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	<title>
	Comments on: How To Manage Lymphedema At Home [12 Ways]	</title>
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	<description>Your Online Resource For Information &#38; Advice On Lymphedema</description>
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		<title>
		By: Jen		</title>
		<link>https://lymphedemalifeline.org/articles/how-to-manage-lymphedema-at-home/#comment-2042</link>

		<dc:creator><![CDATA[Jen]]></dc:creator>
		<pubDate>Sun, 18 Aug 2024 22:38:05 +0000</pubDate>
		<guid isPermaLink="false">https://lymphedemalifeline.org/?p=549#comment-2042</guid>

					<description><![CDATA[In reply to &lt;a href=&quot;https://lymphedemalifeline.org/articles/how-to-manage-lymphedema-at-home/#comment-1783&quot;&gt;Margaret&lt;/a&gt;.

Hi Margaret, the most common ways to manage symptoms are exercise and elevation of the limb, massage, and pneumatic compression or compression stockings. I can&#039;t personally vouch for the effectiveness of a system such as Lympha Press, however there is evidence such compression devices may help with lymphedema. I understand the point your therapist may be making however in that there are many of these devices on the market, and not all are developed with lymphedema in mind. There is actually a clinical studies section on the Lympha Press website if you wish to do more reading around this type of treatment.]]></description>
			<content:encoded><![CDATA[<p>In reply to <a href="https://lymphedemalifeline.org/articles/how-to-manage-lymphedema-at-home/#comment-1783">Margaret</a>.</p>
<p>Hi Margaret, the most common ways to manage symptoms are exercise and elevation of the limb, massage, and pneumatic compression or compression stockings. I can&#8217;t personally vouch for the effectiveness of a system such as Lympha Press, however there is evidence such compression devices may help with lymphedema. I understand the point your therapist may be making however in that there are many of these devices on the market, and not all are developed with lymphedema in mind. There is actually a clinical studies section on the Lympha Press website if you wish to do more reading around this type of treatment.</p>
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		<title>
		By: J.Thomas		</title>
		<link>https://lymphedemalifeline.org/articles/how-to-manage-lymphedema-at-home/#comment-1870</link>

		<dc:creator><![CDATA[J.Thomas]]></dc:creator>
		<pubDate>Sun, 09 Jun 2024 17:47:13 +0000</pubDate>
		<guid isPermaLink="false">https://lymphedemalifeline.org/?p=549#comment-1870</guid>

					<description><![CDATA[Thank you very much]]></description>
			<content:encoded><![CDATA[<p>Thank you very much</p>
]]></content:encoded>
		
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		<title>
		By: Jesse morales		</title>
		<link>https://lymphedemalifeline.org/articles/how-to-manage-lymphedema-at-home/#comment-1803</link>

		<dc:creator><![CDATA[Jesse morales]]></dc:creator>
		<pubDate>Fri, 12 Apr 2024 17:24:17 +0000</pubDate>
		<guid isPermaLink="false">https://lymphedemalifeline.org/?p=549#comment-1803</guid>

					<description><![CDATA[I have lymphedema]]></description>
			<content:encoded><![CDATA[<p>I have lymphedema</p>
]]></content:encoded>
		
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		<item>
		<title>
		By: Margaret		</title>
		<link>https://lymphedemalifeline.org/articles/how-to-manage-lymphedema-at-home/#comment-1783</link>

		<dc:creator><![CDATA[Margaret]]></dc:creator>
		<pubDate>Sun, 24 Mar 2024 19:56:56 +0000</pubDate>
		<guid isPermaLink="false">https://lymphedemalifeline.org/?p=549#comment-1783</guid>

					<description><![CDATA[During my physical last year, my doctor and I decided it was time to try to learn to manage my hereditary lymphedema. I went to months of lymphedema therapy and did a trial of a compression machine. Besides ankle and foot swelling, daily becomes torso swelling also. So  I was prescribed a Tactile FlexTouch Plus with legs and torso components, which apparently sells for $10,000 and my Medicare Advantage Insurance refuses to pay for it, even when provided more data by use of one with just legs components for 30 days.  I&#039;ve been checking blogs looking for alternatives. I could pay for a Lympha Press out of pocket at thousands of dollars less but my therapist says it isn&#039;t designed by someone with lymphedema knowledge and wouldn&#039;t work. Any ideas for managing my condition besides therapy which co-pay is now $40 a session for me so why wanted a machine instead of therapy I learned or by the professional?]]></description>
			<content:encoded><![CDATA[<p>During my physical last year, my doctor and I decided it was time to try to learn to manage my hereditary lymphedema. I went to months of lymphedema therapy and did a trial of a compression machine. Besides ankle and foot swelling, daily becomes torso swelling also. So  I was prescribed a Tactile FlexTouch Plus with legs and torso components, which apparently sells for $10,000 and my Medicare Advantage Insurance refuses to pay for it, even when provided more data by use of one with just legs components for 30 days.  I&#8217;ve been checking blogs looking for alternatives. I could pay for a Lympha Press out of pocket at thousands of dollars less but my therapist says it isn&#8217;t designed by someone with lymphedema knowledge and wouldn&#8217;t work. Any ideas for managing my condition besides therapy which co-pay is now $40 a session for me so why wanted a machine instead of therapy I learned or by the professional?</p>
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