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	<title>Comments on: Fibromyalgia</title>
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		<title>By: becky burns</title>
		<link>http://yourhealthresources.com/fibromyalgia/comment-page-1/#comment-1912</link>
		<dc:creator>becky burns</dc:creator>
		<pubDate>Mon, 19 Jul 2010 03:27:26 +0000</pubDate>
		<guid isPermaLink="false">http://yourhealthresources.com/fibromyalgia/#comment-1912</guid>
		<description>dear robin, my name is becky and i have everything that you have except the tos.my dr. diagnosed me with fibro.about 5yrs.ago andi,ve been on everything you have been on.just last month my dr. upped my dosage of lyrica to 600mgs.a day but i have gained 60lbs. in just 2yrs.,along with my feet swelling.it hurts when i walk sit or stand .i have had 2heel surgeries, one in 08 09 3 knee surgeris the last one being on feb.4th. of 2010.i,m only 5ft1 and now he hhas taken me off my soma,skelaxin and getting him to give me anything differant for pain is like pulling teeth out of a mule.go figure i have seen this dr. for 11yrs. in jan.do you have any thought in this matter that might help me.i,m at my witts end i also have suffered bypollar manic depressive for yrs.i don,t take half the meds. for that because it seems eveything makes me gain weight please help.B.B. in Texas</description>
		<content:encoded><![CDATA[<p>dear robin, my name is becky and i have everything that you have except the tos.my dr. diagnosed me with fibro.about 5yrs.ago andi,ve been on everything you have been on.just last month my dr. upped my dosage of lyrica to 600mgs.a day but i have gained 60lbs. in just 2yrs.,along with my feet swelling.it hurts when i walk sit or stand .i have had 2heel surgeries, one in 08 09 3 knee surgeris the last one being on feb.4th. of 2010.i,m only 5ft1 and now he hhas taken me off my soma,skelaxin and getting him to give me anything differant for pain is like pulling teeth out of a mule.go figure i have seen this dr. for 11yrs. in jan.do you have any thought in this matter that might help me.i,m at my witts end i also have suffered bypollar manic depressive for yrs.i don,t take half the meds. for that because it seems eveything makes me gain weight please help.B.B. in Texas</p>
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		<title>By: robin</title>
		<link>http://yourhealthresources.com/fibromyalgia/comment-page-1/#comment-1847</link>
		<dc:creator>robin</dc:creator>
		<pubDate>Tue, 15 Jun 2010 05:56:54 +0000</pubDate>
		<guid isPermaLink="false">http://yourhealthresources.com/fibromyalgia/#comment-1847</guid>
		<description>I have been dealing w/fibro for yrs. but my PCP is one of those flipping idiots that did not beleive fibro. exisited he kepted saying I just pulled a muscle! WHAT!? has he lost his damn mind? I guess I pulled a muscle in my ass,back,hips,shoulder,legs,arms, ect...... I finally got mad and told him to piss off! and I took it matters in my own hands I started doing research you have got to be your own advocate because believe me no one else knows you but you! and here is my conclusion so far lyrica only works for people not allergic to or cannot tolerate NSAIDS and if you are not careful you will gain alot of weight,it also can cause you to feel like you are completely losing your mind! and dear God I sweat in a cold shower, my hands &amp; feet felt like they were going to exploded the swelling was unbearable! I go for days w/out sleep and sometimes I would do nothing but sleep?! finally after being on 450mg a day for almost a year I told the Dr. NO MORE NO WAY!Iam now of that and feeling better I started taking neurontin(Gabapentin) it is a nerve blocker,mobic,wellbutrin XL 24hr.,trazodone(sleep aide),soma(carisoprodol-muscle relaxer,skelaxin(metaxalone-muscle relaxer)and of coarse lomotil for IBS w/diarrea THANK GOD Iam on of the luckier ones that do not have constipation! Iam sorry for the ones that do! I do have other problems other than fibro I also contend with osteoarthritis,digenitive disk disease,carpol tunnel,bursitis,&amp; major feet problems,hyatial hernia,ect........ for anyone whos insurance won&#039;t cover your meds.appeal it!the feet problem is called plantar facsitis(muscle in the heel of foot)NEED TO SEE ORTHOPEDIC FOOT DOC.it feels like knives