Ladee Empress, you rock!!!! Your husband has no right to call you lazy. Remember that next time he gets a cold & has to stay in bed for a week:) I'm so glad this web site is here, you are the only ones I can turn to and know you understand.
My employer took me out of a job I have been doing for 12yrs and put me elsewhere. They thought it was in my best intrest, right. I was in tears in her office today explaing this new job is to hard/confusing. I need to be in a job that I'm familure with, even my Dr agreed. I told her I was embaressed & humiliated having to ask the same thing over & over again, not to mention all the mistakes I'm making.
I had no problems in my old position. I'm a liablility, it's that simple. The people who are in my old job are terrible, customers complain & they make tons of mistakes. The only difference is they don't have MS!!!! I'm looking to cut my hours & go out on part time disability. Has anyone ever applied for part time disability? Hugs TammyView Thread
Hope everyone's having a great Labor Day weekend & your MS is also on Vacation:) This is a question for those of you who love to fish. I'm an avid fisher WOmen but I find it a lot more difficult these days. I constantly drop things in the water, can barely tie a not & I'm afraid one of these times my whole rod is going to go into the water when I cast:)
I was thinking of tying everything to my vest but that would look pretty stupid. I will have to say I'm still out fishing my husband,LOL Would appreciate any ideas any of you may have. Hugs, TammyView Thread
I get the burns a lot. It is hard to describe to someone who doesn't have MS, but I know exactly what you're talking about. It would be much easier to explain if you could show them a rash or even a little red spot. My feet are a big problem for me. Besides the burning and tingling there are times the pain gets so bad I don't even want to put my feet on the ground cause I know it's really going to hurt. Have you tried Neurotin?
There are so many weird things with this disease. Last night at 3am I woke up with the feeling, like an ant, was biting the back of my leg. I got up, checked the bed & the back of my leg, of course nothing. This lasted about 10mins. Why is it always night when the symptoms seem worse:( You're not alone, I think we can all relate to your symptoms. Hope your feeling better soon. Hugs, TammyView Thread
I'm getting my mri's & seeing my dr in October. I'm getting some pretty serious welts & redness that's lasting 4-5 days. It use to be every once in a while I'd get a welt, now it's every time. I agree about the bee sting feeling:o Thanks for the info. hugs TammyView Thread
I'm at the same point as you. I'm checking into it but no answers yet. Someone told me it takes six months before you start receiving payments & about 2 years before you can apply for medi-cal. What are we suppose to do in the mean time?
I'm on Copaxone & tahts alone is about 10k for 3 mos. What are you on? If I find out anything new I will let you know. Best of luck Hugs TammyView Thread
Sorry you keep relapsing, that sucks. I'm not really driving customers anymore & I'm really getting paranoid driving. I try not to cross the hwy because there has been a few times I didn't notice cars & I've had to slam on my breaks.
My family is great & we just keep laughing. Hope you stay around it's great talking with you. Is there anything they do for Transverse Myelitis? Hugs, TammyView Thread