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		<title><![CDATA[MESH cornwall Forum - All Forums]]></title>
		<link>http://meshcornwall.org/forum/</link>
		<description><![CDATA[MESH cornwall Forum - http://meshcornwall.org/forum]]></description>
		<pubDate>Mon, 06 Feb 2012 04:52:14 +0000</pubDate>
		<generator>MyBB</generator>
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			<title><![CDATA[GOOGLE THREAT on MESH WEBSITE]]></title>
			<link>http://meshcornwall.org/forum/showthread.php?tid=722</link>
			<pubDate>Fri, 19 Aug 2011 19:13:10 +0000</pubDate>
			<guid isPermaLink="false">http://meshcornwall.org/forum/showthread.php?tid=722</guid>
			<description><![CDATA[To anyone who finds themselves here after trying to access the MESH website.<br />
<br />
The warning has been applied by Google after the forums were targetted by spammers. <br />
<br />
There is no malware on the MESH website and we have requested a review of the website by Google.<br />
<br />
<span style="color: #9400D3;"><span style="font-size: medium;">To access the MESH website <br />
open a new tab/page<br />
copy and paste this link - <a href="http://uk.yahoo.com/" target="_blank">http://uk.yahoo.com/</a><br />
search MESH cornwall<br />
click meshcornwall.org</span></span><br />
<br />
Normal service will be resumed as soon as possible<img src="images/smilies/biggrin.gif" style="vertical-align: middle;" border="0" alt="Big Grin" title="Big Grin" />]]></description>
			<content:encoded><![CDATA[To anyone who finds themselves here after trying to access the MESH website.<br />
<br />
The warning has been applied by Google after the forums were targetted by spammers. <br />
<br />
There is no malware on the MESH website and we have requested a review of the website by Google.<br />
<br />
<span style="color: #9400D3;"><span style="font-size: medium;">To access the MESH website <br />
open a new tab/page<br />
copy and paste this link - <a href="http://uk.yahoo.com/" target="_blank">http://uk.yahoo.com/</a><br />
search MESH cornwall<br />
click meshcornwall.org</span></span><br />
<br />
Normal service will be resumed as soon as possible<img src="images/smilies/biggrin.gif" style="vertical-align: middle;" border="0" alt="Big Grin" title="Big Grin" />]]></content:encoded>
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			<title><![CDATA[Wheelchair services Cornwall]]></title>
			<link>http://meshcornwall.org/forum/showthread.php?tid=721</link>
			<pubDate>Mon, 08 Aug 2011 09:08:29 +0000</pubDate>
			<guid isPermaLink="false">http://meshcornwall.org/forum/showthread.php?tid=721</guid>
			<description><![CDATA[From the MESH inbox <img src="images/smilies/biggrin.gif" style="vertical-align: middle;" border="0" alt="Big Grin" title="Big Grin" /> <br />
<br />
The PCT has commissioned Disability Cornwall to find out from wheelchair service users in Cornwall how they can become more involved in shaping services to ensure they continue to improve.<br />
<br />
 <br />
<br />
We have developed a short survey for people to take part in the process. If you are a wheelchair user, or a parent or carer of someone who uses a wheelchair, please tell us your views. Alternatively you can forward this email to relevant individuals or organisations in order to maximise the feedback we receive.<br />
<br />
 <br />
<br />
Please follow the link below to take part. The survey should take no more than 10 minutes and, as an added incentive, we are entering everyone who takes part the chance to win one of two £25 vouchers from Marks and Spencer.<br />
<br />
 <br />
<br />
<a href="https://www.surveymonkey.com/s/TZDLYLX" target="_blank">https://www.surveymonkey.com/s/TZDLYLX</a><br />
<br />
 <br />
<br />
Your views are important. Please take this opportunity to help make wheelchair services in Cornwall an example for others to follow.<br />
<br />
Thank you for taking part <img src="images/smilies/biggrin.gif" style="vertical-align: middle;" border="0" alt="Big Grin" title="Big Grin" />]]></description>
			<content:encoded><![CDATA[From the MESH inbox <img src="images/smilies/biggrin.gif" style="vertical-align: middle;" border="0" alt="Big Grin" title="Big Grin" /> <br />
<br />
The PCT has commissioned Disability Cornwall to find out from wheelchair service users in Cornwall how they can become more involved in shaping services to ensure they continue to improve.<br />
<br />
 <br />
<br />
We have developed a short survey for people to take part in the process. If you are a wheelchair user, or a parent or carer of someone who uses a wheelchair, please tell us your views. Alternatively you can forward this email to relevant individuals or organisations in order to maximise the feedback we receive.<br />
<br />
 <br />
<br />
Please follow the link below to take part. The survey should take no more than 10 minutes and, as an added incentive, we are entering everyone who takes part the chance to win one of two £25 vouchers from Marks and Spencer.<br />
<br />
 <br />
<br />
<a href="https://www.surveymonkey.com/s/TZDLYLX" target="_blank">https://www.surveymonkey.com/s/TZDLYLX</a><br />
<br />
 <br />
<br />
