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    <title>Care Issues</title>
    <link>http://www.spinalcordinjury-paralysis.org/discussions/care-issues</link>
    <description><![CDATA[The nitty-gritty of taking good care and staying healthy.]]></description>
    <language>en-us</language>
    <item>
      <guid isPermaLink="true">http://www.spinalcordinjury-paralysis.org/discussions/care-issues/2012/04/23/1-thing-i-wish-someone-told-me</guid>
      <title>#1 Thing I wish someone told me...</title>
      <link>http://www.spinalcordinjury-paralysis.org/discussions/care-issues/2012/04/23/1-thing-i-wish-someone-told-me</link>
      <description><![CDATA[I have been paralyzed for 14 years and the #1 things that I never heard from any rehab facility, doctor, nurse or physical therapist is how important what you sit on is... ALL the time. I am not just talking about a cushion in your chair, which is obviously really important, but also when you are not in your chair. The two biggest places that no everyone thinks of is putting a seat cushion down in your car if you drive and when you shower.<br />
<br />
When you drive, use a low-profile ROHO seat cushion. This will help absorb the bumps in the road and protect your butt. Even if your shower chair is padded, for those who are paralyzed and others, this is not enough padding. Don&#39;t kid yourself and put down a low-high profile ROHO.<br />
<br />
The three best cushions for your chair I have found in my years of experience (I&#39;ve been through many many cushions) are the following:<br />
<br />
1. ROHO - good for active people in chairs<br />
2. Easy Ride - custom to fit your butt to completely get the pressure off<br />
3. Aquila - has a motor that moves air about to relieve pressure from sitting.<br />
<br />
Take care of yourselves fellow wheelchair users! I wish someone told me these two important life adjustments to prevent skin-breakdowns, so I would like to pass on this wisdom to you. ]]></description>
      <pubDate>Mon, 23 Apr 2012 22:00:38 GMT</pubDate>
      <dc:creator>Wheelchair Traveler</dc:creator>
    </item>
    <item>
      <guid isPermaLink="true">http://www.spinalcordinjury-paralysis.org/discussions/care-issues/2012/04/22/body-temperature-issues</guid>
      <title>Body temperature issues</title>
      <link>http://www.spinalcordinjury-paralysis.org/discussions/care-issues/2012/04/22/body-temperature-issues</link>
      <description><![CDATA[Anyone have any documentation on temperature control issues for people with sci?<br />
<br />
My son has an incomplete sci. We&#39;re dealing with a divorce, and my son&#39;s father isn&#39;t educated on sci. I need information for the lawyer/judge to help set safe conditions for visitation.<br />
<br />
Thanks.]]></description>
      <pubDate>Mon, 23 Apr 2012 00:10:24 GMT</pubDate>
      <dc:creator>Dash</dc:creator>
    </item>
    <item>
      <guid isPermaLink="true">http://www.spinalcordinjury-paralysis.org/discussions/care-issues/2012/04/05/mobility</guid>
      <title>Mobility</title>
      <link>http://www.spinalcordinjury-paralysis.org/discussions/care-issues/2012/04/05/mobility</link>
      <description><![CDATA[<span style="font-size: 14px"><span style="color: #800080">http://www.wimp.com/newdevice/<br />
<br />
Please check out this website. I found it encouraging and facinating. Tell me what you think. I think it&#39;s awesome.</span></span>]]></description>
      <pubDate>Fri, 06 Apr 2012 02:55:00 GMT</pubDate>
      <dc:creator>annette</dc:creator>
    </item>
    <item>
      <guid isPermaLink="true">http://www.spinalcordinjury-paralysis.org/discussions/care-issues/2012/03/27/suprapubic-vs-urostomy</guid>
      <title>suprapubic vs urostomy</title>
      <link>http://www.spinalcordinjury-paralysis.org/discussions/care-issues/2012/03/27/suprapubic-vs-urostomy</link>
