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biancabirsan
i am 18 and i was diagnosed two months ago. two weeks ago i was like a mummy in a wheelchair after 10 relapses in three months. i thought i would be stuck in it forever and that the relapses would never stop.. i started avonex pen, my...
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Written on May 16th, 2013
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104 Views
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Seppe
All of you chronic pain complainers, what have you taken besides narcotics for your pain? Food for thought!
Seppe ...
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Written on May 12th, 2013
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47 Views
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bluemoonbarb
I was diagnosed this past October and I have been on Copaxone since January.
The neurologist told me I must have had it for a couple of years but I didn't notice
it until I could not walk right. I still walk with a limp but I have...
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Written on May 11th, 2013
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156 Views
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mileymai
my mother has had ms for twelve years we need a hoist or stand aid we are desperate at this point. i am her carer but i am also six month pregnant so i cannot move her at all for obvious reasons i will not put my baby at risk my lifting...
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Written on May 10th, 2013
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74 Views
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racedad18
I was just diagnosed with MS I am not sure just what to expect. My Dr. perscribed Copaxone to start with. What should I expect?
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Written on May 9th, 2013
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146 Views
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mrsbuzzkill
In a previous post I discussed my need for exercise and my almost pathological
desire to avoid it. I have collected four scripts from four different mds and still I sit.
Well, I actually contacted the insurance company. They have...
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Written on May 9th, 2013
2 Rate Ups
75 Views
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Seppe
The truth is ALL of my old acquaintances (friends) disappeared almost immediately upon diagnoses. And you know? ... Screw them! The lungs are still expanding and my capillaries are still flowing. Honey's coming home and the grand kids a...
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Written on May 1st, 2013
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194 Views
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Seppe
Was the best MS med you have taken. Mine happened to have been Tysabri. It was amazing how well my MS was under control. I used braces on my legs and a cane to keep me shooting straight. Then after 5 years I tested positive for the JC...
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Written on April 30th, 2013
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212 Views
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mrsbuzzkill
There are many different pains that come along with MS. Physical, emotional, mental, psychological, pick one. One of my initial symptoms were my feet. They would spasm out of control and wake me up out of a sound sleep. My arches would...
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Written on April 25th, 2013
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295 Views
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crazyguineapiglady
So tired of feeling useless, just need to vent, having one of those days when nothing works my body fails me daily no one understands I am stressed to the gills over every thing my house is a constant mess there is so much i want to do...
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Written on April 23rd, 2013
2 Rate Ups
323 Views
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mrsbuzzkill
A few years ago I volunteered to teach a group of teen-agers as part of a religious class, part of which included a visit to a mens homeless shelter. The shelter was only open from 6am to 6 pm, it's main purpose was to provide the men...
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Written on April 23rd, 2013
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172 Views
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mrsbuzzkill
I am channeling some wicked anxiety today,and I know the reason why. My husband, who has been working 4-midnight all winter goes back to the day shift tomorrow. Which means dinner on the table at six, all items cooked and served in...
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Written on April 21st, 2013
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250 Views
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Waxyjack
Okay guys, same story as everyone. I am a 41 year old male who was diagnosed 20 years ago this Thanks Giving. I am now considering anabolic steroids. I would love to hear what everyone thinks...and believe me I know the risk but has...
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Written on April 18th, 2013
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378 Views
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mrsbuzzkill
When I was first diagnosed with ms, medically there was baclofen, steroids and not much else. No ABC drugs, nothing on the table for me to choose from as to where to go from here. The first neurologist was a real dick. He basically said...
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Written on April 17th, 2013
6 Rate Ups
308 Views
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kittybeemine
I had my first Rebif injection yesterday. Really reacted to it and had quite bad flu symptoms. Feeling in a dark place at the moment. I am alone and have no partner and my family is distant. I only have one friend really. My work...
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Written on April 17th, 2013
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239 Views
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kimma546
After a lengthy hospital stay among the many tests, steroids, and plasma I was diagnosed with Ms, but my Dr. thinks its Devics disease. I have gone completely blind I'm my left eye and almost completely in my right. I am losing feeling...
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Written on April 15th, 2013
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238 Views
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jilljer
Hello everyone, my name is Jill and I was diagnosed with relapsing and remitting MS in Feb. 2004 , 9 years ago. I have always been on rebif , and always hesitant about considering a different therapy , afraid of the unknown. My last two...
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Written on April 12th, 2013
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423 Views
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Katie2210
Ive had 2 attacks since december 2011 and have constant tingling/ shock sensation when i flex my head forward and i get numbness sensation quite often due to temperature changes. I researched MS quite alot before i was diagnosed last...
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Written on April 12th, 2013
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465 Views
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Adelis
I read Any Drink that contains Sugar free is Bad for our M.S
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Written on April 11th, 2013
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177 Views
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mrsbuzzkill
This has been an educating winter for all of us in this house. One daughter home, working part time and writing her novel. My husband is working 2nd shift, so he's home 'til 4:00. I, by virtue of being blessed with MS, am here all the...
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Written on April 10th, 2013
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235 Views
Other experience groups that have been combined into this group include: Have Ms, Had Ms Since I Was 21, Have Multiple Sclerosis Ichthyosis Factor 8 Deficiency, Have Multiple Sclerosis, Acute Fulminating, Dont Like Living With Multiple Sclerosis, Have Multiplesclerosis, Bipolar Disorder, Have Ms But Ms Doesn't Have Me, Developed Ms After Giving Birth, Am a Ms Patient, Suffer Fromtrigeminal Neuralgia, Ms and Diverticulitis, Have Multiple Sclerosis, Diagnosed In Nov 08, Have Ms and Pots and Am a Mystery to Doctors, Have Muliple Sclerosish, Am Battliing Multiple Sclerosis, Depression, Have Been Battling Ms Since 1996
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