Your views are important. Please take this opportunity to help make wheelchair services in Cornwall an example for others to follow.<br />
<br />
Thank you for taking part <img src="images/smilies/biggrin.gif" style="vertical-align: middle;" border="0" alt="Big Grin" title="Big Grin" />]]></content:encoded>
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			<title><![CDATA[a little about me]]></title>
			<link>http://meshcornwall.org/forum/showthread.php?tid=446</link>
			<pubDate>Fri, 15 Jul 2011 14:06:58 +0000</pubDate>
			<guid isPermaLink="false">http://meshcornwall.org/forum/showthread.php?tid=446</guid>
			<description><![CDATA[Hi i am a single parent of an 11 year old boy with additional needs.I have had M.E./cfs for 4 years and lately i would say that whilst my brain fog might not be so severe, physically things seem to be getting worse.I have become progressively more isolated as time has gone on and have had to spend alot of energy on trying to get the right help for my son.I look forward tomaking some new friends and hopefully find some support for myself here.]]></description>
			<content:encoded><![CDATA[Hi i am a single parent of an 11 year old boy with additional needs.I have had M.E./cfs for 4 years and lately i would say that whilst my brain fog might not be so severe, physically things seem to be getting worse.I have become progressively more isolated as time has gone on and have had to spend alot of energy on trying to get the right help for my son.I look forward tomaking some new friends and hopefully find some support for myself here.]]></content:encoded>
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			<title><![CDATA[Professor AJ Pinching @ Liskeard 4thJuly]]></title>
			<link>http://meshcornwall.org/forum/showthread.php?tid=441</link>
			<pubDate>Sat, 25 Jun 2011 09:10:58 +0000</pubDate>
			<guid isPermaLink="false">http://meshcornwall.org/forum/showthread.php?tid=441</guid>
			<description><![CDATA[<img src="images/smilies/biggrin.gif" style="vertical-align: middle;" border="0" alt="Big Grin" title="Big Grin" /><br />
<br />
<br />
<div style="text-align: center;"><span style="color: #9400D3;"><span style="font-size: x-large;">A BIG EVENT !</span></span><br />
<br />
<span style="color: #9400D3;"><span style="font-size: large;">Current Perspectives on Chronic Fatigue Syndrome CFS/ME by Professor A J Pinching </span></span><br />
<span style="color: #9400D3;"><span style="font-size: medium;">(a final talk before his retirement)<br />
<br />
<span style="font-weight: bold;">ALL WELCOME </span><br />
Monday 4th July ... 6.30pm The Public Hall LISKEARD PL14 6BW <br />
free parking after 4pm (opposite hall) in the Westbourne car park <br />
£1 (free to accompanying carers) disabled access  and refreshments provided<br />
<br />
DETAILS: E: MESHcornwall@live.co.uk T: 01736 756775</span> </span></div><span style="color: #9400D3;"></span><br />
<br />
<br />
<br />
<br />
Hope to see you there <img src="images/smilies/biggrin.gif" style="vertical-align: middle;" border="0" alt="Big Grin" title="Big Grin" />]]></description>
			<content:encoded><![CDATA[<img src="images/smilies/biggrin.gif" style="vertical-align: middle;" border="0" alt="Big Grin" title="Big Grin" /><br />
<br />
<br />
<div style="text-align: center;"><span style="color: #9400D3;"><span style="font-size: x-large;">A BIG EVENT !</span></span><br />
<br />
<span style="color: #9400D3;"><span style="font-size: large;">Current Perspectives on Chronic Fatigue Syndrome CFS/ME by Professor A J Pinching </span></span><br />
<span style="color: #9400D3;"><span style="font-size: medium;">(a final talk before his retirement)<br />
<br />
<span style="font-weight: bold;">ALL WELCOME </span><br />
Monday 4th July ... 6.30pm The Public Hall LISKEARD PL14 6BW <br />
free parking after 4pm (opposite hall) in the Westbourne car park <br />
£1 (free to accompanying carers) disabled access  and refreshments provided<br />
<br />
DETAILS: E: MESHcornwall@live.co.uk T: 01736 756775</span> </span></div><span style="color: #9400D3;"></span><br />
<br />
<br />
<br />
<br />
Hope to see you there <img src="images/smilies/biggrin.gif" style="vertical-align: middle;" border="0" alt="Big Grin" title="Big Grin" />]]></content:encoded>
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			<title><![CDATA[Expert Patient Programme Merlin Centre]]></title>
			<link>http://meshcornwall.org/forum/showthread.php?tid=435</link>
			<pubDate>Wed, 15 Jun 2011 08:36:01 +0000</pubDate>
			<guid isPermaLink="false">http://meshcornwall.org/forum/showthread.php?tid=435</guid>
			<description><![CDATA[Just to let you all know in case you are well enough to attend. <br />
<br />
It is to be held at the <span style="color: #000080;"><span style="font-size: small;">Merlin Centre every Friday for 6 weeks from 15th July 10.30 - 1pm. <br />
</span></span><br />
The course is for people with long term health problems, it aims to improve your quality of life, learn new skills to manage your condition, meet others and share experiences, communicate better with family, friends and professionals and to feel more in control of your condition.<br />
<br />
Contact: cathie.shipwright@ciospct.cornwall.nhs.uk / 01208 252507 <br />
<br />
