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I Have Multiple Sclerosis

Personal stories and news for people with Multiple Sclerosis. In affiliation with ThisIsMS.com 1,291 People

    It was 2013 and I was 26 years old

    when I was diagnosed. I am now 28. It started out with numbness in my extremities and went to cordination difficulties and weakness ending up in paralysis. I went for help 3 times during this episode... 3rd time i was completely paralyzed and was still sent home with the...
    deleted deleted 26-30 2 Responses Jan 29, 2015

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    A Journey of 30 Years, With MS As a Teacher...

    Hello All, I've been journeying with MS as a constant companion for over 30 years, and facilitate a wellness & support group in CO.  I'm also a retired clinical and transpersonal hypnotherapist.  Like you, through many ups and downs, I've learned a lot about...
    Shabda1 Shabda1 56-60, F 11 Responses Mar 9, 2007

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    I don't have MS but I have a very similar

    condition that works similar but secondary to MS (the affects too) it is called 'Superficial Siderosis of the Central Nervous System' and is caused by an internal bleed releasing iron into the CNS this breaking everything down as it progresses. :(
    Paul2v Paul2v 26-30, M 1 Response Aug 6, 2015

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    How do you treat ms? I have not been diagnosed,

    but my grandma does and I am worried I might.
    Happybri123 Happybri123 18-21, F 1 Response Mar 22, 2015

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    I guess just upset my doctor has me work 30

    week my work is going let me go. I just do not know when. I am so tired even working 6 hrs/ day instead of 8. Ms sucks the life out of you. I do not know what is going to happen I think they are trying get me to quit.
    wolfeeegirl wolfeeegirl 41-45, F 1 Response Jul 1, 2015

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    My Left Arm Stopped Working And I Starrted Walking Like A Drunk

    I was at my laptop. And I reached for a smoke or something. My arm just shot out straight and I couldn't curl it back up again. I held it back to its former position and tried again with the same results. I was just so surprised that I couldnt control my arm. After a while this...
    Beausejour Beausejour 31-35, M 3 Responses Nov 14, 2013

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    When I Became My Disease...

    I have MS.  I was diagnosed at 27.  I had many years including my teens where I had symptoms.  At 20 I bought my first business.  My passion was floral design. My specialty was weddings.  I have done wedding design and coordination for 13 years now. ...
    jenisue jenisue 31-35, F 7 Responses Jan 5, 2008

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    I have Multiple Sclerosis

    and I'm better off than most, blessedly
    AsgardRain AsgardRain 41-45, F 1 Response Jan 19, 2015

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    Depression Alone!

    I have 3 kids 14, 12 & 8. They are the only one's keeping me still breathing every day! I do have a partner we have been with one another for 10yrs now. I love him but, I don't think well I actually got that vibe that that he does'nt care:'( . He takes me to the hospital with...
    lonely5603 lonely5603 31-35 4 Responses Nov 17, 2012

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    msfancypants msfancypants 46-50, F 6 Responses Aug 9, 2012

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    I was diagnosed in 2007.

    I was a long distance runner before my diagnosis and kept it up for years but now I can barely walk and am afraid I will have to go on disability soon. As strong as I try to be I'm scared as hell.
    robbyt3545 robbyt3545 31-35, M 3 Responses Feb 4, 2015

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    MS

    I found out shortly after I had turned 21 that I had Multiple Sclerosis. I was forced to quit my job and quit school. I pretty much had to re arrange my life.  The doctors told me that I had had it before the age of 19 but this was the first time that it had shown itself. I...
    gigglemonster2000 gigglemonster2000 26-30, F 14 Responses Mar 13, 2007

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    I decided to write an update

    since my last entery was a long while ago. I am not taking any MS drugs. However I do take suppliments daily (NAC,B-12, Multi Vitamin, etc.) As well as LDN, an oil every night. I had the CCSVI surgery about 2 years ago. So much that I lost in the first place has been given back...
    Shyness03 Shyness03 18-21, F 1 Response Apr 1, 2015

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    I ******* hate this disease.

