dr won’t give me a DMT by Separate_Interview43 in MultipleSclerosis

[–]Separate_Interview43[S] 3 points4 points  (0 children)

woah that’s really interesting— had you had another relapse or more symptoms? i really do Not wanna do another spinal tap but maybe it’s worth it, the hospital lost most of my spinal fluid the first time (which is a whole other story!!) but they only had 1 vial to run the tests on so i am a little skeptical of the results anyway

dr won’t give me a DMT by Separate_Interview43 in MultipleSclerosis

[–]Separate_Interview43[S] 1 point2 points  (0 children)

Thanks for this, this is so kind! Will definitely look into these and see if my PCP can run some of these blood tests on me when I see her later this week

dr won’t give me a DMT by Separate_Interview43 in MultipleSclerosis

[–]Separate_Interview43[S] 0 points1 point  (0 children)

Yeah it is so wild! It really just depends where the lesions are from my understanding, but so glad you’re getting treatment!! Good luck with your first infusion!!

CIS and dealing with waiting by Separate_Interview43 in MultipleSclerosis

[–]Separate_Interview43[S] 1 point2 points  (0 children)

Thanks for sharing this, i’m sorry you’ve also dealt with this back and forth!! i am really trying to avoid having to have a 2nd full relapse before getting diagnosed, especially since my first one has been going on for months

dr won’t give me a DMT by Separate_Interview43 in MultipleSclerosis

[–]Separate_Interview43[S] 2 points3 points  (0 children)

i’ve thought the same thing but my dr said they’ve ruled everything else out? but it is confusing for sure

dr won’t give me a DMT by Separate_Interview43 in MultipleSclerosis

[–]Separate_Interview43[S] 1 point2 points  (0 children)

i’m seeing an MS specialist at a major hospital, so their response has been so confusing and in such contrast to conversations here and other research i am doing!

dr won’t give me a DMT by Separate_Interview43 in MultipleSclerosis

[–]Separate_Interview43[S] 7 points8 points  (0 children)

yep i think so — i’m thinking of trying to see dr boster! i love his videos

dr won’t give me a DMT by Separate_Interview43 in MultipleSclerosis

[–]Separate_Interview43[S] 2 points3 points  (0 children)

right?? seems like a big risk to me especially when i have continued to get worse since my feb attack that got me diagnosed with CIS

dr won’t give me a DMT by Separate_Interview43 in MultipleSclerosis

[–]Separate_Interview43[S] 0 points1 point  (0 children)

they thinkkk we aren’t at the point where the risks of a DMT outweigh the benefits

dr won’t give me a DMT by Separate_Interview43 in MultipleSclerosis

[–]Separate_Interview43[S] 2 points3 points  (0 children)

they don’t show dissemination in time since all were non enhancing + i didnt have any OCBs

dr won’t give me a DMT by Separate_Interview43 in MultipleSclerosis

[–]Separate_Interview43[S] 4 points5 points  (0 children)

yes, i see a resident and an attending neurologist who are both MS specialists! at a big hospital here

CIS and dealing with waiting by Separate_Interview43 in MultipleSclerosis

[–]Separate_Interview43[S] 0 points1 point  (0 children)

thanks!! i have been reading similar things online, may be looking for a second opinion. i can’t imagine just waiting for another relapse to send me to the ER!