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  <title>Raynaud's Association</title> 
  <description></description> 
  <link>http://www.raynauds.org/support/forums/forum/index.cfm?forumid=1</link> 
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		<title>Painfull fingers</title>
		<link>http://www.raynauds.org/support/forums/forum/messageview.cfm?catid=10&amp;threadid=2510</link> 
		<pubDate>2010-08-30T19:37:35 -05.00</pubDate> 
		<dc:creator>Gerty</dc:creator>
   	    <slash:comments>2</slash:comments> 
		<description><![CDATA[ I was only DXed with Raynaud's a few days ago and even tho I do get pains in my fingers Im not sure what the Raynaud's pain feels like as everything I have read it just say's pain. My pain that I have notice for some 8 months now Is more like arthritis pain mostley in the joints of my fingers but I can close my fingers they do not feel stiff and ache all day long. there is  a 2nd pain that I get on top of this pain and its not there all the time only when my fingers get cold its like they are painfully cold esp in my right hand more then my left hand and more so the very tips of my fingers. My toes just go numb numb and feel very cold but I seem to feel like an arthritis pain in them as well and like a burning pain when they do warm up.Can those of you that get Raynaud's pain as I read not every body gets the pain with Raynaud's describe it the best you can I know pain can be hard to describe at times ]]></description>
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		<title>Infracare socks</title>
		<link>http://www.raynauds.org/support/forums/forum/messageview.cfm?catid=10&amp;threadid=2507</link> 
		<pubDate>2010-08-26T17:30:45 -05.00</pubDate> 
		<dc:creator>ma02127</dc:creator>
   	    <slash:comments>2</slash:comments> 
		<description><![CDATA[ Has anyone tried these socks or heard about them?  I have to see a podiatrist tomorrow and I was looking at their website.  They have a very extensive site for foot care and I bumped into these sox.  They are $19.99/pair.<br /><br />The practice is the New England Podiatry in the Greater Boston Area but they have low cost shipping.  I usually have cold feet problems when in the snow but I know some of you suffer terribly so I wanted to share the information.<br /><br /><a target=_blank class=ftalternatingbarlinklarge href="http://www.ourdoctorstore.com/nep/store/item.asp?ITEM_ID=774&DEPARTMENT_ID=250">http://www.ourdoctorstore.com/...774&DEPARTMENT_ID=250</a><br /><br /><br />Infracare socks are the solution for: cold feet due to diabetes, impaired circulation, peripheral vascular disease (PVD), or Raynaud's disease.<br /><br />These socks are embedded with Bio-materials that work on proven scientific principles to deliver infra-sound waves that warm up your feet.  If you are suffering from cold feet due to a medical condition such as poor circulation, diabetes, Raynaud's disease, use Infracare socks for 2 weeks and you will notice that your feet feel warmer when wearing them <br /><br />Enjoy warm feet the entire day -  Here's how it works: <br /><br />As your body is continuously radiating heat, Infracare socks redirects that heat back to your feet.  Thus they maintain a steady flow of heat to keep the feet warm for the entire period they are worn.  The steady low intensity heat presents no risk of skin burns.  It's a big step forward, as Infracare socks do more than just retain heat....they actively facilitate heat re-transmission back to the feet.<br /><br />There is much more information at the link provided above ]]></description>
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		<title>Ingrown toenails</title>
		<link>http://www.raynauds.org/support/forums/forum/messageview.cfm?catid=10&amp;threadid=2506</link> 
		<pubDate>2010-08-24T23:13:32 -05.00</pubDate> 
		<dc:creator>ma02127</dc:creator>
   	    <slash:comments>4</slash:comments> 
		<description><![CDATA[ Hi everyone<img src="i/expressions/face-icon-small-sad.gif" border="0"><br /><br />I am wondering if anyone else has had to deal with ingrown toenails.  My nails are so weak that they tend to break very low, at least on one side.  I have to wait for them to grow a little before I can start coaxing the nail to grow on top of the toe's soft tissue.  This time, I didn't catch it before it got bad.  In one toe I have been treating what appears to be an open soar on the side on the low nail and it is extremely sore.  I cannot manage it the way I can on my hands.  It's a harder position, bad arthritis and I need eye glasses.  <br /><br />I intellectually link the problem with poor circulation from Raynauds although my feet are not normally affected much.  They just turn colors when my legs are handing off the doctor's table.  I always get the empathetic sigh when they see the various colors I develop with a/c exposure.<br /><br />Has anyone had to go to a podiatrist because of complications of Raynauds? ]]></description>
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		<title>getting a O2 level</title>
		<link>http://www.raynauds.org/support/forums/forum/messageview.cfm?catid=10&amp;threadid=2499</link> 
		<pubDate>2010-08-09T20:46:29 -05.00</pubDate> 
		<dc:creator>skay</dc:creator>
   	    <slash:comments>5</slash:comments> 
		<description><![CDATA[ With my mom's hands and feet involved getting an oxygen level reading is difficult. It use to work on her feet but not that doesn't seem to work either. She goes to the hospital a resonable amount and the nurses are not use to dealing with cases such as hers. Where could I advise them to try to get an O2 level before they totally flip out over the very low reading they are getting? ]]></description>
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		<title>drooling question</title>
		<link>http://www.raynauds.org/support/forums/forum/messageview.cfm?catid=10&amp;threadid=2498</link> 
		<pubDate>2010-08-09T20:43:27 -05.00</pubDate> 
		<dc:creator>skay</dc:creator>
   	    <slash:comments>2</slash:comments> 
		<description><![CDATA[ My mom has both raynauds and scleoderma. She has a problem with drooling a lot. She wanted to know if anyone else had this issue that has either of these conditions. ]]></description>
