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    <title><![CDATA[Ask a Question]]></title>
    <description><![CDATA[Have a question about the AF Community? Get answers from our community members or our community administrator.]]></description>
    <link>http://community.arthritis.org/ask</link>
    
    	
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      <guid isPermaLink="true">http://community.arthritis.org/post/ask/share_your_treatment_experience_on_treatment_report.html</guid>
	
      <title><![CDATA[Share your treatment experience on Treatment Report ]]></title>
      <description>&lt;p class=&quot;MsoNormal&quot;&gt;
&lt;p class=&quot;MsoNormal&quot;&gt;
&lt;p class=&quot;MsoNormal&quot;&gt;
&lt;p class=&quot;MsoNormal&quot;&gt;Hi Deanna and William,&lt;/p&gt;
&lt;p class=&quot;MsoNormal&quot;&gt;I was hoping that in addition to sharing your experiences
here, &lt;span style=&quot;mso-spacerun:yes&quot;&gt;&amp;nbsp;&lt;/span&gt;you can share them on Treatment
Report and assign a treatment result to your experience. &lt;span style=&quot;mso-spacerun:yes&quot;&gt;&amp;nbsp;&lt;/span&gt;Here is what some of the other people posted&lt;o:p&gt;&lt;/o:p&gt;&lt;/p&gt;
&lt;p class=&quot;MsoNormal&quot;&gt;&lt;a href=&quot;http://www.treatmentreport.com/conditions/knee-pain/surgery-knee-replacement/40/29/3&quot;&gt;http://www.treatmentreport.com/conditions/knee-pain/surgery-knee-replacement/40/29/3&lt;/a&gt;&lt;/p&gt;
&lt;p class=&quot;MsoNormal&quot;&gt;We don’t have any information under post replacement pain.&lt;o:p&gt;&lt;/o:p&gt;&lt;/p&gt;
&lt;p class=&quot;MsoNormal&quot;&gt;&lt;a href=&quot;http://www.treatmentreport.com/conditions/knee-post-replacement-pain/60/&quot;&gt;http://www.treatmentreport.com/conditions/knee-post-replacement-pain/60/&lt;/a&gt;&lt;/p&gt;
&lt;p class=&quot;MsoNormal&quot;&gt;I appreciate your time.&lt;o:p&gt;&lt;/o:p&gt;&lt;/p&gt;
&lt;/p&gt;
&lt;/p&gt;
&lt;/p&gt;
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      <pubDate>Mon, 02 Nov 2009 16:57:29 GMT</pubDate>
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      <guid isPermaLink="true">http://community.arthritis.org/post/ask/tkr_5_weeks_ago.html</guid>
	
      <title><![CDATA[TKR 5 weeks ago ]]></title>
      <description>&lt;P&gt;I've been reading the blogs here and I'm amazed at the variety of post-surgery problems that have occurred.&amp;nbsp; I've recently been experiencing shin discomfort but nothing that will inhibit my recovery...I hope.&amp;nbsp; I agree with all the posts about taking your pain meds.&amp;nbsp; They are the only way I get through my therapy.&amp;nbsp; I must be lucky, because my therapy team is fantastic. At the end of my session they were&amp;nbsp;stretching and bending my knee while&amp;nbsp;my leg was hanging off a table.&amp;nbsp; I was told I was&amp;nbsp;&quot;cheating&quot; because I kept lifting my hip off the table and leaning.&amp;nbsp;&amp;nbsp;I told them I had sciatica and it was really hurting&amp;nbsp;me through my hip and lower back.&amp;nbsp; Now they lay me down, stretch and manipulate my knee on my back.&amp;nbsp; The stretching part is more difficult this way for me in regards to the discomfort, but my&amp;nbsp;sciatica doesn't&amp;nbsp;interfer with my progress. Last time they&amp;nbsp;took a measurement I was at a 95 degree bend. I'm diligent about doing bending exercises at home daily between therapy sessions and have learned when I need my pain meds and when I don't. Essentially I have been on my own since the 4th day after surgery and for me found that since I needed to do daily things for myself I became stronger faster than if I had someone do them for me.&amp;nbsp; I know this isn't necessarily true for all, but for me it worked. They also informed me it would take about a year before I would lose the feeling that there is something foreign in my leg. I got that information also from a woman I know who had both of her knees done.&lt;/P&gt;
    &lt;P&gt;I had the pleasure of having my staples out on my 64th birthday..whoopee! For months I had wanted to see a band that was playing close to home and wasn't going to let my surgery stand in the way. That night my good friend prepared dinner for my &quot;helping crew&quot; and they took me to see the band.&amp;nbsp; I only lasted for 45 min. but I did it. Two days later I discovered I could get myself into my truck and I've been mobile every since. Now don't get me wrong, I'm not out galavanting around alot, but I can get myself to therapy and if I need milk and bread I don't have to wait until someone has time to help. &lt;/P&gt;
    &lt;P&gt;One thing I do need help with is getting my cat to the vet today.&amp;nbsp; He's 20lbs and I don't have a prayer of carrying him so one of my good Samaratins is coming to load him in my truck and she'll go with me to haul him around.&amp;nbsp; And...another good thing...my vet will allow me to pay for the visit after I get back to work.&lt;/P&gt;
    &lt;P&gt;I guess all in all I'm trying to say I'm not having a terrible time of recovery..just impatient to get the &quot;rodeo&quot; over and get back to normal.&lt;/P&gt;
    &lt;P&gt;&amp;nbsp;&lt;/P&gt;</description>
      <pubDate>Mon, 02 Nov 2009 13:08:31 GMT</pubDate>
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      <guid isPermaLink="true">http://community.arthritis.org/post/ask/help_i_have_no_ins_and_need_surgery_and_meds.html</guid>
	
