how many people have multiple sclerosis in uk

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//multiple-sclerosis-research.blogspot.com/ ). It's run by some UK neuros/researchers for people with MS. What's nice about this blog is that not only do you get the research abstracts, but they also give some sort of context or commentary as to why you might be interested or how promising they think whatever it is will be. As a bonus, if you have a question about the research, they will often answer it in the comments.

So how long until you think our FDA gives it a thumbs up ? I believe it has been resubmitted or it is close - maybe by the end of 2014 is my thinking. I'm surprised that NICE approved it.

Here is a link for buying tickets on line for a classical concert in aid of Multiple Sclerosis. Society!http://www.etickets.to/buy/?e=6429 All proceeds from ticket sales and raffle go to Manchester MS Society. String ensembles, String Orchestra, Soprano, Baritone and Guitar Quartet! Please come along if you can and help raise awareness of Multiple Sclerosis and hopefully some money for Manchester MS Society too!

How many neurologists have you seen in your quest to be diagnosed/on the way to diagnosis?

Some of these people no doubt suffered no relapses, while others suffered many. Also, of course, some people who are on no DMD have had no relapses. Statistics can be misleading. Nothing can be concluded about you as an individual. However, whatever has happened in the past, I strongly urge you to seek treatment now.

Many of us are in limbo and have symptoms like yours. Many have been trying to get an accurate dx for years. It's awful! You are in good company here. I doubt if any of us can say what the chances are that you have MS. There are so many things that mimic the disease. If you think your doctor has stopped looking, find a good neurologist. Read the health pages here and elsewhere, and don't give up on finding out what is wrong, whether it is MS or something else!

I had an MRI that showed one lesion in my brain, a hemangioma in the thoratic region and some mild degeneration in my cervical spine. I have been feeling ill since Feb 09 and as my condition continues I think I can recall feeling some of these symptoms as far back as 15 years old. I have has pnemonia 2 times and had HPV when I was a teen. I am 30 years old now and have 2 wonderful children and an amazing husband. My question is where do I go from here? What kind of doctors should I be seeing?

Ok, being told different stuff, how many scans do you get in UK? I had first two, I was under the impression there was one more later on to check if baby breech etc. Huge cutbacks since I had my last child 5 years ago, so I'm not sure what's what nowadays...

Might be worth contacting any of the other pain clinics near you if the only treatment option offered at the one you went to was diazepam, which is used in multiple sclerosis primarily for the relief of muscle spasms and spasticity but its definitely not the only treatment option for muscle spasms and spasticity! Hmmm have you considered botox? Hope that helps.....

My thoughts and prayers go out to you. It is so frustrating not to have the answer. People who are unfamiliar with this limboland phenomena, seem to have the hardest time understanding our dilemma - even some if not most doctors. Good luck with your situation and getting a proper diagnosis.

6% had relapsing remitting multiple sclerosis, 9.4% primary progressive multiple sclerosis and 6% clinically isolated syndrome. Nearly 40% of our multiple sclerosis patients with disease duration >10 years (mean = 16.2 ± 5.3 years) remained with no or mild disability (Expanded Disability Status Scale [EDSS] 3). Also, about 30% of patients with relapsing remitting multiple sclerosis showed benign disease evolution (EDSS 3) more than 20 years (mean = 24.0 ± 3.3) after onset.

ask for their opinion? It is not unusual for people to be misdiagnosed as their are so many conditions that mimic MS symptoms. Is this new Neuro running further tests & trying to find out what they feel is causing your symptoms? Keep us updated & ask any questions you may have. Take Care, Karry.

Most of the things I have read about medical research in the UK has been wonderful. That you for posting this link. It gives hope to some out there!

Hi I am a 22 year old College basketball player and I am a new member to this site I joined because I am very concerned I might have Multiple Sclerosis I have very few people I can talk about this to in my life if anyone on this site reading or has knowledge about this or feed back please help me as I am worried sick please here me out! Here is my story..

If it is MS there are things that can help. Most people with MS have problems with urination at some point. The bladder is not tied to the brain so it can be short circuited rather easily. The statistics for men and prostate problems ( not all cancer) increases with age. My brother in law a Doctors says a man has a 50% chance of prostate problems at age 50 years old, 75% at 75 and so on.

How Science Is Solving the Mysteries of Multiple Sclerosis by Howard L. Weiner (Oct 25, 2005) it explains where MS research and treatment has developed.

Multiple Sclerosis Patients Are Missing Out On Drugs Only 40% of people eligible for drugs to combat multiple sclerosis in the UK are actually taking them, says a report from the MS Society. A survey of more than 10,000 adults with MS showed that many were missing out on the seven licensed medicines approved for use. The charity said a lack of information and access to specialists was to blame. It is calling for the government to provide a personalised care plan to every person with MS.

One thing you might consider is finding a forum that has people your age to talk about their parent with MS - the Multiple Sclerosis Society of the UK has a great forum and you can find young people talking about this and much more - http://www.mssociety.org.uk/forum/caring-someone-ms And you can always come back here to ask your questions. Good luck to you both.

s Hospital, Harvard Medical School, is a leading institution in the area of multiple sclerosis, providing comprehensive patient care, innovative technology, and ongoing clinical research trials. The Partners MS Center is equipped to provide the best level of care for MS patients and is committed to continuous clinical and laboratory research, in an effort to discover a cure for multiple sclerosis. This web site is designed for both patients and health care professionals.

s government/veteran website and will have diseases associated with agent orange, studies being conducted past and present, how to apply for compensation, etc.

do you have to have active lesions in the brain on MRI in order to have M.S. My husband was diagnosed with M.S. and is driving himself crazy denying it. He had an MRI of the brain that showed multiple foci of T2 and FLAIR hyperintensity in the white matter of both cerebral hemispheres including approximately 5 small lesions in the periventricular white matter, lovated at the callosal sptal margin and oriented perpendicular long axis of the lateral ventricles.

The 50 plus symptoms in MS symptomology are variable and many non-quantifiable. there are many other diseases that have a presentation of similar symptoms as MS. LPs are not exclusive to MS- close to 90% are, which is not enough for a MS diagnosis. It's like a court trial, where evidence has to be beyond ANY reasonable doubt! Same with EPTs (evoked potential tests) are not exclusive to MS! Neurological exams at the Neuro's office are far from conclusive.

I don't know how bad your MS is, but in some cases, pregnancy has been known to put a MS patient into remission. IVF can be very expensive.

I have had RR multiple sclerosis since I was 10 ish diagnosed (finally) in 2008. Had routine MRi of head and neck last month, everything is stable for 2 years now. Thank you Tysabri! My question is the impression of my mri stated T1 and T2 disease burden is at least moderate ( written for head and cervical MRI). Also JCV negative this whole time can I stay on Tysabri indefintely as long as I am negative?

How many people have multiple sclerosis in uk

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