I realise it is beyond most of us but I do know someone who attended the first session and found the information pack very useful. <br />
The Merlin Centre is at Hewas Water St. Austell PL26 7JF]]></description>
			<content:encoded><![CDATA[Just to let you all know in case you are well enough to attend. <br />
<br />
It is to be held at the <span style="color: #000080;"><span style="font-size: small;">Merlin Centre every Friday for 6 weeks from 15th July 10.30 - 1pm. <br />
</span></span><br />
The course is for people with long term health problems, it aims to improve your quality of life, learn new skills to manage your condition, meet others and share experiences, communicate better with family, friends and professionals and to feel more in control of your condition.<br />
<br />
Contact: cathie.shipwright@ciospct.cornwall.nhs.uk / 01208 252507 <br />
<br />
I realise it is beyond most of us but I do know someone who attended the first session and found the information pack very useful. <br />
The Merlin Centre is at Hewas Water St. Austell PL26 7JF]]></content:encoded>
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			<title><![CDATA[Sharing learnings]]></title>
			<link>http://meshcornwall.org/forum/showthread.php?tid=377</link>
			<pubDate>Sat, 21 May 2011 11:08:30 +0000</pubDate>
			<guid isPermaLink="false">http://meshcornwall.org/forum/showthread.php?tid=377</guid>
			<description><![CDATA[Hi there, <br />
<br />
I have joined this forum so that I can share what I've learned so far with others and maybe learn a bit myself. I am 35yo and first developed cfs/m.e over 7 years ago when I was so bad I couldn't leave the house for weeks at a time to where I am now, having made huge strides in my recovery and am pretty much in the final stages.<br />
<br />
During my quest for health I have tried Mickel Therapy, Reverse Therapy, Lightning Process, EFT, Hypnotherapy, nutrition, Yoga, Tai Chi, Optimum Health Clinic approaches (even doing the practitioner course!), the Crysalis Effect, pacing, and many more as well as reading dozens and dozens of books around the subject and am happy to share my findings / experiences with you via the forum, over the telephone, face to face, whatever.. <br />
<br />
During this time I have seen so many others recover completely using the same tools in a much shorter period of time. It has just taken me longer because I had quite a strong achiever pattern going on in the background, which meant that I would push myself too hard when my energy picked up a little and yo-yo between almost well and almost dead! Pretty sure I've got that one covered now too though.<br />
<br />
If you interested in comparing notes, give me a shout!<br />
<br />
G]]></description>
			<content:encoded><![CDATA[Hi there, <br />
<br />
I have joined this forum so that I can share what I've learned so far with others and maybe learn a bit myself. I am 35yo and first developed cfs/m.e over 7 years ago when I was so bad I couldn't leave the house for weeks at a time to where I am now, having made huge strides in my recovery and am pretty much in the final stages.<br />
<br />
During my quest for health I have tried Mickel Therapy, Reverse Therapy, Lightning Process, EFT, Hypnotherapy, nutrition, Yoga, Tai Chi, Optimum Health Clinic approaches (even doing the practitioner course!), the Crysalis Effect, pacing, and many more as well as reading dozens and dozens of books around the subject and am happy to share my findings / experiences with you via the forum, over the telephone, face to face, whatever.. <br />
<br />
During this time I have seen so many others recover completely using the same tools in a much shorter period of time. It has just taken me longer because I had quite a strong achiever pattern going on in the background, which meant that I would push myself too hard when my energy picked up a little and yo-yo between almost well and almost dead! Pretty sure I've got that one covered now too though.<br />
<br />
If you interested in comparing notes, give me a shout!<br />
<br />
G]]></content:encoded>
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			<title><![CDATA[Forum update]]></title>
			<link>http://meshcornwall.org/forum/showthread.php?tid=376</link>
			<pubDate>Fri, 20 May 2011 16:42:31 +0000</pubDate>
			<guid isPermaLink="false">http://meshcornwall.org/forum/showthread.php?tid=376</guid>
			<description><![CDATA[Hi everyone,<br />
<br />
I have hopefully managed to stop 99% of all the advertising rubbish that was being posted on the forum. Why these people want to ruin a charitable forum like this MESH cornwall is beyond me!<br />
<br />
Anyway I am looking for any volunteers that would like to become Moderators on the forum which would help me keep an eye on things and delete any unsavoury posts. <br />
<br />
Please message me via the forum if you are willing to become a Moderator.<br />
<br />
Chris.]]></description>
			<content:encoded><![CDATA[Hi everyone,<br />
<br />
I have hopefully managed to stop 99% of all the advertising rubbish that was being posted on the forum. Why these people want to ruin a charitable forum like this MESH cornwall is beyond me!<br />
<br />