      <description><![CDATA[Hi, had a sp put in on 10/13/2011 and everyday my stomach swells and pain is constant starts in the stomach and spreads down to the groin then by bedtime goes to the knees. The bladder is emptying. Take ditropan xl, baclofen,nitrofurantoin,cranberry pills and a glass of water with vinegar and aloe everyday. The second urologist says the only way to stop the pain is to have a ilealconduit. I am a c5/6 quad and before the sp&nbsp;I used a ureatha folley for 30 yrs. Does anyone have a urostomy and is it painful 24/7? Would appreciate any feedbackThanks<br />
<br />
Cydnight&nbsp;&nbsp;]]></description>
      <pubDate>Tue, 27 Mar 2012 22:38:08 GMT</pubDate>
      <dc:creator>cyd</dc:creator>
    </item>
    <item>
      <guid isPermaLink="true">http://www.spinalcordinjury-paralysis.org/discussions/care-issues/2012/03/26/bowel-and-bladder-care</guid>
      <title>Bowel and Bladder care</title>
      <link>http://www.spinalcordinjury-paralysis.org/discussions/care-issues/2012/03/26/bowel-and-bladder-care</link>
      <description><![CDATA[My sister met with an accident and is suffering from spinal cord injury . she&nbsp;is a &nbsp;quadriplegia and i need some help with bowel care. ]]></description>
      <pubDate>Mon, 26 Mar 2012 20:46:40 GMT</pubDate>
      <dc:creator>vani</dc:creator>
    </item>
    <item>
      <guid isPermaLink="true">http://www.spinalcordinjury-paralysis.org/discussions/care-issues/2012/03/21/outpatient-rehab</guid>
      <title>Outpatient Rehab</title>
      <link>http://www.spinalcordinjury-paralysis.org/discussions/care-issues/2012/03/21/outpatient-rehab</link>
      <description><![CDATA[Since mid-October my husband has been in outpatient rehab. They are talking about releasing him at the end of March. Has anyone ever left one outjpatient facility and went to a different since they were not satisfied with the outcome of the first facility? Does the insurance companies allow you to do it? In our case we feel they are releasing him before they taught him any true life skills.....any thoughts?]]></description>
      <pubDate>Thu, 22 Mar 2012 03:38:07 GMT</pubDate>
      <dc:creator>Jay</dc:creator>
    </item>
    <item>
      <guid isPermaLink="true">http://www.spinalcordinjury-paralysis.org/discussions/care-issues/2012/03/21/pressure-relief-false-alarms</guid>
      <title>Pressure Relief False Alarms</title>
      <link>http://www.spinalcordinjury-paralysis.org/discussions/care-issues/2012/03/21/pressure-relief-false-alarms</link>
      <description><![CDATA[When I was in the hospital a PT told me I had to do 45 seconds of pressure relief for every 15 minutes in the chair. I started doing that, realized it was nuts and just never thought about it again.<br />
<br />
So now I&#39;m 17 years into the rig as a t-12 para. &nbsp;I&#39;ve done multiple century rides on a bike, have driven cross country a dozen times, have spent YEARS in my chair sitting in front of a computer for work, have spent entire days in a plane (6 trips to Europe and 2 to India) and have NEVER gotten a pressure sore on my arse. If you live a normally active life; &nbsp;transfer a dozen times a day and check yourself after strenuous activity you&#39;re just fine. If you sit and mope you will get pressure sores ( high level quads excluded, of course...).&nbsp;<br />
<br />
There are plenty of real problems out there that need to be addressed, but this one just takes common sense. Move around - use a cushion. nuff said. No need to freak out the newbies about a problem that doesn&#39;t exist.&nbsp;]]></description>
      <pubDate>Wed, 21 Mar 2012 07:51:41 GMT</pubDate>
      <dc:creator>Jama</dc:creator>
    </item>
    <item>
      <guid isPermaLink="true">http://www.spinalcordinjury-paralysis.org/discussions/care-issues/2012/03/09/baclofen-pump-leg-pain-questions</guid>
      <title>baclofen pump leg pain questions</title>
      <link>http://www.spinalcordinjury-paralysis.org/discussions/care-issues/2012/03/09/baclofen-pump-leg-pain-questions</link>
      <description><![CDATA[I am a walking SCI patient due to severe spinal stenosis. I recently had the baclofen pump implanted., Its been 6 weeks now and im experiencing a tremendous amount of leg and back pain.Pre pump i hadsome discomfort but nothing continuous like this. Is this normal until they get the pump dialed in? Any feedback would be greatly appreciated Thanks, Todd]]></description>
