Відео

Thank you for posting. Going thru it now. It's new to me and terrible.

I find the dry mouth totally unbearable. For me it has destroyed my quality of life. I sure don't want to die of cancer but if I could pass in my sleep I would take that any day rather than this.

David, just reconnected with oncology after 11 years with out. dxd myeloma 2000, tandem autologous scts 2000. The new onc, 2 weeks ago, reported believing I am smoldering and isn't pushing tx. 2 days ago got a call from oncs office stating after my newest blood draw he is afraid I am in full blown relapse. asked that I have a pet-ct scan which I have set up appointment for. The only thing he looks at is a cbc, chem panel and kappa lambda light chains and differential. The differential stated unable to calculate ratio due to undetectable concentration of free kappa lambda light chains. when I looked up undetectable it stated this could be a false positive or false negative and the test should be rerun. i am happy to have the pet-ct scan because I've had no bone surveys in 11 years. I have no mm pain which for me is very different than all other pains Ive experienced.. I'm believing this is undetectable is good news so not afraid, but a little nagging in the back of my mind. What is your take or feed back for me if you have any. Thank you Candace Andrews

Thank you for this video. My son has MM and is in remission now for almost 4 years. He thinks about he cancer almost everyday. He is 50 years old - and found out he had MM in 2020. What is this thermos thing that you mentioned in your video? I know he tries to eat healthy, and exercises regularly - he also purchase a sauna hoping this may help as well. He has a good outlook on life, but I know deep down he is worried when it will come back and how aggressive it will be.

Now I’m taking Tavley and now I have no sense of taste and have a hard time swallowing food. My lambda light chains are rising again after having car t therapy. Are there any other options than this bi specific therapy?

My mother has this and she has lost a lot of weight how do I get her to gain more weight? Thanks so much for the video you made

Hello do you eat bread

Can one consume alcohol in case of covid related steriod induced avascular necrosis?

My husband is 63 re entry diagnosed with multiple myeloma, along with servere COPD. He was diagnosed about a month ago. The only reason why they found is they seen a spot on his hip after he slipped and thought he fractured his hip. Now back in November 2023 he had been sleeping when he rolled over felt a pop in his chest he popped it so bad that his sternum is coupled. They believe that the myeloma caused his chest to literally cave in. His thoracic spine is basically gone he goes to chemo gets shots twice a week in his stomach and just recently he started chemo at home on a daily basis in pill form. My question to you is will my husband ever live to walk upright again, will he ever be comfortable, and what can his life expectancy be?! He used to be5'10" now he stands at 5' 1". He weighed 170 now he's 116 lbs. He's way too young for all of this, and aggressively fast. Actually they said that his myeloma hasn't gotten worse, but it's only been a month of treatments. I'm so scared for him. He is such a strong man. Can you please please get back to me?! You are appreciated. Sincerely

Hope you're ok and still fighting this prayers and healing for all ❤🙏

Hi im from papua new guinea, my dad has multiple myeloma and and he had a blood transfusion and after that had swelling feet and after week it went down a bit but they started hardening and hes having numbess in his feet and also his hands

Great info! Are you allowed to drink room temp water during the sauna treatment or abstain until after? What temp have you had in the sauna when you do your session? I'm also fighting cancer that's why I ask.

The body doesn't know the difference between a piece of fruit and a piece of candy. Some veggies have high amounts of carbs which, of course, turns to sugar. This advice is good for people who are healthy, but cancer? That requires more.

What about shots of vitamin c? Is it better than oral? I know iv is best, but expendive

Thanks for this video. I'm 71 and in the Doctors words very fit at 155 lbs and 5.1 A1c. But what got me to the E room was a fractured spine and I spent 30 days in the hospital and rehab. The advice I give to anyone who listens is keep yourself fit, it goes a long way towards your recovery. I don't want be a burden to my wife or adult children or to anyone. Life doesn't owe me one more minute, I am doing chemo and what the Doctor says, it's all you can do. My best to everyone waging this battle.

Where is this info found,?

David,this is the 1st day I watched any of your videos. You have more than a couple. I think there is more to PeopleBeatingCancer than I have seen. I watched a # of your videos. I have a new diagnosis of MM 2/22 of this year. I felt sick ,shortness of breath,weakness, loss of weight. Was admitted to hospital for 18 days of diagnostic testing, Have started chemo in march. Just learning some now. Your videos offer somewhere to learn some more things from your experience. Right now Im thinking of the curcumin diet.

Thank you for all you do!

You're right, I just realized that Mario updated his favorite way to tackle ED and it's crazy! Although what he previously talked about was pretty decent, it was difficult to follow, I just go'ogled the latest by Mario Volpstein, it's so much simpler and potent now!

My father is suffering from stage 4 multiple myeloma....... currently he is on chemo therapy....... suddenly his RBCs and platelets drops.......what to do now

👏🏻

👏🏻

Hi David. What test did you get don’t for genetic testing for diagnosis of multiple myeloma? How much was the treatment cost in Texas? I have had a brain tumor removed frontal lobe meningioma. I have the PTEN and KMT2D variant.

How are you now?

Hi, Can one replace Biphosphonath with AlgaeCal? Our functional medicine doc suggested AlgaeCal, so we can get off Biphosphonath. AlgaeCal is supposed to really improve Bone density

Very helpful, thank you 👍

Are you still alive

Thank you. I was diagnosed in 2019 but I've had Multiple Myeloma since 2016. I am on a maintenance program and I have not yet achieved remission. I am still living and everyday I work harder to improve my life. I live my life with no regrets. I smile and laugh everyday. I truly believe in Progress not Perfection. Thank you again!!!

