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	<title>Comments on: Rheumatoid Arthritis Anger</title>
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	<description>Bringing information &#38; encouragement to fight RA</description>
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		<title>By: Thom Cady</title>
		<link>http://rawarrior.com/rheumatoid-arthritis-anger/comment-page-1/?show=comments-60259</link>
		<dc:creator>Thom Cady</dc:creator>
		<pubDate>Sun, 13 Mar 2011 10:03:20 +0000</pubDate>
		<guid isPermaLink="false">http://rawarrior.com/?p=5071#comment-60259</guid>
		<description>Learning to process anger without increasing harm to ones own body &amp; mind by what one thinks of oneself, mindless chatter-boxes that have &#039;know-it-all attitudes&#039; or &#039;well meaning&#039; along with many physicians who practice medicine without ever getting good at it; may take years of review (connecting-the-dots) to achieve harmony within oneself. The pain is real when it arrives as an unwelcome visitor; however, expecting others to understand is &#039;too draining&#039;.  I have gotten more soft spoken yet bolder with people and physicians after reading insightful experiences and research.  I simply ask both groups &quot;how long have you been practicing medicine?&quot; then quickly get away from the negativity.  If a &#039;know-it-all&#039; is in my home I announce I need my nap now that they will need to come back &#039;sometime&#039;.  If they are calling and will not &#039;shut up&#039;, &quot;I need to go to the bathroom right now and will call you back (sometime)&quot;.  Get away from negative people (who think they are positive)politely but firmly with your need of peace of mind.</description>
		<content:encoded><![CDATA[<p>Learning to process anger without increasing harm to ones own body &amp; mind by what one thinks of oneself, mindless chatter-boxes that have &#8216;know-it-all attitudes&#8217; or &#8216;well meaning&#8217; along with many physicians who practice medicine without ever getting good at it; may take years of review (connecting-the-dots) to achieve harmony within oneself. The pain is real when it arrives as an unwelcome visitor; however, expecting others to understand is &#8216;too draining&#8217;.  I have gotten more soft spoken yet bolder with people and physicians after reading insightful experiences and research.  I simply ask both groups &#8220;how long have you been practicing medicine?&#8221; then quickly get away from the negativity.  If a &#8216;know-it-all&#8217; is in my home I announce I need my nap now that they will need to come back &#8216;sometime&#8217;.  If they are calling and will not &#8216;shut up&#8217;, &#8220;I need to go to the bathroom right now and will call you back (sometime)&#8221;.  Get away from negative people (who think they are positive)politely but firmly with your need of peace of mind.</p>
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		<title>By: Melena</title>
		<link>http://rawarrior.com/rheumatoid-arthritis-anger/comment-page-1/?show=comments-60251</link>
		<dc:creator>Melena</dc:creator>
		<pubDate>Sun, 13 Mar 2011 04:50:08 +0000</pubDate>
		<guid isPermaLink="false">http://rawarrior.com/?p=5071#comment-60251</guid>
		<description>It&#039;s sad to know that other people are going through the same things but yet comforting too.  People and family say that same stuff to me, &quot;if you weren&#039;t under so much stress&quot; &quot;if you just let things go&quot; If, if,if, if I just had a dollar for every if I would be shopping. I wish that people knew how wrong they are and that they are hurting not only me but my husband who feels guilty for being laid off work adding to my stress and my kids who don&#039;t even ask for help with things to not add to my stress. I know that I didn&#039;t cause this disease and I know that stress doesn&#039;t help either.  I just hope that someday people stop and think before the speak and realize that we are all in this together. This has been an eye opening experience for my entire family and we now look at the world and people a lot differently because of it, not that we were uncompassionate people before not we are just more aware of others and their situations.  Great article and advice from everyone.</description>
