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-   -   It's official (again). I'm diseased! (https://www.neurotalk.org/multiple-sclerosis/62653-official-im-diseased.html)

Gazelle 12-03-2008 02:07 PM

It's official (again). I'm diseased!
 
This doc was great. He listened, was very personable, had a sense of humor, explained things well, and felt that without a doubt it was MS. So I have my dx back. (and he laughed when I told him at the end of the visit that I was afraid that I was going to go down there and end up with him telling me I had a hang nail)

I'm diseased officially (again)!!!!! :yahoo::yahoo::yahoo:
(hmm.... maybe the excited people emoticons are kind of strange considering what I'm happy about)

OH..... and I can sign up for a clinical trial with oral medication Fingolimod (FTY720)!
http://clinicaltrials.gov/ct2/show/N...US%3APA&rank=4


http://www.msclinicaltrials.com/index.html

I'm going to talk to the study coordinator. I'd been on Copaxone since 2005 when I got my dx from my second neuro (Dr. Flip Flop's partner). But the chance to try an oral medication, even knowing that it could turn out to be a placebo, is worth a shot (pun intended) as an alternative to daily injections which I hate.

Off to see about getting a "baseline" MRI done for him.

Snoopy 12-03-2008 03:29 PM

WooHoo!! Congratulations on getting your disease back!

:holysheep: That just seemed soooo wrong :eek:

Well at least you fit in quite nicely here :p

dmplaura 12-03-2008 03:57 PM

Ahhhh, so the cape and staff worked huh? :D

Very big congratulations on finding your disease again! :hug:

Gazelle 12-03-2008 04:25 PM

Quote:

Originally Posted by Snoopy (Post 418992)
WooHoo!! Congratulations on getting your disease back!

:holysheep: That just seemed soooo wrong :eek:

LOL Yeah, it does, LeeAnn. Sort of like saying, "Congratulations! I'm so glad you are disabled enough to get your disability benefits." Huh??



Quote:

Originally Posted by dmplaura (Post 419004)
Ahhhh, so the cape and staff worked huh? :D

Very big congratulations on finding your disease again! :hug:

He was deeply impressed with the cape, but I think the staff, which had a Gandalf head on it which, when tapped, emitted halogen bright beams of light and little sparkly bits floating in the beams probably did it. :p



As long as this doc doesn't leave the facility or stop treating MS patients, I'm going to stick with him.

Kitty 12-03-2008 04:27 PM

Congratulations.....I think. What's the proper etiquette for congratulating someone on their disease? :D Just kidding.....I know you're glad to finally have someone agree with what you already knew.

These doctors could learn a lot from us if they would just listen! :rolleyes:

CayoKay 12-03-2008 05:30 PM

Quote:

Originally Posted by Gazelle (Post 419015)
He was deeply impressed with the cape, but I think the staff, which had a Gandalf head on it which, when tapped, emitted halogen bright beams of light and little sparkly bits floating in the beams. :p

if only I could get my Gandalf to do THAT !!

he just makes noise:


honk honk, WHEEEEEEEEEEE!! honk honk, WHEEEEEEEEEE !!


hey, can you take the Fingolimod in ADDITION to the Cop?

hey, I'm so old I remember when it was called Cop1.

to differentiate it from Cop2 and Cop3, other versions of Glatiramer Acetate they were trying out in the clinical trials back in '94 and '95.

so, "At Ease! Stotty!"

don't be un-easy, your dis-ease is in fine form, and we're here to celebrate the resurgence of your diseasement.

:grouphug:

tkrik 12-03-2008 06:00 PM

YIPPPEEEE!!! I am so glad the 3rd time was a charm. I am also glad you liked the dr and he had a sense of humor.

dmplaura 12-03-2008 10:07 PM

Quote:

Originally Posted by Gazelle (Post 419015)
He was deeply impressed with the cape, but I think the staff, which had a Gandalf head on it which, when tapped, emitted halogen bright beams of light and little sparkly bits floating in the beams probably did it.

So.... I hope you didn't cause him Optic Neuritis or something. :holysheep:

JoeMac 12-03-2008 10:49 PM

Happy to hear that the 3rd time WAS the charm Gazelle! Great to hear, and it is SO refreshing to get a doc that actually LISTENS and makes you feel GOOD when you leave the office, it helps us SO much more when we know our docs are like that.........This disease is just TOO crazy and we really NEED that in a doctor.........

I am happy that you have finally found your guy.........:)


Joe



Quote:

Originally Posted by Gazelle (Post 418948)
This doc was great. He listened, was very personable, had a sense of humor, explained things well, and felt that without a doubt it was MS. So I have my dx back. (and he laughed when I told him at the end of the visit that I was afraid that I was going to go down there and end up with him telling me I had a hang nail)

I'm diseased officially (again)!!!!! :yahoo::yahoo::yahoo:
(hmm.... maybe the excited people emoticons are kind of strange considering what I'm happy about)

OH..... and I can sign up for a clinical trial with oral medication Fingolimod (FTY720)!
http://clinicaltrials.gov/ct2/show/N...US%3APA&rank=4


http://www.msclinicaltrials.com/index.html

I'm going to talk to the study coordinator. I'd been on Copaxone since 2005 when I got my dx from my second neuro (Dr. Flip Flop's partner). But the chance to try an oral medication, even knowing that it could turn out to be a placebo, is worth a shot (pun intended) as an alternative to daily injections which I hate.

Off to see about getting a "baseline" MRI done for him.


lady_express_44 12-04-2008 05:39 AM

Well I'm glad you finally have someone who is willing to put a label to it so you can at least start fighting the battle. Sorry to hear it's MS for sure though. :hug:

Cherie


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