Ms symptoms in men

Common Questions and Answers about Ms symptoms in men

multiple-sclerosis

Avatar f tn Hi! I had come across an article that basically stated that men with MS may benefit from testosterone therapy. Have you heard much about this and in what ways could it be of benefit?
211940 tn?1267881266 burning sensation, pain in back and sides, having to frequently go (for a trickle), extremely cloudy urine (orangy-yellow, and very "rank" smelling) Any other, "home remedies" any of you may know of, that I haven't tried yet? Typically, my UTI's last 1-2 days, not 3 weeks.
Avatar m tn I'm not sure where your getting your information from but contrast basically just identifies the active demyelinating lesions from the non-active lesions. New or still active lesions enhance and light up with contrast but old or non-active lesions don't.
Avatar f tn Thanks everyone. I figured I could go out for a couple of minutes, but quickly realized ms or no ms I couldn't stay out in that heat. Thanks for the replies. I thought it might be something you all had experience with.
Avatar n tn Last saturday, my 12 year old daughter complained that her left cheek developed a "cracking" feeling, and began to hurt. Her opposite cheek began to hurt a minute later, and then her nose went numb. Within 5 minutes, she was fine. It happened again later that night. The following day, sunday, she complained about her cheeks going numb or hurting a couple of times throughout the day. She described the numbness as feeling like she doesn't have a cheek.
Avatar m tn Uti's are common in women, but not so much in men. Only about 3% of all men worldwide get UTI's. You are part of that group. Hopefully antibiotics will clear it up and you'll not have to worry about it again. https://www.medicalnewstoday.com/articles/320872.
Avatar m tn My PCP states that he is not worried about MS at this time. He states that it is not that common in men my age and does not feel my symptoms are compatible with MS (no optical problems, no walking issues). At this point he does not want to refer me to a neurologist. I am not worried about ALS, but i am concerned about possible MS. Questions: 1. Does this presentation sound like MS? 2. Do you think a neurological eval is warrented at this time?
Avatar m tn Can i as if anyone knows if there is any possibility of damage to my thyroid from MS. I ask because i have long standing MS symptoms including muscle aches in arms, hands and legs along with severe and permanent loss of sensation in my thighs. My question is really concerning the likelihood a thyroid disorder. I am finding it very, very slow to shift my excess weight. I follow a strict diet and exercise program and over a six month period the weight is moving but very slowly.
Avatar f tn Could it be true the men actually have your pregnancy symptoms as well?? My boyfriend now complains about nausea, heartburn, and fatigue now that I'm pregnant. I laugh at him but he takes it quite serious. Could it really be real?
Avatar f tn my partner was diagnosed with MS in March this year. He is now suffering from urine retention and unable to perform sexually. My question is..
1168718 tn?1464983535 Single lipomas occur with equal frequency in men and women. Multiple lipomas occur more frequently in men.
Avatar n tn what are the first symptoms in men and when do they show after being infected?Few days, weeks,months?
Avatar m tn It will take a neurologist to diagnose MS. No test rules it in or out. Neurologists Specialize so I would get a MS Specialist to begin with. It can take awhile because they are busy. Most good neurologists take awhile to get an appointment. The one I have too 8 months and I was already diagnosed. Your PCP can do a neurological exam that is reflexes, following the finger and such. My PCP did one and found it to be very abnormal pointing to MS. She sent me to a neurologist.
1054985 tn?1257173275 I had my first episode which involved tingling in the left side of body and vision problems. Those symptoms have yet to come back,its been 5 months. However I seem to be twitching more (toes, legs, head, fingers, torso...), I am very tired, have bits of depression. Are these symptoms or just the disease itself? I guess the question is this an episode or just minor things that MS cause. Is a person with MS tired all the time or just during episodes?