seroxat/paroxetine for neurological symptoms?? - LUPUS UK

LUPUS UK

32,210 members28,554 posts

seroxat/paroxetine for neurological symptoms??

brave profile image
10 Replies

Another med to try??although im very anxious,consultant has suggested trying an ssri seroxat for rebalancing the nervous system ,im also very depressed and my brain totally fried and overloaded ,however I cant seem to switch my brain off ,my autonomic system is way out of whack ,heart,stomache,bladder,bowel,blood pressure and more ,have any of you had good experiences with ssris?im VERY worried as I don't like these drugs,thanks all ,brave;)

Written by
brave profile image
brave
To view profiles and participate in discussions please or .
Read more about...
10 Replies
Purpletop profile image
Purpletop

I haven't had these, so I can't comment but still, there is hope that it could well work. I know you hate taking medication and I agree it is worrying when you have to start a new one and read all the side effects etc. But I don't see what else you've got left to try, you're in need of some peace soon so you can start recovering!

brave profile image
brave in reply toPurpletop

;))x

Loopylooby profile image
Loopylooby

Brave can I ask what neurological symptoms you have? I am currently waiting for the outcome of my MRI x

brave profile image
brave in reply toLoopylooby

Where do you want me to start??lol;()to be honest all classic symptoms of M.S with a definite issue with my autonomic nervous system,im waiting to see a consultant in this area,at the moment im taking beta blockers to help migraine and switch of sympathetic activity,and as from today im taking citalopram 10mg as I didn't fancy taking the seroxat (heard to many negatives).For me it looks like I have a condition called dysautonomia,perhaps it came because of lupus ??however this is way more troublesome than anything else at the moment ,im in a sorry old state;( I hope this helps a little loobyloo?take care xp.s my mri was pretty much normal .

Welshexile profile image
Welshexile

Hi Brave

I have been taking ssri (seroxat) at the lowest dose (20mg daily) for the past 10yrs and, for me, the benefits far outweigh any side effects. I was not happy taking them initially, but as I was having a breakdown due to stress of multiple diagnosis and neurological involvement of SLE & APS I too felt they were a 'last chance' and therefore worth trying. I can honestly say they helped , along with CBT & Groups Therapy, to return me to some semblence of normality (mentally at least ;-)). But I know they don't work for everyone, so only you can decide........but don't be scared to give them a trial......you need some light at the end of the tunnel! Hugs x

brave profile image
brave in reply toWelshexile

thankyou ,,,,,well after winding myself up in knots I decided to give citalopram a go second time around as it a newer ssri,and I felt seroxat maybe to potent for my hypersensitive nervous system, I too feel like im breaking down due to stress of ill health;(so after challenging my g.p he said take which ever one you want as they all do the same,,,,,,not really the answer I was looking for ,I will give this one a go ,if not seroxat here I come ,thanks,,,,,,,,can I ask if t settled your nervous system down?as I really don't need anything to wind mine up ,I need calming and balancing with a mood lift ;)

Welshexile profile image
Welshexile

GP's......give me strength grrrrrrrrr! Yes it has settled my nervous system down, but I have been advised by consultant that it probably helps I am able to manage symptoms on the minimum dose. I am on much more of an even keel nowadays - don't get me wrong I still have my 'moments' but they are now manageable. I wasn't ever offered citalopram (probably wasn't available back then) but keep me posted on your progress as it's always good to have alternatives!

brave profile image
brave in reply toWelshexile

I will ,thanks for your support ,really need it at the moment;((I wish you well ,brave;)

Welshexile profile image
Welshexile

anytime hun, that's what we're all here for :-) x

brave profile image
brave in reply toWelshexile

I have to say ,even after reading a not so nice blog this morning where a member felt brushed off by this site ,I feel this site is amazing and I would be lost without it ,thanks for your support x

Not what you're looking for?

You may also like...

Neurological symptoms?

I am having really awful symptoms of vertigo at the moment, whenever I move my eyes left or right...
Maya23 profile image

Tremors, twitching, neurological symptoms

I am officially diagnosed as uctd, but it is called lupus and sjogrens. I have an ana of 1/1280 and...
Kangamum profile image

Neurological symptoms

Hello Has anyone experienced neurological symptoms with SLE? I'm waiting to see neurology but a...
Sunshine634 profile image

Several neurological symptoms

Hi all can anyone relate to some of the symptoms I have been experiencing over the last year...
Queencara78 profile image

INSOMNIA:(((((((

Im overwhelmed at the chronic insomnia that accompanies this vile disease,the more i flare the...
brave profile image

Moderation team

See all
Debbie_kinsey profile image
Debbie_kinseyAdministrator
chelseawong profile image
chelseawongAdministrator
michaellasmith profile image
michaellasmithAdministrator

Top community tags

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.