Multiple Myeloma Diet

I was diagnosed in Aug. 2020 with Multiple Myeloma. Hard to not eat meat and sugar.

Would like to have a copy of the diet for MM. Was diagnosed in May 2022. Not doing the stem cell transplant because of my age. I am 64

I have MDS and would like to try this diet.

I would love to have the diet to help me in my struggle to survive MM many thanks

Can you please send you diet for MM. Thank you.

Can you please forward diet for MM. My husband would require this. Thankyou.

Can this be used for follicular lymphoma too?

I was diagnosed with MM three years ago. I also have kidney failure at same time so I am on dialysis. Please send me diet information. It seems some good food for MM is not compatible with the renal diet.

What is. A good site for the flexatarian diet. I am in treatment and have reached remission. Want to stay there. Help!

I would like your diet for mm

I am a MM patient fighting for 7 years now..would love the MM diet pkz

Bowel cancer diabetic fattyliver damaged liverwould like to know about diet also oestoprosis gut problems underactive thyroid ta

Diet info please

I am private, please. Would love your diet. Kindly, send

I would like the diet. I am in remission for 1 1/2 years

I’m 73 and was diagnosed 2019. I take 10mg. Revilmide. Would like diet info to like longer.

I would like your guide on eating

Would like a guide on what should and should not eat

I was diagnosed in August of 2021 with Smothering Myeloma. I would like to know more about your diet please. Thank you.

hello I have had MM for 4 years I am not able to receive a transplant due to cell damage from the chemo therapy I am actively takin blue seed oil tablets what can I do or take to hlp fight against the MM an is takin black seed oil tablets beneficial

Husband age 49 diagnosed with MM in August- would like nutritional information.

Hi, just diagnosed with MM at 32, please send me your nutritional food plan thank you.

Recently diagnosed MGUS. But kappa light chains keep going up and kidneys are great. Please send diet info. Going to check out your reading recommendations and video. Thank you

I was diagnosed with MM in 2021. I am very interested in your nutritional food plan.

Diagnosed with MM 2021 just had partial kidney removed on revlimid. Please send me your nutritional food plan.

Got multiple Malom2021 got stem cell replaced bone marrow my own September 2022 I was taking 5% Relival only lasted till August 2022 Now back on chemo for 15 weeks. Please help…

MM since 2013,please send diet plan.Thanks

May I have information on the nutritional benefits and diet/lifestyle? I also have had a kidney transplant (9 years) and some CHF problems but am hanging in there. Would like to get into complete remission and if diet will help then I’m all for it. Thanks.

I was diagnosed with MM in 2017, had SCT and on 10 mg Revlamid. I had a relapse in 2019 but have done great since then. I’m turning 65 soon and I’m very interested in Diet and Nutrition info.

I am recently dx with plasmacytoma on R hip and starting radiation soon, bone marrow biopsy just done and do not know results, I’m very fatigued and lots of pain, I am very interested in diet with foods and supplements to improve my nutrition to help me improve the quality of my life, I would appreciate any information you can guide me with, I believe proper nutrition can help. Thank you

[…] anti-myeloma nutrition […]

My husband was diagnosed with mm in 2017, had a sct and is currently on 10mg of revlimid as maintenance. I am concerned about his eating habits and would like some information on how I can guide him in the right direction. His oncologist doesn’t say much about diets.

I would like to get your info. Thanks. I’m on revlimid and doing well.

I had a stem cell transplant in June 2021. I am doing well on Revlemid. Please send me the diet information.

Hello. Just recently diagnosed with MM. Not sure about stages as oncologist didn’t say. Told me that my bone marrow biopsy shows “5 to 10 %” MM. I’m being treated with radiation right now on an area of my rib that the oncologist labeled “ plasmacytoma. Any info you can provide will be very much appreciated. Thank you.