in bottom of feet! PLEASEEEEEE try to stay away from narcotics they will ruin your liver&amp;kidneys lyrica,mobic,and almost any drug that treats fibro.will do that to so have blood tests done at least every 3 or 4 months! to make sure that does not happen to you! also, cymbalta &amp; the other anti-depressants that they give for fibro. is VERY dangerous please watch dosage &amp; side effects! you do not want to O.D.or become suicidal! pain management doc. are great! get one! aquatic theropy is FABULOUS! BY THE WAY,I have TOS thorastic outlet syndrome it only occurs in about 4% of the population &amp; I guess the jokes on me! they want to remove my number 1 rib(it is up in the neck region)&amp; remove the muscles &amp; nerves that surround it from the no.1 rib to the no.4 rib which happens to all be around all the main arteries from your neck area to your heart. and since I have fibro. they feel that it is going to be im-operable unless I start to lose full mobility in my left arm &amp; of coarse Iam left handed so Iam going to see a cardiovascular surgeon &amp; a nerologist so hopefully they can come up with a plan to solve this delema that Iam in. Well,good luck to all &amp; I hope I was helpful if anyone has questions or concerns I have a vast wealth of knowledge on alot of different health concerns I have a mom who has been a trama nurse for 43yrs.&amp; her husband is a doctor currently serving in Iraq.  MAY GOD BLESS EVERYONE AND KEEP YOU WELL!!       AND GOD BLESS AMERICA!!!!!!!  ROBIN</description>
		<content:encoded><![CDATA[<p>I have been dealing w/fibro for yrs. but my PCP is one of those flipping idiots that did not beleive fibro. exisited he kepted saying I just pulled a muscle! WHAT!? has he lost his damn mind? I guess I pulled a muscle in my ass,back,hips,shoulder,legs,arms, ect&#8230;&#8230; I finally got mad and told him to piss off! and I took it matters in my own hands I started doing research you have got to be your own advocate because believe me no one else knows you but you! and here is my conclusion so far lyrica only works for people not allergic to or cannot tolerate NSAIDS and if you are not careful you will gain alot of weight,it also can cause you to feel like you are completely losing your mind! and dear God I sweat in a cold shower, my hands &amp; feet felt like they were going to exploded the swelling was unbearable! I go for days w/out sleep and sometimes I would do nothing but sleep?! finally after being on 450mg a day for almost a year I told the Dr. NO MORE NO WAY!Iam now of that and feeling better I started taking neurontin(Gabapentin) it is a nerve blocker,mobic,wellbutrin XL 24hr.,trazodone(sleep aide),soma(carisoprodol-muscle relaxer,skelaxin(metaxalone-muscle relaxer)and of coarse lomotil for IBS w/diarrea THANK GOD Iam on of the luckier ones that do not have constipation! Iam sorry for the ones that do! I do have other problems other than fibro I also contend with osteoarthritis,digenitive disk disease,carpol tunnel,bursitis,&amp; major feet problems,hyatial hernia,ect&#8230;&#8230;.. for anyone whos insurance won&#8217;t cover your meds.appeal it!the feet problem is called plantar facsitis(muscle in the heel of foot)NEED TO SEE ORTHOPEDIC FOOT DOC.it feels like knives in bottom of feet! PLEASEEEEEE try to stay away from narcotics they will ruin your liver&amp;kidneys lyrica,mobic,and almost any drug that treats fibro.will do that to so have blood tests done at least every 3 or 4 months! to make sure that does not happen to you! also, cymbalta &amp; the other anti-depressants that they give for fibro. is VERY dangerous please watch dosage &amp; side effects! you do not want to O.D.or become suicidal! pain management doc. are great! get one! aquatic theropy is FABULOUS! BY THE WAY,I have TOS thorastic outlet syndrome it only occurs in about 4% of the population &amp; I guess the jokes on me! they want to remove my number 1 rib(it is up in the neck region)&amp; remove the muscles &amp; nerves that surround it from the no.1 rib to the no.4 rib which happens to all be around all the main arteries from your neck area to your heart. and since I have fibro. they feel that it is going to be im-operable unless I start to lose full mobility in my left arm &amp; of coarse Iam left handed so Iam going to see a cardiovascular surgeon &amp; a nerologist so hopefully they can come up with a plan to solve this delema that Iam in. Well,good luck to all &amp; I hope I was helpful if anyone has questions or concerns I have a vast wealth of knowledge on alot of different health concerns I have a mom who has been a trama nurse for 43yrs.&amp; her husband is a doctor currently serving in Iraq.  MAY GOD BLESS EVERYONE AND KEEP YOU WELL!!       AND GOD BLESS AMERICA!!!!!!!  ROBIN</p>
