Guest guest Posted December 8, 2010 Report Share Posted December 8, 2010 First time poster --long-- long time patient(1977). Please excuse the rather ambitious help I am asking the list for. I am here to try to salvage a bad turn of events. I am on a short deadline and both my practitioners who were researching this for me have fallen ill. Myself, I've just now been able to spend part of the day out of bed after a 10 week very acute episode. I am in and out of brain fog even to be able to compose this letter. I am especially interested in hearing from any one who has ever been through the VA system regarding CFS/ME or CEB. Deadline: After waiting 5 years, the Veteran's Administration scheduled me for a hearing with 4 weeks notice and that hearing is Tuesday Dec 14th. That or wait another year. I can submit medical literature as evidence. I am trying to get the VA to accept the co-morbid conditions documented and diagnosed at the time of my discharge but, not considered " rateable " . In fact, when I was diagnosed there was no medical code for the condition and I am also trying to get them to remove the substitute diagnostic code for " Lupus E " for the CFS/CEB. Unfortunately, as I explain later, I am not getting medical assistance from the VA for either treatment, referral, pain management, or documentation even though they are my primary care providers.--(tonight a " foreign trained doctor " at the VA ER refused to forward my insulin and diabetes refills to the pharmacy -- I have to go to another VA hospital when I get where I am going) but I am trying to suppress my incredulity about the effectiveness of rationed healthcare. Anyway,the VA mis-coded me 30 years ago for " Lupus E " and in a Catch-22, I have to " prove " to them that this is was a substitute diagnosis and needs to be changed. I even had my primary-care foreign trained,contracted VA Doctor(sic), tell me there was no such thing as CFS--all here know what he has his head stuck up, but-- I digress. I need a list and/or citation for co-morbid associations with CFS that have been published in the 30+ years since CFS was recognized. I have read several lists of co-morbid findings/associations --but I am unable to relocate and print out. Specifically: Swollen Uvula Tooth loss/gum disease Chronic Epstein-Barr Chronic lower back pain Chronic Sinusitis other than the faceomaxiallary and TMS(?)connection Fibro. Myalg. (FMS)overlapping conditions Demyelenation of nerve sheaths Sleep Apnea/Disturbances Liver Damage/Impairment long and short term. Cytomegalovirus Infection in CFS/CEBVpaitents Eye/vision problems Hypertension Diabetes Effects on autonomic /endocrine regulation. Urticaria/Hives/Rash Organs affected in CFSpaitents. Restless Leg Syndrome. Reflex Distrophy Syndrome(RDS) or " burning skin sensations " Stress levels and stress triggers for CFS acute episodes. I have most of the commonly known associated conditons such as IBS, Headache. Tender points but any and all links/ citations our guidence is invited. I've three days to finalize this collection for presentation. One other point: while the SSA determines if you are capable of " Substantial Gainful Employment " (SGE) the VA has to make a determination of what % of one's time, one are or are not disabled or impaired by one's condition. For what it is worth, So they don't even parallel the SSA ruling regarding CFS and medically observable/measurable finding. Background: When I was diagnosed in 1983 with a suspected immune complex disorder and Chronic Epstein Barr infection it was a year before CFS was announced in the literature. At the time I was under the 200th patient so diagnosed. So they chose a similar condition Lupus for my diagnostic code. I've had to move mountains to get them to understand that I don't have lupus and believe it of not have to prove that I don't ave lupus and that I have CFS/CEB. My onset was abrupt and after receiving a flu vaccination in 1977 where 90% of my brigade(Ft Hood , TX) got ill with what then was diagnoses as " prolonged mono " given the sophistication of medical knowledge at the time. Several of us never got better. I went undiagnosed for 7 years. Several of my past symptoms were more related to Guillain-Barré Syndrome(GBS)this was within a year of the Swine Flu Vaccination debacle of 1976. I have had 3 times over the 34 or so years where I was confined to bed a majority of my days the better part of 18 months at a stretch--Rarely have I been symptom free--For whatever that is worth to my fellow patients. As you may surmise, I am miserable much of the time and surprise even myself I've lived so long with it. A direct reply to my email is best for me as I am on the road for the next 14 hours. Regards and Thank you in advance, Elton Quote Link to comment Share on other sites More sharing options...
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