Multiple sclerosis in young patients

Common Questions and Answers about Multiple sclerosis in young patients

multiple-sclerosis

org/brochures and you can get many publications from The Basic Facts, The History of Multiple Sclerosis, to publications on Newly Diagnosed, Employment issues, Staying Well, Managing Specific Issues, Managing Major changes, And the list goes on and on.

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.

LOMS is usually associated with a faster progression to disability compared to young adult multiple sclerosis (MS) patients. Moreover in patients over 50, MS variants and atypical forms which present a difficult diagnostic problem, may be frequently encountered.

In a third study, optic neuritis with no MRI lesions led to multiple sclerosis at 5 years in 16%, versus 51% of patients with 3 or more MRI lesions (Beck 1997). The 10-year data for this study show multiple sclerosis in 22% without MRI lesions, and in 56% in those with 1 or more MRI lesions. The amount of disability is unrelated to baseline lesion load. In a fourth study, optic neuritis with no MRI lesions led to multiple sclerosis at 5.

We'll soon be launching a Multiple Sclerosis Tracker, which will allow members to track symptoms and treatments related to Multiple Sclerosis. Please leave us a comment if you're interested in this tracker and we'll notify you when it's available.

Stress regulation in multiple sclerosis-current issues and concepts Mult Scler 2007; 13; 143 originally published online Jan 29, 2007 C Heesen, D C Mohr, I Huitinga, F Then Bergh, J Gaab, C Otte and S M Gold "An increasing body of empirical evidence now supports the association between stressful life events and relapses in MS, although this literature is of varying methodological quality and does not permit causal inferences.

48 µmol/L)[18] A 1998 study completed a statistical analysis of 20 million patient records, comparing serum uric acid values in patients with gout and patients with multiple sclerosis. Almost no overlap between the groups was found.[19] Uric acid has been successfully used in the treatment and prevention of the animal (murine) model of MS.

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?

Ojibajo is so right about the patient being more in danger from germs carrier in by the patients. It is known that hospitals are full of nasty stuff, just by the nature of what their business is - taking care of very sick people. Whether we have MS or not, visitors to hospitals should be sure to practice good hand hygiene - washing them thoroughly. We pick up those germs from door knobs, hand shakes, and even elevator buttons everywhere we go, but especially in hospitals (and schools!

It is possible that I had/have undiagnosed multiple sclerosis, and then when I started treatment the interferon kept the MS from progressing?

Thanks, Write2, that helps. We thought originally you were looking for the new approved oral. PPMS, I'm so sorry. LDN is not known to treat the disease, but I understand why your willing to try :( for symptoms. I hope it brings you much needed relief! I'll look for some past discussions on LDN for you. and, link them here. Or, you can always go to "search this community" and type in LDN or low dose, etc.

php Long-Term Study With COPAXONE(R) Indicated Protective Effect On Brain Tissue In Multiple Sclerosis Patients Article Date: 29 Apr 2009 - 7:00 PDT "New data presented provided evidence that long-term treatment with COPAXONE® (glatiramer acetate injection) may offer sustained protection from neuronal/axonal injury.

The new report entitled Treatment Algorithms in Multiple Sclerosis also finds that only 38.8 percent of newly diagnosed patients receive a drug within one year of their first diagnosis. This highlights the substantial room for increased uptake of disease-modifying therapies in newly diagnosed patients.

Hi! I'm posting this here to get some opinions on my current condition. I plan on visiting a neurologist and getting an MRI to confirm/deny things, but I want to see what others think.

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?

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