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		<title>By: Jennie</title>
		<link>http://yourhealthresources.com/fibromyalgia/comment-page-1/#comment-1823</link>
		<dc:creator>Jennie</dc:creator>
		<pubDate>Thu, 27 May 2010 02:40:09 +0000</pubDate>
		<guid isPermaLink="false">http://yourhealthresources.com/fibromyalgia/#comment-1823</guid>
		<description>I was diagnosed 1 year ago w/fibro, mixed connective tissue disease (lupus &amp; schelroderma), herniated discs, osteoarthritis, bulging discs, hyatial hernia, strictions in my esophagus, hives, and signs of reynaud and God knows what else. For the last 3 months I&#039;ve recently have had convulsions (like I&#039;ve been shot with a tazer) on the floor convulsing and my breathing becomes labored and my primary says is all phsycological and having a terrible time trying to  see a neurologist. June 1 I will have a new primary. I have medicare. Fighting to get referral after referral, due to the pain, I am now seeing a pain management dr. He has prescribed lyrica, ms contin and hydrocodone. My primary (dr moron) just kept giving me hydrocodone (10.325 7Xday) My right leg is constantly in exruciating pain. Only with the new combo in my leg feeling relief cause of pain mgmt dr. Now I can&#039;t afford lyrica and don&#039;t know what I&#039;m going to do. Reading the other meds on this site helps. I stretch alot, use a rolling pin on my legs, heating pad, yoga and little walking helps. But sometimes the bottom of my feet feel so bruised and can hardly walk. I sleep approx. 4 to 5 hrs at night, now. I can deal with that instead of 3 hr nights. My insurance suggested instead of lyrica there is ethosuximide or fibronal. Left message with pain mgmt dr.. Had my whole family read about fibro and the rest for support. They are good to me. God Bless those without the support. I will pray for you. I will take any suggestions or love to hear from anyone with the same as me. Oh, found out that traditional medicare can allow you to see any specialist. It&#039;s like a PPO (80/20) insurance. Mayo clinic will take you tomorrow with trad. medicare (no hmo&#039;s). Open enrollment is Nov 1st unless, financially troubled, you can switch immediately with a visit to social security office and apply. God Bless you all. I know the pain and how it turns you life upside down. Don&#039;t give up and don&#039;t be afraid to try new medication. Jennie</description>
		<content:encoded><![CDATA[<p>I was diagnosed 1 year ago w/fibro, mixed connective tissue disease (lupus &amp; schelroderma), herniated discs, osteoarthritis, bulging discs, hyatial hernia, strictions in my esophagus, hives, and signs of reynaud and God knows what else. For the last 3 months I&#8217;ve recently have had convulsions (like I&#8217;ve been shot with a tazer) on the floor convulsing and my breathing becomes labored and my primary says is all phsycological and having a terrible time trying to  see a neurologist. June 1 I will have a new primary. I have medicare. Fighting to get referral after referral, due to the pain, I am now seeing a pain management dr. He has prescribed lyrica, ms contin and hydrocodone. My primary (dr moron) just kept giving me hydrocodone (10.325 7Xday) My right leg is constantly in exruciating pain. Only with the new combo in my leg feeling relief cause of pain mgmt dr. Now I can&#8217;t afford lyrica and don&#8217;t know what I&#8217;m going to do. Reading the other meds on this site helps. I stretch alot, use a rolling pin on my legs, heating pad, yoga and little walking helps. But sometimes the bottom of my feet feel so bruised and can hardly walk. I sleep approx. 