		<content:encoded><![CDATA[<p>It&#8217;s sad to know that other people are going through the same things but yet comforting too.  People and family say that same stuff to me, &#8220;if you weren&#8217;t under so much stress&#8221; &#8220;if you just let things go&#8221; If, if,if, if I just had a dollar for every if I would be shopping. I wish that people knew how wrong they are and that they are hurting not only me but my husband who feels guilty for being laid off work adding to my stress and my kids who don&#8217;t even ask for help with things to not add to my stress. I know that I didn&#8217;t cause this disease and I know that stress doesn&#8217;t help either.  I just hope that someday people stop and think before the speak and realize that we are all in this together. This has been an eye opening experience for my entire family and we now look at the world and people a lot differently because of it, not that we were uncompassionate people before not we are just more aware of others and their situations.  Great article and advice from everyone.</p>
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		<title>By: Kelly Young</title>
		<link>http://rawarrior.com/rheumatoid-arthritis-anger/comment-page-1/?show=comments-51838</link>
		<dc:creator>Kelly Young</dc:creator>
		<pubDate>Sun, 23 Jan 2011 22:35:54 +0000</pubDate>
		<guid isPermaLink="false">http://rawarrior.com/?p=5071#comment-51838</guid>
		<description>Patrice, you make many important points here and I hope your words are read by many. There is much reason to be angry but like you, I try to channel it into changing things ofr the future of RA. On behalf of our children and grandchildren - so when these bad things still happen, I call it my &quot;rocket fuel&quot; to keep me going!</description>
		<content:encoded><![CDATA[<p>Patrice, you make many important points here and I hope your words are read by many. There is much reason to be angry but like you, I try to channel it into changing things ofr the future of RA. On behalf of our children and grandchildren &#8211; so when these bad things still happen, I call it my &#8220;rocket fuel&#8221; to keep me going!</p>
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		<title>By: Kelly Young</title>
		<link>http://rawarrior.com/rheumatoid-arthritis-anger/comment-page-1/?show=comments-51827</link>
		<dc:creator>Kelly Young</dc:creator>
		<pubDate>Sun, 23 Jan 2011 21:57:40 +0000</pubDate>
		<guid isPermaLink="false">http://rawarrior.com/?p=5071#comment-51827</guid>
		<description>right, Suzi.  Who would say this to Michael J Fox or a breast cancer patient? I agree that the RA patients I&#039;ve met are the kindest most patient people  - for the most part - probably due to living with horrendous pain. </description>
		<content:encoded><![CDATA[<p>right, Suzi.  Who would say this to Michael J Fox or a breast cancer patient? I agree that the RA patients I&#8217;ve met are the kindest most patient people  &#8211; for the most part &#8211; probably due to living with horrendous pain.</p>
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		<title>By: patrice</title>
		<link>http://rawarrior.com/rheumatoid-arthritis-anger/comment-page-1/?show=comments-51767</link>
		<dc:creator>patrice</dc:creator>
		<pubDate>Sun, 23 Jan 2011 17:00:34 +0000</pubDate>
		<guid isPermaLink="false">http://rawarrior.com/?p=5071#comment-51767</guid>
		<description>Angry, yes I do get angry at times. Not as often as I used to. I&#039;ve learned to process the anger and handle it differently. I also moved to a better climate because of the disease. And so my family is over 500 miles away. Since I&#039;ve had the symptoms since I was 19 and not diagnosed until I was 40 after seeing many docs I did get angry alot. The frustration of not knowing what exactly I was dealing with did not help. In those years I had 4 children and not being able to keep up with them at times or having to hold my baby and scoot down the stairs on my butt cuz I couldn&#039;t walk yeah that did make me angry. Having to crawl to the bathroom again cuz I couldn&#039;t walk. And having a husband who is now deceased think I was faking it to get out of  doing things even though I still ran, played tennis, and worked out when I could. That pissed me off! Or the cavalier attitude of the docs and their dispensing of pain meds. Sometimes