Jeny,
Thank you for responding to my question. I wondered if I was the only one.
I used to be like JJ-but too much has happened since my diagnosis. I live in constant nerve pain. I can't leave the house. And now, with the latest diagnosis of Lymphocytic colitis, and the fact that it is chronic, it's hard to feel upbeat.
I don't want an anti-depressant, because I already take too many medications.
I agree-MS really does bite. It's very hard on families.
Sheila
I too feel like I over react when everything isn't perfecto at home. I have 3 kids ages 14, 11, and 9. So that can be stressful! Lol. And yes....our poor husbands take a brunt at times. I really wish I could be more like you JJ! I try my best to. I think positively but just get angry or worry very easily.
I taked with the neuro about this wondering if I should ake an antidepressant to help calm me down some. I'm afraid all this stress I put on myself is causing my MS to worsen. I ant be good :(. I just don't want to have to take the medicine because I know I'm not depressed...just a little OCD. Lol
This disease bites and hate that my family has to suffer too.
Jeny
I have MS "without visible lesions", so I can't address stress related to lesions, but we all have stress in our lives.....some of us, more than others.
And I feel your doctor isn't taking you seriously.
And I agree with you, stress does worsen MS.
I've had MS exacerbations after stress.
When I told my MS Specialist in February, that I was depressed, felt overwhelmed, she offered me a prescription for an anti-depressant, and as she wrote the 'script, she smiled and said, "And your problems are bigger than everyone else's?"
I feel the same way.....like giving up. I developed Lymphocytic colitis, I'm down to 74#s, and my MS Lifelines nurse came out a few weeks ago, and I have limited areas of fat that I am allowed to inject.
So, I have two weeks left of the new Rebidose injector, and I don't know if I will continue. I told Accredo to put my refills on hold, until I see my MS Specialist at the end of June.
I think I'm sorry I was ever diagnosed.
Well my doctor is blaming my stress for the lesions... I know that stress can worsens MS but I dont think it can cause lesions :(
i am on the verge of giving up .. i dont want to know whats wrong anymore :(
Tracy,
I feel the same way-very little patience. And I am very emotional.
Stress is also a very huge part of my life, and I agree, it is a factor. You work a lot of hours. So, that makes it even harder.
Sheila
Yes I have found myself to be very emotional at times. Can cry at the drop of a hat. while I have more patience with myself I do not have any patience with others!
Stress is a huge part of my life and I think that is a factor - I was off this weekend - the first one since February and the last till August and found myself in a much better mood, even though I worked around the house harder than I do at my job. Also found that my legs are in better shape today and walking is much easier - Oh to be able to quit the part time job and only work 5 days a week! SIGH!
Tracy