can anyone tell me their experience of taking baclofen. met someone today who has been able to give up using her sticks and can now walk fairly normally without ....
I was put on a 40mg a day dose of prednisone for ms has anyone had any bad experiences during or after taking this medication?
If anyone can help me with this, i am really really worried about it.
About 3 months ago i noticed a stiffness in my thumb on my right hand, it loosened ....
hi i am almost 31 and i have been having some of the symptoms of ms and i am really scared i have 3 young children and i dont want to be going trough this but i ....
I am hoping you can give me some advice about the bout of optic neuritis you had, as I was told on Friday thats whats wrong with my right eye. I was also told my ....
Have had problems with ataxia for about 10 years (mild) but after a bad viral infection 14 months ago it has worsened. Most noticable when walking slow, standing ....
This is my first time on here and I am in desperated need to share my experiances and hope that others on here can share theirs with me, as I have ....
Hi i'm 38yrs old and recently took what i thought was aura (from migraine) vision affected with a halo of colours and blurred vision inside the halo. 1hr later this ....
I wonder if anyone has had this before as i cant find it on google or on this site..??
I have a dull pain in my right hip/thigh and what feels like ....
Hi, just wanted to talk with people who understand as not many have so far my end! My 'story' began 10 yrs ago at 22 when I was diagnosed with ME/Chronic Fatigue ....
Is it possible to show signs of ms disease on a cervical MRI and no signs on the brain MRI
I just want to thank you for the short, very inclusive article on MS. I was diagnosed in 2006 on my birthday...I was turning 56. The right side of my body went ....
I'm just browsing here as I believe I'm having symptoms of M.S but feel it's being overlooked.
Last year I had about 7 weeks of tingling and burning ....
Sister diagnosed 21 yrs ago. Neurologist says the MS has run it's course and no MS nodules are present. She has fluid in the brain which cannot be drained because ....
[b:d171d3f96f]hi there ive been through similar problems too had 2 mri s and a lumber( not had results yet) my own dr plus pain clinic dr r saying with all the symptons ....
I had my one and only (so far anyway) known episode 10 years ago, when my ankle refused to move as quickly as it should have!! After a couple of weeks of me constantly ....
I have had MS for 12yrs and since 2007 when I have been unable to transfer I have had such nerve/neuro pain. Its like my legs and bottom have been burning ....
I was partially diagnosed last year and have so far opted not to pursue a conclusive diagnosis. I have enough information to explain what seemed like a truly random ....
It’s true, I’ve had this disease for such a very long time and yet I’m dong so very well. I walk around knowing how unbelievably fortunate I am, as if I won the ....
30 years of living with ms and it’s going as well as could be expected. The new medicines came too late for me, but as it turns out, I didn't need them anyway ....
hi i was just wondering if anyone could give me any advice ive been suffering various disabling symptoms which have become more severe over the past almost five ....
I was diagnosed with MS in 1993, following an MRI scan in 1987 and repeat in 1993. Both showed multiple lesions in the white matter. In 2001 I asked for further ....
I have been on this site daily since joining and am having great difficulty in finding anyone out there who are having problems with diagnosis and what they done ....
Hi everyone, well I am getting referred to another neuroligist at a different hospital to last time. ( Hopefully he will do new tests instead of using results from ....
I have went through almost every person on this site. I thought it was a disscussion site where you could find out from people like yourselve about the illness with ....
Well im almost 2 years down the line now and unable to work at the grand age of 35!! I have a fab husband and 3 fantastic children who all help me on my bad days, ....
I have had MS for over thirty years. I have the relapsing remitting type. It all started when I was 19 I had Optic Neuritis, I was on a campsite, I had just finished ....
I was dx'd with RRMS December of 2005. Since that time, I began Copaxone. Within the last 11 months, I've had a total of 3 exacerbations--1 I was hospitalized and ....
I have already submitted an account of my MS, which I have had for over thirty years. What I was lookinf for was any reaction to my article.
Best wishes from Julia ....
I awoke one morning in the winter of 1979/80 with tingling toes. It only lasted a couple of hours. I didn't see my GP -- he'd have laughed me out of the surgery. ....
I would like to thank you so much for taking the time to respond to me.. I really appreciate it.
I have since seen a neuroligist and I hate to say it, through the ....
Hi, to Jaqueleine and the person who wrote the message on 30.5.06.
I too am here, because I looked for information on treatment options. I was diagnosed with MS ....
I was diagnosed in 1996 but had ms since 1982 with not many 'attacks' since, until 1996 when i was left like a baby, unable to write, speak except for yes & ....
I too feel sorry for you unsuccessful diagnosis, but once diagnosed, carry on, it's not the end of the world although that'#s what i felt like, but 20 years down ....
- Conditions A
- Conditions B
- Conditions C
- Conditions D
- Conditions E
- Conditions F
- Conditions G
- Conditions H
- Conditions I
- Conditions J
- Conditions K
- Conditions L
- Conditions M
- Conditions N
- Conditions O
- Conditions P
- Conditions Q
- Conditions R
- Conditions S
- Conditions T
- Conditions U
- Conditions V
- Conditions W
- Conditions X
- Conditions Y
- Conditions Z
Disclaimer: Patient.co.uk has no control over the content of any external links. Inclusion does not imply endorsement by Patient.co.uk.