4 to 5 hrs at night, now. I can deal with that instead of 3 hr nights. My insurance suggested instead of lyrica there is ethosuximide or fibronal. Left message with pain mgmt dr.. Had my whole family read about fibro and the rest for support. They are good to me. God Bless those without the support. I will pray for you. I will take any suggestions or love to hear from anyone with the same as me. Oh, found out that traditional medicare can allow you to see any specialist. It&#8217;s like a PPO (80/20) insurance. Mayo clinic will take you tomorrow with trad. medicare (no hmo&#8217;s). Open enrollment is Nov 1st unless, financially troubled, you can switch immediately with a visit to social security office and apply. God Bless you all. I know the pain and how it turns you life upside down. Don&#8217;t give up and don&#8217;t be afraid to try new medication. Jennie</p>
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		<title>By: dolores</title>
		<link>http://yourhealthresources.com/fibromyalgia/comment-page-1/#comment-1753</link>
		<dc:creator>dolores</dc:creator>
		<pubDate>Wed, 14 Apr 2010 19:37:25 +0000</pubDate>
		<guid isPermaLink="false">http://yourhealthresources.com/fibromyalgia/#comment-1753</guid>
		<description>i read judy&#039;s info of her&#039;, and i can relate to what she is saying. i&#039;ve have lupus and fibro,since 2005 when the doctors confirmed my pain. i&#039;ve gotten off the meds that they perscribed and switched to medical marijuana. it takes away the pain alot guicker and makes me fell alot better not to mention,lots of laughter. i still have to work at dealing with the pain buti don&#039;t have to worry about constapation.that is so difficult,hated it. oxycontin is not the answer, it puts everything to sleep and the pain is still there. i will always have pain and can have relief for a alittle while with marijuana but i won&#039;t have to deal with the catastrophy that meds leave behind. my doctor blessed me with my decision. i don&#039;t look like death anymore, but i do have to watch my intake of food. it makes you hungry,when before i did not want to eat because the meds kept me from going to the bathroom. i do eat healthy, i don&#039;t eat alot of junk, but now i know i can eat and no problem having it come out. well i hope this helps someone with their pain,it&#039;s not for everyone, i&#039;m working at this myself cause i don&#039;t want to use pain pills that can do more harm than good.</description>
		<content:encoded><![CDATA[<p>i read judy&#8217;s info of her&#8217;, and i can relate to what she is saying. i&#8217;ve have lupus and fibro,since 2005 when the doctors confirmed my pain. i&#8217;ve gotten off the meds that they perscribed and switched to medical marijuana. it takes away the pain alot guicker and makes me fell alot better not to mention,lots of laughter. i still have to work at dealing with the pain buti don&#8217;t have to worry about constapation.that is so difficult,hated it. oxycontin is not the answer, it puts everything to sleep and the pain is still there. i will always have pain and can have relief for a alittle while with marijuana but i won&#8217;t have to deal with the catastrophy that meds leave behind. my doctor blessed me with my decision. i don&#8217;t look like death anymore, but i do have to watch my intake of food. it makes you hungry,when before i did not want to eat because the meds kept me from going to the bathroom. i do eat healthy, i don&#8217;t eat alot of junk, but now i know i can eat and no problem having it come out. well i hope this helps someone with their pain,it&#8217;s not for everyone, i&#8217;m working at this myself cause i don&#8217;t want to use pain pills that can do more harm than good.</p>
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		<title>By: Your Medical Resources &#187; Fybromyalgia &#8211; Relief From the Pain</title>
		<link>http://yourhealthresources.com/fibromyalgia/comment-page-1/#comment-1742</link>
		<dc:creator>Your Medical Resources &#187; Fybromyalgia &#8211; Relief From the Pain</dc:creator>
		<pubDate>Thu, 08 Apr 2010 16:23:19 +0000</pubDate>
		<guid isPermaLink="false">http://yourhealthresources.com/fibromyalgia/#comment-1742</guid>
		<description>[...] Fybromyalgia Fybromyalgia &#8211; Mayo Clinic [...]</description>
		<content:encoded><![CDATA[<p>[...] Fybromyalgia Fybromyalgia &#8211; Mayo Clinic [...]</p>
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		<title>By: julie</title>
