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Hi everyone, I'm new to the forum, in June 2022 I got what I presume was a viral illness, with symptoms such as fever, cough, throat pain and slight dysphagia.
All symptoms besides the dysphagia subsided until I got tired moving for a new job and, between July and August, I first developed fatigue, slight uncoordination and muscle spasms and, later, quite severe brain fog, insomnia and some visual disturbances (feels like stars in my vision when standing up). Around September the dysphagia sensation ceased.
During all this period I have had a higher than normal resting heart rate and blood pressure, episodes of intense throat pain and paresthesia radiating to my arm and chest, cluster headaches and occasional mild fever.
I have been diagnosed with POTS ten years ago and some symptoms feel like they could be related, I also have a cecocentral scotoma from presumed optic neuritis, which developed around the time of the POTS diagnosis and worsened half a year ago.
For a week, at the local university hospital, I have done tests (MRI, EEG, spinal tap) for many conditions but the only finding was a 14mm pineal cyst (which grew in size since my last MRI in 2014). My doctor told me I may have ME/CFS or some type of MS.
Has anyone experienced some of these less ME-specific symptoms (dysphagia, slight feeling of uncoordination, tachycardia and throat pain)? Also I was wondering, does the onset pattern match ME/CFS?
All symptoms besides the dysphagia subsided until I got tired moving for a new job and, between July and August, I first developed fatigue, slight uncoordination and muscle spasms and, later, quite severe brain fog, insomnia and some visual disturbances (feels like stars in my vision when standing up). Around September the dysphagia sensation ceased.
During all this period I have had a higher than normal resting heart rate and blood pressure, episodes of intense throat pain and paresthesia radiating to my arm and chest, cluster headaches and occasional mild fever.
I have been diagnosed with POTS ten years ago and some symptoms feel like they could be related, I also have a cecocentral scotoma from presumed optic neuritis, which developed around the time of the POTS diagnosis and worsened half a year ago.
For a week, at the local university hospital, I have done tests (MRI, EEG, spinal tap) for many conditions but the only finding was a 14mm pineal cyst (which grew in size since my last MRI in 2014). My doctor told me I may have ME/CFS or some type of MS.
Has anyone experienced some of these less ME-specific symptoms (dysphagia, slight feeling of uncoordination, tachycardia and throat pain)? Also I was wondering, does the onset pattern match ME/CFS?