I was recently diagnosed with MS at age 27 and have not dealt with it in the proper way yet. I occupy my time and thinking with 2 jobs and school and so I have limited time to think about it. The only time I do think about it is on infection nights. I believe that because Ive had these pains for so long and was misdiagnosed many times that this disease has become part of my life in which I block out. I feel alone in which noo one understands and has their own opinions but are not supportive. My question is how do I get to that point of acceptance so that I can to something about it other than just taking medications? Also what are other things can I do other than the meds?
Posts You May Be Interested In
I was diagnosed with Epilepsy when I was 10. I am currently 20 years old am at a point in my life where I am starting to lose hope on having my seizures controlled because throughout my life I have tried multiple medications but the ones that worked my body used to and then would stop. The longest Ive been free of them was only 5 months. Im trying to find something in my life truly worth living...
I miss traveling with my husband. Has anyone found a specific site regarding cruising for widow/widowers or any sightseeing trips. Not interested in being with couples and kids,,,I realize a cruise ship will have a portion size of families and couples, but perhaps they also put together a part of the cruise ship for groups of widows/widowers????