My boyfriend’s mother has crohn’s disease and she has had some problems with it. She recently took a vacation to visit us (12 hrs away), and the day she got back home she went to the hospital for chemotherapy treatments. She told my b/f that it was nothing to worry about that it was just treatment for her crohn’s. I don’t know much about crohn’s/treatments, but I have never heard of chemotherapy as a form of treatment for this disease. She has lied to him once before when she was having renal failure and she told him that it was just a simple kidney infection. Is chemotherapy a treatment used for crohn’s disease?

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I’m passinga kidney stone – have passed them for 13 years – since I was about 24. Anyway, this one is a painful son of a gun…..and it’s near the ‘final frontier’ – just wondering if you have any advice as to how to get it out. I am drinking lots and lots of water….and I have been doing my normal morning workouts….but it’s quite achey……and in the past, Doc’s have told me that ‘movement’ is key – so walking, exercise, etc is good, if you can do it.

I do think I have a pretty high threshold for pain……but the gnawing pain is really getting old.

The largest stone I’ve ever passed is the size of half of an Advil…..which is pretty big…..and I’m concerned that this one is larger…..

I’m an old pro with it comes to passing kidney stones, but if you have any advice, I’m all ears (or eyes since we’re reading it here.)
When I was going through chemotherapy (Jan-July 2007) I was taking Allopurinol…..and I must admit, while it’s a good chemo-for-cancer drug, it is also used to eliminate the formation of kidney stones/gout. Anyway, I felt that during that time, my kidneys felt great….no pain at all. Not sure why doc didn’t prescribe this for me….but I think once this/these pass, I’ll have to go and have it prescribed…..I can’t live like this…

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I remember reading somewhere that there were four stages of treatment for systemic lupus erythematosus I think it was like
I-corticosteroids
II-?
III-?
IV-Immunosuppressors, chemotherapy, etc

I was wondering if there was anything like this on the internet or whether I am confusing it with the kidney affected stages? (I doubt it but you never know…)

Thanks in advance for any info, and please be sure to set up a link to where you got your info

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I am a ten year breast cancer survivor; stage I, 1.7cm, no lymph node involvement, estrogen positive to me; I had as treatment 17 CMF chemotherapy, 45 Neupogen shots, 30 radiation treatments and a quadrantectomy. My balance seemed to be off during my second chemo treatment. I told my doctor, I fell often. And in 2001 I fell down stairs, broke a tib/fib, titanium rods implanted and ended up with DVT. I have been walking with a cane since then.Last year was treated for an ear infection, serous otitis media, At the emergency room the doctor said I had bubbles on my eardrum. I was admitted to the hospital, and isolated. One doctor came in and said I had MRSA. I didn’t know what that was. I was treated with many antibiotics and the only one that worked was oxacillin. I was discharged after three days. Afterwards, everything changed. I had two failed 17 year old root canals, numerous antibiotics, kidney stone,more antibiotics, ear doctor treated with more antibiotics, saw a neurologist, said I have cerebellar ataxia. Another said I didn’;t. One neurologist said I had fear of falling. One said it was peripheral neuropathy. One said it was PTSD. I was thankful last year to hear that I did not have a neuro-degenerative disease. I left the state to celebrate, with my walker, my cane and a change of clothes. The third day, I fell off a foot high porch and broke the calcaneous bone and did a 2+ sprain on the left ankle. I returned back to my home with the goal of relearning to walk. However, I again became more imbalanced, my right eye started twitching and wouldn’t stop. The eye doctor today tells me it is convergence. The eye doctor last year, told me nystagmus. I call it my scarry eye and continue to do vestibular therapy. Two months ago, I went on another journey to try and save my life and the quality of my life. A neurosurgeon told me, I have never seen that part of the brain completely gone. You need to go to a stroke center. Another doctor told me I might have a connective tissue disease. I tested positive for anti nuclear AB. Yes, I do have arthiritis. If I have something else I don’t know. Last month I made an appt. with a gastroenterologist, because of unusual bloating and unable to urinate completely. No pain at this point. A week later I end up in the Emergency Room: told you have a 2mm kidney stone; it is in the ureter and should pass into the bladder, you should see a doctor in three days. I saw a urologist, CT scan of abdomen and pelvis. He said maybe you will pass it, if not we will do a lithotripsy and place a stent. By the end of the week I ended up in the ER again. I was admitted. The 2 mm stone now was 5.8 mm and in the ureter. I was given pain meds and stayed in the hospital so my 80 year old mother didn’t have to witness me birthing a stone, Everrbody said it was nothing. I tell you it was painful. Before I was discharged from the hospital, the doctor told me a CT scan revealed it was in my bladder. That all should be okay. I have strained urine, looking for a stone, The urologist says the stone is still in the ureter, and the radiologist read the report wrong. Today, a doctor says, good news, no blood in the urine, Today, I still have problems with bloating and voiding fully. I already have problems with vestibular dysfunction and I believe that this is compromising my life. Symptoms: can’t walk or stand for very long, can’t walk forward without holding on. I do well in a swimming pool but sometimes, even it can be difficult. Is it the ear? IS it another disease? I am exhausted and need help? My eyes have a hard time focussing. I try to exercise, stationary bike and swimming every other day. I used to be a very active person who helped others. Please, someone help me. It is difficult being in this body.Every day I don’t know what it will be like when I get up, good or bad, confident or fright.

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I’m trying to figure out what this really is. My mom has breast cancer. Last week, she was really sick. She went to the emergency room, and she they found a kidney stone. It was pretty big, but they sent her home after she was starting to feel better.
Today, they used that ultrasound machine to break it up, and she came home fine for a while. About fifteen minutes ago, she got really sick again. They are taking her back to the emergency room now.

My question is… is it really the kidney stone that is causing her this pain, or could it be more complicated/breast cancer related? I don’t think you are normally rushed to the ER twice in two weeks for a kidney stone. I’m really worried that it spread, or something worse. Can someone help me? Is it just a very bad kidney stone with complications, or something else? Can breast cancer have anything to do with kidney stones?

Also: my mom is about half-way through her chemotherapy treatment, and her tumor has been shrinking.

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