Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS)


advertisement
Reply
 
Thread Tools Display Modes
Old 12-15-2006, 02:18 PM #1
RSD_Angel's Avatar
RSD_Angel RSD_Angel is offline
Member
 
Join Date: Oct 2006
Location: Greene, NY
Posts: 153
15 yr Member
RSD_Angel RSD_Angel is offline
Member
RSD_Angel's Avatar
 
Join Date: Oct 2006
Location: Greene, NY
Posts: 153
15 yr Member
Default Ok questions ot all us RSD'ers

ok.. as you all know or might not know for the past going on 2 mos, i have been having bad vertigo spells.. they have gotten better and dont last for weeks this time, but i still get them for no reason. I went to my ENT thinking that its because of my menieres and he said nope that it could be migraine related(dont have head pain , or head aches with pain but didnt question him) he sent me to a neurologist and he did a CT (wanted an MRI but cant bc of the stim's) and saw him yesterday, and said normal ct, dont know whats going on, I dont need to see you agian , unless these get worse again.

I left there balling my head off. The nite before the appt, i had a bad spell.. i was up till 2 with my foot bc it was hurting so bad adn i had my head in my pillow watching a lifetime movie and all of the sudden the tv started so pull... like it was rubber and the colors were streching too... and i still have that funky feeling in my head . He didnt seem to care or think it was anything... i called my mom on my cell and she was like WHAT.. and i was like, mom im not making this **** up .. i dont want these, why would i be seeing freekin docs and having to leave concerts bc of these.. grrr... ok before i start crying again.

I see my PCP on monday to see what he thinks now that the neuro doesnt want to see me again and wishes me luck.

Do any of you guys have this and its been related to your RSD or could this be MS?? I have bad eye pressure when i get the spells and have to push on my temples., and blurry vision and cant concentrate... ?? Not the typical vertigo spells i normally have with my menieres. They just go away after the dizzy spell or the meds works. With these ones, they linger and the meds DONT work at all!

HELP!! I cant handle the unpredictibility of these and RSD too!!

Thanks!!

Amber

PS.. good news.. is I got a 93 and exempt from taking the final in my College Statistical math class !! )
RSD_Angel is offline   Reply With QuoteReply With Quote

advertisement
Old 12-16-2006, 12:31 AM #2
allentgamer's Avatar
allentgamer allentgamer is offline
Senior Member
 
Join Date: Sep 2006
Location: Toon Town USA
Posts: 1,023
15 yr Member
allentgamer allentgamer is offline
Senior Member
allentgamer's Avatar
 
Join Date: Sep 2006
Location: Toon Town USA
Posts: 1,023
15 yr Member
Default What a bummer

Hi Amber,

I too have the dreaded menieres, and get the spins from it baaaaaad. Only lately I too have been getting the spins, the same kinda vertigo but not menieres. It has to be from the RSD, one of my docs told me that RSD can mess with any nerves in your body, even your hearing

So it is quite possible that is exactly what is happening. I just had the scan also with a neg that it is from menieres. So only thing is left is dental or RSD.

I hope you quit spinnin, and dont spin again for a while. It is one of the most worst helpless feelings in the world. I will be prayin for ya

big hugs
allen

PS: Grats on the 93!!

Last edited by allentgamer; 12-16-2006 at 12:32 AM. Reason: add ps
allentgamer is offline   Reply With QuoteReply With Quote
Old 12-18-2006, 08:55 PM #3
moonstar moonstar is offline
Member
 
Join Date: Sep 2006
Location: brentwood,ny
Posts: 310
15 yr Member
moonstar moonstar is offline
Member
 
Join Date: Sep 2006
Location: brentwood,ny
Posts: 310
15 yr Member
Default Wow!!

I Just Saw An Ent Today Due To Vertigo For Over A Month (i Think) Now And He Saw Nothing Wrong But Is Sending Me For More Tests Next Week..never Thought It Might Be From The Rsd ....silly Me...everything Seems To Be Connected To That.. Have Also Had 5 Min-strokes With No Answers To Why??? All Those Tests I Went Thru Came Out That Nothing Is Wrong Also... I Am Just One Big Mystery To All The Drs I See....so Why Do I Bother??? I Guess For The Hope That One Day I Will Get An Answer And Maybe Some Help For All The Pain That Is Taking Over My Life... Glad To Kknow I Am Not Alone But So, So,so Sorry That Anyone Else Feels The Way That I Do....hugs To Us All.. Maybe Next Year Things Will Get Easier?? Let's Hope So.. Moonstar
moonstar is offline   Reply With QuoteReply With Quote
Reply


Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off


Similar Threads
Thread Thread Starter Forum Replies Last Post
A couple of questions RE: TOS Rachael Thoracic Outlet Syndrome 16 02-07-2007 05:53 AM
Palm Oil questions Lara Vitamins, Nutrients, Herbs and Supplements 4 11-01-2006 05:07 PM
Specific Questions To Ask The Doc?? hideej76 Reflex Sympathetic Dystrophy (RSD and CRPS) 3 10-27-2006 07:06 PM
b12 questions lahgarden Vitamins, Nutrients, Herbs and Supplements 18 10-03-2006 05:32 PM
SCS questions beth Reflex Sympathetic Dystrophy (RSD and CRPS) 11 09-30-2006 10:07 PM


All times are GMT -5. The time now is 08:21 AM.

Powered by vBulletin • Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise v2.7.1 (Lite) - vBulletin Mods & Addons Copyright © 2024 DragonByte Technologies Ltd.
 

NeuroTalk Forums

Helping support those with neurological and related conditions.

 

The material on this site is for informational purposes only,
and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider.


Always consult your doctor before trying anything you read here.