I would wish that certain ones would have this disease for a day, the worse flare up day. Than they would have a grasp on what they are treating. And not treat you like some addict looking for a fix! I was in the medical field for years and I do know that they treated many patients the same way I was not unusual. That in it self made me very angry. I take very few allopathic meds so when I do ask for something a red light should go on but does it NO! They all of a sudden want to send me to a pain clinic. I don&#039;t have the kind of pain that I feel warrants a pain clinic. And when I need one I will ask for it. I get very angry because to get any thing across to my doc or her PA I have to be very adament about the situation. I have learned over the years both with my disease and with my medical training how to handle the flare-ups and other problems by myself. I&#039;m not a patient who calls my doc for every little thing to complain about. Maybe it&#039;s because I remember having those kind of pts myself and how they were perceived as crack pots. And I certainly don&#039;t want that on my chart. So it&#039;s a catch 22 you&#039;re damned if you do and you&#039;re damned if you don&#039;t. It really makes me angry that we are all lumped into one bunch and they don&#039;t see us as individuals with different needs, different levels of pain tolerance, and progression of joint deterioration. I&#039;ve had a few good docs they were the ones who had some sort of autoimmune dx themselves. I&#039;ve had people actually say to me that they have never seen me in any distress do to the RA. They think it&#039;s not real . My answer to them is I have good days and bad days. And after all these years I&#039;ve learned to hide it well. I guess they aren&#039;t perceptive enough to see the swelling of my fingers and wrists or when I&#039;m limping,and moving slower than normal.  So now I handle my anger differently,I&#039;ve found that the things I do now work for me and diffuse the anger a little but not much! But that&#039;s what keeps me going the anger and to prove others wrong about this disease.Thanks.</description>
		<content:encoded><![CDATA[<p>Angry, yes I do get angry at times. Not as often as I used to. I&#8217;ve learned to process the anger and handle it differently. I also moved to a better climate because of the disease. And so my family is over 500 miles away. Since I&#8217;ve had the symptoms since I was 19 and not diagnosed until I was 40 after seeing many docs I did get angry alot. The frustration of not knowing what exactly I was dealing with did not help. In those years I had 4 children and not being able to keep up with them at times or having to hold my baby and scoot down the stairs on my butt cuz I couldn&#8217;t walk yeah that did make me angry. Having to crawl to the bathroom again cuz I couldn&#8217;t walk. And having a husband who is now deceased think I was faking it to get out of  doing things even though I still ran, played tennis, and worked out when I could. That pissed me off! Or the cavalier attitude of the docs and their dispensing of pain meds. Sometimes I would wish that certain ones would have this disease for a day, the worse flare up day. Than they would have a grasp on what they are treating. And not treat you like some addict looking for a fix! I was in the medical field for years and I do know that they treated many patients the same way I was not unusual. That in it self made me very angry. I take very few allopathic meds so when I do ask for something a red light should go on but does it NO! They all of a sudden want to send me to a pain clinic. I don&#8217;t have the kind of pain that I feel warrants a pain clinic. And when I need one I will ask for it. I get very angry because to get any thing across to my doc or her PA I have to be very adament about the situation. I have learned over the years both with my disease and with my medical training how to handle the flare-ups and other problems by myself. I&#8217;m not a patient who calls my doc for every little thing to complain about. Maybe it&#8217;s because I remember having those kind of pts myself and how they were perceived as crack pots. And I certainly don&#8217;t want that on my chart. So it&#8217;s a catch 22 you&#8217;re damned if you do and you&#8217;re damned if you