I developed neuralgia on the left side of my face and took co-codamol for pain relief. Within 24 hours this side had swollen drastically. I went to hospital and was given a course of steroids to reduce the swelling. I was diagnosed as being allergic to codeine.
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how do you cope? One year ago I fell downstairs (vertigo) fractured my neck and had severe pain in upper left arm, felt like a very bad bruise and a swollen but not broken wrist. Neck healed, pain in my upper arm remained and could move it but not do up bra etc without severe pain. Had an injection in my shoulder - made it worse. 11 months on I fell down a shorter flight of stairs (return of vertigo!) on to same bad shoulder/arm. Now frozen and pain from neck to finger tips all the time and even worse at night. Can't take oral pain relief tablets has anyone tried pain relief patches? The pain is so bad I can't do anything and I am getting seriously depressed and being driven to despair, its like being in constant childbirth labour! constantly having to massage my arm including from elbow to wrist and palm of hand into fingers. Given conflicting advice by every medical person seen so far. Seems it is likely multiple problems but still no MRI, xray shows no broken bones in shoulder. Read most of the discussions, not many triggered by injury unless I have missed those. Any support groups locally in Cornwall where we could at least cry openly!
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I am 34 year old NZ mum and I had CES about 3 years ago, after 3 operations and lots of physio and exercise I returned back to work, bit by bit, slowly working my way up to full time over the period of 8 months. I actually feel pretty fortunate and feel that Iv made a pretty amazing recovery, I got the mobility of my right leg back (it was dragging) although this is still very numb and weak, it appears normal to those around me, and I no longer walk funny, and my bladder only seems to play badly up certain times of the month (by play up I mean weakness and high frequency) the pain is pretty good too....compared to what it use to be like. The night before my first urgent operation I had hot cold sensations filling my legs,it felt like they were being dipped in warm or cold water, it was one of the strangest things I have ever felt, I hadn't realised that going to the bathroom every few min was a warning sign (I actually thought I must of been pregnant). Anyway recently I'm getting cold patches (large patches) and weird almost pleasant cold tingling around the butt and the back of the legs and wondered if anyone else gets similar sensations?, I hate rushing back to the docs and don't want to live in fear that the CES will raise its ugly head again, I also want to avoid too many more MRIs as I have already been exposed to far to much radiation from these. Was really just hoping that another CES patient could tell me their ongoing symptoms and issues that they have just managed to live with.
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I have two options: Ellipse Excision (most invasive) and Curettage and Electrodesiccation (least invasive). Derm says with C and D she is not able to tell me if after the surgery all basal cell carcinoma are removed as there is no pathology testing. I'm nervous thinking about what I want the most. Has anyone on the Cancer board had either of these two surgeries. If so, which one was most successful?
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I was diagnosed 3 years ago at the age of 20. I was in total shock.At that point I was blacking out 3-5 times a day, constantly dizzy and struggling with the pain in my spleen.Along with the pv my haemotologist told me I am iron deficiant and cannot take iron tablets as it will make my haemoglobin shoot through the roof and risk me having a stroke or heart attack.so now I'm constantly tired and weak. I am just on 2 aspirin a day as doctor was worried about putting me on other medication as I'm quite young and is scared about the side effects on me (as if I'm not terrified enough).now my spleen has tripled in size and is a constant struggle to do daily things with my toddler, I'm starting to feel like I should just get it removed.has anyone had this done? And how did it effect you after the operation and then in daily life?
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It's has increased in size and it's hard and painful to pressure.
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I have quite a deep cyst on my right butt cheek. It's been there for over 5 years now and I am planning on getting it removed. It has never secreted any pus as it is quite deep under the skin but when I feel around the area I can feel that it's quite wide and deep under the surface! I guess the big question is will it leave a large dent or will it sink in once the cyst is removed? I know it doesn't sound like a big deal but I really don't want a large dimple or dent there!
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Can you have breathing problems from smoking weed?
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Ok well I'm sat up as I'm typing this, I've been a heavy cocaine user for the past 2 years. Put been using for 15 years. Sat here now my eye is weeping water I've bad headache side of my face is in sore.
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I am hoping to find other parent's that also have an adult with Down Syndrome. I am finding that there is several subjects for baby's etc. but very little groups that focus on "adults with Down Syndrome".
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