The long wait.
This is just a venting post but if anyone has advice or experiences to share, I’d love to hear.
I was referred to a POTS clinic in November last year, the one in Cornwall U.K. had closed so I will need to travel a fair distance to another county. My GP told me that the wait was around a year.
I had a couple of questions for the clinic and the cardiologist emailed me back himself directly to say that the wait is more like 2yrs, so I could be looking at 2028. They are clearly overwhelmed as the clinic he runs is covering multiple counties, but I was very grateful for his candid and polite response.
At 44 I feel like being much older leaves less time to find answers and the older you get especially as a woman, the less interested doctors are in assisting your ailments. Over the past 10yrs I have experienced first hand the misogyny that sadly exists within the medical industry.
For context, I am diagnosed with MCAS/HIT, CFS, Long-Covid, hypermobility and ADHD combined, but also have suspected SFN.
I did consider taking out some form of credit and going private for POTS/Dys. I wonder if there are any places anyone could recommend, especially in the West Country area would be helpful. I don’t know if I can wait 2yrs, but of course private is incredibly expensive.
Any advice welcome or if anyone just wants to share their own experiences please do. Thanks all. 🩷