    Anyone here who's opinion is different?
    DaveShaved DaveShaved 51-55, M 2 Responses Jan 16, 2015

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    Some days r fine But some days r just like what

    the hell!!! It's like it likes to play tricks on yu!!! I hate it(•.•)
    jinna69 jinna69 31-35, F 10 Responses Dec 3, 2014

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    Heads You Win, Tales I Lose

    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 ****. He basically said whatever you have now is all you will have...
    mrsbuzzkill mrsbuzzkill 51-55 5 Responses Apr 17, 2013

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    Infusion day. Hopefully this is one of the

    times it kicks in without messing me up too much. I am sick of getting stuck with needles, though.
    painterchick painterchick 36-40, F 1 Response Jul 31, 2015

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    My Husband Has Multiple Sclerosis And My Heart Is Breaking

    When I first met my husband I knew of the condition multiple sclerosis; I knew the treatment methods, the steroid trips to the hospitals, I knew the diets and the preventative measures to help battle this ongoing incurable and debilitating disease. What I did NOT know was how...
    MrsTeri MrsTeri 22-25, F 20 Responses Jun 20, 2012

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    I am a 47 year old male.

    I was dx with MS in 2013. I am and was the bread winner of my family of 4. In the last 2 years my MS has gotten worse my gait is terrible and my cognitive skills have worsened. I worked in the medical field for 14 years. My co-workers, clients and doctor think I need to get on...
    ceisinger ceisinger 46-50, M 1 Response Feb 2, 2015

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    The Spinal Tap

    I was still shaking from the spinal tap. The medical term is “lumbar puncture.” Any combination of words that contains “spinal” and “puncture” was going to terrify me. It did. From working in a law firm that handled personal injury cases, I...
    ZenGrrrl ZenGrrrl 41-45, F 26 Responses Apr 3, 2006

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    I’m 26 years old and I was diagnosed with MS

    about a year and a half ago. I’m very asymptomatic, this means my symptoms may go unnoticed. Weakness in my legs and arms, and lack of sensitivity in my face are included on the symptoms I felt. 4 months ago I started the Gilenya treatment, the one and only drug I have ever...
    isa88 isa88 26-30, F 2 Responses Feb 3, 2015

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    So hard to start a relationship with someone

    with me having MS. Each year I have been going downhill Has anyone heard of a uphill?
    Agilezs Agilezs 61-65, F 2 Responses Sep 3, 2015

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    I was diagnosed with m.

    s in 1999 hardest 2 things I had to learn to deal with were 1. Understanding that people without m.s cannot relate to the condition AT ALL!. its not their fault how could they possibly understand a hidden illness or understand that the symptoms that they can see are the tip of...
    ledgie1975 ledgie1975 36-40, M 1 Response Jun 20, 2015

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    Had a fairly good day today

    but now the fatigue has set in...but I still have to feed the kids and get them to bed. ugh
    painterchick painterchick 36-40, F 3 Responses Nov 23, 2015

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    The Human Chain I entered the Neuro Dept,

    checked in, then do what I always do- go to then restroom. On my way back to the waiting room I passed a lady in a wheelchair kind of waving to get someone's attention. I noticed and stopped, asking her if she needed the rest room. She should her head yes. So I wheel my walker...
    mrsbuzzkill mrsbuzzkill 51-55 Jul 18, 2014

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    Heavy...

     Thats one way to describe it. My limbs especially my lower extremities feel heavy, as if they are being tied down by weights. The worst part of dealing with this disease is how unpredictable it can be. Sometimes I have more then enough energy for the day and other times I...
    Nunyabuziness Nunyabuziness 31-35, M 26 Responses Mar 12, 2010

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    It's very difficult having a condition

    where you look fine on the outside but feel bad. People look at you and think " well she looks fine, what's her problem?" MS is definitely not a fun disease to have. First of all it is very difficult to diagnose. Then, they have to find the right medication that works for you. I...
    deleted deleted 26-30 4 Responses Jul 1, 2014

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    My Long Ms Journey

    I consider myself to be one of the "luckier" MS ones. For the most part my MS has been what they used to call benign MS. For me that meant I got away with hiding my MS and being the Queen of Denial. Looking back I, along with my friends and family, can remember all sorts of...
    JfromOC JfromOC 51-55, F 5 Responses Oct 30, 2007

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    Good day ! My husband has MS.

    It was benign MS, after 10 yrs MS attacked his both eyes and became blurred almost loss of vision. Then after several treatments w/ steroids hoping for his eyesight to come back, unfortunately it didn't work. Right-after that, numbness of his arms happened and his both legs is...
    Andrea0328 Andrea0328 36-40, F 1 Response Feb 3, 2014

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    I do not know if I have MS.

    My mother had it and passed away in 2008 from complications related to the illness. I've been having strange symptoms and curious to hear others. Recently, for the past few days my left arm tingles and goes numb. The left side of my face goes numb every on and off but mostly...
    dynamic71 dynamic71 41-45, M 6 Responses Apr 11, 2015

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    A Lack Of Understanding Of MS!!!

