Any help gladly welcomed

Hi Shelly,

Sorry you are being bounced around. It’s so frustrating and an added stress that you don’t need.

Perhaps it’s just as well you are seeing a Neuro - hopefully you’ll get a diagnosis. I’ve had the rainbows (scintillating scotoma) and squiggles in the past and still often have all the other symptoms you describe- they seem to be ubiquitous on this site.

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Thanks @sputnik2…I need to be determined because I need to make a plan going forward because this currently impacting my life so much I just feel that if I get to the bottom of what’s going on I can adjust and adapt better…if that makes sense?
If family or friends ask what’s wrong and I describe VM they usually react by saying that’s not too bad and if I go to bed for a few days it will get better so to describe it as debilitating at the moment seems a bit OTT but for me anyway it really is debilitating xx
This site has been the first thing that actually throws light on my situation I am so thankful xxx

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