I had to tell my doctor that I was going to see a blood specialist doctor because I had anemia and he kept telling me that not to worry about that it was not that bad. I then went to an oncologist and she order several blood test and she to me that I had multiple myeloma. Please when you feel something is not right don't wait for a doctor to tell not to worry seek help.
How are you now have they managed to help you with your myeloma. I think it's what is happening to me please 🙏 could you give me any advice i would be grateful. Thanks hope you are doing good
@@mooneymooney1565 Always get a sencond, opion some doctors are just making money for the hospitals they work at but there are a few great doctors out there that will lead you in the right direction.
Yes doctors are extremely primitive individuals , usually getting their degrees in medicine just to be secured in life but not because of loving the field of medicine or because they want to help patients.
I’ve always had issues especially with bone joint pain but for months now it has progressively gotten so much worse. I’m 27 and I’m barely able to get up and go work I have to take pain medicine to make it through the day. My whole back, ribs, hips, shoulders, and arms and legs are in excruciating pain without it. I’ve been having terrible skin bumps that won’t heal and rashes all over the place that keep getting more frequent and worse. I realized I’ve had several swollen lymph nodes for a while but they are in places doctors don’t typically check. I smell horrible. Im so weak and fatigued way beyond normal, I’m getting terrible headaches and the main thing that actually scared me the most to get to the dr asap, aside from all my symptoms progressing getting worse, is my kidneys are hurting terribly and I realized that can be associated with a bad body smell. Some of the lab works they have done twice now have shown my rbc low, platelets low, monocytes low, and then my wbc almost in the low range but my baby white blood cells have been really high. And my kidney function is just almost in the low range. The only way I can describe it is I literally feel like my body is shutting down. I had a biopsy a few years ago on a liver growth and they missed it and it was inconclusive and with at least that and all of my symptoms being so sick I would have thought the doctors would be taking me more seriously. The doctors seem to keep riding me off and it’s such a hopeless feeling. And my primary doctor just said I have anemia I had to basically beg him to just send me to a hematologist because I just know this is not normal for me and there has to be something going on it’s been months and it’s only getting worse and worse. I have an appointment in two days with a hematologist/oncologist please if you see this please say a prayer that they will take me seriously and help me get to the bottom of this. 🙏🏼
I have Kappa at 84 so my doctor asked me if i had bone pain. I played rugby cricket and gymnast for years. I have pain everywhere and wouldn't have the first clue what bone pain was.
I was experiencing so many symptoms, even had an abnormal cbc at the er twice and so i went to the doctor last week, i ended up with a diagnosis of anemia and blood work was only slightly off but i know my body. I know its more to it for me
Started getting tingling on my bum cheek that went pain near the coccyx, this then went to a pain in my lower back with numbess and tingling. This has gone to hip aches and numbness heaviness in arms legs and tingling in jaw with the odd dizziness. Had blood tests they were fine and waiting on MRI scan results
hi there how are you . four months ago my blood test show more protein in the my blood test . and hematologist. took sample .and biopsy from my spine . and full blood test and full sonography and full s scan . he said my disease is m gus . and he didnt give me any medication. only said after 6 month another blood test and urine test . sometime toes pain and arm pain no to much i dont need pain killer . i am on the diet no more red meat. i eat 4 times a week fish & brown rice & tuna & more beans & lentils . brown bread & no sugar and more salad. i am non-alcohol & non smoker . please give me more information for help and what is best diet food i am 61 years old men from australia country thank you
I have fatigue, bone pain, numbness and pain in arms, legs. I'm just 22 its going to be 2 weeks and these symptoms are not going away. My doctor thought I had something in head or in nerves he planned a CT, an xray of neck vertebrae, TSH, blood sugar but all these tests came out absolutely fine. I have some stomach and heart Issues as well nowadays.
Have your doctor run a test called SPEP (serum protein electrophoresis). If you have a monoclonal protein on that test, you could have multiple myeloma. It is an inexpensive test to run.
I found Chris Beats Cancer in August and started his protocol in September. My numbers were going up like crazy but since starting that protocol my numbers are going back down and I have a ton of energy where I used to sleep most of the day.
