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dawney-t

I Love My Neurologist!

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dawney-t

Well this morning I went to see my neurologist for my 6 monthly appointment. I love him to bits, he is just so human and helpful.

 

When I first saw him in October 2003 he was very abrupt, said he could find nothing neurologically wrong with me, that in his opinion I was depressed (actually said, "you look depressed"!) and prescribed me Citalopram. Luckily for me at that time he did refer me for a VEP as I was having vision problems. I say luckily because that came back showing demyelination on my left optic nerve so he followed it up with a brain MRI which showed "areas of demyelination consistent with MS". This was all over a year ago and I have seen him 3 times since and he has changed from Mr Ogre to Mr Wonderful.

 

He has decided to take me off Amantadine and put meon Modafinil as the Amantadine doesn't appear to help my fatigue at all.

 

I bravely asked him if he could tell me more about my MRI scan and he couldn't have been nicer. Said he didn't actually have the scan with him but would make sure he had it for next time and we could go throug it together, but according to the report I had "multiple lesions in every area of my brain, particular the ventricular ........" (missed the last word). He did a thorough clinical examination (to compare how things had progressed in the last six months) and has arranged another appointment for December where he wrote on the note for the receptionist, "make sure that x-ray package is available".

 

So although not good news about the scan report I was quite happy with my consultation and am looking forward to studying my scan in December.

 

I just wish all neuros were like him.

 

:angel: Dawn


MS diagnosed May 2004, PPMS diagnosed July 2004

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crispy

Hi Dawn, :angel:

 

Glad to hear your appointment went well, and it sounds as though you have a good one there. If you feel that someone is at least looking out for you, and treating you with respect, that has to help a little.

 

All the best,


................................ :dog: ........................................

All the best,

Chris P

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stranding

Hi Dawn

 

I'm also very pleased to hear you found your :angel: transformed to an :sadwalk: today. Makes such a huge difference to how you feel when they show any sort of listening response and will answer your questions, whatever they have to tell you, doesn't it?.

 

I'm interested he's changed you to Citalopram which is what I've been on for the last few months. It has workied magically with me and no side effects noticed except a slight very blurring of vision at first for about 10 days.

 

And I've also been on Modafinil now for several years (from the time when it was licensed only for narcolepsy, and anyone else had to take a chance if they wanted to risk it).

 

Think the recommended dose is 2 a day (is that what he's given you?) but I normally take just one mid-morning, unless I'm expecting an extra tiring day or am going to be driving home late (always avoid doing that now if at all possible) when I will have one in the morning and a second no later than 4 pm if possible. The effects are supposed to last for 6 hours, and that seems about right, so anything later will stop me sleeping. When I started, with 2 a day, within 3 days I began to get really jittery & jumpy hyperactive & couldn't sleep, as if I'd overdosed on strong black coffee, so it's been one daily since.

 

Works very well most of the time, and wish I could take it earlier in the morning to help wake up, but then I'd be nodding off by the afternoon, so I put up with it that way round.

 

It was brave to ask to see the MRI...(I wouldn't have even thought of doing that) and he's willing to show you too. It might be strange to see it, I suppose...?? Well, good luck for next time & hope he's still in his :hehehe: mood! Fancy you going with those cold feet with all the toes gone ... So brave of you!!! :smarty:

 

Ann :smarty:


Remember to KYPU at all times...

(Keep Your Pecker Up)

Ppms 20-ish years.

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dawney-t

Thank you Chris and Ann for your replies.

 

Now Ann, much as I love you, you must pay attention!!!

 

1. I've been on Citalopram since November 2003 (since the first time I saw neuro).

 

2. My appointment this morning was before doing my forfeit, therefore feet were intact at the time. Good job too as he spent some time prodding them and brushing pins along them.

 

Interested to hear about your experience with Modafinil though. He told me it is an amphetamine type drug. I'll probably go as hyper as my 10 year old son is. I'm not sure what dose he's prescribing. I have to go see my GP in a couple of weeks to get the prescription.

 

I'll let you know.

 

Now concentrate in future as they'll be questions afterwards!!!

 

:angel: Dawn


MS diagnosed May 2004, PPMS diagnosed July 2004

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Lula_lulabel

Hi Dawn

 

You are sure lucky to have a neuro with an ounce of humanity in him...

I am still waiting for one of them to come along... as it stands... I am expected to drive an hour there and an hour back to see mine... and he aint helpfull at all, lol!

Second to that I will have to see the Consultant Neurologist that I had repremanded for treating me unfairly... (and that went right up thru the cheif exec and my MP) I don't know how to face him... and he's such an arrogant person!)

He has said that I can have modafinil for my sleep attacks... but my next appointment is December!

 

So in all I am over-the-moon with your result, and take it as a positive thing, that there are some understanding neurologists still about, (might have to move house tho, to get one,lol)

 

sending hugs love Lula xxx


sprinkling magic all around

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stranding

Hi Dawn

...you must pay attention!!!

:oops::sorry: !!!

:bow: :bow: :bow: 'Umble grovels and bosom beating for not taking that in properly (put it down to complete scattiness :gaga:


Remember to KYPU at all times...

(Keep Your Pecker Up)

Ppms 20-ish years.

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