		<link>http://yourhealthresources.com/fibromyalgia/comment-page-1/#comment-1688</link>
		<dc:creator>julie</dc:creator>
		<pubDate>Thu, 25 Feb 2010 05:34:52 +0000</pubDate>
		<guid isPermaLink="false">http://yourhealthresources.com/fibromyalgia/#comment-1688</guid>
		<description>I  have had fibromyalgia for some time now, and have started recently to have severe pain in the bottom of my feet, it feels like they are severely bruised, mostly on the heel area,it subsides when i get off my feet for a while. I also have severe back pain right in the area where my bra goes across my back , on the right side, mostly, i took lyrica for a while it helped tremendously, but my ahccs insurance wont cover it , so i am out of samples, and the withdrawal of it was terrible, hope someone finds a cure for this horrible disease, I wouldnt wish it on my worst enemy.</description>
		<content:encoded><![CDATA[<p>I  have had fibromyalgia for some time now, and have started recently to have severe pain in the bottom of my feet, it feels like they are severely bruised, mostly on the heel area,it subsides when i get off my feet for a while. I also have severe back pain right in the area where my bra goes across my back , on the right side, mostly, i took lyrica for a while it helped tremendously, but my ahccs insurance wont cover it , so i am out of samples, and the withdrawal of it was terrible, hope someone finds a cure for this horrible disease, I wouldnt wish it on my worst enemy.</p>
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		<title>By: Pat</title>
		<link>http://yourhealthresources.com/fibromyalgia/comment-page-1/#comment-1679</link>
		<dc:creator>Pat</dc:creator>
		<pubDate>Wed, 17 Feb 2010 22:48:18 +0000</pubDate>
		<guid isPermaLink="false">http://yourhealthresources.com/fibromyalgia/#comment-1679</guid>
		<description>Having suffered with this for years, I finally found a medical professional who understands it. You cannot describe it unless you have it.I am now taking along with painkillers, flexeril,mobic,  have just started on lyrica.  I still have bad days, but I MAKE myself stay active.  Even if I have to roll out of bed.  I work fulltime, and find I need to have something to get up and moving for.  I am not saying that I have days I am not bedridden, because there are some.  My sympathies to all. Exercise helps, even though at times I just can&#039;t.  Who wants to be the woman who complains about their aches and pains all day?  I hurt right now but it is controlled.  I have an active family, but some week ends I just have to REST!</description>
		<content:encoded><![CDATA[<p>Having suffered with this for years, I finally found a medical professional who understands it. You cannot describe it unless you have it.I am now taking along with painkillers, flexeril,mobic,  have just started on lyrica.  I still have bad days, but I MAKE myself stay active.  Even if I have to roll out of bed.  I work fulltime, and find I need to have something to get up and moving for.  I am not saying that I have days I am not bedridden, because there are some.  My sympathies to all. Exercise helps, even though at times I just can&#8217;t.  Who wants to be the woman who complains about their aches and pains all day?  I hurt right now but it is controlled.  I have an active family, but some week ends I just have to REST!</p>
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		<title>By: Judy Morrison</title>
		<link>http://yourhealthresources.com/fibromyalgia/comment-page-1/#comment-1664</link>
		<dc:creator>Judy Morrison</dc:creator>
		<pubDate>Thu, 04 Feb 2010 02:40:22 +0000</pubDate>
		<guid isPermaLink="false">http://yourhealthresources.com/fibromyalgia/#comment-1664</guid>