I fractured my patella & when they xray my knee they found a bone lesion above my knee..now I'm getting pain in both feet the top bone of my feet severe pain & bottom stiffness I don't know if it's poor circulation or neuropathy..or other what kind of test should I request
Where I am, doctors don’t even bother listening to you. And when you try to come back on it they become nasty. It’s been a moment since I feel my body wrong, like something isn’t right but nobody listens to me even though I have visible chonic symptoms like anemia, easy bleedings or bleeding that doesn’t go away, nausea, fatigue and weakness, sleeping issues, bruises, night sweats, painful armpits lumps, fever that doesn’t really go away, infections.. Last time I did blood test my platelets number was really low, same with my red cells and my white blood cells number was really high, nobody paid attention to it…And since months now I have bone/joints pain with edema. But my parents say it’s just in my head. Since doctors don’t listen to me I really hope it’s in my head..
My total blood protein tests have been between 8.3-8.5 every year for at least 7 years. They are stable but still higher than normal. Is this concerning? My cbc and calcium levels are normal.
Heck the protein count…it’s really important and if you can have that test by doctors try searching if in your state you have the chance to buy them without referral
Hi. My globulin is 4.5, my total protein is 8.5, and my albumin/globulin ratio is 0.8. Would you say this is concerning? I also have high Lyphocytes, am anemic, etc.
@@camillebambi6449 did blood work on me the other day. My ana was normal, but my c protein is elevated and a few other things. Is it possible for ana to show normal and still have lupus?
@@amandanichols1988 definitely. Also i had chronic elevated CRP for years but negative ANA and i still have bad rheumatoid arthritis (I am sero-negative). All autoimmune diseases are really hard to diagnose because no one will have all positive tests. And once you have one autoimmune disease, you can get another really easily. I'm currently being tested for lupus (again), MS and multiple myeloma after having a mini stroke at 33. Protein electrophoresis would be your best test. Helped me get diagnosed with RA.
Thank you 😊 I'm so sorry to hear you are going through all of that. My RA factor didn't show anything, i dont think. I still havent heard from the dr about what they think it is. Just saw my results on the patient portal. I'm sure it is probably an autoimmune disease. I hope you are able to get a proper diagnoses yourself. I will be sure to ask for the test you recommended 😊
My doctor notice my protein was a little elivated and commented that my protein was slightly elivated and was sure its nothing to worry about but still sent me to an oncologist
They didnt listen to my partner they told him he wasnt ill and to go back to work a few weeks of returning to A&E we found out he has AML 😢 this was 6 weeks ago hes having chemo right now. 😢😢😢
I'm almost 27 yrs old and I'm having so much pain. I'm fighting off my other cancer and now I got these hip, hand and spinal pain. Not to mention I'm always sleepy but that could also tie in with my mental disorders lol. I'm in so much pain but I don't look like I ever would be.
A German doctor finally diagnosed my brother after all the Army docs sent him back out in the field! They didn't want to have the responsibility of a soldier with MM, medical retirement, etc... disgusting!
A Chinese Doctor diagnosed my cancer right away when all the other Doctors where telling me it was all in my head! Chinese and most Asian Doctors are very thorough and compassionate.
I had to tell my doctor that I was going to see a blood specialist doctor because I had anemia and he kept telling me that not to worry about that it was not that bad. I then went to an oncologist and she order several blood test and she to me that I had multiple myeloma. Please when you feel something is not right don't wait for a doctor to tell not to worry seek help.
How are you now have they managed to help you with your myeloma. I think it's what is happening to me please 🙏 could you give me any advice i would be grateful. Thanks hope you are doing good
@@mooneymooney1565 Always get a sencond, opion some doctors are just making money for the hospitals they work at but there are a few great doctors out there that will lead you in the right direction.
I'm currently on vitamin and natural things you can order on line do some research and you be surprise all the things you can take for cancer .
Unfortunately, Most doctors don’t listen to their patients ...
Pretty much had to hit mine in the head with a verbal bat to get him to listen to me. They're all the same. Their effing egos make them deaf.
Yes doctors are extremely primitive individuals , usually getting their degrees in medicine just to be secured in life but not because of loving the field of medicine or because they want to help patients.
Some don’t even tell patients their diagnosis
You can ask for tests.
@@shereehi5539 and if they refuse, insist they document in your chart why
I was diagnosed with MM on my first visit to an orthopedist for my post polio symptoms. He said he saw me in the hall, and knew immediately.
