Posts Tagged ‘find’

i am currently on i. v dilaudid and have no insurance. is yhere any where for me to get help with out insurance?

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    When my wife, well ex-wife, filed for divorce, I guess I was supposed to receive divorce notices on the matter. I do not ever recall receiving these and am not sure what one even looks like. Are these notices something everyone receives when they get a divorce? What do they even say? Can I find the ones I supposedly received?

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      I’ve always been curious about the details of the proceedings in my parent’s divorce. What is the easiest way for someone to a) locate and b) get their hands on an old case file like this?I’ve looked online at the public records and they don’t go back to 1975. Any other way to search?ps- not asking if you think i should do this; asking HOW.

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        I live in OC, california. Going through divorce. Can anyone recommend me a divorce attorney, one good with custody negotiation and battle. Tell me your experience of attorney and what you like about him or her.

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          Western medicine has completely failed me. I deal with chronic pain, fatigue, muscle cramps, brain fog, etc. , that is pretty constant but with a clear cyclical component. It is, according to all available tests, physicals, and evaluations of other kinds, NOT fibromyalgia, chronic fatigue syndrome, stress, depression, MS, lupus, rheumatoid arthritis, celiac disease, or any other of myriad disorders Western doctors are halfway familiar with. I’m not a hypochondriac or an attention seeker, and this issue is really affecting my quality of life. MY best guess is myofascial pain, but I’m not sure. I definitely have the ropey knots of trigger points, but pressing them brings relief in a “good pain” kind of way, not discomfort. The knots can never be worked out with massage, though. I don’t have any tender points in the traditional sense. For awhile I really wanted a diagnosis, something to validate what I was going through and open up treatment options. Now I really just want it to stop. So what kind of title should I look for beside the name of a practitioner? I want someone highly trained in several forms of alternative medicine, not just an acupuncturist or herbalist. Interesting, Dave. I suppose it’s the lack of a centralized accrediting system I was wondering about – is there, in fact, no such agency at all, or is there one agency more widely respected than others? It’s hard to imagine that there is no body widely recognized as the authority, even though there clearly are charlatans out there. If there is one widely respected body, I’d like to know which agency that is. I’m not sure how one would use the placebo effect knowing what it is. Once you know something is a placebo, haven’t you effectively guaranteed its ineffectiveness? As an analogy, you can’t undo a disbelief in Santa Clause. Interesting, Dave. I suppose it’s the lack of a centralized accrediting system I was wondering about – is there, in fact, no such agency at all, or is there one agency more widely respected than others? It’s hard to imagine that there is no body widely recognized as the authority, even though there clearly are charlatans out there. If there is one widely respected body, I’d like to know which agency that is. I’m not sure how one would use the placebo effect knowing what it is. Once you know something is a placebo, haven’t you effectively guaranteed its ineffectiveness? As an analogy, you can’t undo a disbelief in Santa Clause. Edit: Just wanted to let you know I didn’t give the thumbs down. I appreciate any thoughtful answers and never thumbs down real responses. Sorry, Gary Y. , didn’t mean to offend. I thought it would be clear from the context that “in this instance” was implied, though it was not written. And yes, in this instance, Western medicine HAS completely failed me. Doctors have been all too happy to order bloodwork and then shake their heads and shrug when it comes back negative. I had a neurologist tell me that I couldn’t POSSIBLY have MS because I had a negative brain MRI – so I asked about spinal lesions, and asked why the MS Society said five percent of MS patients showed no brain lesions. His response? He said, “The MS Society lies,” and went on to say checking for spinal lesions would be a possibility if I’d had vertigo. My response? “Vertigo is on the list of my symptoms I just handed you!”Far too many people seem to go into medicine with no curiosity, and that’s not the field you should go into if you’re not curious. I’m not picking on doctors – far too many people in EVERY field are incompetent, my own included.

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