Hi All. Thank you all for your kind words and thoughtful support. I can't tell you how many times I wrote a thread to post and scratched it because I guess I just wasn't ready to talk about it. Besides, we didn't how bad it was or what the out look was going to be so there really wasn't anything to say. I wasn't trying to hi jack the other thread but this whole experience has really given me some new perspectives and I really related to Leafy's question.
In response to the inquiries about how we found out...here's the story.
My husband is 49 and has always had problems with his lower back. However, last January the pain got a little worse so I encouraged him to go to the doctor. Her response was he needed to loose weight as usual. I'm not fond of this doctor as she's said some pretty unprofessional things to me in the past. Anyways, even though he does have the typical belly most men his age have, over all his health is pretty good and I felt he deserved more attention about the issue than he got.
At that point, I insisted he try my doctor and get a second opinion which he did. She listened and thought it might be a muscle spasm. To treat it, my doctor gave him something for pain, exercises to do at home and started him with physical therapy. However, after two weeks nothing was working, in fact, the exercises & PT made the pain worse and the drugs she prescribed didn't even dull the pain. It was so bad he literally could not sit down. After a couple of weeks of this, the doctor ordered an MRI and while it showed a possible pinched nerve, there was also an abnormality on one of the vertebrae they felt needed further attention. A contrasting MRI was ordered which showed there was metastasizing in the bone in several areas. She advised us she felt there was a chance of cancer and that she had already consulted with an Oncologist who ordered a cat scan as well as a full skeletal x-ray and tons of blood work. At that time a non confirmed diagnosis was made of the Multiple Myeloma but the Oncologist wanted to wait for the last of the testing (a bone biopsy and 24 hour urinalyses) to get a final confirmation and find out what stage. We found out the results yesterday which confirmed the Multiple Myeloma and that it's in stage 3. The doctor advised us the stage is irrelevant though because his kidneys are clear and his bones are not brittle enough for him to experience breakage yet and with the treatment shouldn't get to that point. The treatment plan which was started yesterday has an 80% success rate and he assured us he has lots of patients living fairly normal lives in a state of remission.
For those who are unfamiliar, Multiple Myeloma is a cancer of the blood that attacks the bone with lesions, damages the marrow and destroys the kidneys. Broken bones are very common as is kidney failure. All of his other organs and lymph nodes tested clean as well. The only reason it's considered stage 3 is because he has lesions in several places such as his ribs, collar bone, spine, pelvis and skull.
I feel so terrible that for weeks he has been walking around whacked out on Valium and Vicodin and the only way he can comfortably relax is to lay in the recliner on a heat pad. Not once has he missed a day of work until last Friday after a bone marrow biopsy. He even went to work yesterday after the first infusion. In addition to the chemo he's taking, he's also receiving medications to help rebuild his bones and immune system. The amazing thing is too, he won't loose his hair, experience nausea, or get sick in any way from the chemo. Eventually the pain from the bones will disappear and he will be able to live a fairly normal routine. I can't believe he went to work yesterday after his first infusion and kept saying he felt great. I know science has made great strides but it's truly amazing at how far it has really come.
Needless to say, the past 3 weeks have been a nightmare. I've had to keep a smile on my face and a positive outlook when I'm around him but the whole time my stomach is constantly in knots and that feeling that our world was coming down around us was constant.
Each night as I lay in bed, I spend hours listening to him sleep and worry about how this will all play out. While yesterday's news was both the most positive we've had in weeks and the best we could have received, I know our lives won't ever be the same and as grateful as I am that this is a treatable condition it's all just incredibly sad to me.
judiegal6
neetsiepie
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