don&#8217;t. It really makes me angry that we are all lumped into one bunch and they don&#8217;t see us as individuals with different needs, different levels of pain tolerance, and progression of joint deterioration. I&#8217;ve had a few good docs they were the ones who had some sort of autoimmune dx themselves. I&#8217;ve had people actually say to me that they have never seen me in any distress do to the RA. They think it&#8217;s not real . My answer to them is I have good days and bad days. And after all these years I&#8217;ve learned to hide it well. I guess they aren&#8217;t perceptive enough to see the swelling of my fingers and wrists or when I&#8217;m limping,and moving slower than normal.  So now I handle my anger differently,I&#8217;ve found that the things I do now work for me and diffuse the anger a little but not much! But that&#8217;s what keeps me going the anger and to prove others wrong about this disease.Thanks.</p>
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		<title>By: Suzi</title>
		<link>http://rawarrior.com/rheumatoid-arthritis-anger/comment-page-1/?show=comments-51732</link>
		<dc:creator>Suzi</dc:creator>
		<pubDate>Sun, 23 Jan 2011 13:43:37 +0000</pubDate>
		<guid isPermaLink="false">http://rawarrior.com/?p=5071#comment-51732</guid>
		<description>Oh my goodness, whoever said that anger causes RA must have worked under the direction of Sigmund Freud. When I go to my rheumatoid doctor and see all these people come in with walkers and canes to assist them I highly doubt it was the &quot;anger&quot; in their lives that brought them to this point. Some of these people are the sweetest people I have ever met. I had cancer back in 2000 at the age of 40. Did anger cause my cancer, too? If this rheumatoid does take my life earlier than expected, then perhaps, it will read in my obituary, &quot;She suffered from a life of anger which caused her rheumatoid arthritis&quot; lol. I don&#039;t think so. Thank you for letting me share!</description>
		<content:encoded><![CDATA[<p>Oh my goodness, whoever said that anger causes RA must have worked under the direction of Sigmund Freud. When I go to my rheumatoid doctor and see all these people come in with walkers and canes to assist them I highly doubt it was the &#8220;anger&#8221; in their lives that brought them to this point. Some of these people are the sweetest people I have ever met. I had cancer back in 2000 at the age of 40. Did anger cause my cancer, too? If this rheumatoid does take my life earlier than expected, then perhaps, it will read in my obituary, &#8220;She suffered from a life of anger which caused her rheumatoid arthritis&#8221; lol. I don&#8217;t think so. Thank you for letting me share!</p>
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		<title>By: Michael Patterson</title>
		<link>http://rawarrior.com/rheumatoid-arthritis-anger/comment-page-1/?show=comments-51679</link>
		<dc:creator>Michael Patterson</dc:creator>
		<pubDate>Sun, 23 Jan 2011 06:42:50 +0000</pubDate>
		<guid isPermaLink="false">http://rawarrior.com/?p=5071#comment-51679</guid>
		<description>Thanks, Tracey!  Good attitude.  Things are actually much better since I wrote that, but I think I still needed to hear that!</description>
		<content:encoded><![CDATA[<p>Thanks, Tracey!  Good attitude.  Things are actually much better since I wrote that, but I think I still needed to hear that!</p>
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		<title>By: Tracey</title>
		<link>http://rawarrior.com/rheumatoid-arthritis-anger/comment-page-1/?show=comments-51549</link>
		<dc:creator>Tracey</dc:creator>
		<pubDate>Sat, 22 Jan 2011 08:50:27 +0000</pubDate>
		<guid isPermaLink="false">http://rawarrior.com/?p=5071#comment-51549</guid>
		<description>Hi Michael,
I know where you&#039;re coming from - I mourn my losses, I used to play guitar - and I&#039;ve watched it disappear with so many other things I used to be able to do. Badminton, anything with a racquet, even handwriting is becoming a chore (and I&#039;ve got 7 exams to do this year - I&#039;m studying!). I&#039;m also a graphic designer, but can&#039;t do that anymore (notice I haven&#039;t given up on that completely I didn&#039;t say &#039;I was a graphic designer&#039;!).
The trick is to replace the things you can&#039;t do with things you can do.
