Desperately Trying to Get Diagnosed
I already posted this in the Neurology sub, but I wanted to post it here, too, as my symptoms seem relevant to autoimmune as well:
I have been sick for 9 months now. I was 23, no other known health problems, then suddenly I got extremely fatigued for about 2 weeks back in November– then I started getting muscle spasms, too. Now, I have been chronically fatigued for 9 months, & nothing eases the fatigue– there are only things that make it worse. Sleep does nothing, caffeine does nothing, rest does nothing… but if I don’t sleep, or miss a meal, or do any amount of exercise, or use my brain for more than very basic functions, my fatigue gets worse & it can take a few days to recover if I push myself too far. In addition, I have muscle spams only on the right side of my body that are triggered by physical activity. They make walking pretty impossible because my right leg has major random muscle contractions that I can’t control– walking makes my fatigue & spasms worse, anyways.
On top of all of that, I have brain fog, too. I used to work as a junior scientist in a lab researching muscular dystrophy at the University of Minnesota– I’d just graduated from college with a B.S. in biochemistry 6 months before all this started happening. Basically, I am trying to say that I really enjoyed being mentally stimulated and I liked to work out complex problems. Now, if I try to stimulate myself mentally, I can’t concentrate at all and I get really, REALLY tired. I get kind of confused and my short-term memory has gone to crap. I literally don’t even hear when people are talking to me unless they specifically get my attention first– my poor husband will tell me an entire story and my brain doesn’t even pick up that someone was talking if I’d been doing something other than talking to him when he began telling his story. I feel awful every time he has to ask, “Did you hear what I just said?” & that’s the first time I even registered his voice.
So now, I’ve seen several doctors (4 neurologists, a rheumatologist, 2 PCPs, an endocrinologist, & a psychotherapist). I have had a few abnormal test results that apparently don’t actually mean anything– which makes me wonder why the doctors had me pay to have them done in the first place. I had high insulin & C-peptide levels when I was tested in November (not a diabetic), but then it was never tested again. I had high Epstein-Barr Virus antibody titers in January, but then I was never tested again. I had high antibody titers against antistreptolysin O (Group A Strep) in June, but was told that didn’t mean anything (then why did the doctor order this test!!!). I had low acylcarnitine levels in January, then I was tested again in June and they were even lower, but I switched from a rheumatologist (who thought this was significant but didn’t know what it meant exactly) to a neurologist, and the neurologist literally ignored me when I mentioned it to him. So, there’s my 5 abnormal test results that apparently mean nothing, because the doctors I’ve spoken to either ignore them entirely or tell me that they are insignificant. I’ve never had mono (epstein-barr virus) or strep throat (antistreptolysin-O) before either, at least I’ve never thought I did or been diagnosed with either of them before, so idk why my antibody titers would be high (IgG antibodies for both, so the ones that indicate a previous infection but not a current one).
I was diagnosed with Functional Movement Disorder by a neurologist very recently for my muscle spasms only (not the fatigue & brain fog, so these are still 100% unresolved issues). He told me to get physical therapy, then told me most patients see a dramatic decrease in symptoms within 2-3 PT sessions & total & permanent absence of symptoms within 4-5 months. I got physical therapy for 4 months earlier this year (late December – mid-April), but I assumed that was not specifically targeting my muscle spasms & was more to prevent muscle atrophy, so I thought that this new PT was going to specifically target my symptoms. So, I saw the physical therapist that he highly recommended to me, & she told me that she looked over the previous physical therapists’ notes, and said she’d have done exactly the same therapy with me for Functional Movement Disorder. So like… what the hell, honestly? Did the doctor not know that I’d received PT for 4 months already? I called his office yesterday explaining that the new physical therapist just told me I’d basically already received treatment for the thing he diagnosed me with & that obviously it didn’t work after 4 months the first time, so it would be ridiculous to do the exact same thing again hoping for different results (still waiting on a call back regarding this). Also, the physical therapist he recommended ignored me when I told her at least 4 times during our 40-minute appointment that I crash if I push myself too hard, then she pushed me way too hard, & I had a horrible crash– she actually managed to induce new, worse symptoms in me because she pushed me too hard. Great, I really love being ignored by people who are supposed to be helping me & then ultimately being made sicker by them because they ignored me (sarcasm).
I have a whole slew of other, smaller symptoms, but these are the big ones. My question now is this: How on Earth do I get Mayo Clinic to accept me as a patient? My rheumatologist referred me to Neurology at Mayo & I was denied. Then a few days ago I tried to self-refer to Internal Medicine at Mayo as a last-ditch effort because I’d heard of someone who was rejected with a doc referral but got in on self-referral, & I got an email this morning saying I was rejected from Internal Medicine, too.
Do I just have to wait until I’ve been sick for years and years like all the other people I’ve read on here who have stories of finally getting diagnosed? I do not want to keep wasting my time with doctors who ignore what I say & keep telling me they don’t know what’s wrong with me without giving me any advice on what to do next. I am beyond frustrated that I have spent thousands of dollars I do not have only to still be at square 1 of diagnosis. My only thought of how to get diagnosed is to go to Mayo Clinic (Rochester, as I live in MN– I cannot afford to travel farther), but they are too full of other desperate people trying to get their diagnoses, and I can’t get in.
