What be your first symptoms to Multiple sclerosis? and what did you do in the order of it ? are you pedals stool bound ? are you on medication? Thanks all
Answers:
A lot of family first obtain optic neuritis approaching I did.
The eye doctor saw the optic neuritis and he told me that in attendance be a hit and miss I have MS. The neurologist did an MRI and told me the likelihood that I have MS be contained by the 50-75% variety. I begin reading adjectives something like MS symptoms and know that I particularly have it. A subsequent MRI be loaded next to lesion. I afterwards go blind in my vanished eye, suffered excrutiating stomach-ache, could just totter, have slurred speech, cognitive problems and memory problems. A few months next adjectives the symptoms that I described go away. I took Copaxone for a few years. I go sour it and very soon help yourself to lone LDN (Low Dose Naltrexone). I am not wheelchair bound. I live a pretty typical natural life despite have MS. While some those become profoundly artificial by the disease, others enjoy pretty benign cases. But MS is importantly unpredictable.
I started next to optic neuritis. My ophthalmologist know that more than partially of the populace who attain ON develop MS, so he recommended I jump final to my doctor and rota an MRI. Done and done, and they explain to me I enjoy probable MS. After a second MRI a few months after that, and comparison between the two showing that I'm getting more lesion on the brain and they can next confirm MS.
I'm on Copaxone. I enjoy to transport the shot every daytime, but it have the smallest side effects. Not to mention you can preserve it at room heat for up to a month. The drug have held bad any other symptoms so far. We shall see.
-cj
My first symptoms be ably previously I be in reality diagnoised near MS. About 7 years prior I experienced my legs numb and thought I have pulled something in my fund, the doctors sent me for an MRI of my brain, which showed nought wrong. This be support within 1986. Seven years subsequently I become awfully dizzy, standard lamp head and until that time the expire of that hours of daylight I be powerless to surface my not here leg. But separating those years, I also have optic neuritis several times, tripping while walking up steps and my arms falling asleep for hours at a time.
WHEN I WAS DIAGNOSED I WAS HAVING AN EXACERBATION, MAKING IT DIFFICULT TO WORK, I WAS WALKING DOWN A LONG HALLWAY INTO A LARGE GARAGE AND WHEN MY EYES BEGAN TO ADJUST TO THE VERY LARGE DIM LITE ROOM (16 BAYS) I FELL TO GROUND AND STARTED GETTING A CRAZY BUZZ IN MY HEAD WHICH THEN WENT ON FOR DAYS AND I FINALLY WENT TO DOCTORS WHERE A NURSE PRACTIONER CAUGHT IT BY WATCHING ME WALK SENT ME FOR AN MRI AND THE REST IS HISTORY. BUT THE FIRST SYMPTOM I CAN RELATE BACK TO MS WAS ABOUT A YEAR BEFORE MY DX MY LEFT EYE BEGAN TO TURN IN, I WAS DRIVING FROM MASS TO VA AND HAD TO WHERE A PATCH OVER ONE EYE TO KEEP MY VISION CLEAR. I WAS INITIALLY PRESCRIBED AVONNEX WHICH HAD MANY SIDE EFFECTS THAT I DIDNT TAKE WELL TOO, I WAS THEN CHANGED TO COPAXONE WHICH I HAVE BEEN ON FOR A FEW YEARS NOW AND HAVE BEEN EXACERBATION FREE SINCE STARTING WITH THE COPAXONE TREATMENT.
I also started near Optic Neuritis. Had double delirium, both eyes going in contrasting direction. I be put on IV Steroids, told I some nature of inflammationon my brain and sent home after 3 days. No one made any mention of MS. Ten years next have trouble near urination and gait. Had an MRI and tada finally a diagnosis.
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Answers:
A lot of family first obtain optic neuritis approaching I did.
The eye doctor saw the optic neuritis and he told me that in attendance be a hit and miss I have MS. The neurologist did an MRI and told me the likelihood that I have MS be contained by the 50-75% variety. I begin reading adjectives something like MS symptoms and know that I particularly have it. A subsequent MRI be loaded next to lesion. I afterwards go blind in my vanished eye, suffered excrutiating stomach-ache, could just totter, have slurred speech, cognitive problems and memory problems. A few months next adjectives the symptoms that I described go away. I took Copaxone for a few years. I go sour it and very soon help yourself to lone LDN (Low Dose Naltrexone). I am not wheelchair bound. I live a pretty typical natural life despite have MS. While some those become profoundly artificial by the disease, others enjoy pretty benign cases. But MS is importantly unpredictable.
I started next to optic neuritis. My ophthalmologist know that more than partially of the populace who attain ON develop MS, so he recommended I jump final to my doctor and rota an MRI. Done and done, and they explain to me I enjoy probable MS. After a second MRI a few months after that, and comparison between the two showing that I'm getting more lesion on the brain and they can next confirm MS.
I'm on Copaxone. I enjoy to transport the shot every daytime, but it have the smallest side effects. Not to mention you can preserve it at room heat for up to a month. The drug have held bad any other symptoms so far. We shall see.
-cj
My first symptoms be ably previously I be in reality diagnoised near MS. About 7 years prior I experienced my legs numb and thought I have pulled something in my fund, the doctors sent me for an MRI of my brain, which showed nought wrong. This be support within 1986. Seven years subsequently I become awfully dizzy, standard lamp head and until that time the expire of that hours of daylight I be powerless to surface my not here leg. But separating those years, I also have optic neuritis several times, tripping while walking up steps and my arms falling asleep for hours at a time.
WHEN I WAS DIAGNOSED I WAS HAVING AN EXACERBATION, MAKING IT DIFFICULT TO WORK, I WAS WALKING DOWN A LONG HALLWAY INTO A LARGE GARAGE AND WHEN MY EYES BEGAN TO ADJUST TO THE VERY LARGE DIM LITE ROOM (16 BAYS) I FELL TO GROUND AND STARTED GETTING A CRAZY BUZZ IN MY HEAD WHICH THEN WENT ON FOR DAYS AND I FINALLY WENT TO DOCTORS WHERE A NURSE PRACTIONER CAUGHT IT BY WATCHING ME WALK SENT ME FOR AN MRI AND THE REST IS HISTORY. BUT THE FIRST SYMPTOM I CAN RELATE BACK TO MS WAS ABOUT A YEAR BEFORE MY DX MY LEFT EYE BEGAN TO TURN IN, I WAS DRIVING FROM MASS TO VA AND HAD TO WHERE A PATCH OVER ONE EYE TO KEEP MY VISION CLEAR. I WAS INITIALLY PRESCRIBED AVONNEX WHICH HAD MANY SIDE EFFECTS THAT I DIDNT TAKE WELL TOO, I WAS THEN CHANGED TO COPAXONE WHICH I HAVE BEEN ON FOR A FEW YEARS NOW AND HAVE BEEN EXACERBATION FREE SINCE STARTING WITH THE COPAXONE TREATMENT.
I also started near Optic Neuritis. Had double delirium, both eyes going in contrasting direction. I be put on IV Steroids, told I some nature of inflammationon my brain and sent home after 3 days. No one made any mention of MS. Ten years next have trouble near urination and gait. Had an MRI and tada finally a diagnosis.