Anyway I am looking for any volunteers that would like to become Moderators on the forum which would help me keep an eye on things and delete any unsavoury posts. <br />
<br />
Please message me via the forum if you are willing to become a Moderator.<br />
<br />
Chris.]]></content:encoded>
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			<title><![CDATA[Forum problems!]]></title>
			<link>http://meshcornwall.org/forum/showthread.php?tid=373</link>
			<pubDate>Thu, 12 May 2011 19:53:00 +0000</pubDate>
			<guid isPermaLink="false">http://meshcornwall.org/forum/showthread.php?tid=373</guid>
			<description><![CDATA[<span style="font-size: large;">The forum has been targeted lately by numerous unscrupulous people flooding the forum with advertising. This has caused some functions not too work, I am doing my best to rectify the problems caused by these unsavoury people.<br />
In the the future I will have to reluctantly change the way people join the forum so that they can post on the forum once they have been cleared by admin.  </span>]]></description>
			<content:encoded><![CDATA[<span style="font-size: large;">The forum has been targeted lately by numerous unscrupulous people flooding the forum with advertising. This has caused some functions not too work, I am doing my best to rectify the problems caused by these unsavoury people.<br />
In the the future I will have to reluctantly change the way people join the forum so that they can post on the forum once they have been cleared by admin.  </span>]]></content:encoded>
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			<title><![CDATA[New to mesh]]></title>
			<link>http://meshcornwall.org/forum/showthread.php?tid=348</link>
			<pubDate>Tue, 26 Apr 2011 07:12:13 +0000</pubDate>
			<guid isPermaLink="false">http://meshcornwall.org/forum/showthread.php?tid=348</guid>
			<description><![CDATA[Hi my name is karen and have had M E for 11 years now, have managed to work as self employed (cant work for other people as cant keep up) but have recently had nasty setback due to operations.]]></description>
			<content:encoded><![CDATA[Hi my name is karen and have had M E for 11 years now, have managed to work as self employed (cant work for other people as cant keep up) but have recently had nasty setback due to operations.]]></content:encoded>
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			<title><![CDATA[Audio books.]]></title>
			<link>http://meshcornwall.org/forum/showthread.php?tid=167</link>
			<pubDate>Tue, 05 Apr 2011 17:55:42 +0000</pubDate>
			<guid isPermaLink="false">http://meshcornwall.org/forum/showthread.php?tid=167</guid>
			<description><![CDATA[Hi,<br />
I was wondering if any other person is using audio books as I personally have found them a god send<img src="images/smilies/angel.gif" style="vertical-align: middle;" border="0" alt="Angel" title="Angel" /><br />
I bought an Amazon Kindle but found any type of reading a real demand on my energy<img src="images/smilies/angry.gif" style="vertical-align: middle;" border="0" alt="Angry" title="Angry" /><br />
I found I can download audio books from Audible.co.uk and transfer them from my computer onto the Kindle and its bliss<img src="images/smilies/heart.gif" style="vertical-align: middle;" border="0" alt="Heart" title="Heart" /><br />
I've listened to Ken Follets Pillars of the Earth ( about 40hrs) and am now listening to Frank Herberts Dune, which I had read many years back.<br />
The discovery of the audio books has been a revelation for me and has helped me get through many hours whilst poorly.<br />
If anyone wants further advice I will be more than willing to help. <img src="images/smilies/biggrin.gif" style="vertical-align: middle;" border="0" alt="Big Grin" title="Big Grin" />]]></description>
			<content:encoded><![CDATA[Hi,<br />
I was wondering if any other person is using audio books as I personally have found them a god send<img src="images/smilies/angel.gif" style="vertical-align: middle;" border="0" alt="Angel" title="Angel" /><br />
I bought an Amazon Kindle but found any type of reading a real demand on my energy<img src="images/smilies/angry.gif" style="vertical-align: middle;" border="0" alt="Angry" title="Angry" /><br />
I found I can download audio books from Audible.co.uk and transfer them from my computer onto the Kindle and its bliss<img src="images/smilies/heart.gif" style="vertical-align: middle;" border="0" alt="Heart" title="Heart" /><br />
I've listened to Ken Follets Pillars of the Earth ( about 40hrs) and am now listening to Frank Herberts Dune, which I had read many years back.<br />
The discovery of the audio books has been a revelation for me and has helped me get through many hours whilst poorly.<br />
If anyone wants further advice I will be more than willing to help. <img src="images/smilies/biggrin.gif" style="vertical-align: middle;" border="0" alt="Big Grin" title="Big Grin" />]]></content:encoded>
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			<title><![CDATA[Just joined]]></title>
			<link>http://meshcornwall.org/forum/showthread.php?tid=165</link>
			<pubDate>Tue, 29 Mar 2011 18:43:27 +0000</pubDate>
			<guid isPermaLink="false">http://meshcornwall.org/forum/showthread.php?tid=165</guid>