I’ve always had issues especially with bone joint pain but for months now it has progressively gotten so much worse. I’m 27 and I’m barely able to get up and go work I have to take pain medicine to make it through the day. My whole back, ribs, hips, shoulders, and arms and legs are in excruciating pain without it. I’ve been having terrible skin bumps that won’t heal and rashes all over the place that keep getting more frequent and worse. I realized I’ve had several swollen lymph nodes for a while but they are in places doctors don’t typically check. I smell horrible. Im so weak and fatigued way beyond normal, I’m getting terrible headaches and the main thing that actually scared me the most to get to the dr asap, aside from all my symptoms progressing getting worse, is my kidneys are hurting terribly and I realized that can be associated with a bad body smell. Some of the lab works they have done twice now have shown my rbc low, platelets low, monocytes low, and then my wbc almost in the low range but my baby white blood cells have been really high. And my kidney function is just almost in the low range. The only way I can describe it is I literally feel like my body is shutting down. I had a biopsy a few years ago on a liver growth and they missed it and it was inconclusive and with at least that and all of my symptoms being so sick I would have thought the doctors would be taking me more seriously. The doctors seem to keep riding me off and it’s such a hopeless feeling. And my primary doctor just said I have anemia I had to basically beg him to just send me to a hematologist because I just know this is not normal for me and there has to be something going on it’s been months and it’s only getting worse and worse. I have an appointment in two days with a hematologist/oncologist please if you see this please say a prayer that they will take me seriously and help me get to the bottom of this. 🙏🏼
Thanks for sharing, you’re strong!
I have Kappa at 84 so my doctor asked me if i had bone pain. I played rugby cricket and gymnast for years. I have pain everywhere and wouldn't have the first clue what bone pain was.
I was experiencing so many symptoms, even had an abnormal cbc at the er twice and so i went to the doctor last week, i ended up with a diagnosis of anemia and blood work was only slightly off but i know my body. I know its more to it for me
Did you get a definitive diagnosis?
How are you doing now?
pls check your B12
pls check your B12.
I am having a health scare as-well, hope it all ends up ok. I probably shouldn’t watch all these RUclips videos, just scaring myself.
Started getting tingling on my bum cheek that went pain near the coccyx, this then went to a pain in my lower back with numbess and tingling. This has gone to hip aches and numbness heaviness in arms legs and tingling in jaw with the odd dizziness. Had blood tests they were fine and waiting on MRI scan results
Hope u r doing well brother ❤what does doctor said after mri report
What was it?
how do you know what is bone pain .or muscle pain ?
When you experience bone pain, you will know. Just like a real contraction for women, when its time, you know.
hi there how are you . four months ago my blood test show more protein in the my blood test . and hematologist. took sample .and biopsy from my spine . and full blood test and full sonography and full s scan . he said my disease is m gus . and he didnt give me any medication. only said after 6 month another blood test and urine test . sometime toes pain and arm pain no to much i dont need pain killer . i am on the diet no more red meat. i eat 4 times a week fish & brown rice & tuna & more beans & lentils . brown bread & no sugar and more salad. i am non-alcohol & non smoker . please give me more information for help and what is best diet food
i am 61 years old men from australia country
thank you
Hi! Please send us an email to support@healthtree.org and our team will help you!
Include Tumaric
I was having fatigue and went in for blood work and found kidney failure. Renal biopsy revealed MM.
How are you now Tim? What were your symptoms for kidneys? God bless hope your ok
I hope you got the best treatment and now in remission
Only fatigue? What else?
Praying for a mircle my sister has this please God
🙏🏾🙏🏾🙏🏾🙏🏾🙏🏾🙏🏾🙏🏾
🙏🙏🙏
🙏🙏🙏🙏🙏🙏🙏🙏🙏🙏🙏🙏🙏🙏🫶🫶🫶🫶🫶🫶🫶🫶❤️❤️❤️❤️❤️❤️❤️❤️
My 67yo brother also just diagnosed.
can you explain what kind of myeloma
thankyou for very informative Vedio
Thanks for watching!
I have fatigue, bone pain, numbness and pain in arms, legs. I'm just 22 its going to be 2 weeks and these symptoms are not going away. My doctor thought I had something in head or in nerves he planned a CT, an xray of neck vertebrae, TSH, blood sugar but all these tests came out absolutely fine. I have some stomach and heart Issues as well nowadays.
Have your doctor run a test called SPEP (serum protein electrophoresis). If you have a monoclonal protein on that test, you could have multiple myeloma. It is an inexpensive test to run.
I found Chris Beats Cancer in August and started his protocol in September. My numbers were going up like crazy but since starting that protocol my numbers are going back down and I have a ton of energy where I used to sleep most of the day.
Maybe polycythemia vera
Did you find a diagnosis?
Go direct for a bone marrow test and a CT scan
When you’re a veteran and go to the V.A. it’s always dismissed as PTSD or allergies
😢
I fractured my patella & when they xray my knee they found a bone lesion above my knee..now I'm getting pain in both feet the top bone of my feet severe pain & bottom stiffness I don't know if it's poor circulation or neuropathy..or other what kind of test should I request
Your primary care needs to get you into a oncologist and let him handle it
Thanks
Where I am, doctors don’t even bother listening to you. And when you try to come back on it they become nasty.
