Do you live in a place with too few MS Specialists? If that is the case I can see why he can't see you. The ER will not be much help, they usually refer you to a Neurologist or tell you to see your own. Do you have a good Primary Care? Mine treats symptoms when the specialists are too busy.
Alex
Hi and welcome to our little MS community,
Firstly let me just say..............OMG, do you need a better neurologist! I can see you in 2-3 months for a person dx with MS, is just not good enough! Most relapses are over in that time frame, so if you are in one it will be way too late for IVSM to shorten the attack and on top of that you have a history of seizures, sorry but your neurologist is important and i would be replacing him just for his lack of availability.
Please consider finding an MS neuro, who will give you his/her time when you actually need it and not when it fits his schedule, because everyone will tell you, that MS simply does not care what anyone's schedule is, it never cooperates or plays nice with others and you basically need someone who can fit in with your MS. Think about it!
If your dx and stopped taking your meds, does that mean your not taking any disease modifying drugs too?
The rule of thumb for if your having a relapse, is that any return of sx's, worsening of sx's and or experiencing something new, for no less than 24/48 hours can be indicating your relapsing and you are recommended to see a (preferably your) neurologist. I would also recommend you see a neurologist to discuss your reasons for not taking the seizure meds, and what that might mean long term and if you have only been treating the seizures and not the disease, to also discuss your DMD options.
I do not know the rules in your country, so i'm sorry I can't help you with how to find an alternative MS neuro, apart from advising you to contact your local MS society and asking them for some recommendations.
Please keep us informed of how you get on :o)
Cheers.............JJ
Hi there & welcome, I am a bit shocked by your Neuro not helping but telling you to go to ER.....hmmmmm. Have you told him about the eye pain as well because it could be Optic Neuritis...he needs to check that out or refer you straight to an Opthamologist.
Is he a MS Specialist? I know that many Neuro's don't treat sensory symptoms with something like IV Sulomedrol. I have only recently been dx'd with MS so hopefully someone will chime in with some advice for you.
The Meds you were on were they DMD for the MS or anti seizure medications?
Take Care,
Karry.
From what I understand MS symptoms come and go. Maybe that is what has happened... I think if they couldn't get me in, I would go to ER or start my meds again.. Sorry, I am new to this!