multiple myeloma message boards

mmrf honorary board

the mmrf honorary board is comprised of high-profile public figures who help to raise funds and promote awareness for multiple myeloma research. the mmrf honorary board is comprised of high-profile public figures who help to raise funds and promote awareness for multiple myeloma research. skip to content in the text message or by contacting

online multiple myeloma forum: cancer resources

multiple myeloma discussions. visit our online multiple myeloma forum to research helpful cancer topics and obtain valuable feedback and support. you are not alone in your fight against cancer. join today to find the additional information and resources you need to make an informed decision.


i was diagnosed with having multiple myeloma several months ago. does anyone diagnosed with multiple myeloma have any pain, if so where, and do you have any bone pain? also does anyone with mm have elevated calcium levels? any help would be greatly appreciated. - thanks for the information on pain medications, i am

multiple myeloma forums and blogs that prove youre not alone

finding support online: multiple myeloma blogs, forums, and message boards medically reviewed by seunggu han, md on july 29, 2019 written by stephanie watson multiple myeloma is a rare disease. blogs by, about, and for people who

please help by clicking on add your myeloma blog to make sure yours is added. if you dont have a blog and you want one, write to me by clicking on the contact link. by the way, please make it easy for people to comment on your blog by not requiring a login or account creation.

mimmick multiple myeloma

do not consider message boards as medical advice. never delay or disregard seeking professional medical advice from your doctor or other qualified healthcare provider because of something you have read on webmd. you should always speak with your doctor before you start, stop, or change any prescribed part of your care plan or treatment.

discussion boards cancer survivors network

please remember that these discussion boards are a public forum, which means open to the public i.e. non-csn members and the content can be found via internet search engines.

all loss of a spouse to multiple myeloma messages

it has been a week ago since i lost my husand to multiple myeloma. i can't help feeling guilty, as i feel i should have done more for him. i had taken care of him for 3 and a half years. they did not expect him to make it back when he was first diagnosed, but he fooled everyone. the last week before

multiple myeloma

had a quiet new year's eve. wrote a tongue in cheek family newsletter for my sibs and started it with: it was the best of years, it was the worst of years. that covers it. i realized it was in 2004 that my doctor said i had an elevated protein that could indicate multiple myeloma. i couldn't imagine living ten years--yet here i am and very

all what to expect in end stage multiple myeloma messages

on jul 27, 2010 7:44 pm mmsurvivor wrote: i have sent you a private reply but i was told i had end stage in 2004 mid october. my symptoms were extreeeeeme pain, inability to walk, extreme loss of arm use, 95% kidney failure. high calcium levels, hemaglobin of 6 white count and paltelets way below

multiple myeloma treatment questions

i was diagnosed with multiple myeloma in october, 2017. my mm manifested itself in my kidneys no bone fractures or other tumors which have returned to normal function after an induction treatment of velcade, cytoxin, and dex every week for approximately 8 months.

8 types of multiple myeloma

multiple myeloma is the second most common type of blood cancer, but not all multiple myeloma cases are the same. learn more about the types of multiple myeloma and how they differ.

forum: multiple myeloma forum

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multiple myeloma

my mom was just recently diagnosed with multple myeloma and was scheduled for a bone marrow transplant at johns hopkins hospital. unfortunately, during the process they discovered that she had contracted hepatitis b. dr's said that this may have come from one of her blood transfusions. don't they test all

relapsed/recurrent multiple myeloma: symptoms, causes

if you have multiple myeloma, theres a good chance it will come back after successful treatment. when this happens, its called recurrent or relapsed. if it doesnt respond to treatment or

can someone describe end stage myeloma for me?

multiple myeloma is a terrible, painful and horrible disease. my prayer is for someone to come up with a cure so that no other son or daughter, wife or husband, grandson or granddaughter, will ever have to see their loved one fade away to skin and bones, and have the suffering my dad endured.

multiple myeloma forums, multiple myeloma message boards

do i have multiple myeloma? questions and discussion to help forum members determine if they may have multiple myeloma, smoldering multiple myeloma, or mgus. 157 topics 851 posts last post by ron harvot on sun dec 08, 2019 2:43 pm; weekly polls weekly polls of the myeloma beacon's readers on topics related to multiple myeloma.

all multiple myeloma messages

i am caregiver to my wife who has been diagnosed with multiple myeloma in october 6, 2016. she has undergone autologous bmt stem cell transplant without blood transfusions. almost after a month an mri revealed a plasmacytoma at the l4 level of her spine. further tests noted many lytic lesions

physician reviewed medical information on multiple myeloma

multiple myeloma overview. multiple myeloma is a blood cancer in which plasma cells grow out of control. healthy plasma cells come from the bone marrow and play a key role in your immune system.

multiple myeloma hub article on lenalidomide bmy message

multiple myeloma mm often progresses from an asymptomatic phase, called smoldering multiple myeloma smm . the risk of progression is 10% per year, however the presence of adverse prognostic factors can lead this to increase to 25%. the current standard of care for smm is observation.

multiple myeloma forums, multiple myeloma message boards

the multiple myeloma forums at the myeloma beacon are an independent community of myeloma patients, caregivers, and others interested in multiple myeloma. independent, up-to-date news and information for the multiple myeloma community.

multiple myeloma symptoms, diagnosis, treatments and

read about other experiences, ask a question about multiple myeloma, or answer someone else's question, on our message boards: i can not get a diagnosis. please help. tell us your medical story. share your misdiagnosis story. what is the best treatment for this? see all the forums. article excerpts about multiple myeloma