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		<title>ulcer</title>
		<link>http://www.raynauds.org/support/forums/forum/messageview.cfm?catid=10&amp;threadid=2490</link> 
		<pubDate>2010-07-23T12:27:35 -05.00</pubDate> 
		<dc:creator>SamD</dc:creator>
   	    <slash:comments>5</slash:comments> 
		<description><![CDATA[ I was wondering can you get an ulcer under your finger nail? I have only had one ulcer and that was a really long time ago, but I can't remember if you can get them under your nails. This has been like this for a while now. My Rhuemy did see it back in June and told me to be careful not agaviate it. But I cant leave it alone its hard feeling and it hurts. I have appointment with him in august will mention it again to hime.Plus let hiom know I am having pain still and I am taking my lyrica three times a day still. And its not helping. I so wish I could relax sometimes and that my neck and shoulders would stop hurting. Well I have rambled on sorry. Just let me know what you think please.. Sam ]]></description>
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		<title>New and Tired!</title>
		<link>http://www.raynauds.org/support/forums/forum/messageview.cfm?catid=10&amp;threadid=2482</link> 
		<pubDate>2010-07-07T21:50:47 -05.00</pubDate> 
		<dc:creator>4girls</dc:creator>
   	    <slash:comments>3</slash:comments> 
		<description><![CDATA[ I'm 39, wife, mom of 4 and feel like I am going completely crazy!  I have a wonderful precious primary care doctor, but lately things seem a little odd and I'm not sure if even he knows what is going on.<br /><br />December I was diagnosed with Raynauds.  No other symptoms at that time, but at the beginning of this summer I feel like I'm falling apart.  I woke up one morning with the bottom of my foot swollen and felt like I was standing on a small ball as I walked.  Dr. looked at it, ordered an RA test, lupus, and both came back negative.  It stayed swollen for an entire week and the swelling worked its way to the top of my foot and toes. After that subsided 2 weeks later my neck began to feel like someone hit me in the throat.  After 2 days that went away.  Woke up 2 days later and right beneath my chin was huge!  He doesn't think my foot, neck ,and chin are related ....but I feel like they are.  They are all affecting the right side of my body.  I have no symptoms on the left at all.<br /><br />I am running a low grade temperature between 99.3 and 99.5 which makes me move slow.  <br /><br />Am I NUTS.....and what advice do you have in moving forward with other doctors?<br /><br />thank you and this website is a blessing!  I just found it today! ]]></description>
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		<title>New bruises</title>
		<link>http://www.raynauds.org/support/forums/forum/messageview.cfm?catid=10&amp;threadid=2477</link> 
		<pubDate>2010-07-02T01:05:31 -05.00</pubDate> 
		<dc:creator>pcarroll</dc:creator>
   	    <slash:comments>2</slash:comments> 
		<description><![CDATA[ I've had Raynauds forever!  Over the last few years I notice a small pain in my fingers or feet and then itching.  Next thing I know there is a bruise which lasts for several hours.  Note: this is not the transient purple finger, its a certifed bruise.<br /><br />Today I had the same sensation (while I was walking and doing absolutely nothing with my fingers).  Now I have a bruise that equals 1/3 of my finger and its stilll here going on 14 hours.<br /><br />This kinda freaks me out.  I read about avoiding cold.  However I can be completely warm and stress free, and no, I don't smoke tobacco, but I still get the numbness and white fingers.  I get it in my toes everytime I take a shower.  Mind you, I take hot showers so why would that happen?<br /><br />Any insight anyone can give me regarding the bruising or reason for numbness in a hot shower would be appreciated to the depths of my heart.<br /><br />Maybe Michael Jackson wore the glove because he had unilateral Raynauds, think so ? ]]></description>
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		<title>other medications</title>
		<link>http://www.raynauds.org/support/forums/forum/messageview.cfm?catid=10&amp;threadid=2466</link> 
		<pubDate>2010-06-16T15:19:58 -05.00</pubDate> 
		<dc:creator>tulip</dc:creator>
   	    <slash:comments>3</slash:comments> 
		<description><![CDATA[ My mum has just been diagnosed with Reynaud's and has hit a bit of a problem with other meds.She bought decongestant tablets and had to take them back as she can't take them,same with cold and flu capsules.Is there a list of over the counter medicines she can take anywhere?<br /><br />tulip ]]></description>
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	<item>
		<title>Purple feet</title>
		<link>http://www.raynauds.org/support/forums/forum/messageview.cfm?catid=10&amp;threadid=2463</link> 
		<pubDate>2010-06-14T16:32:02 -05.00</pubDate> 
		<dc:creator>Lorgirl</dc:creator>
   	    <slash:comments>3</slash:comments> 
		<description><![CDATA[ Hi<br /><br />Newbie here.  I have been diagnosed with Raynauds.  Most likely secondary, yet no other symptoms as of yet of anything else.<br /><br />When I first noticed I had this, my fingertips on one hand felt numb due to being very cold.  Since I started paying attention to this, my hands (mainly fingers) on occasion will turn reddish and sometimes a little purple. <br /><br />The problem I seem to be having is more in my feet and is making me wonder if it is really Raynauds in my feet or something different.  My whole foot tends to go purple even when I am not very cold.  Plus, it is usually only when I'm sitting.  I was sitting at work today at my computer and both feet were purple.  When I got up to walk somewhere, I looked at the bottom of my feet and they were totally white with small patches of red.  If I held my foot up for a bit, the reddness would come back.  My feet weren't cold, numb or painful.  Does this sound like Raynaud's? <br /><br />Thanks ]]></description>
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