It’s been a moment since I feel my body wrong, like something isn’t right but nobody listens to me even though I have visible chonic symptoms like anemia, easy bleedings or bleeding that doesn’t go away, nausea, fatigue and weakness, sleeping issues, bruises, night sweats, painful armpits lumps, fever that doesn’t really go away, infections..
Last time I did blood test my platelets number was really low, same with my red cells and my white blood cells number was really high, nobody paid attention to it…And since months now I have bone/joints pain with edema. But my parents say it’s just in my head.
Since doctors don’t listen to me I really hope it’s in my head..
Get a 2nd, 3rd, 4th opinions. See a different doc.
How are you feeling now?
Everything you described is what I’m going through.
GO ASAP TO A SPECIALIST. HEMATOLOGY AND ONCOLOGY PLEASE!!
My total blood protein tests have been between 8.3-8.5 every year for at least 7 years. They are stable but still higher than normal. Is this concerning? My cbc and calcium levels are normal.
Heck the protein count…it’s really important and if you can have that test by doctors try searching if in your state you have the chance to buy them without referral
Hi. My globulin is 4.5, my total protein is 8.5, and my albumin/globulin ratio is 0.8. Would you say this is concerning? I also have high Lyphocytes, am anemic, etc.
Also have been having hip and back pain. And pain in my should all on the same side. Heart palpitations, etc
@@amandanichols1988 you should be checked for lupus.
@@camillebambi6449 did blood work on me the other day. My ana was normal, but my c protein is elevated and a few other things. Is it possible for ana to show normal and still have lupus?
@@amandanichols1988 definitely. Also i had chronic elevated CRP for years but negative ANA and i still have bad rheumatoid arthritis (I am sero-negative). All autoimmune diseases are really hard to diagnose because no one will have all positive tests. And once you have one autoimmune disease, you can get another really easily. I'm currently being tested for lupus (again), MS and multiple myeloma after having a mini stroke at 33. Protein electrophoresis would be your best test. Helped me get diagnosed with RA.
Thank you 😊 I'm so sorry to hear you are going through all of that. My RA factor didn't show anything, i dont think. I still havent heard from the dr about what they think it is. Just saw my results on the patient portal. I'm sure it is probably an autoimmune disease. I hope you are able to get a proper diagnoses yourself. I will be sure to ask for the test you recommended 😊
Now, I have ALL the symptoms. I am a senior. lol.
So could osteoporosis scan actually be multiple myeloma?
Have your parathyroid hormone level checked along with calcium. PTH is what it’s called and obviously calcium level too.
Overactive parathyroid glands leach calcium out of your bones causing osteoporosis and will eventually cause a multitude of problems in your body.
My doctor notice my protein was a little elivated and commented that my protein was slightly elivated and was sure its nothing to worry about but still sent me to an oncologist
Love this
Wunderbar!
Can a doctor run this blood test even if there is no apparent reason calling for it?
These blood level tests are standard CMP when you get your annual physical.
They didnt listen to my partner they told him he wasnt ill and to go back to work a few weeks of returning to A&E we found out he has AML 😢 this was 6 weeks ago hes having chemo right now. 😢😢😢
I'm almost 27 yrs old and I'm having so much pain. I'm fighting off my other cancer and now I got these hip, hand and spinal pain.
Not to mention I'm always sleepy but that could also tie in with my mental disorders lol. I'm in so much pain but I don't look like I ever would be.
Sorry you have to go through that bro. How are you feeling now?
I will pray for you 🙏
Sometimes Chronic kidney disease could be actually Multiple Myeloma.
My uncle passed away from this 2 years ago,,
Pray for ur uncle🙏.. What are the symptoms he had at that time.. Is it not early diagonosed..
Bro I’m 28 and I’m convinced now I have cancer.
Get your blood work done.
That's why German doctors are the best
A German doctor finally diagnosed my brother after all the Army docs sent him back out in the field! They didn't want to have the responsibility of a soldier with MM, medical retirement, etc... disgusting!
A Chinese Doctor diagnosed my cancer right away when all the other Doctors where telling me it was all in my head! Chinese and most Asian Doctors are very thorough and compassionate.
best at what? lol
cell transplant side effects
How are you
My dr didn't believe me.
Or you can be a 36 year old nurse and these things also seem normal 😮💨😩