      <pubDate>Sat, 10 Mar 2012 03:10:37 GMT</pubDate>
      <dc:creator>Todd</dc:creator>
    </item>
    <item>
      <guid isPermaLink="true">http://www.spinalcordinjury-paralysis.org/discussions/care-issues/2012/03/09/shower-commode-chairs---need-new-one-for-new-roll-</guid>
      <title>Shower commode chairs - need new one for new roll in shower.</title>
      <link>http://www.spinalcordinjury-paralysis.org/discussions/care-issues/2012/03/09/shower-commode-chairs---need-new-one-for-new-roll-</link>
      <description><![CDATA[Hi -&nbsp; am looking for a good shower/commode chair for my son who is a 6&#39;4&quot; c4 quad.&nbsp; He is able to do quite a bit of self care and we are finishing a new roll-in shower for him.&nbsp; What would any of you recommend and&nbsp; who has used this commode / shower chair AdVAnced Folding Shower/Commode Chair <a href="http://www.allegromedical.com/bathroom-assists-c517/advanced-folding-shower-commode-chair-p561141.html">http://www.allegromedical.com/bathroom-assists-c517/advanced-folding-shower-commode-chair-p561141.html</a>.&nbsp; WHen his shower is finished and we have a new chair, it will be the first time in a year that he&#39;s had a SHOWER !!&nbsp; WOO HOOO!!!! (don&#39;t think that he hasn&#39;t been bathed in all this time though! :) )<br />
<br />
Would love to hear thoughts and any shower chairs and anyother thoughts / best practices for shower / self care you all may have.<br />
<br />
]]></description>
      <pubDate>Fri, 09 Mar 2012 20:33:45 GMT</pubDate>
      <dc:creator>SMG</dc:creator>
    </item>
    <item>
      <guid isPermaLink="true">http://www.spinalcordinjury-paralysis.org/discussions/care-issues/2012/03/06/gadgets-cell-phones</guid>
      <title>Gadgets/ cell phones</title>
      <link>http://www.spinalcordinjury-paralysis.org/discussions/care-issues/2012/03/06/gadgets-cell-phones</link>
      <description><![CDATA[My 68 year old dad is a recent spinal cord injury (C5,C6 incomplete)&nbsp; We are looking for recommendations for gadgets that will make it easier for him to read, write and make phone calls.&nbsp; He has wrist movement, arm movement, but no finger movement.&nbsp; I have not found a phone yet that he can turn on/off without having to push a button and that is totally voice activated.&nbsp; I&#39;m also concerned that his voice is still weak and he will have difficulty with voice activiation.&nbsp; Please let me know what&#39;s worked for you!<br />
<br />
]]></description>
      <pubDate>Tue, 06 Mar 2012 20:37:37 GMT</pubDate>
      <dc:creator>Cindy</dc:creator>
    </item>
    <item>
      <guid isPermaLink="true">http://www.spinalcordinjury-paralysis.org/discussions/care-issues/2012/01/19/utis-that-wont-stop</guid>
      <title>uti's that won't stop!</title>
      <link>http://www.spinalcordinjury-paralysis.org/discussions/care-issues/2012/01/19/utis-that-wont-stop</link>
      <description><![CDATA[I have a neurogenic bladder due to a spinal cord injury...L4-L5....cauda equina<br />
syndrom. My URO said that I would be a good case for a bladder augmentation<br />
surgery.<br />
Anyone out there have any advice?<br />
Any advice would be very helpful.<br />
Thanks,<br />
Gene]]></description>
      <pubDate>Thu, 19 Jan 2012 17:45:22 GMT</pubDate>
      <dc:creator>gene701@msn.com</dc:creator>
    </item>
    <item>
      <guid isPermaLink="true">http://www.spinalcordinjury-paralysis.org/discussions/care-issues/2012/01/11/recurrent-uti-in-spinal-cord-injury------help-need</guid>
      <title>RECURRENT UTI IN SPINAL CORD INJURY------HELP NEEDED</title>
      <link>http://www.spinalcordinjury-paralysis.org/discussions/care-issues/2012/01/11/recurrent-uti-in-spinal-cord-injury------help-need</link>