			<description><![CDATA[Hi. Just found this forum and I'd like to say hello. <br />
<br />
I'm pretty much recovered now. I'm probably about 70-80% on the M.E. scale. It's certainly been a difficult illness but I've come through the worst of it.<br />
<br />
Although I'm not yet fully recovered, so still unable to work. Walking is still very tiring and occasionally I still need to rest during the day. But I can drive and and I'm independent, so I'm very thankful that I'm nearly recovered.]]></description>
			<content:encoded><![CDATA[Hi. Just found this forum and I'd like to say hello. <br />
<br />
I'm pretty much recovered now. I'm probably about 70-80% on the M.E. scale. It's certainly been a difficult illness but I've come through the worst of it.<br />
<br />
Although I'm not yet fully recovered, so still unable to work. Walking is still very tiring and occasionally I still need to rest during the day. But I can drive and and I'm independent, so I'm very thankful that I'm nearly recovered.]]></content:encoded>
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			<title><![CDATA[Hi Everyone]]></title>
			<link>http://meshcornwall.org/forum/showthread.php?tid=164</link>
			<pubDate>Tue, 29 Mar 2011 13:50:11 +0000</pubDate>
			<guid isPermaLink="false">http://meshcornwall.org/forum/showthread.php?tid=164</guid>
			<description><![CDATA[Hi, I was diagnosed with ME about 6 years ago by Prof. Pinching after 17 years of being fobbed off by Drs.  I had Glandular fever aged 14, which I took a long time to get over, then I had Chicken pox at 21, Fertility treatment until 24 and after the resulting little girl (wonderful!) I was on my last legs.  Was then told I was lazy and to go to the gym so that I would feel better <img src="images/smilies/angry.gif" style="vertical-align: middle;" border="0" alt="Angry" title="Angry" />.  This resulted in being virtually housebound, caring for my daughter, trying to hold a part time job, very depressed and barely able to look after myself.  So now I am 37 and my daughter is 13, its been a hard 13 years especially the first few not knowing why I wasnt coping like other mums<img src="images/smilies/huh.gif" style="vertical-align: middle;" border="0" alt="Huh" title="Huh" />. My Husband is brilliant but he works full time to try to keep a roof over our heads and I am unable to work or claim any benefits to help.  I have up until about 18 months ago managed ok with the advice from Prof. P.  However since my dad died I have gone backwards dramatically, so am now having visits from the Occ. Therapist.  Finding the pacing very hard, and also writing all activities down is making me feel worse at the moment, I dont seem to be able to get any energy to build up enough to go out for a short walk with our greyhound.  I cant remember the last time I felt well.  Feel quite depressed that I have gone backwards after all these years.  I generally have always kept positive an happy but it is difficult lately.  Sorry to moan so much, I will cheer up soon<img src="images/smilies/cool.gif" style="vertical-align: middle;" border="0" alt="Cool" title="Cool" />]]></description>
			<content:encoded><![CDATA[Hi, I was diagnosed with ME about 6 years ago by Prof. Pinching after 17 years of being fobbed off by Drs.  I had Glandular fever aged 14, which I took a long time to get over, then I had Chicken pox at 21, Fertility treatment until 24 and after the resulting little girl (wonderful!) I was on my last legs.  Was then told I was lazy and to go to the gym so that I would feel better <img src="images/smilies/angry.gif" style="vertical-align: middle;" border="0" alt="Angry" title="Angry" />.  This resulted in being virtually housebound, caring for my daughter, trying to hold a part time job, very depressed and barely able to look after myself.  So now I am 37 and my daughter is 13, its been a hard 13 years especially the first few not knowing why I wasnt coping like other mums<img src="images/smilies/huh.gif" style="vertical-align: middle;" border="0" alt="Huh" title="Huh" />. My Husband is brilliant but he works full time to try to keep a roof over our heads and I am unable to work or claim any benefits to help.  I have up until about 18 months ago managed ok with the advice from Prof. P.  However since my dad died I have gone backwards dramatically, so am now having visits from the Occ. Therapist.  Finding the pacing very hard, and also writing all activities down is making me feel worse at the moment, I dont seem to be able to get any energy to build up enough to go out for a short walk with our greyhound.  I cant remember the last time I felt well.  Feel quite depressed that I have gone backwards after all these years.  I generally have always kept positive an happy but it is difficult lately.  Sorry to moan so much, I will cheer up soon<img src="images/smilies/cool.gif" style="vertical-align: middle;" border="0" alt="Cool" title="Cool" />]]></content:encoded>
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			<title><![CDATA[On Line diary 'Twitter']]></title>
			<link>http://meshcornwall.org/forum/showthread.php?tid=163</link>
			<pubDate>Sat, 26 Mar 2011 19:15:26 +0000</pubDate>
			<guid isPermaLink="false">http://meshcornwall.org/forum/showthread.php?tid=163</guid>