I was diagnosed in May 2022 w/smoldering myeloma.
Have progressed to MM as of September 2022.
Very interested in your books & diets!
28 years in remission WOW!
Good for you—love to learn from you. (Just turned 67)

I’m 86 yrs old just diagnosed w MM myeloma just wondering about the pAin I will be experiencing in the future months. If I over due I get pain in my back and neck fatigue yes. Look forward to hearing from you🙏☘️☘️🙏

[…] Anti-angiogenic nutrition […]

[…] Multiple Myeloma Diet- Before, During, After Therapy Myeloma Diet in Three Easy Steps Multiple Myeloma Diet Multiple Myeloma Diet- Flaxseeds/Budwig […]

[…] Myeloma Diet, Supplement – A How-To Guide Multiple Myeloma Survivor Diet – Multiple Myeloma Diet- Before, During, After Therapy Myeloma Diet in Three Easy Steps Multiple Myeloma Diet […]

Diagnosed with stage one in August 2022 after four years with Smoldering MM. Now in treatment. Can you send me the Flex diet? Thank you!!

[…] To learn more about your Myeloma Diet as a therapy click now- […]

[…] Multiple Myeloma Diet- Before, During, After Therapy Myeloma Diet in Three Easy Steps Multiple Myeloma Diet Multiple Myeloma Diet- Flaxseeds/Budwig […]

[…] To learn more about your Diet as a Multiple Myeloma Therapy click now- […]

Thanks for being willing to share your journey and wisdom! It is inspiring to know there are people who significantly outperform the statistics out there. I’ve been diagnosed with SMM and would like to slow progression to MM for as long as possible. Please send your nutrition guide.

Hello. I am 54 and I have been diagnosed in March 2021, chemo for 1 year and in remission now. Only 5 mg Revlimid per day. Also morphine and gaba for my pain.
Can u email me a nutrition guide please. My oncologist said nothing about how important is the diet. Thank you

I was diagnosed with MM March 2022, been on Revlamid, Velcade, Darzalex and dexamethisone since, and going for SCT end of September. Please send me your diet details. Thank you!

[…] Multiple Myeloma Diet […]

I’ve switched from store bought milk, to organic goat milk from a neighbor who sells it ( full fat); also, his eggs. I don’t drink alcohol, soda, commercial juices; mostly water. The goat milk is for cooking and cereal
I try to stick to fruits and veggies, but I have a sweet tooth and I bake quite a bit

I am interested in learning more. I have had two stem cell transplants and I still have evidence of disease albeit a smaller amount than prior to the transplants.

[…] For example, I may talk up the basics of my anti-cancer diet and the general benefits of the Mediter… […]

Please can you send details on the
diet. Many thanks.

Please send me information on the Flexitarian Diet.
Thank you

Like nutritional info

I need to know in regards to the flexitarian diet

I have been in remission for 71/2 years after a stem cell transplant. Would you send me the nutrition diet.

I have MM. had stem cell transplant In Sept. 2021 and am now in complete remission. Please send nutritional guide. Stomach doesn’t tolerate many foods except carbs. Thank you.

Hi, have been diagnosed with MM in June 2021 and on derma infusion since June 21 . Progress is good . Would like to know more from you about diet , etc on how to beat this disease. Am 72 with no other prior diseases.

I would like to know more about The flexitarian diet. I would also like to know more about the coaching program.
Thanks so much

I would like to sign up. Please send me whatever forms you need. And who to write the check to.

I live on Ritz crackers and chocolate milk and ensure Suplement for the last 9 months. Any other food makes me nauseous, just the smell of food cooking makes me vomit. I’m very weak and tired all the time.

Hi there!
My husband was diagnosed 5/2021 with MM. He is status post SCT. Not quite 30 days yet. In his medical notes I saw deep vgPR1 after 7 months of VRD. What diet should I start him on to keep him in remission. He is igG lambda. Im still reading and trying to understand this cancer. I appreciate any advice.

Could you please send nutritional guide. Thanks so much!

Please send guide and if you have book provide info on how to get. I want to read it all!😊 Thank you

Hello. A friend has MM and CKD. Please send nutrition guide. Thank you!

I was diagnosed with MGUS in April 2021 – I’m interested in learning how to better take care of myself

Just found out husband has stage 3 MM, please send any information, thank you

I have MM. Please send me your nutrition guide.