    My son got married on Tuesday and we had to go to the marriage office before hand. I parked outside the door in a disabled space as my ability to walk is not too great. I knew that i would be standing off and on all day so i took a walking stick with me. As i got out of my car...
    ClimberJeff ClimberJeff 51-55, M 4 Responses Nov 14, 2013

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    I am in the chair getting my 32nd infusion

    as I write this. I was diagnosed 3 years ago. I was diagnosed at the same age as my mother was when she was diagnosed. I still work full-time and raise my two little ones. Everyone tells me how strong I am. I don't feel strong. I just do what I need to do. What else can one do...
    painterchick painterchick 36-40, F 1 Response Jul 1, 2015

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    Does anyone take copaxone

    or glatopa? How long does it a 20mg injection to be fully absorbed and when can I inject into the same area again? I'm thin so my options are a bit limited.
    7MattW 7MattW 31-35, M 3 Responses Oct 5, 2015

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    The doctors recently diagnosed me with MS.

    How do you manage this. Any tips will be helpful. Today I have started my rounds of Steroids.
    Regina1931 Regina1931 18-21 1 Response Oct 29, 2015

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    So does anyone here have other "issues" besides

    MS. I have: Migraines Idiopathic thrombocytopenic purpura Diabetes
    DaveShaved DaveShaved 51-55, M Feb 8, 2015

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    Year 8

    And I'm still not used to it. Every year comes with a new frustrating symptom that I must adapt to and figure out how to live a normal life with it and make it as unnoticable as possible.  From the spasms and tremors to the loss of strenght and control, I have to hold...
    Nunyabuziness Nunyabuziness 31-35, M 18 Responses Oct 7, 2010

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    My Story-in A Nutshell

    Well, I'm 26 and was just officially diagnosed with MS on June 9th. However, I've suspected I had it for about 4 years now. All doctors and specialists I've seen just treated me like an overweight, depressed, hypochondriac. Telling me my symptoms stemmed from depression, weight...
    TattooedMissez TattooedMissez 26-30, F 17 Responses Aug 17, 2011

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    Has anyone with MS had their vision randomly go

    black for a few seconds? As if someone flicked a light switch off and then back on.
    Idontwanttosendyouapic Idontwanttosendyouapic 18-21, F 2 Responses Jan 2

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    Symptoms Ignored...

    In my last post I detailed how I was diagnosed with Multiple Sclerosis. During my hospital stay and the weeks after, I had a lot of time to think about symptoms I may have had in the past. Now that I know what's wrong with me, I see that the symptoms started long ago. Being...
    ChicaBee503 ChicaBee503 26-30, F 3 Responses Feb 6, 2013

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    Relapsing Remitting Ms - Maybe Progressive

    I have the kind where after my last attack I didn't get back to my previous baseline.  How I feel right now, I would have never gone to work before... but since this appears to be as good as it gets, I resumed my life. My last brain lesion was the size of a golfball...
    Wiccad Wiccad 41-45, M 7 Responses Jun 1, 2007

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    My whole life is falling apart

    before my own eyes...well when there working.
    fuckms fuckms 36-40, M 1 Response Jun 16, 2015

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    Happybri123 Happybri123 18-21, F 2 Responses Mar 19, 2015

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    In 2012 I went on the trip of a lifetime to

    Canada on a working holiday. When I came home, I was depressed and watched an awful lot of TV. So when my left eye became sore, and my vision became blurry I ignored it. Until I woke up completely blind. I was diagnosed with optic neuritis. I was told that it would get better on...
    bjoffo bjoffo 22-25, F 2 Responses Nov 16, 2015

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    I'm Never Giving Up On Life.

    November 17th, 2012, I was diagnosed with MS. At the time I was 15. My reaction was hardly a reaction at all. I haven't really heard of the disease, and knew nothing about it. The first two months I was in denial. I'm too young to have this. They made a mistake. Then reality...
    Shyness03 Shyness03 18-21, F 8 Responses Nov 28, 2013

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    I was dx n 2009 with r.

    r.ms. I've done all kinds of therapies & changed my diet. I take daily vitamins 7 anti inflammatory suplements 2 help me. I did Copaxone 1 year.. shots sucks & it did'nt help much. 4 the last 4 years i've beeb doing Chemotherapy 1 x a month 7 getting Botox n my knees every 3 mos...
    sparradia sparradia 41-45, F 2 Responses Oct 21, 2014

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