<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"
	xmlns:content="http://purl.org/rss/1.0/modules/content/"
	xmlns:dc="http://purl.org/dc/elements/1.1/"
	xmlns:atom="http://www.w3.org/2005/Atom"
	xmlns:sy="http://purl.org/rss/1.0/modules/syndication/"
	
	>
<channel>
	<title>
	Comments on: How to enjoy a conversation after brain injury	</title>
	<atom:link href="https://www.jumbledbrain.com/holding-conversation-brain-injury/feed/" rel="self" type="application/rss+xml" />
	<link>https://www.jumbledbrain.com/holding-conversation-brain-injury/</link>
	<description>Discover - Empower - Thrive</description>
	<lastBuildDate>Wed, 30 Mar 2022 20:25:51 +0000</lastBuildDate>
	<sy:updatePeriod>
	hourly	</sy:updatePeriod>
	<sy:updateFrequency>
	1	</sy:updateFrequency>
	
	<item>
		<title>
		By: michelle.munt@yahoo.co.uk		</title>
		<link>https://www.jumbledbrain.com/holding-conversation-brain-injury/#comment-1251</link>

		<dc:creator><![CDATA[michelle.munt@yahoo.co.uk]]></dc:creator>
		<pubDate>Thu, 18 Oct 2018 10:31:29 +0000</pubDate>
		<guid isPermaLink="false">https://www.jumbledbrain.com/?p=571#comment-1251</guid>

					<description><![CDATA[In reply to &lt;a href=&quot;https://www.jumbledbrain.com/holding-conversation-brain-injury/#comment-1249&quot;&gt;Heather&lt;/a&gt;.

Heather thanks so much for saying this. It&#039;s always refreshing to hear from someone you hasn&#039;t got a brain injury themselves, but wants to help those who do. Yes you are right about compassion and understanding needing to be higher on the agenda, and I do hope that the more we talk about it, the better we can make the situation.]]></description>
			<content:encoded><![CDATA[<p>In reply to <a href="https://www.jumbledbrain.com/holding-conversation-brain-injury/#comment-1249">Heather</a>.</p>
<p>Heather thanks so much for saying this. It&#8217;s always refreshing to hear from someone you hasn&#8217;t got a brain injury themselves, but wants to help those who do. Yes you are right about compassion and understanding needing to be higher on the agenda, and I do hope that the more we talk about it, the better we can make the situation.</p>
]]></content:encoded>
		
			</item>
		<item>
		<title>
		By: Heather		</title>
		<link>https://www.jumbledbrain.com/holding-conversation-brain-injury/#comment-1249</link>

		<dc:creator><![CDATA[Heather]]></dc:creator>
		<pubDate>Thu, 18 Oct 2018 04:46:27 +0000</pubDate>
		<guid isPermaLink="false">https://www.jumbledbrain.com/?p=571#comment-1249</guid>

					<description><![CDATA[Thank you so much for writing this, and all the articles I&#039;ve been reading. My boyfriend has TBI and after reading this I wonder if I have shown enough care and patience with him. He hides the symptoms from me very well and only rarely asks me to explain what I mean, so I don&#039;t always know when he is struggling. Just as people with disabilities/mental health issues need compassion and more community outreach/awareness/SUPPORT, we definitely need that same thing for TBI survivors. We should start teaming up causes to get more people supporting all of these. Keep writing!]]></description>
			<content:encoded><![CDATA[<p>Thank you so much for writing this, and all the articles I&#8217;ve been reading. My boyfriend has TBI and after reading this I wonder if I have shown enough care and patience with him. He hides the symptoms from me very well and only rarely asks me to explain what I mean, so I don&#8217;t always know when he is struggling. Just as people with disabilities/mental health issues need compassion and more community outreach/awareness/SUPPORT, we definitely need that same thing for TBI survivors. We should start teaming up causes to get more people supporting all of these. Keep writing!</p>
]]></content:encoded>
		
			</item>
		<item>
		<title>
		By: michelle.munt@yahoo.co.uk		</title>
		<link>https://www.jumbledbrain.com/holding-conversation-brain-injury/#comment-447</link>

		<dc:creator><![CDATA[michelle.munt@yahoo.co.uk]]></dc:creator>
		<pubDate>Sat, 18 Feb 2017 12:36:34 +0000</pubDate>
		<guid isPermaLink="false">https://www.jumbledbrain.com/?p=571#comment-447</guid>

					<description><![CDATA[In reply to &lt;a href=&quot;https://www.jumbledbrain.com/holding-conversation-brain-injury/#comment-444&quot;&gt;David Cropp&lt;/a&gt;.

