Brisk reflexes - one symptom too many?

As an introduction, I hope you don’t mind if I start with a list of my symptoms (!!!) …

dizziness (occasional bouts of this for about 15 years, now becoming more common);

fatigue (really aware of this for last 2-3 years);

a range of aches and pains (rib cage pain on and off most days for last 15 months, upper arm pain that feels like I’ve been weight lifting (on and off for about 12 months) and recently pains in lots of random places, including wrists and ankles. I’ve also been a long term migraine sufferer and have had quite a few headaches recently

sensory problems - lost feeling in one toe for about 6 weeks last year, now often get tingling feeling in my toes and occasionally right down my left arm

memory/ concentration problems (getting really behind at work, just feel I’m not coping with stuff I’ve always been able to do)

depression and anxiety (now on antidepressents which help me sleep but haven’t had much in the way of other effects - my Dr prescribed them saying that ‘depression can lead to perceptions of pain’ but I’ve always felt that I’m depressed because I feel so awful, not the other way round!)

very severe eye pain - have had this three times since Dec. - it felt like a toothache but in my eye. I don’t think I had any vision problems so don’t think it was optic neuritis but could have been??? My doc did a blood test for temporal (or giant cell) arteritis which was negative.

clumsiness (every now and then I drop things, out of the blue - like I have dropped my toothbrush in the middle of cleaning my teeth three times in the last few months)

and I think that’s about it until today’s new discovery … that I have ‘brisk reflexes’ - I went to see an osteopath to see if that could help all the aches and pains and she tested them. She is going to write a letter to my GP asking for me to be referred to a neuro. Hooray! at last someone is on my side!

So, I don’t know if all this is MS or not - I realise it could be other things but a possible MS diagnosis been in my mind for nearly a year now and I’ve wanted a referral to neuro for ages, even if just to rule neuro stuff out. I just never seem to be able to ask when I go to the GP because there is always a new theory and something different she wants to test. Am I right, though, that brisk reflexes are a definite sign of neuro problems? Is this just one symptom too many to ignore that possibility? I would SO like some answers as I’ve been thinking I’ve been going mad for ages now. I know I come across to docs as a hypochondriac but I really am experiencing all these symptoms and I just want to know what’s wrong, even if that means an MS diagnosis. Having said that, I’ve started worrying myself today that I could also potentially have a brain tumour - if you Google brisk reflexes the options that come up are MND (don’t think I have that), AIDS (definitely don’t have that), MS and brain tumour. Here I go again - no wonder the doc thinks I’m a hypochondriac.

Anyway, I guess this long post is just to say does this sound like it could be MS? OR anything else? I’ve made an appointment with the doc but its not for another week and a half. I could ask for an emergency appointment but I guess I don’t need that and anyway, it would probably be with a different doc. Despite putting everything down to depression, my own doc has been quite supportive. She’s organised x-rays and loads of blood tests so it hasn’t just been the ‘your depressed’ route. By the way, I am on calcium and vit D because of a premature menopause. When I had the eye pain, she tested for vit D levels and they are very slightly low, despite the supplements but it’s nothing significant and not likely to be the cause of any symptoms.

Sorry, this has been such a ramble but I’ve been in pieces today and just need to share it all with someone. If you’ve kept reading this far, thank you very much. :slight_smile:

Hi lilacgirl, if not already done,may I suggest you tell the Dr you think there is more going on and you would appreciate a refferal to a neurologist. Maybe take the written list of all your symptoms to your g.p so you don’t’ get side tracked, you sound like you have a lot of tell tale signs from my own experience of MS. The only way I found out is with an MRI I had several CT scans on my neck back knees referral to orthapedics etc etc to no avail over a 3 year period.

Good luck xx

Hi Pollypocket

Thank you for your message - it really helps just to know there are people out there who are on my side. I think there won’t be a problem with the neuro referral at my next GP appointment as I will have the letter from the osteopath saying I need one. I have also starting writing a list of all my symptoms, with dates/ variations etc so that I can take that with me to future appointments. It probably sounds silly but I have been wary of saying I think I could have MS up till now in case my doc thinks I have Googled MS symptoms and made them up to match (and then not take them seriously) - sometimes I even come round to believing that myself! I just wanted her to come to that conclusion herself based on what I told her about the symptoms. I did once say ‘could it be something neurological?’ but she said there weren’t any neurological disorders that matched my symptoms, so I didn’t take it further. It’s really silly because I’m usually quite an assertive person and I have worked in the NHS so it’s not as though I’m afraid of doctors. This has just seemed a difficult one to handle.

Anyway, another week and a half and hopefully I’ll be on the next stage of the journey towards finding out what’s wrong. Thanks so much for your support.

Lilacgirl x

You are doing the right thing writing down when things happen. I persevered for 4 years and had no idea they were going to diagnose me with MS. That was a year ago. I was relieved in many ways as I actually felt like I was being taken seriously and that I wasn’t going crazy. I have very brisk reflexes on many occasions, one dr that tried them got kicked in the face which was rather embarrassing. I hope the neurologist can help you but don’t expect this to be a quick process as it does take them a long time to investigate. Take care Barney