			<description><![CDATA[;)Hi all,<br />
having just relapse again I've decided to keep some sort of online diary the easiest being Twitter. <br />
If anyone  wants to follow me my search name is pmclarke5, its to see how I improve and also to see where I'm going wrong.<br />
Cheers Paul. <img src="images/smilies/smile.gif" style="vertical-align: middle;" border="0" alt="Smile" title="Smile" /><hr />
Or search name is @pmclarke5<br />
not quite sure.<br />
Cheers Paul]]></description>
			<content:encoded><![CDATA[;)Hi all,<br />
having just relapse again I've decided to keep some sort of online diary the easiest being Twitter. <br />
If anyone  wants to follow me my search name is pmclarke5, its to see how I improve and also to see where I'm going wrong.<br />
Cheers Paul. <img src="images/smilies/smile.gif" style="vertical-align: middle;" border="0" alt="Smile" title="Smile" /><hr />
Or search name is @pmclarke5<br />
not quite sure.<br />
Cheers Paul]]></content:encoded>
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			<title><![CDATA[Hi from a nother new guy.]]></title>
			<link>http://meshcornwall.org/forum/showthread.php?tid=140</link>
			<pubDate>Wed, 09 Mar 2011 13:28:16 +0000</pubDate>
			<guid isPermaLink="false">http://meshcornwall.org/forum/showthread.php?tid=140</guid>
			<description><![CDATA[Hey,<br />
<br />
After finally getting fed up with my local doctors and getting refered to Prof Pinchings dept, i figured i'd sign up on th MESH forums aswell.<br />
<br />
I'm Nick 35 and in Cornwall. I was diagnosed with ME/cfs about 8 years ago now. the doctor explained that she didnt believe in ME but if she did then that is definatley what i had....<br />
<br />
That was my first of many negative experiences with GP's. Since then i have slowly done away with making doctors visits as i always come away from them somewhat disheartened as if i must be a little mad in the head to suggest my severe tiredness and confusion is an illness.<br />
<br />
My illness tends to come and go where i may be fine for months as long as im careful and then over a period of a few days i can feel a knowing ache or my eyes start blurring or i get severe numbness in my legs along with the usual fatigue. having to prop myself up against a wall to do the dishes is my latest telltale sign<img src="images/smilies/smile.gif" style="vertical-align: middle;" border="0" alt="Smile" title="Smile" />. <br />
<br />
Im lucky that im self employed and limit myself to 15 to 20 hours a week. I occasionally manage the gym or walks etc but they are often responsible for huge relapses. i havent had any severe confusion or "brain fog" in a while. it used to get so bad that i couldnt speak coherently. <br />
<br />
Guilt was a big problem for me for a long time thinking that i must be just lazy or unfit or something and my siblings not understanding was hard to deal with.<br />
<br />
Staying inside and not being social led to a number of anxiety problems and i guess a bit of depression however, i seem to be really on top of those negative aspects these days. <br />
<br />
Im lucky to have a partner who is very patient and understanding (plus a degree in counselling helps lol).<br />
<br />
other silly or maybe important things ive noted are<br />
<br />
*i take omeprazole for jumpy acid and if ever i stop taking it i ALWAYS get my ME/cfs symptoms back for weeks and weeks<br />
<br />
*I have signs of having had glandular fever but have no re3collection of this<br />
<br />
*illness started as severe flu after wild camping in the lake district however the doctors tell me not to even consider lyme's disease as its really rare.( this i have tried fighting as prior to thgis i was an outdoor instructor and spend many weeks of a year in wales/scotland hill walking and camping etc etc).<br />
<br />
*I disagree that CBT is effective in treating ME and have found the easist way is to start by doing NOTHING and then slowly create a routine and add to my daily routine and just monitor how im feeling.<br />
<br />
Anyways. this was only meant to be a quick introduction and a chance to say hi but guess im feeling vocal today.<br />
<br />
Its great to have found a forum linked to this and i really cant believe i didnt think about looking for one before.]]></description>
			<content:encoded><![CDATA[Hey,<br />
<br />
After finally getting fed up with my local doctors and getting refered to Prof Pinchings dept, i figured i'd sign up on th MESH forums aswell.<br />
<br />
I'm Nick 35 and in Cornwall. I was diagnosed with ME/cfs about 8 years ago now. the doctor explained that she didnt believe in ME but if she did then that is definatley what i had....<br />
<br />
That was my first of many negative experiences with GP's. Since then i have slowly done away with making doctors visits as i always come away from them somewhat disheartened as if i must be a little mad in the head to suggest my severe tiredness and confusion is an illness.<br />
<br />