David it&#039;s so difficult isn&#039;t it. I&#039;m glad you found new work but I can completely understand how that environment makes it hard.]]></description>
			<content:encoded><![CDATA[<p>In reply to <a href="https://www.jumbledbrain.com/holding-conversation-brain-injury/#comment-444">David Cropp</a>.</p>
<p>David it&#8217;s so difficult isn&#8217;t it. I&#8217;m glad you found new work but I can completely understand how that environment makes it hard.</p>
]]></content:encoded>
		
			</item>
		<item>
		<title>
		By: David Cropp		</title>
		<link>https://www.jumbledbrain.com/holding-conversation-brain-injury/#comment-444</link>

		<dc:creator><![CDATA[David Cropp]]></dc:creator>
		<pubDate>Fri, 17 Feb 2017 13:22:00 +0000</pubDate>
		<guid isPermaLink="false">https://www.jumbledbrain.com/?p=571#comment-444</guid>

					<description><![CDATA[Oh, Michelle, where to start? I was never much of a talker anyway. Before my injury my job involved going to customers sites to repair or modify their plant or equipment, as I would see the same person on each visit I would build a relationship with that person and there would always be a period of catching up as we worked. I hadn&#039;t realized but it&#039;s those conversations that I miss, because of my ABI I lost my job. I got another job now, but it&#039;s noisy and dusty, so we have to wear hearing protection and a respirator mask, this makes conversation impossible. At break times most of my co workers sit looking at their phones, so not much conversation there either.

What I did enjoy was during my outpatient rehab, each therapy session would start with the therapist steering me into a conversation with no pressure to start the therapy session. They would listen to what I had to say and let the conversation flow naturally. I guess that was as much a part of the therapy as was the actual therapy. It also didn&#039;t hurt in the way it was enjoyable to be able to converse without pressure.

Family conversations tend to be carried on en mass and not one to one and therefore difficult to follow because of the overload of information. I often joke that I&#039;ve been kept out of the loop over some situation and they will say that&#039;s what we talked about last week at the restaurant when we all had lunch together.

I have a couple of neighbors who I converse with on a regular basis, so this seems to satisfy that part of life when a little chat is what&#039;s needed.

Also there are my TBI, ABI pals on Twitter and their respective blogs, it&#039;s those little tweets or reading their blogs that helps to make me feel like part of a community. Thanks Michelle, I&#039;m sure your blogs are a comfort to many people with a brain injury, knowing that they are not alone]]></description>
			<content:encoded><![CDATA[<p>Oh, Michelle, where to start? I was never much of a talker anyway. Before my injury my job involved going to customers sites to repair or modify their plant or equipment, as I would see the same person on each visit I would build a relationship with that person and there would always be a period of catching up as we worked. I hadn&#8217;t realized but it&#8217;s those conversations that I miss, because of my ABI I lost my job. I got another job now, but it&#8217;s noisy and dusty, so we have to wear hearing protection and a respirator mask, this makes conversation impossible. At break times most of my co workers sit looking at their phones, so not much conversation there either.</p>
<p>What I did enjoy was during my outpatient rehab, each therapy session would start with the therapist steering me into a conversation with no pressure to start the therapy session. They would listen to what I had to say and let the conversation flow naturally. I guess that was as much a part of the therapy as was the actual therapy. It also didn&#8217;t hurt in the way it was enjoyable to be able to converse without pressure.</p>
<p>Family conversations tend to be carried on en mass and not one to one and therefore difficult to follow because of the overload of information. I often joke that I&#8217;ve been kept out of the loop over some situation and they will say that&#8217;s what we talked about last week at the restaurant when we all had lunch together.</p>
<p>I have a couple of neighbors who I converse with on a regular basis, so this seems to satisfy that part of life when a little chat is what&#8217;s needed.</p>
<p>Also there are my TBI, ABI pals on Twitter and their respective blogs, it&#8217;s those little tweets or reading their blogs that helps to make me feel like part of a community. Thanks Michelle, I&#8217;m sure your blogs are a comfort to many people with a brain injury, knowing that they are not alone</p>
]]></content:encoded>
		
