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International Myeloma Foundation
International Myeloma Foundation
International Myeloma Foundation
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Founded in 1990, the International Myeloma Foundation (IMF) is the first and largest global organization focusing specifically on multiple myeloma. The IMF’s reach extends to more than 525,000 members in 140 countries worldwide. The IMF is dedicated to improving the quality of life of myeloma patients while working toward prevention and a cure.

Your support helps us provide a wide range of programs and services to the myeloma community in the areas of Research, Education, Support, and Advocacy.

The International Myeloma Foundation is a 501(c)(3) organization.
Learn more at www.myeloma.org
Комментарии
@kmarie1351
@kmarie1351 День назад
I love the metaphor of myeloma being a small animal in a cage.
@18168587
@18168587 День назад
A man diagnosed in 2011 received VRD for 6 cycles, then AutoHSCT. relapses in July 2023. receives VRD for 4 cycles, second AutoHSCT. maintenance lenalidomide.
@debbietaylor1922
@debbietaylor1922 3 дня назад
Why didn't this video list EARLY symptoms of MM? Instead of just saying 'early detection yay'
@michelsooriah692
@michelsooriah692 5 дней назад
There is hope
@heidipucci9078
@heidipucci9078 8 дней назад
Thanks for sharing your story. ❤ I have recently been diagnosed with Smoldering Multiple Myeloma, I too have a high M spike and also I have the Free light chains. How many years did you say you went by until the myeloma became more active and you started therapy? Also, when you went through the induction was it really hard on your body? What symptoms did you have from the chemo? Thank you guys!
@a914freak
@a914freak 10 дней назад
So if you were smoldering your bone marrow biopsy must have been less then 20% involvement correct?
@matthewgraham2546
@matthewgraham2546 10 дней назад
I'm 72 years old have MM with fractured vertebrae so I am thankful for the videos. Some of the accents are a little hard to understand so the sub titles are very helpful.
@SoheilaLapeyre-wm7sd
@SoheilaLapeyre-wm7sd 10 дней назад
How lucky you are!
@Gfordnut
@Gfordnut 13 дней назад
Go Dr Abonour, that's my Myeloma Specialist, he's the best!!
@lmcdonough2293
@lmcdonough2293 14 дней назад
❤❤❤
@heidipucci9078
@heidipucci9078 15 дней назад
Very informative,thank you
@sfeeneygirl
@sfeeneygirl 18 дней назад
Thank you Dr. Durie
@IMFMyeloma
@IMFMyeloma 19 дней назад
Have a question? The IMF's InfoLine team consistently provides callers with the best information about multiple myeloma in a caring and compassionate manner. Infoline@myeloma.org 800-452 CURE (2873) US & Canada 1-818-487-7455 Worldwide
@IMFMyeloma
@IMFMyeloma 19 дней назад
Have a question? The IMF's InfoLine team consistently provides callers with the best information about multiple myeloma in a caring and compassionate manner. Infoline@myeloma.org 800-452 CURE (2873) US & Canada 1-818-487-7455 Worldwide
@IMFMyeloma
@IMFMyeloma 19 дней назад
Have a question? The IMF's InfoLine team consistently provides callers with the best information about multiple myeloma in a caring and compassionate manner. Infoline@myeloma.org 800-452 CURE (2873) US & Canada 1-818-487-7455 Worldwide
@IMFMyeloma
@IMFMyeloma 19 дней назад
Have a question? The IMF's InfoLine team consistently provides callers with the best information about multiple myeloma in a caring and compassionate manner. Infoline@myeloma.org 800-452 CURE (2873) US & Canada 1-818-487-7455 Worldwide
@IMFMyeloma
@IMFMyeloma 19 дней назад
Have a question? The IMF's InfoLine team consistently provides callers with the best information about multiple myeloma in a caring and compassionate manner. Infoline@myeloma.org 800-452 CURE (2873) US & Canada 1-818-487-7455 Worldwide
@ElephantsRock19
@ElephantsRock19 20 дней назад
Can mass spectrometry take the place of a bone marrow biopsy?
@matthewgraham2546
@matthewgraham2546 20 дней назад
I'm stage 3 had a fractured vertebrae and surgery. I'm 72 years old and in great shape, is 5 years a typical survival rate.
@anonymousbutterfingers7564
@anonymousbutterfingers7564 20 дней назад
A number of posts below (i.e. entered before 07/07/24) mention that "... my oncologist has not explained all these options ...". My experience is that it is extremely important to have MM specialist looking at your case. Not just an oncologist or a transplant specialist or a hematologist but somebody whose main focus is multiple myeloma. I understand that a smaller hospitals may not have such people. If this is the case try to find somebody you can see 3-4 times per year in a larger city/hospital or even somebody you can meet on line. The point is that MM is an area of very active research, there are dozen (or more) options to go with, new drugs are approved every year and not every doctor has time to follow it up.
@sunnshine321
@sunnshine321 21 день назад
Would that signify that losing weight extend remisión?
@intelligenttechnologies2476
@intelligenttechnologies2476 16 дней назад
I would love to know this aswell.
@richardhowe898
@richardhowe898 21 день назад
Thank you
@VithikaNag
@VithikaNag 23 дня назад
Thank you!
@dr.satyabratasahoo5644
@dr.satyabratasahoo5644 23 дня назад
Good
@dr.satyabratasahoo5644
@dr.satyabratasahoo5644 23 дня назад
Nice
@ceceliabrunott1015
@ceceliabrunott1015 24 дня назад
Thank you. A great overview!