      <title><![CDATA[HELP! I HAVE NO INS AND NEED SURGERY AND MEDS! ]]></title>
      <description>Hello,
&lt;div&gt;&lt;br&gt;
&lt;/div&gt;
&lt;div&gt;I am at a loss! &#160;Can Somebody PLEASE tell me how I can get the help I need. &#160;I don't have insurance, I receive a VERY small check from ssi each month, I am in IMMINENT NEED of a second hip replacement, I have RA in every joint and i need to be under a drs care! I need Meds! &#160;I have a three yr old son who is now in the custody of my family because i cannot care for him and when I gave them temp custody the dept of child and family took away my medicaid! &#160;I dont know what to do, I am only 36 and i fear if I dont get this surgery and the medication i need my quality of life is going to suffer tremendously!&lt;/div&gt;
&lt;div&gt;&lt;br&gt;
&lt;/div&gt;
&lt;div&gt;Thanks for any and all input.&lt;/div&gt;
&lt;div&gt;&lt;br&gt;
&lt;/div&gt;
&lt;div&gt;Sincerely,&lt;/div&gt;
&lt;div&gt;&lt;br&gt;
&lt;/div&gt;
&lt;div&gt;Jennifer C.&lt;/div&gt;
</description>
      <pubDate>Fri, 23 Oct 2009 15:14:32 GMT</pubDate>
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      <guid isPermaLink="true">http://community.arthritis.org/post/ask/electric_pain_feeling_.html</guid>
	
      <title><![CDATA[Electric pain feeling  ]]></title>
      <description>&lt;P&gt;&lt;STRONG&gt;&lt;FONT size=4&gt;I have Fibromyalgia, osteoathritis, tendonitis, PTS, migraines, cronic asthma, depression, had total knee replacement back in 2008 only on right knee. I have&amp;nbsp;been disabled since 1992. I'm only 47. I keep having shooting pains in my back, the upper part towards shoulders It feels like someone shot electicity rod in my back. It seems to paralyze me for a few seconds and also makes me jerk like I've just been tazered. Does anyone else have this problem? Or could someone explain this.&lt;/FONT&gt;&lt;/STRONG&gt;&lt;/P&gt;
    &lt;P&gt;&lt;STRONG&gt;&lt;FONT size=4&gt;&lt;/FONT&gt;&lt;/STRONG&gt;&amp;nbsp;&lt;/P&gt;
    &lt;P&gt;&lt;STRONG&gt;&lt;FONT size=4&gt;&lt;/FONT&gt;&lt;/STRONG&gt;&amp;nbsp;&lt;/P&gt;
    &lt;P&gt;&lt;STRONG&gt;&lt;FONT size=4&gt;Thanks&lt;/FONT&gt;&lt;/STRONG&gt;&lt;/P&gt;
    &lt;P&gt;&lt;STRONG&gt;&lt;FONT size=4&gt;Robin-Ohio&lt;/FONT&gt;&lt;/STRONG&gt;&lt;/P&gt;</description>
      <pubDate>Wed, 21 Oct 2009 23:35:32 GMT</pubDate>
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      <guid isPermaLink="true">http://community.arthritis.org/post/ask/embrel_research.html</guid>
	
      <title><![CDATA[Embrel research ]]></title>
      <description>&lt;P&gt;I am doing some research for my dad and I have 2 questions to post:&lt;/P&gt;
    &lt;P&gt;1)&amp;nbsp; Dad has been on Embrel for 6 years and has just qualified for Medicare.&amp;nbsp; He now believes he will have to pay for Embrel out of his pocket (expensive) so he has decided to stop taking Embrel.&amp;nbsp; He hasn't had any swelling or rashes occur yet (symptoms he&amp;nbsp;had when he began taking Embrel) but he said he wasn't feeling well overall.&amp;nbsp;&amp;nbsp;Should&amp;nbsp;we be concerned about his discountinued use of Embrel (other than the obvious swelling/rash, etc.)?&lt;/P&gt;
    &lt;P&gt;2)&amp;nbsp; Does anyone know for sure that&amp;nbsp;Medicare won't cover Embrel and if yes&amp;nbsp;does anyone know what the next step is?&amp;nbsp; I find it hard to believe that there is no way to have this necessary drug covered.&amp;nbsp; I suppose secondary insurance is next. . .???&lt;/P&gt;
    &lt;P&gt;Thank you in advance for any advice on these issues!&lt;/P&gt;
    &lt;P&gt;&amp;nbsp;&lt;/P&gt;
    &lt;P&gt;&amp;nbsp;&lt;/P&gt;</description>
      <pubDate>Sun, 27 Sep 2009 14:20:03 GMT</pubDate>
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      <guid isPermaLink="true">http://community.arthritis.org/post/ask/total_knee_replacement_pain.html</guid>
	
