Multiple Sclerosis (MS) Support Group
This community is a place where members can discuss current events and weigh in on what's going on in the world.
This community is a place where members can discuss current events and weigh in on what's going on in the world.
You falling are very concerning. Have you mentioned this to your doctor? Have they seemed concerned about why you fall? I would fall, just seemed like my legs were not there anymore and fall. That was one of my first symptoms that scared me. Please think about mentioning them to your medical team.
I'm currently seeing a new neurologist and getting a second opinion about everything. I've had MS symptoms for years now and have been to my neurologist repeatedly but he always just increased my anti-convulsants. I finally got my PCP to give me a new referral because even she was starting to get convinced that it might not be epilepsy at all.
I am having to use my phone to answer. It doesn't work like my computer as far as being able to answer each one of you personally becuz it only shows my post. However I know what you guys have said so I will try my best.
I do wonder sometimes about seizures since the eye thing is so uncontrollable and no matter how hard I try I can't make it stop.I heard from the neuro office today. They want me to see a general neuro first before I see the MS specialist. The neuro said that I do have symptoms of MS he needs to have something more concrete. I don't want to see the neuro he referred me to. I told his assistant this becuz I am afraid of neuros due to the one who made me feel like a fool 4 years ago. She told me I could see my regular doc and tell him all my symptoms and get an MRI of brain and spine. If they showed lesions then I could call her and she would talk to the doc and get me in to see him. So hopefully things will work out.
I can tell you that it does make me feel a little better to know that what I experienced was most likely warning signs. With you guys describing yours...well they definitely sound similar. I know I should have gone straight home after church yesterday to rest. I chose to ignore the extreme fatigue I felt right after spending 15 minutes fighting with all I had to keep my eyes open. But I went out shopping and came home and cooked a big meal. Well I woke up today feeling like death warmed over. I felt all over sick. I was extremely fatigued, muscles hurt all over my whole body..not just left side. Left side lymph node under jaw was swollen again ribs right under breasts were and still are very achy. Had to stay home instead of going shopping with my mom, aunt and cousin. At least I was able to rest...feeling somewhat better but toes are having a danceathon tonight and it is making my front of my feet hurt, left knee and hip hurtingand my legs and feet are moving to their own beat.totally can not control this either. vicodin helped earlier so I might take another one in a bit. all this waiting for docs is gonna turn me into a junkie!!
Thanks all of you for taking the time toanswer my post and share with me....Irish
Oh yea, I get that all the time. As soon as the weird warm feeling starts I try to get to a sitting position because I have no idea what the end result will be (fainting, falling, sudden exhaustion etc). After panicing a few friends and family and having unnecessary amulances called, I have learned to warn people that if I suddenly sit down to just leave me be for 20 minutes and don't call 911.
WOW! I am happy that you feel the same exact thing! I mean I am not happy that you have to suffer through it...but it makes me feel justified because this happened again today right before the eye thing started again. The eye thing started and lasted like 20 minutes and like you, right after I was so exhausted I fell into a deep sleep that lasted for 2 hours.
When the eye thing started I mentioned to my mom and aunt that the eye thing was starting again and my a aunts response was to tel my mom to look at how cute her dog looked asleep on a pillow.And my mom said for me to try not to force my eyes open because it could make it worse. I can't believe how my aunt is acting about this whole thing I am going through especially since I was her biggest supporter when she found out she had a brain tumor and then went through a 7 hour surgery to remove it. Now 2 years later I am still her biggest supporter. Her own kids are not as understanding as I am. Sometimes I get so sick of so called caring family and friends.....thats nothing but a big fat ugly joke!!!
Thank you for the reassurance!...... Irish
I don't blame the people for their lack of understanding, I usually think "I hope I never treated anyone like that back in the day when I didn't know about MS." I figure, they really 'just don't get it'.
I am sorry you are having so many troubles with the issues. I hope you get the dx figured out soon.