Comments on: Symptoms – Part 3 | My First Vertigo Attack http://www.mymenieres.com/2008/11/15/symptoms-part-3-my-first-vertigo-attack/ The story of my Diagnosis of Meniere's Disease and Resources that may help Thu, 24 Jun 2010 21:39:44 +0000 http://wordpress.org/?v=2.9.2 hourly 1 By: admin http://www.mymenieres.com/2008/11/15/symptoms-part-3-my-first-vertigo-attack/comment-page-1/#comment-440 admin Thu, 18 Mar 2010 15:53:06 +0000 http://www.mymenieres.com/?p=10#comment-440 Believe me when I tell you that I understand your frustration. Fortunately my symptoms seem to be more intermittent now than they were. Unfortunately, I have developed joint pain and from the testing now, they say it is either Rheumatoid Arthritis or Lupus. They suspect it is likely RA. I feel like there isn't a single aspect of my daily life that isn't affected by either that or my Meniere's. The thing is, it's made me re-evaluate th things I should be spending my time with somewhat. I hope you can find treatments that will lessen your symptoms and hope very much that you can find some things to do that you enjoy and focus on the good things. (I know, it's hard not to focus on the bad, but it doesn't take you to a good place.) That much said - it's good to vent! In fact at one point my head was bursting with so much information about this disorder I felt compelled to start writing it up on this site. In some ways it's been therapeutic to do so. Finding others that can understand help as well and I would highly recommend you to stop by the <a href="http://www.menieres.org/forum/index.php" rel="nofollow">Meniere's forum</a> at http://www.menieres.org/forum/index.php if you haven't already. Believe me when I tell you that I understand your frustration. Fortunately my symptoms seem to be more intermittent now than they were. Unfortunately, I have developed joint pain and from the testing now, they say it is either Rheumatoid Arthritis or Lupus. They suspect it is likely RA. I feel like there isn’t a single aspect of my daily life that isn’t affected by either that or my Meniere’s.

The thing is, it’s made me re-evaluate th things I should be spending my time with somewhat. I hope you can find treatments that will lessen your symptoms and hope very much that you can find some things to do that you enjoy and focus on the good things. (I know, it’s hard not to focus on the bad, but it doesn’t take you to a good place.)

That much said – it’s good to vent! In fact at one point my head was bursting with so much information about this disorder I felt compelled to start writing it up on this site. In some ways it’s been therapeutic to do so.

Finding others that can understand help as well and I would highly recommend you to stop by the Meniere’s forum at http://www.menieres.org/forum/index.php if you haven’t already.

]]> By: Adi http://www.mymenieres.com/2008/11/15/symptoms-part-3-my-first-vertigo-attack/comment-page-1/#comment-439 Adi Wed, 17 Mar 2010 19:28:42 +0000 http://www.mymenieres.com/?p=10#comment-439 I have Menier's disease. It has made my life hell. I don't know how to live with it. I don't enjoy anything anymore. When every pleasurable experience is intrupted by a fucking fluid in your years... how can you enjoy life... I have Menier’s disease.
It has made my life hell. I don’t know how to live with it. I don’t enjoy anything anymore. When every pleasurable experience is intrupted by a fucking fluid in your years… how can you enjoy life…

]]>