I am retired nurse ,have researched & found pts with MM require increased amts of vitamin B12 .Eating only small amts of red meat will cause iron & vit b12 deficiency which is essential for DNA.heart ,nerve & blood maintenance.Vegans & vegetarians are at high risk of vit B12 def which not diagnosed early & treted results in Pernicious Anaemia.I have a friend MM diabetic,under-treated for b12 def ,treated with chemo now 12 mths when told originally 6 wks .She is has had 2 iron infusions in last 6 mths..I would be interested to hear your views & if you have every been tested for genetic mutation MTHFR .

Hi, I was diagnosed in June 2021 with MM and am currently receiving RVD. SCT when my numbers are where my doctors would like them.
Would you please send me your nutrition guide.
No one ever emphasizes how important diet is.
Thank you!

Very informative and realistic. Please send nutrition, cannabis and intro guides.

How do I get Long Term Nutrition Plan

Recently diagnosed mm, started RVD, possibly SCT. I would love your nutrition guide.

Hi David,
Please email me the nutrition guide. Thank you and God bless.

I had stem cell transplant January 2020. Currently in remission. Please send me the MM nutrition guide.

Hi David. I was diagnosed with MM on June 2020. Had a bone marrow transplant in December 2020. On remission at this moment. Can you send me a copy of MM nutrition guide? Thanks.

Thank you. Was never told that nutrition was important as a myeloma patient. Can you send me your nutrition information.

Thank you. Was never told that nutrition was important t as a myeloma patient. Can you send me nutrition information.

Is ASA good to take?

Thanks for this great information David. Can you please send me the MM CC nutrition guide.

Very good contribution to better lifestyle..copy of your information wold be welcomed. Thank you.

Good afternoon and thank you for the informative information. May I have copy of your diet and CBD related recommendations. Thank you.

I would like a copy of the diet.Being tested for MM

Is there a charge for you to email me a plan. I have SM and bounce with MM

Hi, I would appreciate a copy of your dietary recommendations. I was diagnosed SMM 2years ago but some weird things happening to my body..
thank you.

Please send me the guidei

Please send me the guide.

I am a caregiver for my 86 year old mother diagnosed with MM, she is on dialysis now because of it, please tell me what foods are best for her. Thank you for this article…..God bless., Karen

Please send me the guide

I would like to receive the MM CC nutrition guide

I would love to know more about MM Nutrition Dieet🙏

Please send the MM CC nutrition guide. I am fairly recently diagnosed, and have received absolutely no support from the doctors regarding nutrition or diet. I would appreciate anything you could share at this point. Thanks. Have a beautiful week. Dave

I am very happy to learn about your diet. I am almost done with my treatments of mm. 3 mores weeks. And I know that diet is very important but we have to know what to eat and not eat. So thank you again . I will do my best to read about it . My cancer came back to normal after 7 months but the doctor want to do the treatments for a year for controlling it better.i hope you can understand my English because I am from Quebec Canada. But I leave here for many years but I do speak French still a lot with my family. I am 74 years old. My cancer was in my spine only whe we begin the treatments. I am on revlimid.

I’m newly diagnosed and am learning as much as I can. Can you please share the diet you’ve developed with me? Thank you for your encouragement.

Hello, I have just been diagnosed with MGUS and very much appreciate your mention of Dr. Li’s work. I would be grateful for any information you might share about your own nutritional wisdom. Thanks

Hi David. I am a 9 year survivor having been diagnosed with SMM. I had a AST five years ago and relapsed 3 years later. I am currently in CR. I am fit and eat a pretty good diet but would appreciate a copy of your flexarian diet. Thanks so much.

hopefully that product will be nice

David is my coach and has shared his experiences and suggestions for me and many others. He does his best to support MM patients. He is a Living example of successful fighting

Hi David. I’m 52 and was diagnosed with SMM a year ago. I’m IgA Kappa and have an m-spike of 0.9 and 0.2. (Total of 1.1). I was working with a nutritionist who had me on the “Mitchell Page Diet and a daily routine of over 70 pills/supplements. My numbers have remained stable but did not go down as the nutritionist said they would with the regime he had me on. I am now seeing a new nutritionist. I’ve only had my initial consult, but the gist is that I’ll do the AIP diet for a month along with food sensitivity testing and a select and more targeted supplement intake. After a month, I will be able to add back certain foods I was able to eliminate so long as I don’t show an inflammatory response. I would love to learn more about your program to make tweaks. Thanks in advance for sharing your potentially life saving protocol.