I can&#039;t use the computer graphics software anymore - but I&#039;ve discovered that I&#039;m rather good at Tax and accounting. It feels a bit sad to go from creative to accounting, but what can I say, I&#039;m enjoying it! (mainly because I can do it and I&#039;ve achieved something!) Plus i can do it on my own terms - online, from home wearing my pink pyjamas and my blue bed socks with purple polka dots! (seriously - I have them on now).
I think it&#039;s important to stop your world from closing in too much - I have a tendancy toward being a bit of a hermit, so I try to resist that, but on my own terms.
I can&#039;t peel potatoes any more - so I learned to cook them with their skin on - turns out it&#039;s healthier - who knew!
I don&#039;t want to sound too &#039;pollyanna&#039; as my husband puts it, but I&#039;m having a flare-up kind of week yet still feeling positive - so I&#039;m paying it forward.
Hope you find a few replacements for your losses - keep looking they&#039;re out there.
Cheers
Tracey.</description>
		<content:encoded><![CDATA[<p>Hi Michael,</p>
<p>I know where you&#8217;re coming from &#8211; I mourn my losses, I used to play guitar &#8211; and I&#8217;ve watched it disappear with so many other things I used to be able to do. Badminton, anything with a racquet, even handwriting is becoming a chore (and I&#8217;ve got 7 exams to do this year &#8211; I&#8217;m studying!). I&#8217;m also a graphic designer, but can&#8217;t do that anymore (notice I haven&#8217;t given up on that completely I didn&#8217;t say &#8216;I was a graphic designer&#8217;!).</p>
<p>The trick is to replace the things you can&#8217;t do with things you can do. </p>
<p>I can&#8217;t use the computer graphics software anymore &#8211; but I&#8217;ve discovered that I&#8217;m rather good at Tax and accounting. It feels a bit sad to go from creative to accounting, but what can I say, I&#8217;m enjoying it! (mainly because I can do it and I&#8217;ve achieved something!) Plus i can do it on my own terms &#8211; online, from home wearing my pink pyjamas and my blue bed socks with purple polka dots! (seriously &#8211; I have them on now).</p>
<p>I think it&#8217;s important to stop your world from closing in too much &#8211; I have a tendancy toward being a bit of a hermit, so I try to resist that, but on my own terms.</p>
<p>I can&#8217;t peel potatoes any more &#8211; so I learned to cook them with their skin on &#8211; turns out it&#8217;s healthier &#8211; who knew!</p>
<p>I don&#8217;t want to sound too &#8216;pollyanna&#8217; as my husband puts it, but I&#8217;m having a flare-up kind of week yet still feeling positive &#8211; so I&#8217;m paying it forward.</p>
<p>Hope you find a few replacements for your losses &#8211; keep looking they&#8217;re out there.</p>
<p>Cheers</p>
<p>Tracey.</p>
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		<title>By: Tracey</title>
		<link>http://rawarrior.com/rheumatoid-arthritis-anger/comment-page-1/?show=comments-51547</link>
		<dc:creator>Tracey</dc:creator>
		<pubDate>Sat, 22 Jan 2011 08:30:43 +0000</pubDate>
		<guid isPermaLink="false">http://rawarrior.com/?p=5071#comment-51547</guid>
		<description>Hi Barbara,
I agree that stress can trigger flares in RA, I&#039;ve seen it in my own case. I worked full time in one organisation where I thoroughly enjoyed my co-workers, while working to tight deadlines, doing creative work and dealing with a range of other potential &#039;stressors&#039; but I didn&#039;t feel stressed because the work environment was essentially positive (actually downright fun!) When I left to work part time with a different organisation, doing the same type of work with similar &#039;stressors&#039; my RA flared to the point I was forced to give up work. The difference was the work environment, the second place was positively toxic and I reacted to it accordingly.
The same thing happened with my two pregnancies, the first I worked for a government bureaucracy with a very negative environment, my blood pressure was very high until I was told by my doctor to stop work. The second pregnancy, I was self employed, working on big budget projects and meeting tight deadlines, but had a pleasant work environment - no problem with blood pressure at all and worked right up to baby&#039;s arrival (and started back with baby in tow very soon after!)