My illness tends to come and go where i may be fine for months as long as im careful and then over a period of a few days i can feel a knowing ache or my eyes start blurring or i get severe numbness in my legs along with the usual fatigue. having to prop myself up against a wall to do the dishes is my latest telltale sign<img src="images/smilies/smile.gif" style="vertical-align: middle;" border="0" alt="Smile" title="Smile" />. <br />
<br />
Im lucky that im self employed and limit myself to 15 to 20 hours a week. I occasionally manage the gym or walks etc but they are often responsible for huge relapses. i havent had any severe confusion or "brain fog" in a while. it used to get so bad that i couldnt speak coherently. <br />
<br />
Guilt was a big problem for me for a long time thinking that i must be just lazy or unfit or something and my siblings not understanding was hard to deal with.<br />
<br />
Staying inside and not being social led to a number of anxiety problems and i guess a bit of depression however, i seem to be really on top of those negative aspects these days. <br />
<br />
Im lucky to have a partner who is very patient and understanding (plus a degree in counselling helps lol).<br />
<br />
other silly or maybe important things ive noted are<br />
<br />
*i take omeprazole for jumpy acid and if ever i stop taking it i ALWAYS get my ME/cfs symptoms back for weeks and weeks<br />
<br />
*I have signs of having had glandular fever but have no re3collection of this<br />
<br />
*illness started as severe flu after wild camping in the lake district however the doctors tell me not to even consider lyme's disease as its really rare.( this i have tried fighting as prior to thgis i was an outdoor instructor and spend many weeks of a year in wales/scotland hill walking and camping etc etc).<br />
<br />
*I disagree that CBT is effective in treating ME and have found the easist way is to start by doing NOTHING and then slowly create a routine and add to my daily routine and just monitor how im feeling.<br />
<br />
Anyways. this was only meant to be a quick introduction and a chance to say hi but guess im feeling vocal today.<br />
<br />
Its great to have found a forum linked to this and i really cant believe i didnt think about looking for one before.]]></content:encoded>
		</item>
		<item>
			<title><![CDATA[new!]]></title>
			<link>http://meshcornwall.org/forum/showthread.php?tid=139</link>
			<pubDate>Tue, 08 Mar 2011 11:07:29 +0000</pubDate>
			<guid isPermaLink="false">http://meshcornwall.org/forum/showthread.php?tid=139</guid>
			<description><![CDATA[Hello. I was diagnosed with post viral fatigue syndrome in Feb 2009. At the time I was living in London, working 3 jobs and studying for an MA........ I had to give that life up after struggling with money having not been able to work or study! I thus moved back to live with the parents (at the age of 30!) near Launceston, and although I had a good summer (2010) health wise (managed!!), I am now worrying about relapsing. Following a cold a few weeks ago, I have returned to a state of fog, sleep problems, exhaustion, dependancy on caffine...... I could go on..... Although my GP is understanding, he has said that life will be like this for possibly ever....... Thus, I thought it time to make contact with other people who will understand my symptoms and not make me feel like an idiot for being tired all the time......so, HELLO......<img src="images/smilies/smile.gif" style="vertical-align: middle;" border="0" alt="Smile" title="Smile" />]]></description>
			<content:encoded><![CDATA[Hello. I was diagnosed with post viral fatigue syndrome in Feb 2009. At the time I was living in London, working 3 jobs and studying for an MA........ I had to give that life up after struggling with money having not been able to work or study! I thus moved back to live with the parents (at the age of 30!) near Launceston, and although I had a good summer (2010) health wise (managed!!), I am now worrying about relapsing. Following a cold a few weeks ago, I have returned to a state of fog, sleep problems, exhaustion, dependancy on caffine...... I could go on..... Although my GP is understanding, he has said that life will be like this for possibly ever....... Thus, I thought it time to make contact with other people who will understand my symptoms and not make me feel like an idiot for being tired all the time......so, HELLO......<img src="images/smilies/smile.gif" style="vertical-align: middle;" border="0" alt="Smile" title="Smile" />]]></content:encoded>
		</item>
		<item>
			<title><![CDATA[New to MESH]]></title>
			<link>http://meshcornwall.org/forum/showthread.php?tid=138</link>
			<pubDate>Mon, 28 Feb 2011 11:55:15 +0000</pubDate>
			<guid isPermaLink="false">http://meshcornwall.org/forum/showthread.php?tid=138</guid>
			<description><![CDATA[Hi, my name is Linda and I have just found MESH through Facebook, so am about to join.  I have had ME for over 20 years but only diagnosed in 2007 and since July 2007 have been unable to work.  Hoping that this forum will help.]]></description>
			<content:encoded><![CDATA[Hi, my name is Linda and I have just found MESH through Facebook, so am about to join.  I have had ME for over 20 years but only diagnosed in 2007 and since July 2007 have been unable to work.  Hoping that this forum will help.]]></content:encoded>
		</item>
		<item>