		<description>I have had Firbromyalgia for 29 years.   I also have had chest pain and gone to hospital and had all the heart testing with no sign of heart attack.  I have excercised at Curves and gone to Water Arobics.  Cannot stress the body too much but walk everyday for 25-40 minutes and that helps but when starting out have lots of pain in feet and as I get halfway home the pain lessens.  I am always in pain in every part of my body and can&#039;t take Nsaids as they give me diarrhea and lots of bad gas and also pain in the kidneys.  I have tried Amatriptoline 10mg and 25 but they make me so drousy and worsen my vision.  I am legally blind with Macular Degeneration which I got in my late 40&#039;s as in my case it runs in my family and I have Hereditory Macular so lost my licence to drive in l996 and I have Osteo Arthritis and two knee replacements, so I have been through the mill with Diagnosis of 18 of 18 pressure points for Fibro. I have multiple problems and lots to cry about but  the way I deal with pain is mild excercise and busy my self with other things and try not to dwell on myself too much, whic is very hard to do.  I rest everyday for 1 1/2 hrs anywher from 3:00 p.m. to or by 5:30 for an after dinner rest.  Rest is important but you always get up feeling like you have just fallen off the back of a truck and into a ditch.  Just get up and get moving and keep moving and when I can&#039;t take the pain anymore I take 2 Tylenol extra strength and then take two more 12 hours later to break the pain pattern.  You just have to think positive.

The sleeping is a problem but sometimes I drink a couple glasses of wine or rum is fine anytime of year and takes the pain away temporarily.  Not to become accustom to drinking but now and then it works.  It&#039;s good to have a partner or family member or friend that can read the symptons of Fibro and that&#039;s important having someone who understands   what you are going through for  support  when you need to vent a little.  But you can&#039;t moan and groan too much it drives people away from you.  I guess we just have to not smoke, eat healthy and have faith that there are sometimes spells when you have relief   Not everyone can be so lucky as me to have a undrstanding partner.  It&#039;s something you just have to learn to deal with, but definitely mild excercise rather than taking medication which wrecks havoc with your kidneys and causes bowel problems is part of the answer.   There doesn&#039;t seem to be a cure. It certainly messes your mind up but if you can joke about it that helps also.  Just remember, laugh and the world laughs with you, cry and you cry alone.  I always recall that saying when I have a pity party with myself.  Good luck and keep the  faith.  JM   pardon any spelling errors as I am visually impared.</description>
		<content:encoded><![CDATA[<p>I have had Firbromyalgia for 29 years.   I also have had chest pain and gone to hospital and had all the heart testing with no sign of heart attack.  I have excercised at Curves and gone to Water Arobics.  Cannot stress the body too much but walk everyday for 25-40 minutes and that helps but when starting out have lots of pain in feet and as I get halfway home the pain lessens.  I am always in pain in every part of my body and can&#8217;t take Nsaids as they give me diarrhea and lots of bad gas and also pain in the kidneys.  I have tried Amatriptoline 10mg and 25 but they make me so drousy and worsen my vision.  I am legally blind with Macular Degeneration which I got in my late 40&#8242;s as in my case it runs in my family and I have Hereditory Macular so lost my licence to drive in l996 and I have Osteo Arthritis and two knee replacements, so I have been through the mill with Diagnosis of 18 of 18 pressure points for Fibro. I have multiple problems and lots to cry about but  the way I deal with pain is mild excercise and busy my self with other things and try not to dwell on myself too much, whic is very hard to do.  I rest everyday for 1 1/2 hrs anywher from 3:00 p.m. to or by 5:30 for an after dinner rest.  Rest is important but you always get up feeling like you have just fallen off the back of a truck and into a ditch.  Just get up and get moving and keep moving and when I can&#8217;t take the pain anymore I take 2 Tylenol extra strength and then take two more 12 hours later to break the pain pattern.  You just have to think positive.</p>