@user-lv6jq5tw7c
@user-lv6jq5tw7c 25 дней назад
Sir kindly talk about one side hemorrhagic plural effusion in myloma patients
@IMFMyeloma
@IMFMyeloma Месяц назад
Have a question? The IMF's InfoLine team consistently provides callers with the best information about multiple myeloma in a caring and compassionate manner. Infoline@myeloma.org 800-452 CURE (2873) US & Canada 1-818-487-7455 Worldwide
@IMFMyeloma
@IMFMyeloma Месяц назад
Have a question? The IMF's InfoLine team consistently provides callers with the best information about multiple myeloma in a caring and compassionate manner. Infoline@myeloma.org 800-452 CURE (2873) US & Canada 1-818-487-7455 Worldwide
@heidipucci9078
@heidipucci9078 Месяц назад
Strong couple and strong survivor❤
@amyjenkins9187
@amyjenkins9187 Месяц назад
What did your blood work look like?
@user-ex8lo7jd8v
@user-ex8lo7jd8v Месяц назад
Use subtitles
@fatherabdul
@fatherabdul Месяц назад
Thank You
@madonnaarsenault4452
@madonnaarsenault4452 Месяц назад
I have one kidney due to donating the other one. Recently, the one kidney is now at stage 3 kidney failure as Acute Kidney Injury unspecified, and diagnosed with MGUS and experiencing much pain, weakness, fatigue, and numbness and tingling. Is there anything different to consider with one kidney?
@henrysmom1742
@henrysmom1742 Месяц назад
My mother has myeloma and her doctor always knocks her out for the BMB.
@rob1016ny
@rob1016ny Месяц назад
Thank you on behalf of the rest of us.
@TessRico-ty7qq
@TessRico-ty7qq Месяц назад
GOD bless Tom, praying for my complete physical healing for GOD is my JEHOVAH RAPHA, my DIVINE HEALER, AMEN🙏🙏🙏
@davidjrbechtol4411
@davidjrbechtol4411 Месяц назад
I had to go to a different doctor and they found out I had multiple myeloma. The first doctor Dr almond ran me around for 7 months and said I just wanted pills even though I was working
@KigurumiAlice
@KigurumiAlice Месяц назад
Does it cause GVHD like Monocolonial antibodies 😮
@3Davy
@3Davy Месяц назад
My father also but but he’s cancer therapy did work.But hè died from a influenza virus in the hospital,and I think my brother has infected him😢😢😢😢.
@azalia423
@azalia423 Месяц назад
I have Mgus attributed by my oncologist to long term use of sertraline, an SSRI. After withdrawal, I've developed neuropathy and tinnitus, occasional shooting nerve pains and brief migraines.
@deeb3315
@deeb3315 Месяц назад
Adrienne is such an inspiration!
@chellesswell974
@chellesswell974 Месяц назад
Thank you for sharing your story. I've been diagnosed for mgus and have constant bone pain in my leg, but I no on ever investigates. I'm very concerned about it hearing your story is motivating me to press the issue and beg or demand a Ct scan ASAP
@Deidroni
@Deidroni Месяц назад
Thank you Dr. Joe for your clarity on bi-specifics. Your explanations are the best. Maybe on the next video, skip the background music. It’s a little distracting.
@hillsidevalley5468
@hillsidevalley5468 Месяц назад
does this work in del17p ?
@kiwioffgrid2437
@kiwioffgrid2437 Месяц назад
This sounds disgusting and damaging. Russian roulette.
@donnah5378
@donnah5378 2 месяца назад
Thank you 🙏🏾 😊
@sudhanshusahu251
@sudhanshusahu251 2 месяца назад
my mother patient of Multiple Myeloma aged 63 year old last year went through ASCT and now she is under maintenance therapy with linolidamide 10mg for 21 days and one week rest again repeated but now she is frequently suffering from anxiety, fatigue and constipation she is not fit as like she was well before transplant is there any other therapy in maintenance can be give like immunotherapy or some thing else with low side effects and fatigue after ASCT she has not given any immunizations what are the immunizations which she has to take
@rockinrandyful
@rockinrandyful 2 месяца назад
Hi Beth! Toronto Canada. Diagnosed 13 months ago and post T-Cell transfushion. MyHebogloben has responded from 72 0n Febuary 28th to last weeks reading of 124! I can walk and move around again seemingly as free as I did before my symptoms began in March of 2023. I am so thankful and along with some fantastic care I have recieved from the medical community here in the Kitchener, Ontario region, it is my belief that my positive attitude was second in things that have supported this positive response and speedy recovery that I have and am experiencing. humbly said! I had my Stem cell transplant complleted on January 4th 2024 and again my Hemogloben went from the low 70's On average since January to 90 on Mar 28th with a 13 point increase in one week ending on March 28th. My Oncologist whom I seen 1 week ago informed me she wished to start me on a maintance program after a one month break from last week. My investigations so far on what to expect in the mediications involved in such a maintence progtam has left me somewhat anixious on what to expect as it appears we are on the edge of a whole new round of medications to be introduced through research and even some new considerations within the medical field on different considerations on which avenue one professional verses the other may lead their individual patients. Any general consideration or guidelines you could share with me that would put me in a position to be understanding of the different choices I will be discussing with my care team?