			</item>
		<item>
		<title>
		By: michelle.munt@yahoo.co.uk		</title>
		<link>https://www.jumbledbrain.com/holding-conversation-brain-injury/#comment-144</link>

		<dc:creator><![CDATA[michelle.munt@yahoo.co.uk]]></dc:creator>
		<pubDate>Thu, 27 Oct 2016 08:58:14 +0000</pubDate>
		<guid isPermaLink="false">https://www.jumbledbrain.com/?p=571#comment-144</guid>

					<description><![CDATA[In reply to &lt;a href=&quot;https://www.jumbledbrain.com/holding-conversation-brain-injury/#comment-143&quot;&gt;Jo Wood&lt;/a&gt;.

Jo you are absolutely right, I agree with everything you said! We have had an experience which is unique, and we are learning things that others have no idea about.]]></description>
			<content:encoded><![CDATA[<p>In reply to <a href="https://www.jumbledbrain.com/holding-conversation-brain-injury/#comment-143">Jo Wood</a>.</p>
<p>Jo you are absolutely right, I agree with everything you said! We have had an experience which is unique, and we are learning things that others have no idea about.</p>
]]></content:encoded>
		
			</item>
		<item>
		<title>
		By: Jo Wood		</title>
		<link>https://www.jumbledbrain.com/holding-conversation-brain-injury/#comment-143</link>

		<dc:creator><![CDATA[Jo Wood]]></dc:creator>
		<pubDate>Thu, 27 Oct 2016 08:17:29 +0000</pubDate>
		<guid isPermaLink="false">https://www.jumbledbrain.com/?p=571#comment-143</guid>

					<description><![CDATA[Hello, I too can find conversations difficult, I find once I start to talk I can ramble on and on with so much detail that I can lose myself and don&#039;t know what I am actually talking about. That can be embarrassing, &#039;oh what was I talking about?&#039; I have been seeing a speech therapist, as I lost my speech at the beginning of my illness, seizure and brain surgery, its recovering now but still, stumbles over words and my voice can get stressed in conversations. The speech therapist has taught me to speak with less words, getting to the point, not rambling on, you can get your point across with less words. Learning to listen to others and responding correctly too, it&#039;s quite a task at times and leaves you with &#039;brain strain&#039; some anxiety and fatigue. It would be so much easier to just sit and say nothing, I have thought many times, &#039;what&#039;s the point, my speech is slurred, I have nothing to say, I am boring now&#039; but that is exactly the point, we are not boring &#039;wow&#039; we have a lot going on, so what if it comes out laboured and rambled, we are giving it go. We will only get better by trying. So don&#039;t give up, don&#039;t be defeated by words, take advice. Prepare and practice, listen, keep your words to the point, you will get there. Some days you just have to be brave.]]></description>
			<content:encoded><![CDATA[<p>Hello, I too can find conversations difficult, I find once I start to talk I can ramble on and on with so much detail that I can lose myself and don&#8217;t know what I am actually talking about. That can be embarrassing, &#8216;oh what was I talking about?&#8217; I have been seeing a speech therapist, as I lost my speech at the beginning of my illness, seizure and brain surgery, its recovering now but still, stumbles over words and my voice can get stressed in conversations. The speech therapist has taught me to speak with less words, getting to the point, not rambling on, you can get your point across with less words. Learning to listen to others and responding correctly too, it&#8217;s quite a task at times and leaves you with &#8216;brain strain&#8217; some anxiety and fatigue. It would be so much easier to just sit and say nothing, I have thought many times, &#8216;what&#8217;s the point, my speech is slurred, I have nothing to say, I am boring now&#8217; but that is exactly the point, we are not boring &#8216;wow&#8217; we have a lot going on, so what if it comes out laboured and rambled, we are giving it go. We will only get better by trying. So don&#8217;t give up, don&#8217;t be defeated by words, take advice. Prepare and practice, listen, keep your words to the point, you will get there. Some days you just have to be brave.</p>
]]></content:encoded>
		
