Entering a debated area here. I have anxiety attacks and panic attacks
: I KNOW what causes them
1. acid reflux, possibly combined with oesaphageal dysmotility
2.traumatic events: the aftermath: i had one on Monday and, intermittently, have felt anxious ever since
3. Valium rebound probably. I am on a medium sized doseage.
4. Being in a mini-relapse. I know all these factors are linked and are causative
I have had all the heart checks and have diagnosis of severe oesaphageal dysmotility through a multitude of tests: barium swallow, endoscopy/gastroscope,nuclear medecine stomach emptying test, stage manometry; I also have acid rebound(not identified As NERD or GERD because i could not tolerate the 24 hour ambulatory ph manomenty test). Not a nice mixture; though i try to remain positive. I have chosen to remain on Nexium because they mainly control the diagnosis of nccp(non-cardiac chest pain)caused by acid reflux and regurgitation, which i experienced BEFORE going on Nexium, so if there is rebound there, it is only PARTLY caused by Nexium rebound issues. i have high stomach acid(detected by sodium bicarb test), NOT low stomach acid(I know there is an endless debate about this, and people, wanting to help, which is kind, have suggested all kinds of other tests, one of which was incompetently administered, the administrator having not even HEARD of a Proton Pump Inhibitor, like Nexium, etc-PPI, so as this involved putting a capsule down ur throat on a string with no medical supervision present; thanks but no thanks!
I am not interested therefore in getting into the debate re whether it is high or low stomach acid; that is my choice. Like most people I NEED(for psychological well-being ) to BELIeVE certain things, when there are conflicting opinions; i do not want medical opinion or suggestions for treatment, because i have tried all the sensible and some less sensible ones. I probably sound defensive, but I don't want to get into a further cycle of worry/anxiety about this; and am (just)coping for the moment, sometimes better than others depending on symptom severity and amount of sleep/rest.
I do NOT have dysautonmia; i have looked it up and do not satisfy enough criteria; though i probably DO have a cns/ans problem. However, the language to describe these syndromes changes all the times, not just with scientific/medical developments(obviously), but with FASHIONS, ie. going towards a psychiatric/psychological model, or towards a (primarily) physiological one; or , much more usefully, though scarily, a middle ground of neuro-psychological(most people do not want to hear re this and I am nOT interested, am afraid, in the bigger debate about the psychosomatic v. the viral/physiological model.) But I noticed that the symptoms that, for instance, the (I think) UK based website "No more Panic" as well as the expected panic attack/anxiety symtoms, lists severe exhaustion states!I DO believe i have an m.e type illness, as i have a nearly consistently slightly low white blood cell count and, once only, borderline neutropaenia(slighly low neutrophils). i do not choose to be tested for viruses(though these tests ARE available in the UK if you fight for them; they are in the NICE guidelines)or to take a/vs(these are NOT avilable on the NHS, NICE guidelines).Again, i am not interested in entering the uK debate re the NICE guidelines, though have read the full, around 300 page document and know what is in them and how to use them to my advantage and how to have a dialogue with my G.P re them and their limitations.
So why am i posting this thread?
Just to hear from others who have some/all of the above symptoms and who have been diagnosed with postviralfatiguesyndrome(like me), m.e/cfs(like me later; they use them interchangeably, but is a PRE current NICE guidelines physiological dx)- for MUTUAL SUPPORT really.
thanks Steve("Stevenski")
: I KNOW what causes them
1. acid reflux, possibly combined with oesaphageal dysmotility
2.traumatic events: the aftermath: i had one on Monday and, intermittently, have felt anxious ever since
3. Valium rebound probably. I am on a medium sized doseage.
4. Being in a mini-relapse. I know all these factors are linked and are causative
I have had all the heart checks and have diagnosis of severe oesaphageal dysmotility through a multitude of tests: barium swallow, endoscopy/gastroscope,nuclear medecine stomach emptying test, stage manometry; I also have acid rebound(not identified As NERD or GERD because i could not tolerate the 24 hour ambulatory ph manomenty test). Not a nice mixture; though i try to remain positive. I have chosen to remain on Nexium because they mainly control the diagnosis of nccp(non-cardiac chest pain)caused by acid reflux and regurgitation, which i experienced BEFORE going on Nexium, so if there is rebound there, it is only PARTLY caused by Nexium rebound issues. i have high stomach acid(detected by sodium bicarb test), NOT low stomach acid(I know there is an endless debate about this, and people, wanting to help, which is kind, have suggested all kinds of other tests, one of which was incompetently administered, the administrator having not even HEARD of a Proton Pump Inhibitor, like Nexium, etc-PPI, so as this involved putting a capsule down ur throat on a string with no medical supervision present; thanks but no thanks!
I do NOT have dysautonmia; i have looked it up and do not satisfy enough criteria; though i probably DO have a cns/ans problem. However, the language to describe these syndromes changes all the times, not just with scientific/medical developments(obviously), but with FASHIONS, ie. going towards a psychiatric/psychological model, or towards a (primarily) physiological one; or , much more usefully, though scarily, a middle ground of neuro-psychological(most people do not want to hear re this and I am nOT interested, am afraid, in the bigger debate about the psychosomatic v. the viral/physiological model.) But I noticed that the symptoms that, for instance, the (I think) UK based website "No more Panic" as well as the expected panic attack/anxiety symtoms, lists severe exhaustion states!I DO believe i have an m.e type illness, as i have a nearly consistently slightly low white blood cell count and, once only, borderline neutropaenia(slighly low neutrophils). i do not choose to be tested for viruses(though these tests ARE available in the UK if you fight for them; they are in the NICE guidelines)or to take a/vs(these are NOT avilable on the NHS, NICE guidelines).Again, i am not interested in entering the uK debate re the NICE guidelines, though have read the full, around 300 page document and know what is in them and how to use them to my advantage and how to have a dialogue with my G.P re them and their limitations.
So why am i posting this thread?
Just to hear from others who have some/all of the above symptoms and who have been diagnosed with postviralfatiguesyndrome(like me), m.e/cfs(like me later; they use them interchangeably, but is a PRE current NICE guidelines physiological dx)- for MUTUAL SUPPORT really.
thanks Steve("Stevenski")