MS Connection

I'm having serious issues with my memory. It's starting drive me crazy and I'm becoming extrememly depressed with no one to talk to. I'm tired with all of this. I'm actually looking out for help and counseling. I need someone who I can talk to about it. Partner and Family don't understand,  Read More

MS = Multiple Sclerosis or My Savior I choose the latter. Loving yourself as God loves us-unconditionally-is what helps us not to blame or shame ourselves for the diagnosis of what the flesh says, "It's all my fault...if only...why, why,why?" and so on. I believe the acronym "MS" can become, to those of us… Read More

I have received two connections requests that appear to be suspect, please contact me so I may give you the info. Has any other woman recieved connection requests trying to connect through other means than her a ms connections, if yes please add your name as a reply, thanks. Read More

Hey there guys,My name is Robert Welsh. I’m 29 years old and currently being treated for my first big flare up of ms at swedish medical center in denver. I don’t have a 100 percent diagnosis as of yet but should shortly. My symptoms started in my hands with numbness in every digit and progressed to lhermittes… Read More

I would very much like to remarry. I have been divorced for over 3 years, but with fatigue it is difficult to get out and actually be in places where my Knight in Shining Armor might be. I work a full time job and still have to do the day to day stuff that has to be done to maintain my dwelling place and me. I… Read More

 Hi fellow MS family and friends! I have been battling MS for 10 years now and in the beginning, when I was on Copaxone, I was able to work out for 45 minutes every day… Now that I am on Tysabri for the last eight years I no longer have the stamina to work out  and I have gained a fear of over doing it. My… Read More

How many of you experienced this intimacy issue from your significant other (wife/husband) and what did you do about it?   Read More

For me, I’ve found a love for poker.  It’s a game that challenges my mind, not my body.  It combines my strengths – psychology, math, chess, etc.  Not only is it great fun, but very social.  I have found that there are local live home/bar games everywhere/every night.  If I want to play and not go out, there… Read More

Ok so been put through nothing but b.s. from my so called family to my so called friend's. All they have done is mess with my head. They even had my abusive x stop by. I hate every single one of them. They've been stalking me talking trash about me and just doing everything in there power to try and get me to… Read More

I have been living with MS now for almost 20 yrs. I love my coffee in the morning. I was told when I was first diagnosed that coffee would help with the fatigue. I am trying to be more aware of what I put in my body. I have been told now that I should not drink coffee. What do you think? Read More

I have a mom, a nurse no less, who just doesn''t "get" that cognitive impairment is real.  Whether its not being able to focus and cook with noise and other people around or difficulty in dealing with too much stimuli.  It's a "mental block" or being silly.  After having her falsetto-mimic my request for being… Read More

I’m not sure if this falls under daily life or not.  My mother has MS. 20 years now. In February she had a urinaly infection and the doctor she saw never looked at the result and a week later ended up in the ER. She has since gotten much much worse. She is to the point of needing assisted living and I’m not… Read More

I have attempted to make this post a couple of times. But hopefully I got it this time. I am terrified of summer heat, I tend to have additonal MS symtoms in the summer time and I have constantly been told to stay cool, but i feel like a captive in my own home. I still work but feel so weak during this time of… Read More

There is a very good and simple to understand web site - Everyday Health.com - type in multiple sclerosis and you will find many articles about MS (ie: how to find a good MS neurologist, questions to ask, etc).  Of course they also have information about other diseases and medical conditions. Read More

Finally I have not one but two worker's. That way I know that I'm taken care of right. I have to thank God for it. I know that my family isn't happy because they've been trying to destroy my life. They've harassed me and neglected me then tried to convince me that if I went in for my back surgery I'd be… Read More

I was supposed to meet with this lady and my social worker at the nursing home at 12 but then she came at 10 and Maria knows how I've been saying I've been being gas lighted or stalked. Now this has gone on for 3 years. So about 2 months ago a realtor sent me a text with his card. Then the woman who came was… Read More

My memory is probably my worst symptom.  Having so many App choices, is there one that MS folks have found especially helpful in remininding them of either important meetings, to-do lists, dealing with their MS, etc? Thanks. Read More

Ok so after I fired my nephew he got mad and told me that I didn't give a crap about him nor my great niece's. And he said that he spent $1500 n my house and wanted it back. Then demanded it then said he was taking the title to my truck until I paid him. I don't mind him hanging onto something as collateral… Read More

Hi all I'm still stuck in a nursing home. They're aware of what's been happening to me at home in regards to my nephew and then the rest of the family gang stalking me to neglecting me as well as the neglect and bullying and being taken advantage of. See before it was just little ol me. Then my friend Peter… Read More

To be honest, I just pray to God that I wish that I didn't have MS. It's just something that I have to deal with on a daily basis. I have to have an aide, my nurse aide is cool. I hate that I've had to fire four aides. Not trying to be depressing but if you want to be my aide, come to work. My back does bother… Read More