Tl;dr: Anyone have any tips on how I can get into Mayo Clinic – Rochester after being denied entry into both Neurology (w/ doctor referral) & Internal Medicine (self-referral)? Thank you so much for any advice.
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I def disagree. It shined a needed light on Lyme disease which is needed. I did not think they looked crazy. Brain on Fire and the other one is also excellent but perhaps living it minute by minute makes a difference.
Sorry I am late, I have and had many issues with different cyber systems, in fact , in Michigan I lost my LPN license due to upgrades MiPlus. A story in itself. Sorry for your neurological issues. I understand. I retired from nursing in 2006, for a few years neuropathy. Luckily I love research(in fact, I believe research has more positive therapeutic affects than half the medical service. ) Yes, I always learn much in the research. Computers, texts, files, magazines, people, etc. For my neuropathy,(plus I have a substantial medical library at home), yes to use standard medical institutional services. It is difficult to sort out the more science based professional medical staff , at times medical university complex, other times that special physician is found at a middle sized city or small city. In fact, in my latest bout of neurological problem(dizziness), I assessed over 200 different neurologist in Michigan(looking for a radiological-neurologist), failed but did my best in finding that professional to validate an earlier MRI to brain. Health is an integrated affair. The best choices of a medical professional one can trust. I was fortunate, in my second bout(dizziness), young physicians did an excellent job(in ER) to give me the best possible start in understanding the new symptoms. Later I was not so fortunate, a lesser quality base in the physician. Plus I rely on my educational habits and instincts. (Worked in medicine for 20 years). For starters, it is critical one find the best word to describe ones illness. Dizziness is too vague and usually much of the information on inter-net is lay bulk with little substance. I rely on my medical library and ICD codes and NIH for start. Also impressed with medical stories in Medscape. Yes, in early phase of 3 years of dizziness, some spasm. I started my Adult Male MVI. Also based on the medical information, I add Fish Oil, Tumeric(science based medical herbal), and glucosamine/chondraitin effective for muscular aches . All are based on genetic sensitivity. There is regular progress in biotech. regarding biomarkers and biotargets…hope for vague neurological problems. I was ready to opt for a nursing home at initial of my dizziness symptoms. But the dizziness did not tax my driving ability. Plus I do regular research regarding BPPV and dizziness, a noted paper was from Dr. Martin A. Samuels, M.D. Chairman of Neurology Harvard Medical School…..it is a constant search, never to lose hope, so long the symptoms do not tax ADL's. Plus to keep my spirit, spirituality(what seems effective), I have a support family in the Philippines, a big plus in my over 3 year bout of dizziness. Plus Mayo Chat ….a professional connection, digital communication, one is in constant battle to sort out the waste. Hang in there, plus we all know, there is always genetic mutations constantly going on….possibly at times for better. JIM retired nurse…lately based on research changed my blood pressure medicine(Norvas), a high degree of sa dizziness for folks over 60, based on research, no medical service person flagged this dynamic. JIM>>>>>>
@jczarkowski1270 Hi Lioness here Im retired L.P.N. from Pa.After my work fracture I decided to retire went back but didn't work out This is a great group I give people what knowledge I can made alot of friends online here youll enjoy hearing about what serious problems they have how upbeat they are in face of pain
@jen12contact Colleen Young connect director she gave some info to another person.who was desperate.
Sorry about all your problems. I went to Mayo for Microscopic Colitis. Could not get a decent answer anywhere. Call and make an appointment at Mayo. It should not take long for them to see you. Maybe a month or two. They will want extensive medical records pertaining to your dilemma. It could be dystonia since the disease effects every inch of your body. Not a fun disease. I have pain with mine, but never had the problem of not hearing people. Regards, Dorothy
I agree with others, holistic/integrative approaches best. Along with an over 3 year bout of dizziness, initially had some issues with leg and lower back pain. Luckily, the issues of pain for the most part resolved; first conventional/traditional assessments, (I never had much luck with NSAIDs, probably not sensitive to the chemistry there), but found turmeric quite effective and a balance day(some movements/30 minutes around the house and farm) and of course initially get imaging and labs. And somewhere in there, a supportive interaction with others that are worthy of positive support in ones life. JIM>
Hi jczarkowski1270 I found a tea that helps with inflammation its ginger-tumeric tea from Trader Joe's I have fibromyalgia back problems now with bulging disc so am seeing neurosurgeon Sept 14 hope he helps . Have a good day
I am so sorry for your frustrating predicament , maybe your luck will change and you will see the right person…..it has to be a place where they are dedicated to find out what the dickens is wrong with you…..all the best of British luck…..Beryl
What I find interesting … is one of the BIG reasons people do not want socialized medicine is the terribly long waits for treatment or surgery. But it seems like we are heading in the exact same direction … can't get in to see a dr.,our medical treatments are guided by the insurance co's … or big pharma, Treatment and drugs have astronomical costs, hospitalization and medical treatment are the cause of MOST bankruptcies in the US, but WE DO NOT WANT SOCIALIZED MEDICINE!!!!!!!
Barbarn Good question I never thought of it that way but your right its just not called by that name .