I am a patient at the Pain Clinic in Sir Charles Gairdner Hospital. For a year and a half, I was receiving treatment from one specific doctor who determined all of my condition was psychological and would not give me treatment because one of my diagnoses was FND. They wouldn’t investigate or consider any other option or offer me treatment. Any symptoms that I had were put in the bracket of FND.
So, on top of that, I was continually asking for a second opinion and to have a new doctor. For a year and a half, I was stuck with that doctor, with me continually asking staff for a new doctor, them saying to me, yes, you’re entitled to a second opinion. I’d ask for them to organise that and nothing would happen. Then I’d tell them again what was going on. There was a vicious cycle of that going on and I stayed in that situation for a year and a half.
Eventually, I got a new doctor assigned to me, who said I had multiple diagnoses apart from FND. By that time, Neurology had been told that my condition was psychological, so they obviously (being told that), thought that of me.
So, once I got the new doctor, I had to start again at the bottom of the list. So, in that time, my GP had sent me for tests. What follows is my diagnoses.
•I have a large hiatus hernia and dysphagia, diagnosed through a barium meal by my GP.
•I also have high protein and low iron in my blood.
•I also have multi-level degeneration in my spine from my cervical spine all the way to my lower spine.
•I have canal stenosis and foraminal stenosis in my cervical, thoracic, and lower spine.
•I have spondylosis throughout my spine.
•I have degenerative disc disease throughout my spine.
•I have one of my discs that has broken right down to nothing, and I have six bulging discs.
•I also was diagnosed with muscle atrophy, diagnosed by a doctor within that hospital while I was still seeing the first pain clinic doctor at Sir Charles. I was diagnosed me with muscle atrophy and muscle fatigue but they did nothing about it.
Although I now have the new doctor and I have all of those diagnoses, I’m at the bottom of all of the lists, waiting to get treatment for all of those, including muscle atrophy, biopsy, and nerve conduction studies.
The problem with now trying to seek help for all of those conditions is that the hospital themselves spent one and a half years telling the neurology teams that all my pain was psychological, and it seems, now that is how they only see me.
So I am now, especially with my muscle atrophy which is now visible, not even able to get a biopsy and nerve studies to help me get treatment.
At least now, it’s good that I have the new doctor, but I believe it’s not like they’ve tried to make up for time and help me. The new doctor said straight away, I’ll pop you on the list for needles into the spine for pain relief and will send away a referral to neurosurgery. The point is, they spent the year and a half telling them it’s psychological, and I believe now they don’t know what to think of me. This thing has come through, but all this time they’ve spent telling them that it’s psychological.
"Impact of misdiagnoses for one and a half years"
About: Sir Charles Gairdner Hospital / Pain Management Clinic Sir Charles Gairdner Hospital Pain Management Clinic Nedlands 6009
Posted by septembersr77 (as ),
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Update posted by septembersr77 (the patient) last month