Thought I'd come here for a bit of advice
I am 49 female and for the last few days have been experiencing numbness in my face - like when a dentist does a filling. My tongue and gums are also numb
I have had numbness in the hands for years, possibly due to a compressed nerve in my neck (diagnosed as tennis elbow, then spondylosis via mri, my feet also tingle with strange feelings in my knees
I don't have any pain anywhere apart from occasional lower lumber and mid back pain.
I don't have any double vision, slurred speech.
I walk a lot and keep relatively fit
I've done some research hence being here. I know that it generally affects younger people, but can arise in my age group.
I've read that if the problem is MS that it could take months/ years to get a proper diagnosis and that there isn't much treatment available.
Early next year I will be 50 and I am planning a massive long-awaited holiday to America and Canada, however, I am fully aware that if I go to the Drs and they refer me to a neurologist I then can't get travel insurance due to having an 'undiagnosed condition'
I've looked at the medicines available and they seem to prevent flare-ups by 30-50% but most of the treatment is physio, exercise, cognitive therapy etc (self managed)
I don't know if I have MS, but if I go to the DRs and get a referral - then my 50th birthday gift won't happen
Any advice - have I read the treatments wrong - is there a point going to the Drs at this point - how long do referrals take
Thanks for your help
How do I get about getting a diagnosis when since the 80's and several house moves I have been unable to have any referral for further tests.
Back in the mid 80's my GP told me he suspected I had MS only the Neurologist I was referred to just duplicated the basic tests that the GP had already done.
When I asked for a referral for further investigations he told me that all my symptoms were due to anxiety.
30 years down the line I am no nearer to finding out what is wrong with me despite my midwife during one labour in 1983 said that MS had been put on my notes to inform staff on other shifts that they needed to be aware of my Multiple Sclerosis as it was already causing difficulties.
I asked about this when seeing GPs further down the line and they said they knew nothing about this.
My P.I.P. application was turned down due to lack of evidence so how do I get this?
A week ago today I was diagnosed with MS after 6 months of consultations and tests. I kind of expected the out come as I had looked up some of my symtoms so wasn't much as a shock to me, however since having this confirmed I feel I have been experiencing a lot more symptoms like headaches, tiredness and aching. I didn't feel any of these before being diagnosed, I only ever had slight numb tingling
did this happen to anyone else, I think my anxiety is the main cause of this since I have been doing lots of reading on MS
Can anyone give me any advice?
I started having neurological symptoms when I was 18 this is 17 years ago. It started with vertigo, blurred vision and painful tingling in my legs and arms - later face too. I also had numbness in different areas on my left side. Cheek, arm, back, leg. I also have hyperacusis which began back then. It would all flare up for a couple of weeks or so. I'd feel so so tired, and wobbly. Or it would be one thing or another. I had an Mri scan at 18 which was normal. I saw a neurologist back then too who's only comment was that my reflexes were 'brisk'. They didn't find anything to be very concerning and sent me home. I've continued to have these symptoms and flare ups ever since. But they did go away almost completely for the best part of 10 years. They have been an annoyance but otherwise I've been able to ignore them.
Now for the last few months they have returned with an annoying vengeance. There is nothing that awful about them, I can still walk, I slur my words a bit and I forget words a lot. Even names of people I know really well - which is weird. If it's really bad I have to take time of work, but I still function ok, it just is horrible. Anyway,I had a flare up of it all, but this time I had such a strange feeling in my head that I can't even explain it, it was horrendous tingling but also, an intense sort of of pressure and a cold/pricklyness. This has led to me to the docs as I couldn't sleep.
I've since seen an ENT specialist, because the ear and vestibular symptoms point to Ménière's disease. However, I've got no permanent hearing loss. And the other body symptoms are still not explained.
A had a recent MRI to check for acoustic neuroma, and I asked for a copy of the report. No acoustic neuroma, and nothing noted to account for my symptoms. But it says 'prominent perivascular spaces noted in basal ganglia and white matter' I've done some research on this and I'm hoping some of you might hence know why I am concerned about this. ...The ENT specialist thinks I probably have a 'Ménière's type of thing', but he would have expected hearing loss by now, so agrees with me that MS could be a concern. He thought that my mri scan doesn't completely rule out MS but neither does it confirm anything.
I've had this for so long now, that surely the mri would have shown a lesion if it was MS? But I'm also unconvinced that it is menieres. And, after googling about what my Mri report said - feeling all the more bewildered and In the dark. None of my symptoms are disabling, but they certainly aren't pleasant, and they scare me to death. I don't want to waste NHS resources, but I think I would like to see a neurologist again.
Do you think I should raise my concerns about MS with the doctor and get a referral ?
Two weeks ago the diagnosis came through. After months of tests and being told different diagnosis (including that it could be in my head) part of me was, dare I say it, relieved.
Now though, reality has set in and I am trying to face it, but I'm really struggling. Every time I sit down to research it, I last around five minutes before shutting down the computer and crying.
Aside from that, my biggest decision is revolving around what DMD to go on. I have talked with my neurologist and she is talking about putting meon Rebif. Although she is a great support, I have been given so many leaflets and so much information that its just a complete overload! But she really is pushing rebif, and to be honest I do like the sound of the rebismart machine, if I have to use a needle everyday, I really don't want to have to see it.
If anyone could provide me with any advice or help I would really appreciate it. Is anyone on rebif? Or used to be ?
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