			<title><![CDATA[prof pinching referral]]></title>
			<link>http://meshcornwall.org/forum/showthread.php?tid=137</link>
			<pubDate>Tue, 15 Feb 2011 15:53:40 +0000</pubDate>
			<guid isPermaLink="false">http://meshcornwall.org/forum/showthread.php?tid=137</guid>
			<description><![CDATA[I have just been referred to prof pinching - clinic in Liskeard - does anyone know what happens at your appointment? will any help be offered? I am at my wits end - feeling worse with every day - cant cope much longer! so holding on until my appointment......<br />
<br />
any advice welcome!]]></description>
			<content:encoded><![CDATA[I have just been referred to prof pinching - clinic in Liskeard - does anyone know what happens at your appointment? will any help be offered? I am at my wits end - feeling worse with every day - cant cope much longer! so holding on until my appointment......<br />
<br />
any advice welcome!]]></content:encoded>
		</item>
		<item>
			<title><![CDATA[Any support groups in Truro or Falmouth]]></title>
			<link>http://meshcornwall.org/forum/showthread.php?tid=134</link>
			<pubDate>Wed, 19 Jan 2011 16:19:32 +0000</pubDate>
			<guid isPermaLink="false">http://meshcornwall.org/forum/showthread.php?tid=134</guid>
			<description><![CDATA[Hi,<br />
<br />
I was wondering if there are any support groups in Truro or Falmouth for people who suffer from ME/CFS? <br />
<br />
I am on Job Seekers at the moment as I am waiting for my appeal against ISA to happen, when I went on Job Seekers i got put onto a programme called Plus which helps people who have got an illness/disablity get ready for work and the lady who I see is very helpul as she has got an illness similar to ME/CFS and told me to see if there are any support groups I can join, so here I am.<br />
<br />
If anyone knows of a suuport group or any extra help I would be very grateful.<br />
<br />
If there isnt any support groups in Truro or Falmouth and someone would want to set one up with me then message me.<br />
<br />
Hope everyone is having a good day.<br />
<br />
take care, and thank you for reading.<br />
<br />
Laura]]></description>
			<content:encoded><![CDATA[Hi,<br />
<br />
I was wondering if there are any support groups in Truro or Falmouth for people who suffer from ME/CFS? <br />
<br />
I am on Job Seekers at the moment as I am waiting for my appeal against ISA to happen, when I went on Job Seekers i got put onto a programme called Plus which helps people who have got an illness/disablity get ready for work and the lady who I see is very helpul as she has got an illness similar to ME/CFS and told me to see if there are any support groups I can join, so here I am.<br />
<br />
If anyone knows of a suuport group or any extra help I would be very grateful.<br />
<br />
If there isnt any support groups in Truro or Falmouth and someone would want to set one up with me then message me.<br />
<br />
Hope everyone is having a good day.<br />
<br />
take care, and thank you for reading.<br />
<br />
Laura]]></content:encoded>
		</item>
		<item>
			<title><![CDATA[Question]]></title>
			<link>http://meshcornwall.org/forum/showthread.php?tid=128</link>
			<pubDate>Wed, 01 Dec 2010 00:40:18 +0000</pubDate>
			<guid isPermaLink="false">http://meshcornwall.org/forum/showthread.php?tid=128</guid>
			<description><![CDATA[Good day, I've got a brief query. Does anybody see a slight lag using this forum every time they get access? It normally takes a minimum of five seconds or so for me to view the home page.<br />
<br />
Many thanks<br />
Marisa <br />
======================================<br />
meshcornwall.org rocks! | <a href="http://www.squidoo.com/tvwebi-review" target="_blank">TvWebi Review</a>]]></description>
			<content:encoded><![CDATA[Good day, I've got a brief query. Does anybody see a slight lag using this forum every time they get access? It normally takes a minimum of five seconds or so for me to view the home page.<br />
<br />
Many thanks<br />
Marisa <br />
======================================<br />
meshcornwall.org rocks! | <a href="http://www.squidoo.com/tvwebi-review" target="_blank">TvWebi Review</a>]]></content:encoded>
		</item>
		<item>
			<title><![CDATA[Advertising]]></title>
			<link>http://meshcornwall.org/forum/showthread.php?tid=126</link>
			<pubDate>Mon, 22 Nov 2010 18:02:24 +0000</pubDate>
			<guid isPermaLink="false">http://meshcornwall.org/forum/showthread.php?tid=126</guid>
			<description><![CDATA[There has been a few individuals lately using the MESH Cornwall Forum for commercial purposes, this is not allowed.  As I come across them I will delete the posts and ban the offending individuals.<br />
If you do come across such posts please do let me know via the messaging system, thank you.<br />
<br />
Chris.]]></description>
			<content:encoded><![CDATA[There has been a few individuals lately using the MESH Cornwall Forum for commercial purposes, this is not allowed.  As I come across them I will delete the posts and ban the offending individuals.<br />
If you do come across such posts please do let me know via the messaging system, thank you.<br />
<br />
Chris.]]></content:encoded>
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