Added: 4 years ago
From: WashingtonDeceit
Views: 25,358
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  • my mom died from multiple myeloma and she was only 49 when that happened i was only 9 yrs old now i am 11 yrs old..

    its hard for a girl to go thru that like me :(

  • My mom is 78 she had a bone biopsy

    The dr thought she may have MM

    They are doing another scan of her

    Bones she has no energy tired all the time

    Is anemic has very bad back aches and paines in her neck a vitamin D deficiency

    Does this sound like MM?

    They said she had MGUS

  • You are the best!!!! Thank you!

  • the burzynski clinic in texas has gene treatments for myeloma. check them out.

  • nice

  • very useful for students, thx!

  • my mom has got MM...we are now 8 Years after Diagnosis

  • I have multiple myeloma and it is terrible. When they found I had it, they were not giving me months or days, they were giving me seconds. It's been about a year and 3 months and I am doing pretty well. I have 3 compact fractures in my back, kidney failure, and went from about 6 feet tall to maybe 5 foot 7 inches. It's no fun.

  • @elgatoshadow how are you going? have you found a treatment?

    

  • informative video but i find it boring coz of slowed speaking of the speaker...it is just like I'm about to sleep...not energetic...but the info shared was good..

  • my mother died from this. She survived nearly 7 years with it. It is a horrible thing to die from. 

  • thanks dude!

  • My mother died of this. She was 46.

  • well MM has a bad pronostic only 10% make it through 5 years since diagnosed...

  • Google "9/11 Cancers"

  • I just got word today that one of my best friends has this disease. it has really been hard for us though we remain hopeful as we are blessed to be near great cancer treatment facitlities in utah. Interestingly enough, he fits into the .000016 % of cases being that he is only 27 years old. Thanks for allowing me to better understand what is going on.

  • I was dianosed with MM at 47. At the time they gave me 18 to 36 months with a 25% chance of making it to 5 years. That was Nov.1997. Faith, family, great medical care and I am actually better now than when diagnosed. No treatments for 5 years and pain free. I give Him all the glory & praise! His grace and goodness....all things are possible!

  • Very useful information more is available at myelomaforums d o t com

  • Thank you for the post, i`m carrying out a market research about a new product to control this disease. It has been very helpful and made me understand graphically a bit of how multiple myeloma take place.

  • fantastic. very informative. helps to understand myeloma clinical features, great work!

  • Thank you so much for posting this. My dad was recently diagnosed with multiple myeloma and I'm trying to learn as much as I can about this disease.

  • My Mother,with 72 years old,an energetic and almost workaholic person, is sick now,

    an hematologist,said,maybe she had Multiple Myeloma, This is an horrible disease,maybe worst than cancer, because is virtually incurable, You can beat the cancer if it found in early stages, not the same with multiple Myeloma, In Poor countries like mine,the story is even worse,there are no Radiotheraphy machines, there are no Chemotherapy medicines, etc..

    Pray for my mother please..¡

  • My prayers are with your Mother. May God cure her.

  • Thanks a lot for your prayers,

    we have faith

    every day of life is a God's gift...

  • my dad has multiple myloma im 12 hes 45 has it at a young age

  • well man, i fell terribad about your mother, i will pray for her.

    by the way Multiple Myeloma is a kind of cancer for the record... an ungly one i must say

  • My nana is the type who goes and picks up a hundred sandwiches and drives them around to homeless people in the city. Recently our family was devastated to find out that she had Multiple Myeloma, and it makes me so sad to know that this has only been viewed 36 times! Please help stop this awful, painful experience for families just like mine by donating to the international myeloma foundation and spread the word about this terribly awful cancer.

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