Sometimes dealing with MS is just too much to cope with. I try to keep going, put it on the sidelines best I can and live my life. The last week has just been a lot. Results of my MRI shows moderate to severe arthritis with effusions/cysts in both hips (from steroids). So on to an orthopod for treatment recommendations. Yesterday went for urology studies and they were cancelled because I have another UTI ( second in two months and never had one before that). Back on antibiotics and more studies next week. Then yesterday afternoon was called to tell me that my sleep study shows I have sleep apnea now and have to use cpap mask. Being fitted Monday. My walking is getting progressively worse, stairs are scary.
It seems like all of a sudden things are getting worse at a fast pace. Steroids I had recently did nothing. so many different systems of my body are being affected.
Has this been anyone else's experience? Has it continued at this pace or slowed down again? Have symptoms lessened like when you have a relapse? I've had bad relapses and come back to almost baseline over time but this feels different from that, more a steady decline. It's scary.
Only good part is that I can now get reapproved for Modafinil since I have confirmed sleep apnea. My insurance has been denying appeals since the beginning of the new year. My fatigue is so much worse without it. Trying to see something positive in all this.
** Moderator's note - Spacing added between paragraphs for easier reading. Many people with MS have visual difficulties that prevent them from reading large blocks of print. **
It seems like all of a sudden things are getting worse at a fast pace. Steroids I had recently did nothing. so many different systems of my body are being affected.
Has this been anyone else's experience? Has it continued at this pace or slowed down again? Have symptoms lessened like when you have a relapse? I've had bad relapses and come back to almost baseline over time but this feels different from that, more a steady decline. It's scary.
Only good part is that I can now get reapproved for Modafinil since I have confirmed sleep apnea. My insurance has been denying appeals since the beginning of the new year. My fatigue is so much worse without it. Trying to see something positive in all this.
** Moderator's note - Spacing added between paragraphs for easier reading. Many people with MS have visual difficulties that prevent them from reading large blocks of print. **
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