[…] Multiple Myeloma Diet […]

Wow! I have MM. I was diagnosed in August 2015.
I am very interested in your
information, diet & exercise
program. How do I learn more?

My husband Don had a solitary plasmacytoma on his C5 disc and had surgery in December 2020 followed up with radiation. He has now been diagnosed with MGUS and we would like information, please. Thank you!

Please send me information for my husband, Bob, who was diagnosed last July and is now three months after autologous stem cell transplant. He is doing very well.

Do I have to become a mm coach in order to get the book and materials on the nutrition? I was diagnosed with MM this past February and will be having a SCT in July.. wanting to know more in the nutrition and foods to eat that will help this.

Very good video

I was recently diagnosed with mm. I am starting a RVD treatment then the stem cell transplant. Any advice or help with my diet? Thank you!

Where do you get your supplements resveratrol and curcumin Brand name How do you take them!

Venison ( lean meat ).

[…] Multiple Myeloma Diet […]

Hi David,

I have recently been diagnosed with Multiple Myeloma Stage 3 and I am leaning toward not doing the autologous Bone Marrow Stem Cell Transplant.

I would like your thoughts on this and I would like to know at what Stage you were diagnosed.

Thank you,

Tricia

I have had MM fir 6 years. Had a stem cell transplant 5 1/2 years ago. I am interested in learning about your flexatarian diet.

Hello David, thank you for posting this web on your own journey with dealing with MM, i think it was divine intervention that brought me here. My questions are actually for a loved one. Firstly, thank you for bringing up the MM specialist since the person i am speaking for does not have a specialist only an oncologists, who has been seeing him for over 1 year now, he will actually be getting a 2nd opinion because it seems that his body is not responding well now to Revlimid, his liver enzymes has been trending up and so he had to stop Revlimid 25mg for 1 session and was started on Vemlidy 25mg, it brought down the enzymes but once he started regimen again with Revlimid his enzymes now went up again, do you think the felxitarian diet will help him with this and help his liver? His doctor diagnoses him with smoldering MM so ue is not in late stage yet but now his current tx is affecting his liver. Secondly, do you have any tips to help with insomnia? He has been taken off dexa bit still has hard trouble sleeping and uses ambian everyday to be able to get at least 4hrs sleep. Thank you.

Hi, I would like to know more about multiple myeloma. I was diagnosed last year with mm.

Hello there,

You have an incredible story and it is EXTREMELY rare to hear of anyone discuss links between food and mm. In fact I have actually been told to eat fast food because it might make me feel better mentally! Additionally, while getting chemo I’ve been (almost) forced to eat cake and drink lemonade by the staff. Currently, I’m the ONLY patient in my clinic who has disagreed with these food/beverage offerings. I was diagnosed with stage 1 mm on 23rd march 2020. Currently I am on day +30 post sct. For most of my time since diagnosis I have followed a similar diet to what you have outlined (mostly plant based). My diet is like a cross between fruitarian and Mediterranean foods. Occasionally I eat small quantities of meat. Usually when I eat meat it is after a session with my personal trainer. Interestingly, since swapping over to plant based foods I have noticed massive improvements to my health despite going through chemo. I lost 14kg, gained 8% muscle mass, no flem, no inflammation, better digestion, no dandruff, no bloating/ gas, and feel quite energetic. Last year I typed up a weekly meal plan with some common dishes I eat regularly. Would you be willing to read through my documented meals and offer some advice on where I could improve/ what I could change etc?
Cheers, Dan

Thanks so much for this information

HalloIs thwrw a fb group.I will learn everything about alternativ treatmen for MM so curious.Thwrw is hope.Ilivemyself with MM

I want to learn more and join your group. I am an MM patient and want to learn more about your success,

Hi, because I had a lot of side effects from vevlimid,valtrex,and Dex the steroid and I am 79 years old I can’t have sct. I also have diebetes,hypertension, severe Arthritis. constants dirreaha problem any suggestions?

Hi, because I had a lot of side effects from vevlimid,valtrex,and Dex the steroid and I am 79 years old I can’t have sct. I also have diebetes,hypertension, severe Arthritis. Cordless is a constant problem any suggestions?