Going permanently blind in my left eye. That was a hard symptom to miss for me. Sadly was also my very first and initial relapse that led to my diagnosis. Still blind in that eye - I now live in fear of going fully blind. Not sure what I would do with my life if that happened.
I didn't see this email til I decided to go thu unanswered ones to try to lower the large amount of emails in my box. This was a nice video.Thanks for posting. My earliest symptoms of MS were MS hugs and some arm sensory feeling. I didn't think much about these. I asked my doctor what this chest tightening was which i got now and then, he said they were probably muscle contractions-he didn't know. I found out on the internet after I was diagnosed. My first major symptom was Transverse Myelitis. I knew right away what it was. My daughter had this three years previously and she was dx'd with MS. Never occurred to me I would have it also. I was 57 in 2007. Since then. I can't say I have had any other noticeable symptoms. I do have some OAB issues, but as I have aged these have become a little worse. On the other hand I had five children so in isn't so unusual to have these bladder issues. I am 71 now and bladder issues are not unusual either for those without MS. So If you ask what was my last MS relapse, I really cannot say. I get hugs now and then. Not sure they are a relapse. I was on meds for 12 years. and over a year ago I came off them. My MRI show no new lesions. I had no active lesions when I was diagnosed and may have had them a long time but never new. I feel weak now and then but I am not into exercise which is probably most of my problem. I don't know what a definite relapse is.
Lawrence Hofer here I got MS back in 2013 first thing was double vision went to see Lady she was working with our LORDS holly spirit she fixed it next was couldn't walk got LEMTRADA doing monthly blood work to check how my body is doing after getting that deadly drug now I am with lady that's been working with herbs OUR LORDS meds cooking out herbs 1st drink was to clean my body and rebuild now I'm on drink to remilenate my nerves
It's nice to see that I am kind of normal with my MS. That the confusion I sometimes feel is common and I'm not going mad!
You're not alone with that feeling John!
Thank you for this video, it always helps to see and hear other people facing the same struggles and how they deal with it.
You're welcome, Linda. Glad you liked it, do you have any tips for dealing with relapses?
Going permanently blind in my left eye. That was a hard symptom to miss for me. Sadly was also my very first and initial relapse that led to my diagnosis. Still blind in that eye - I now live in fear of going fully blind. Not sure what I would do with my life if that happened.
This was such a helpful film. I was diagnosed Feb 2020 and am so pleased that my confusion over what maybe a relapse is normal. Thank you for this!
Thanks Susan - you're welcome. So glad you found it helpful!
I didn't see this email til I decided to go thu unanswered ones to try to lower the large amount of emails in my box. This was a nice video.Thanks for posting. My earliest symptoms of MS were MS hugs and some arm sensory feeling. I didn't think much about these. I asked my doctor what this chest tightening was which i got now and then, he said they were probably muscle contractions-he didn't know. I found out on the internet after I was diagnosed. My first major symptom was Transverse Myelitis. I knew right away what it was. My daughter had this three years previously and she was dx'd with MS. Never occurred to me I would have it also. I was 57 in 2007. Since then. I can't say I have had any other noticeable symptoms. I do have some OAB issues, but as I have aged these have become a little worse. On the other hand I had five children so in isn't so unusual to have these bladder issues. I am 71 now and bladder issues are not unusual either for those without MS. So If you ask what was my last MS relapse, I really cannot say. I get hugs now and then. Not sure they are a relapse. I was on meds for 12 years. and over a year ago I came off them. My MRI show no new lesions. I had no active lesions when I was diagnosed and may have had them a long time but never new. I feel weak now and then but I am not into exercise which is probably most of my problem. I don't know what a definite relapse is.
What relapse advice would you give? Comment below ⬇️
Lawrence Hofer here I got MS back in 2013 first thing was double vision went to see Lady she was working with our LORDS holly spirit she fixed it next was couldn't walk got LEMTRADA doing monthly blood work to check how my body is doing after getting that deadly drug now I am with lady that's been working with herbs OUR LORDS meds cooking out herbs 1st drink was to clean my body and rebuild now I'm on drink to remilenate my nerves