<p>The sleeping is a problem but sometimes I drink a couple glasses of wine or rum is fine anytime of year and takes the pain away temporarily.  Not to become accustom to drinking but now and then it works.  It&#8217;s good to have a partner or family member or friend that can read the symptons of Fibro and that&#8217;s important having someone who understands   what you are going through for  support  when you need to vent a little.  But you can&#8217;t moan and groan too much it drives people away from you.  I guess we just have to not smoke, eat healthy and have faith that there are sometimes spells when you have relief   Not everyone can be so lucky as me to have a undrstanding partner.  It&#8217;s something you just have to learn to deal with, but definitely mild excercise rather than taking medication which wrecks havoc with your kidneys and causes bowel problems is part of the answer.   There doesn&#8217;t seem to be a cure. It certainly messes your mind up but if you can joke about it that helps also.  Just remember, laugh and the world laughs with you, cry and you cry alone.  I always recall that saying when I have a pity party with myself.  Good luck and keep the  faith.  JM   pardon any spelling errors as I am visually impared.</p>
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		<title>By: patti williams</title>
		<link>http://yourhealthresources.com/fibromyalgia/comment-page-1/#comment-1603</link>
		<dc:creator>patti williams</dc:creator>
		<pubDate>Mon, 28 Dec 2009 21:30:56 +0000</pubDate>
		<guid isPermaLink="false">http://yourhealthresources.com/fibromyalgia/#comment-1603</guid>
		<description>sorry for the mis-spelling of some of my words above as I am having difficulty right now with my vision.</description>
		<content:encoded><![CDATA[<p>sorry for the mis-spelling of some of my words above as I am having difficulty right now with my vision.</p>
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		<title>By: patti williams</title>
		<link>http://yourhealthresources.com/fibromyalgia/comment-page-1/#comment-1602</link>
		<dc:creator>patti williams</dc:creator>
		<pubDate>Mon, 28 Dec 2009 21:27:58 +0000</pubDate>
		<guid isPermaLink="false">http://yourhealthresources.com/fibromyalgia/#comment-1602</guid>
		<description>I was diagnosed with fibro. about 6-7 months ago after suffering with pain for about 1 year. i had back surgery about 4 years ago. about two months prior to diagnosis i got mono (EBV) and cytomegaly (CMV) virus I also had positive ANA test they ruled out lupus.  I have been hospitalized two times with chest wall pain and placd on cardiac floor which they know very little about fibro. I am a RN so I know such. they actually put me through angiogram, stress testand whole nine yards of test. I told them i felf this as due to my fibro. after the third day of them just giving me dilaudid IV my MD showed up and increased my lyrica from 150mg a day to 300mg a day i am haviving probs. now with double vision and beeing very dizzy and sleepy, i still work full time as a dialysis nurse so im unable to take my lyrica until i get home, im also on cymbalta 60mg every day and xanax 2mg three times a day for panic disorder.  I am allergic to NSAIDS.  they did try soma which didnt help.  please i need advise from some of you that have dealt with this disorder longer than i have. i am also at the point where i feel i cant continue to work full time.......please someone respond with any advise.....thank you patti</description>
		<content:encoded><![CDATA[<p>I was diagnosed with fibro. about 6-7 months ago after suffering with pain for about 1 year. i had back surgery about 4 years ago. about two months prior to diagnosis i got mono (EBV) and cytomegaly (CMV) virus I also had positive ANA test they ruled out lupus.  I have been hospitalized two times with chest wall pain and placd on cardiac floor which they know very little about fibro. I am a RN so I know such. they actually put me through angiogram, stress testand whole nine yards of test. I told them i felf this as due to my fibro. after the third day of them just giving me dilaudid IV my MD showed up and increased my lyrica from 150mg a day to 300mg a day i am haviving probs. now with double vision and beeing very dizzy and sleepy, i still work full time as a dialysis nurse so im unable to take my lyrica until i get home, im also on cymbalta 60mg every day and xanax 2mg three times a day for panic disorder.  I am allergic to NSAIDS.  they did try soma which didnt help.  please i need advise from some of you that have dealt with this disorder longer than i have. i am also at the point where i feel i cant continue to work full time&#8230;&#8230;.please someone respond with any advise&#8230;..thank you patti</p>
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