I read an article from Research 1st today about orthostatic intolerance and thought I should share the information in case someone else is having the same problems. Research 1st is a project of The CFIDS Association of America. I copied this next bit from their website, "Research1st, a project of the CFIDS Association of America, the world's largest organization dedicated to making chronic fatigue syndrome widely understood, diagnosable, curable and preventable. CFS is also known as chronic fatigue and immune dysfunction syndrome (CFIDS) or myalgic encephalomyelitis (ME, ME/CFS, or CFS/ME). We’re intensifying efforts across the field to build a critical mass of rigorous research that validates the biological basis for CFS and leads to improved methods of diagnosis and treatment."
Now back to the original reason for this post. The article came about because a woman asked a question on the Facebook site of the CFIDS site and Research1st did some investigation of the question and got back to her. The article "Is It Anxiety or OI?" I think they did a good job answering the question posed by the woman. The gist of it is that they showed a difference in what is SOMATIC (physically real) not PSYCHOSOMATIC (all in your head!) For so long I took care of people that came into the hospital thinking that they were making it up, having a breakdown, seeking drugs etc. but I didn't think it was 'real'. I think that as a health care provider I have learned more about these disorders, CFIDS, FM,RLS, etc by having been diagnosed with them then I ever did as a professional.
I have been having problems with orthostatic intolerance for many years and was told a long time ago that I was having 'panic/anxiety' issues and when that didn't work orthostatic hypotension/hypertension. I would walk into a building and my heart would start pounding and I would become short of breath, head would swirl, legs get weak, and down I would go. Never mind that prior to walking into the building I was fine and I was fine within minutes of the episode! It made no difference if I was going shopping, to church, work or whatever it would occur! Most times I wasn't stressed or anxious at all just doing what I was doing. I would get light headed rising up from a chair, short of breath walking from the kitchen sink to the livingroom, or go to bed at night and have episodes of tachycardia and shortness of breath. Most episodes were new around any type of even light physical activity. Interesting thing was they didn't happen frequently enough it would be come an issue and if I went to the doctor complaining about the tachycardia and the other issues they looked at me like I was nuts.
Read the article! I was happy to see that they did some research to help the woman...and the rest of us out.
I started this blog in 2010 because of a need to vent about my fibromyalgia and other chronic issues. I continue to blog on health and wellness related issues in hopes I can help just one other person to understand that they aren't alone. I was an RN for 37 years but when I got sick I didn't have a clue about what was going on with me. I still don't at times...I am a work in progress I like to say. What I write about is my personal opinion and probably not backed by medical research.
Showing posts with label CFS. Show all posts
Showing posts with label CFS. Show all posts
Tuesday, June 21, 2011
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