bond, of the Dana-Farber Cancer Institute.
my dad