
Goodness knows where I got this with all the social distancing and hand washing!
I've had bouts like that during the pandemic, Maz, but they were due to hay fever and responded well to Beconase nasal spray.
Sounds like you've been fobbed off even if they are telling the truth. If you haven't been accepted for further treatment and not on any waiting list, then you are off the NHS radar. We know the NHS is under pressure but it isn't a reason not to accept a patient for investigation. You plainly have something wrong with you and when you know what it is then you can deal with it. Like Ian says, I'd opt for further investigation and get some information about your problem. Good luck, Stephen.PanBiker wrote: ↑15 Oct 2020, 10:19 If I was you I would be pressing for another opinion. Putting the ball back in you court for a testing plan that by their own admission is probably not going to be successful or relevant is not good enough. You need better than this Stephen you are still a youngish bloke and should not be abandoned. Time to become a bit awkward it's your life!
Already had EMG https://en.wikipedia.org/wiki/Electromy ... omyography which is what I think you're referring too. It raised as many questions as answers. I've already had a second opinion of sorts, my mother had what appeared to be the same condition, diagnosed and treated under a seperate Hospital (Blackpool) she was given a diagnosis of IBM (Inclusion Body Mysoitis) but there was some doubt. Theres no real treatment. Its certainly a neuro-muscular aliment which is a quagmire of different conditions and symptoms.Marilyn wrote: ↑16 Oct 2020, 00:47 It doesn’t sound right to me either Pluggy. They should find out at what level your degeneration is coming from, be it peripheral muscles or deep nerves ( not just with a muscle biopsy, but with electrical stimulation/conduction tests).
I think we all feel for you. No wonder your happy thoughts have gone AWOL.
Good news about your PIP payments but a bit of a shocker with HIBM. I'd never heard of this condition but have now looked it up on the internet. It says there are medicines available to help you cope with the symptoms. Nag your GP to get some help, don't suffer needlessly. Best wishes for the future.Pluggy wrote: ↑16 Oct 2020, 12:19 I've already had a second opinion of sorts, my mother had what appeared to be the same condition, diagnosed and treated under a seperate Hospital (Blackpool) she was given a diagnosis of IBM (Inclusion Body Mysoitis) but there was some doubt. There is no real treatment. Its certainly a neuro-muscular ailment which is a quagmire of different conditions and symptoms.
I've got the positives back after a period of being down. Being recently accepted for the enhanced rate of PIP helped. It pays almost as much as I was earning mending computers.