			</item>
		<item>
		<title>
		By: michelle.munt@yahoo.co.uk		</title>
		<link>https://www.jumbledbrain.com/holding-conversation-brain-injury/#comment-141</link>

		<dc:creator><![CDATA[michelle.munt@yahoo.co.uk]]></dc:creator>
		<pubDate>Tue, 25 Oct 2016 12:38:32 +0000</pubDate>
		<guid isPermaLink="false">https://www.jumbledbrain.com/?p=571#comment-141</guid>

					<description><![CDATA[In reply to &lt;a href=&quot;https://www.jumbledbrain.com/holding-conversation-brain-injury/#comment-140&quot;&gt;Helen Caligiuri&lt;/a&gt;.

I used to attend a group with the charity Headway. They were all lovely people, but sometimes would get stuck in their own thoughts and issues. To begin with I found that hard, especially when I kept being told mine wasn&#039;t as bad, like it&#039;s a competition. But in time I realised that it was meant in a supportive way and they were trying to encourage me. 
In a way I found it useful for it not to be all about my struggles for a bit, and like how I write this blog, I made my time there more about supporting them than me. When you know something you said or did helped in some small way, and feeling you get is irreplaceable. ]]></description>
			<content:encoded><![CDATA[<p>In reply to <a href="https://www.jumbledbrain.com/holding-conversation-brain-injury/#comment-140">Helen Caligiuri</a>.</p>
<p>I used to attend a group with the charity Headway. They were all lovely people, but sometimes would get stuck in their own thoughts and issues. To begin with I found that hard, especially when I kept being told mine wasn&#8217;t as bad, like it&#8217;s a competition. But in time I realised that it was meant in a supportive way and they were trying to encourage me.<br />
In a way I found it useful for it not to be all about my struggles for a bit, and like how I write this blog, I made my time there more about supporting them than me. When you know something you said or did helped in some small way, and feeling you get is irreplaceable. </p>
]]></content:encoded>
		
			</item>
		<item>
		<title>
		By: Helen Caligiuri		</title>
		<link>https://www.jumbledbrain.com/holding-conversation-brain-injury/#comment-140</link>

		<dc:creator><![CDATA[Helen Caligiuri]]></dc:creator>
		<pubDate>Tue, 25 Oct 2016 12:25:54 +0000</pubDate>
		<guid isPermaLink="false">https://www.jumbledbrain.com/?p=571#comment-140</guid>

					<description><![CDATA[I always find I get caught up in the details. I then struggle to be pithy and to the point. So, I ften talk about what I&#039;m watching, what film I&#039;ve just seen......and often conversations with some others with brain injuries are the most painful. They have their agenda and they aren&#039;t interested in mine. But they don&#039;t tell you what their agenda is they just steer everything to cater to theirs. Do you spend any time with others with an ABI? It&#039;s a real challenge.]]></description>
			<content:encoded><![CDATA[<p>I always find I get caught up in the details. I then struggle to be pithy and to the point. So, I ften talk about what I&#8217;m watching, what film I&#8217;ve just seen&#8230;&#8230;and often conversations with some others with brain injuries are the most painful. They have their agenda and they aren&#8217;t interested in mine. But they don&#8217;t tell you what their agenda is they just steer everything to cater to theirs. Do you spend any time with others with an ABI? It&#8217;s a real challenge.</p>
]]></content:encoded>
		
			</item>
	</channel>
</rss>