Brother i got disphagia during tomotherapy Which is unbearable Plz tell me 1,should istop taking radiation after 10 n 5 are left,? 2. Tell me complete excercises. How much time will it take for complete recovery. Plz reply soon

Did you do a stem cell transplant with Malphalan chemo? If so, what side effects did you experience? Any relapse?

Horrible video!

Can this be used for Neuroendocrine tumor?

My best friend Matthew just died from MM on January 17th. He suddenly stopped taking his Chemo meds about a year ago. I asked why he stopped taking them. He said that they made his head feel too heavy & that he refused taking them. Then about a year later, he claimed he was in remission. It all felt very odd to me. Then about a few months ago, he started having neck pain that was AGONIZING & he slept on a recliner. He went in to get help with that to no avail. Then he called me on January 9th. He began crying because he was in pain. I have never heard him cry before. Then all of a sudden, his texts & phone calls stopped. Then a couple weeks later, I got a text from his wife, stating that he had died on the 17th & now all his friends & I are going to his funeral on Feb 12th. It all happened so fast & so sudden. My advice to anyone going through this, is to LISTEN TO YOUR DOCTORS & TAKE YOUR MEDS!!!!! GET SECOND OPINIONS AS WELL & READ UP ON YOUR ILLNESS

thank you for your post ,martin from in the UK ,one has a ct on friday the 26th, ,one is 2 weeks on iron pills because of anemia,but still strugeling to stay awake, unyet can not sleep at. night ,one has uses an electric wheel chair for 13 months now ,as walking is so hard , one has rib pain and a rash on legs ,like flat red spots ,my thorasic spine can hurt a lot and my iliac crest around the hips,and lumber spine, als one's knees wake me with a lot of pain, Once again thank you, and peace to you, my friend best regards martin,

David ...you mentioned "Silky Wormwood"? Is it the same as Artemisia Annua?

I was diagnosed with tongue cancer in the Fall of 1984 & underwent 3 chemotherapy treatments, 1 per month. In the first half of 1985 I had 2 surgeries, a tongue resection & 2 radical neck dissections to remove lymph nodes from my neck. In the later part of 1985 I had radiation therapy to the front of my lower face & neck. I am still alive, January 2024, but over the last 2 years I have developed peripheral neuropathy in both arms and in my left leg, supposedly due to the radiation but possibly also due to chemotherapy.

I have been diagnosed with MGUS, could it be a good idea suplrmenting with curcumin just im case it develops to MM?

Drop your mail plz 🙏

I am 88 years old, quite healthy and energetic. My annual medical tests discovered multiple myeloma in my bone marrow. I immediately went to MD Anderson in Houston. MDA did exhausting tests and confirmed the presence of multiple myeloma. However, I have no aches or pains. I am doing all normal chores and am living a normal lifestyle. I eat and drink well. Sleep well. I have good balance and do not need any walking aids. I can walk up to a quarter mile before I have to rest for a minute or two and then good to go. MDA watches me closely with blood tests. No medications have been prescribed whatsoever. I do have CKD 3 and I watch my diet and the nephrologist checks me out every 3 months. I drive, perform daily duties, and shopping without difficulties but carefully without assistance. I will be 89 in April 2024. WHAT FUTURE CAN I EXPECT? Is my question. I have lived a very active life. Your response will be greatly appreciated.

are you still beating your cancer? i hope so .i just wonder because it has been so l9ng since you put 9ut a video.

Any way to get the Nutrition guide?

Thanks for the video. I have been curious about it but cant find anything on the subject until I came across your video.

Thank You 💛

Hi David... I also have Multiple Myeloma, for about 15 months and in Remisión NOW.. I am taking curcumin plus Revlimid 10mgs as maintenance ; are you taking also Revlimid OR Only Curcumin??.. Thanks for your response.

Please give an idea of measurement, such as half a teaspoon, whole teaspoon full per day. Thanking you.

Fuirt n veggies lose weight

I have MM & my journey has been a real bitch, there's no polite way to communicate this; sorry. I've had two Bone Marrow Transplants & now my ParaProtein's are on the rise again. I'm only 55 years old & I feel like I have been cheated by life. I feel like this isn't my time. I feel like I contracted this horrid condition 25-30 years too early. Anyway, that's my rant ..... I'll be beginning my next line of treatment in a few weeks, but right now, I'm experiencing extreme fatigue due to the lack of oxygenation in my blood (from an excess of Plasma Cells: not enough Red Blood Cells) .... However, the worstest of the worstest of the worst part of my journey, has been the Peripheral Neuropathy in my feet. It drives me crazy. Crazy to the point where I want ALL LIFE ON EARTH to suffer, then die. I am serious. Sometimes it gets me so angry, I truly wish it would happen ! ..... What HELPS ME, is knowing that other people understand my pain & discomfort from direct experience. Looking at me, you'd think I'm perfectly healthy; but inside, I am dying - this is a fact ..... In addition to this, everyone's journey is unique & MM can become instantly aggressive overnight & finish you off. Just because you hear stories of people living to be 1M years old with MM, doesn't mean that YOU, specifically YOU, will live to be 1M ..... So, what I've learned is --> leave nothing for tomorrow, it may never come. Fulfil your dreams, your desires & your bucket list !!!!!

What are the dosage protocols?

Thanks for your valuable information and congratulations for be a MM survivor... How much curcumin supplement do you recommend daily?.. I am taking 8 grs in 2 times, by morning and before sleeping.

I have been diagnosed with smoldering myeloma. Although I am in the early stages, it is already causing a steadily worsening anemia. My hematologist is recommending a four month course of "RVD Light", which he says he has tried on many patients with good results. I worry about potential side effects, especially cardiovascular risks, but your video has given me some encouragement to give it a try. Best wishes.