multiple sclerosis treatment johns hopkins

treatment of High-Dose Cyclophosphamide for Moderate to Severe Refractory Multiple Sclerosis. It was a 3 day treatment much like Chemo, my immune system was wiped out, and my blood counts taken to near zero. I spent 3 weeks having my blood counts being brought back up. Since then the unwelcome visitor has been quite and all subsequent MRI's and blood work have confirmed that the MS I HAD is in remission!

While a clinical trial testing vitamin D supplements in multiple sclerosis patients is underway at Johns Hopkins and elsewhere, most of the evidence of its efficacy currently comes from animal studies. Vitamin D may prevent or ease symptoms of MS according to results of a recent study. PMCID: PMC3876241 -Free Article- Hope this helps.

Hi All, I have several neurological symptoms including about 30 lesions on a brain MRI scan. I've gotten several diagnoses from different doctors including multiple sclerosis - but nothing definitive from the dozens of tests run. Can someone tell me who is considered the top doctor for DIAGNOSING multiple sclerosis in the U.S. ? I'm willing to travel to any state. Thanks for any help you can give.

Hi all....I had my appts. with Johns Hopkins last week and I'm so happy I went there. My slides from my last FNA, done 3-4-10, that showed atypia susp. for papillary cancer, were sent to Johns Hopkins for their cytopathologists to review. I met with an endocrinologist who specializes in the thyroid (not diabetes) and also had another ultrasound and bloodwork.

The best advice I can provide is that you and your doctors seek consultation with a group of physicians who have engaged in research and reported on their experience with this disease. One such group is at the Johns Hopkins Medical Center in Baltimore. Contact information follows. Orden, Roy Anthony. Timble, Hersha. Saini, Sarbjit S. Johns Hopkins Bayview Medical Center, Baltimore, Maryland., Division of Allergy and Clinical Immunology, Johns Hopkins School of Medicine, Baltimore, Maryland.

30 AM – Forum Starts Hyatt Regency Century Plaza 2025 Avenue of the Stars Olympic Ballroom (Plaza Level) Please join us for this unique opportunity to speak with our MS doctors about the advances that have been made in multiple sclerosis research and patient care. Thanks to your generous support, we are even closer to finding a cure for this debilitating disease.

I have no idea and my docs have no idea whats wrong with me. In sum - developed peripheral neuropathy 2.5yrs ago and it was very painful. My feet burn constantly, but in 2006 I could hardly walk, had serious weakness in all extremities and could hardly walk up a flight of stairs at 31yo. I had plasma electrophoresis 2 yrs ago and I barely recall one abnormal result and it was for Ig -something. I don't remember if it was IgM, IgG, etc.

// clinicaltrials.gov /ct2/show/NCT01024777?

I met with my doctor this morning and found out that my pathology went to Johns Hopkins for consultation. I also received my final pathology report which states: Right ovary: Fragments of membranous ovarian tissue with cystic changes showing mucinous glandular epithelium with rare atypical areas and mitotic activity, suggestive but not entirely diagnostic of borderline low-malignant potential mucinous cyst. Follow-up is recommended.

S. News top ten neurology hospitals in the country, which includes the Mayo Clinic, Johns Hopkins in Baltimore, Methodist Hospital in Houston, UCLA, and Boston Mass. Neurontin and Lyrica help nerve pain, I take the latter, but it's awfully potent.

After about a month in Shady Grove the symptoms have gotten worse, all ability to use any muscles are completely gone. He was transferred to Johns Hopkins in Baltimore and has now been in the hospital for about 14 months. He has absolutely no ability to use any of his muscle functions. He has a breathing tube and a tube for feeding. As far as his brain, he is completely functionally. Can anyone help restore this man to who is once was. He has gotten pneumonia several times.

She has to go to Johns Hopkins to have a lymph node removed and checked. shes really scared, not sure what to expect.

Wow! to both of these. The OCT scan is very interesting and I wonder when they will be finished with their trial studies? That is a relatively simple test to complete from what I just read. Please let us know how it goes and what they find. Now, about the GA - I had to check to make sure I understood it - you have a gluten intolerance, aka Celiac Disease, right?

Please join us for this unique opportunity to speak with our MS doctors about the advances that have been made in multiple sclerosis research and patient care. Thanks to your generous support, we are even closer to finding a cure for this debilitating disease.

a distribution somewhat atypical for multiple sclerosis and most likely due, in a patient of this age, to leukoaraiosis. The lack of patchy signal abnormality in the corpus callosum, cervical spainal cord and infratentorial compartment is also somewhat unusual for multiple sclerosis, although it remains within the differential diagnosis for the visualized lesions. Other etiologies such as vasculitis could also be considered.' So of course I looked up 'leukoaraiosis.

I now have new problems - brain fog, poor hand coordination, poor vision in my left eye, constant spinning, poor balance to mention a few. They suggested I go to Johns Hopkins for another opinion. (I am going in two weeks.) They have put me in touch with a Chiari NS at Johns Hopkins and I'm going in two weeks. I am miserable and unable to do any activities. I would like some input as this has just put my life on hold. Any comments would be greatly appreciated.

It is really a shock to get this diagnosis and then you worry when the symptoms are not getting better with treatment. But, please be patient with the treatment as it will eventually work and her symptoms will calm down. Is she still in the hospital? The disease is not curable but it can be slowed down as Deb has already explained.

m at a loss at how to find a good specialist. Should I be looking for someone who works with Johns Hopkins in Baltimore (as it has been mentioned frequently on this site)? How would I even find out who would use JH to read my biopsy? I'd love ACTUAL recommendations for professionals in the Suburban Maryland area to perform and interpret the FNA, and provide treatment and surgery, if necessary. Thanks, D.

my sister (24) was diagnosed Multiple Sclerosis in 2010, responded to steroid. now she suffered sudden & complete loss of vision in her left eye. she has been put on SOLUMEDROL. please suggest any available treatment modalities world over ? chances of return of vision ??

i had been diagonised with multiple sclerosis in the year 2001. now i am not able to walk. i am also not able to see clearly. my speech is also not clear. i think my type of ms is primary progressive since my condition has worsened gradually. pl suggest some medicines or other alternative therapy.

Multiple sclerosis treatment johns hopkins

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