      <title><![CDATA[Total Knee Replacement Pain ]]></title>
      <description>&lt;FONT size=3&gt;I had a total knee put in 03/31/09 after 3 ACL's over the years.&amp;nbsp;&amp;nbsp;After 6 months, the pain is about as distracting as prior to the procedure. I really wasn't ready for that. Everytime I met with the Surgeon, I would express how happy I will be when the pain is gone. He never disclosed that there was a possibility the pain would remain. But at least it is stable and I don't fall down any longer. My right knee was scheduled for a total in November, but I have postponed it until I work this thing out. I am glad I found this forum. I thought it was just me...&amp;nbsp;&amp;nbsp; Hope we all get better....&lt;/FONT&gt;</description>
      <pubDate>Sat, 26 Sep 2009 00:21:39 GMT</pubDate>
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      <guid isPermaLink="true">http://community.arthritis.org/post/ask/question_about_the_right_shoes_and_walking.html</guid>
	
      <title><![CDATA[question about the right shoes and walking ]]></title>
      <description>Buying the right shoes...running or walking ones?&amp;nbsp; Was hoping to buy online or would it be better to get fitted?&amp;nbsp; I am 35 years, and the arthritis is in my feet, knees, hips, hand mostly.&amp;nbsp; I am trying to find an easy way and unsure how much I push. I went walking and feet and knees really hurt today.&amp;nbsp; Swimming is not an easy access for me? ideas for shoes and exercise...and do I stop before I even start if the pain is already there?&lt;br&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;br&gt;
</description>
      <pubDate>Tue, 22 Sep 2009 13:58:03 GMT</pubDate>
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      <guid isPermaLink="true">http://community.arthritis.org/post/ask/is_this_the_way_it_is.html</guid>
	
      <title><![CDATA[Is this the way it is? ]]></title>
      <description>&lt;P&gt;For years I have known I&amp;nbsp; have arthritis.&amp;nbsp; However, it was not until I tore my miniscus that I was actually diagnosed.&amp;nbsp;&amp;nbsp; Recently my dr did blood work to be able to tell if it was RA or not.&amp;nbsp; I came back neg. for Ra.&amp;nbsp; However, my pain is in the joints of both hands, my shoulders, my lower spine, both of my hipts,both knees, and my toes.&amp;nbsp;&amp;nbsp; The worst being hips and knees.&amp;nbsp; Also, I have lots of pain in all of my lower muscles...even my butt muscles.&amp;nbsp; My calves and thgih muscles are always sore.&amp;nbsp; When I stand after sitting or laying for even a short time, it is difficult moving....and never really seems to loosen up ...always feelins sore and stiff.&amp;nbsp; Bending t oeven lower myself onto the lue is difficult.&amp;nbsp; The only thing the Dr., did..was give me celebrex and send me on my way.&amp;nbsp; &lt;/P&gt;
    &lt;P&gt;I am 45 and can barely go up or down a flight of stairs.&amp;nbsp; Is this normal?&amp;nbsp; Is this the way its just going to be forever?&amp;nbsp; I thought oesto was the lessor of the two arthritisis.&amp;nbsp; &lt;/P&gt;
    &lt;P&gt;Comments, opinions, advice?&amp;nbsp; anything will help.&amp;nbsp; &lt;/P&gt;</description>
      <pubDate>Mon, 21 Sep 2009 23:35:20 GMT</pubDate>
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      <guid isPermaLink="true">http://community.arthritis.org/post/ask/ra_and_hives.html</guid>
	
      <title><![CDATA[RA and Hives? ]]></title>
      <description>I was diagnosed with RA over 2 years ago and was taking Methotrexate and Humira very successfully. No side effects and my RA all but disappeared. A few months ago I went off Methotrexate, but was still taking Humira every two weeks. This month I missed a dose and have since been battling severe hives all over my body. I don't know if the two are related. I have not eaten anything out of the ordinary and do not have any new beauty products in my regimen. Could the hives actually be a &quot;flare?&quot; &amp;nbsp; &lt;br&gt;
</description>
      <pubDate>Mon, 21 Sep 2009 10:43:12 GMT</pubDate>
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