hyperadrenergic

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A late diagnosis is frustrating me. 🙁

I had a spinal tap on New Years Eve for possible IIH. My opening pressure was normal, but then there were the blood tests. I received a call from my neurologist’s office the following week to let me know all of my spinal tap results were fine. I asked the nurse if the doctor had reviewed my blood work results that had been sent to me the previous evening. I’m no doctor, but I do know how to google. As far as I could tell, my results were positive for Lupus. I explained that my mother has Lupus and she had been comparing all of my symptoms to her own for months now. All nurse could say was that the doctor had not reviewed my blood work results and they would have to get back with me the following day. The day came and went with no call. I had an appointment with another doctor, so I sent him the results thinking he could explain it better than google. Nope. He told me that it might be indicating some early on set rheumatoid arthritis. I thought that was strange since I tested negative for rheumatoid arthritis in those same blood work results. I moved on in assumption that I was just reading too many medical websites. 42 days after my spinal tap, also after another physical visit to the neurologist, I got an unexpected call. They finally realized that no one called to tell me that I did in fact test positive for Lupus and now they would like to refer me to a rheumatologist. I know I should be grateful for a diagnosis, as some people wait for years, but I’ve been appealing my short term disability case and I’m down to a matter of days before I’m out of time to gather all of the documentation. Wouldn’t you know that the neurologist’s office has failed to fill out the physicians statement for weeks now. I have called, my rep has called, I even physically walked in a blank copy along with a copy of what my primary doctor had written, so they could better understand my history. I was promised by the nurse practitioner that she would fill it out over the weekend. She didn’t. When I called to check on it again the receptionist let me know that they still had the blank copy I provided last week. As much as I hate to waste my mental energy on it all, my anxiety has a hold of me. Can’t sleep. # #Anxiety #Lupus #hyperadrenergic #LivingWithPOTS #PanicDisorder #Depression #Labyrinthitis #IrritableBowelSyndromeIBS #GastroesophagealRefluxDisease

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Anyone else with hyperpots often have invisible facial flushing?

What I mean by that is just that your face will feel MUCH warmer than the rest of your body combined, but there’s just no actual visible redness of the face. I experience this a lot, and would love to hear any tips you guys might have on how to deal. Also, idk if this happens to anyone else, but when my face gets to that point of hotness I get crazy irritable. #AutonomicDysfunction #Dysautonomia #hyperPOTS
#hyperadrenergic
#hyperadrenergicpots
#PosturalOrthostaticTachycardiaSyndrome

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Those of you with hyperpots, do you have your bed raised, and if so does it seem to help?

My doctor told me that every time I lay down flat, I’m just making it harder for myself to get up. So I have bed risers raising the top portion of my bed, but I feel as if I’ve had more blood pooling in my legs since raising my bed.
#PosturalOrthostaticTachycardiaSyndrome
#hyperPOTS #hyperadrenergicpots #hyperadrenergic #Dysautonomia #AutonomicDysfunction

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