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The Watercooler
something isn't sitting right with-me, could use some feedback pls
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<blockquote data-quote="Hound dog" data-source="post: 434946" data-attributes="member: 84"><p>Jena</p><p></p><p>Bottom line.</p><p></p><p>No matter what it is, or even if it is a combination of things, you need and have a right to be certain about your diagnosis. If there is question, then it needs to be cleared up one way or the other. Because NO doctor can effectively treat you if he doesn't know ALL that is going on.</p><p></p><p>This is why I get so ticked when fam docs and specialists don't communicate back and forth and share information like they should. I also get major ticked when docs don't take the <strong>time to read</strong> the patient's medical hx too. In recent years I've gotten to where I don't even fill in the forms when I see a new doctor concerning hx.....what's the point? They never read it anyway. So instead, I tell them in person, or have it written down for them by date ect. The latter they seem to find the most helpful. </p><p></p><p>So if you have doubts, and obviously you do, then you keep pushing for answers until those doubts are cleared up. You are your own best advocate. </p><p></p><p>Having lived with Lyme's Hope should be able to give you valuable info on it.</p><p></p><p>((hugs))</p></blockquote><p></p>
[QUOTE="Hound dog, post: 434946, member: 84"] Jena Bottom line. No matter what it is, or even if it is a combination of things, you need and have a right to be certain about your diagnosis. If there is question, then it needs to be cleared up one way or the other. Because NO doctor can effectively treat you if he doesn't know ALL that is going on. This is why I get so ticked when fam docs and specialists don't communicate back and forth and share information like they should. I also get major ticked when docs don't take the [B]time to read[/B] the patient's medical hx too. In recent years I've gotten to where I don't even fill in the forms when I see a new doctor concerning hx.....what's the point? They never read it anyway. So instead, I tell them in person, or have it written down for them by date ect. The latter they seem to find the most helpful. So if you have doubts, and obviously you do, then you keep pushing for answers until those doubts are cleared up. You are your own best advocate. Having lived with Lyme's Hope should be able to give you valuable info on it. ((hugs)) [/QUOTE]
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something isn't sitting right with-me, could use some feedback pls
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