Hi everyone, I have been having symptoms lately that look and sound a lot like MS. I’ve been told by doctors that this is their main concern but they’re really limiting my ability to walk, go outside and live my life. I had a spine and head MRI without contrast as outpatient, then I was admitted to hospital for 4 days where I had a second spinal MRI with contrast and a Lumbar Puncture. This was all done just before Christmas (I was discharged on the 23rd) and was told I’d have an appointment with neurology as an outpatient. I just found out that appointment isn’t until the end of March 😢 I know how much the NHS is really struggling at the moment but to be in hospital, poked and prodded then left in the lurch for 3 months is so scary. I haven’t had an MS diagnosis and know very little about what the scans show. Does this sound like a normal timeline for you? Should I be questioning this? If you have been diagnosed recently via the NHS in the UK I’d especially like to hear how this was for you. I’ve been put on some medication for neuro pain and been told to do some bladder control exercises from an MS charity website in the meantime. I’m feeling a bit lost and scared 😞 thanks to anyone who reads and responds!