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-   -   Neuro appointment today (https://www.neurotalk.org/multiple-sclerosis/47222-neuro-appointment.html)

hollym 06-05-2008 09:55 AM

Yay for you LeeAnn!!! So glad you found some relief. Sounds like your old neuro is a better fit, too.



Uh, DM, I think you're thinking of NEMO, not NMO!

Snoopy 06-05-2008 12:15 PM

Quote:

Originally Posted by hollym (Post 293429)
Sounds like your old neuro is a better fit, too.

He is. I just needed to figure that out the hard way :rolleyes: :D

weegot5kiz 06-05-2008 04:48 PM

glad the meds are helping snoopy,

ok ladies may i ask a personal question, snoopy mentioned hormonal changes, my question is does the monthly visit affect your MS, if so i am sorry about that, and sorry if this is none of my beewaxs, its just something i had not thought of till she typed that.

Snoopy 06-06-2008 07:03 AM

Quote:

Originally Posted by weegot5kiz (Post 293701)
glad the meds are helping snoopy,

ok ladies may i ask a personal question, snoopy mentioned hormonal changes, my question is does the monthly visit affect your MS, if so i am sorry about that, and sorry if this is none of my beewaxs, its just something i had not thought of till she typed that.

Thanks, Frank :)

Frank, You could start a thread and ask your question but the female population may or may not answer ;)

I have known for quite sometime that hormonal changes affect MS but it's always nice to get confirmation from your neuro.

The topic of hormonal changes and MS symptoms come up quite a bit on MS forums but since your a guy you probably don't pay attention to those threads :D

If your interested here is some information on this topic from the National MS society:
http://www.nationalmssociety.org/abo...use/index.aspx

sassy 06-06-2008 07:07 AM

Snoop, I hope the T is what finally gets you some relief.

Pain can be so debilitating.

Snoopy 06-06-2008 07:16 AM

Quote:

Originally Posted by sassy (Post 294027)
Snoop, I hope the T is what finally gets you some relief.

Pain can be so debilitating.

Thanks, Brenda.

You are so right about pain - it can be debilitating and just plain exhausting. And, like many of us, I don't have time for pain to interfere with my days :rolleyes:

Riverwild 06-06-2008 07:34 AM

Glad to hear that you are back to a doc you like LA!

I hope the increase in the Trileptal helps! It's got to suck being in pain all the time :mad: Fortunately, I haven't had to deal with that as a part of my MS ( yet?)

As our Doctor Mary said so succinctly: Better living through chemistry!

ewizabeth 06-06-2008 08:50 AM

That is great news Snoopy!!! :) :hug: :hug: :hug: I remember when I had migraines for so many years, and nothing would touch the pain for me. I was thrilled when Topamax finally helped. I'm off of it now, but at least I know I have something if pain starts to be more of a problem for me again.

I hope it continues to help you for as long as you need it.

RW,

I remember when Mary used to say that. ;) I totally agree!

weegot5kiz 06-08-2008 12:59 PM

thank you snoopy, it only took me 3 days to figure out where I had posted this question,,, egads:eek:,

the link was good too thank you,

hopefully i didnt cross the gender line, its mostly woman here and I respect a lot of you more than you all will know. lots of you have had this illness longer or dealing with more disabilities, and yet your senses of humor, are beyond belief, i just really admire a lot of you all on here, many a time the smile on my face was put there by something one of you Ladies have typed, thanks, and if i did cross that line just let me know i wont pry,


peace


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