Should also note that RA was diagnosed between babies, so the second one was a case of going off all meds prior to pregnancy. Luckily I had no RA pain during pregnancy. (I was told that this could be due to large quantities of cortisone women produce naturally during pregnancy).
Anyway bit off topic - What I do know is that for me - stress does play a big part in RA flare-ups, and I agree with you that this could have been extrapolated by some to mean anger. But, I don&#039;t think the anger/stress caused the RA to start with, (especially given that I was 12 when I contracted the virus that is supposed to have caused my Juvenile RA).</description>
		<content:encoded><![CDATA[<p>Hi Barbara,</p>
<p>I agree that stress can trigger flares in RA, I&#8217;ve seen it in my own case. I worked full time in one organisation where I thoroughly enjoyed my co-workers, while working to tight deadlines, doing creative work and dealing with a range of other potential &#8216;stressors&#8217; but I didn&#8217;t feel stressed because the work environment was essentially positive (actually downright fun!) When I left to work part time with a different organisation, doing the same type of work with similar &#8216;stressors&#8217; my RA flared to the point I was forced to give up work. The difference was the work environment, the second place was positively toxic and I reacted to it accordingly.</p>
<p>The same thing happened with my two pregnancies, the first I worked for a government bureaucracy with a very negative environment, my blood pressure was very high until I was told by my doctor to stop work. The second pregnancy, I was self employed, working on big budget projects and meeting tight deadlines, but had a pleasant work environment &#8211; no problem with blood pressure at all and worked right up to baby&#8217;s arrival (and started back with baby in tow very soon after!)</p>
<p>Should also note that RA was diagnosed between babies, so the second one was a case of going off all meds prior to pregnancy. Luckily I had no RA pain during pregnancy. (I was told that this could be due to large quantities of cortisone women produce naturally during pregnancy).</p>
<p>Anyway bit off topic &#8211; What I do know is that for me &#8211; stress does play a big part in RA flare-ups, and I agree with you that this could have been extrapolated by some to mean anger. But, I don&#8217;t think the anger/stress caused the RA to start with, (especially given that I was 12 when I contracted the virus that is supposed to have caused my Juvenile RA).</p>
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		<title>By: Kelly Young</title>
		<link>http://rawarrior.com/rheumatoid-arthritis-anger/comment-page-1/?show=comments-51447</link>
		<dc:creator>Kelly Young</dc:creator>
		<pubDate>Fri, 21 Jan 2011 19:15:01 +0000</pubDate>
		<guid isPermaLink="false">http://rawarrior.com/?p=5071#comment-51447</guid>
		<description>Go Warrior Sandie! I enjoyed reading this Sandie since I&#039;ve been there done that with doctors too! Doing the same thing with my anger - sometimes I call it the &quot;rocket feul&quot;! This stuff like what you say and some parents &lt;a href=&quot;http://rawarrior.com/joint-examinations-with-rheumatoid-arthritis/&quot;&gt;have commented on today&#039;s blog post &lt;/a&gt;- is not acceptable and must change. We&#039;ll be determined enough to make it happen. Thanks. :D</description>
		<content:encoded><![CDATA[<p>Go Warrior Sandie! I enjoyed reading this Sandie since I&#8217;ve been there done that with doctors too! Doing the same thing with my anger &#8211; sometimes I call it the &#8220;rocket feul&#8221;! This stuff like what you say and some parents <a  href="http://rawarrior.com/joint-examinations-with-rheumatoid-arthritis/">have commented on today&#8217;s blog post </a>- is not acceptable and must change. We&#8217;ll be determined enough to make it happen. Thanks. <img src='http://rawarrior.com/wp-includes/images/smilies/icon_biggrin.gif' alt=':D' class='wp-smiley' /> </p>
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