always something new with MS: dealing with... - My MSAA Community

My MSAA Community

9,440 members21,224 posts

always something new with MS

Suzipoohbear profile image
14 Replies

dealing with transgeminal neuralgia at the moment.

Written by
Suzipoohbear profile image
Suzipoohbear
To view profiles and participate in discussions please or .
14 Replies
greaterexp profile image
greaterexp

I’m so sorry. What are you doing for it?

Peruzzot profile image
Peruzzot

Hope you're feeling better soon.

RoyceNewton profile image
RoyceNewton

Umm what is that?

PWilli profile image
PWilli

I'm so sorry. I hope the pain is controlled or at least lessened. Hope you feel better soon!

Pam

BettysMom profile image
BettysMom

trigeminal not transgeminal

Oh, I hate that! Hope it goes away quickly!

jimeka profile image
jimeka

Ouch, painful, hope the pain killers work.

jennie62 profile image
jennie62

I hope you have the right med to keep the pain at bay. My neuro prescribed Oxtellar for me and it sure helps-unless I run out then it comes back quickly! Sending hugs and prayers your way. Hope you are pain free!

Jennie62

erash profile image
erash

Sending healing thoughts 🙏

I have TN (trigeminal neuralgia) after yrs of tegretol, I had gamma knife surgery that has been effective for the past 5+ yrs

Wishing you wellness

janetb1968 profile image
janetb1968

That sounds awful xxxxxx ❤️

hairbrain4 profile image
hairbrain4

Prayers that you feel better soon!

lbenmaor profile image
lbenmaor

I will pray that you feel better.

Warmly,

Leslie

Taylorsmom profile image
Taylorsmom

Hi Suzipoohbear ! I'm so sorry that you're going through this, I just had to Google it because I had no idea what it was. Is this something new for you?

Suzipoohbear profile image
Suzipoohbear

I haven't been on here for awhile. Still dealing with the transgeminal neuralgia. My dose of Gabapentin has been increased a couple of times. Of course, with this pandemic thing I have not been able to see my cardiologist nor my neurologist...so cannot look into any other treatments. I hope this shutdown ends soon....I even have a half completed root canal that was stopped due to the darn shutdown, so I am eating even more carefully. All I can say at this point is ARGHH!

Not what you're looking for?

You may also like...

Always something new with MS...

So recently I've noticed that I startle with loud sounds more than usual. I looked into this and...
erash profile image

Remember…it’s not always MS

For 2 months I kept telling myself that the reason I was feeling so bad was because of my MS. I...
Amore55 profile image

New community member with new MS memoir

Hi everyone! I was diagnosed with MS in 2009 after developing dizziness, visual changes, and taste...

New MS DMT

Hello everyone, I found out yesterday about a new DMT called kesimpta (ofatumumab). Like Ocrevus it...
Allen5280 profile image

Convinced I have MS but diagnosed with something else

Hi, At age 27 I went to the neurologist after having strange symptoms for about a year. I...

Moderation team

See all
johnMSAA profile image
johnMSAAPartner

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.