      <description><![CDATA[I am male quad with c5-c6 injury since 2003 Dec.I have neurogenic bladder and since last 6 yrs I never cath and I rarely developed UTI.From july 2010 I started developing UTI.I took oral antibiotics but UTI keeps coming back.My urologist asked me to cath once a day ,take cranberry pills and D-manose.I&nbsp;normally use hit my stomach and pee in urinal,but my residual urine bladder is 300 cc.My&nbsp;oral antibiotics are getting resistant.I also went on supressive therapy of 50mg at night of antibiotic for 6-months and I was UTI-free.As I stoped the night treatment ,UTI came back in 1-month<br />
<br />
Please can anyone&nbsp;suggest how they are managing their UTI&#39;S]]></description>
      <pubDate>Thu, 12 Jan 2012 04:38:51 GMT</pubDate>
      <dc:creator>khawaja</dc:creator>
    </item>
    <item>
      <guid isPermaLink="true">http://www.spinalcordinjury-paralysis.org/discussions/care-issues/2012/01/02/baclofen-pump</guid>
      <title>Baclofen Pump</title>
      <link>http://www.spinalcordinjury-paralysis.org/discussions/care-issues/2012/01/02/baclofen-pump</link>
      <description><![CDATA[At 17 I suffered from a SCI, in a vehicle accident. I am a T-6 paraplegic. However, I suffered from severe spasms ever since. My spasms are so bad they get in the way of me trying to move. Medications for my spasms do not do anything I have taken all kinds of medicines and none help. Yet, my doctors and therapist talked to me about the pump and after a struggle, they convinced me. First I went to try on a trial of. This trial was temporarily, it allowed me to feel how my legs and body would be without spasms. I felt relief, during the trial. For the first time I could eat, without spasms in my stomach and didn&rsquo;t have to worry about getting a spasm when I moved. Nevertheless, I feel nervous about getting, surgically a baclofen pump. Things that worry me are infections and refilling the pump.&nbsp;]]></description>
      <pubDate>Tue, 03 Jan 2012 04:43:48 GMT</pubDate>
      <dc:creator>Gloria</dc:creator>
    </item>
    <item>
      <guid isPermaLink="true">http://www.spinalcordinjury-paralysis.org/discussions/care-issues/2011/12/06/how-about-healing-the-body-when-one-is-allergic-to</guid>
      <title>How about healing the body when one is allergic to EVERYTHING possible and have a sci, tbi to name a few items</title>
      <link>http://www.spinalcordinjury-paralysis.org/discussions/care-issues/2011/12/06/how-about-healing-the-body-when-one-is-allergic-to</link>
      <description><![CDATA[I would dearly love to know if any other sci/tbi people have run into problems dealing with allergic reactions. &nbsp;I just finished a series of patch tests and was told that EVERYTHING I USE UP TO AND INCLUDING MY GLOVES, MY CUSHIONS, MY CHAIR, MY CLOTHES, EVERYTHING VIRTUALLY was triggering rashes on me and that I had to change everything. &nbsp;Anybody out here who can give me some clue as to what gear I should try to find to use in order to continue functioning??? &nbsp;If I cant use anything except cotton/natural substances/no dyes (the worst allergies were triggered by any and all blue dyes, and several other items....most of which i had no knowledge of being exposed to in the first place...) what do I try to find - a movers dolly??? &nbsp;]]></description>
      <pubDate>Tue, 06 Dec 2011 21:42:29 GMT</pubDate>
      <dc:creator>An</dc:creator>
    </item>
    <item>
      <guid isPermaLink="true">http://www.spinalcordinjury-paralysis.org/discussions/care-issues/2011/11/22/bladder-care</guid>
      <title>Bladder Care</title>
      <link>http://www.spinalcordinjury-paralysis.org/discussions/care-issues/2011/11/22/bladder-care</link>
      <description><![CDATA[My level of injury is C5,C6,C7 due a road accident 10 years back,i am with indwelling catheter since then,my bladder capacity has come down to 75ml and can&#39;t use intermittent catherisation.Can i use indwelling catheter permanently?<br />
<br />
Please let me know your thoughts.]]></description>
      <pubDate>Tue, 22 Nov 2011 12:27:14 GMT</pubDate>
      <dc:creator>Krs</dc:creator>
    </item>
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