Re: Capaisin

[Guest guest]

That is interesting that capaisin is a pain killer. A couple years ago I tried cayenne pepper to help with numbness in the extremities. The pepper is supposed to help circulation and warm up the fingers & toes. It didn't help with the numbness but it did seem to aggravate the L'Hermitte's sign in my neck.

Anyway, it seems that something like capaisin might aggravate pain.

--Mr. Dana F. Utz utzdana@... https://home.comcast.net/~utzdana/

[Guest guest]

SEE.i have wayyyy to much in common with ms.Why can they not just find something

already?I really hate this.Im so sorry you have to deal with the skin

sensitivity to.Theres nuthn fun about that.Big hugz,cassy

[akyba@...] wrote:

I get skin sensitivity too, sometimes it is like a hot/cold reversal...my

arm might tough the wall, which I KNOW is cold, but it feels like fire and I

ll jump like I've been burned. The LDN has helped, it used to be much worse.

..like if Robbin came up and touched my arm it HURT!

Just more MonSter fun I guess...

Hugs

Akiba

-- Re: Re: Capaisin

Thanks for sharing Dana.It aggrates my skin.One of my newest symptoms has

been skin sensitivity.Usually from light touch,clothing,bedding.Sends me

into spasms and jerking.Well this stuff burns the crap out of my skin.For

hours,then it eases up a little and burns like I just put it on.My doc had

meutting it on my hips,so when I went to sleep (I can only sleep on my side)

so the normal pain I have in my hips was way more then it was on top of the

burning.Who knows maybe it was aggravating the nerves.hugz,cassy

[utzdana@...] wrote:

That is interesting that capaisin is a pain killer. A couple years ago I

tried cayenne pepper to help with numbness in the extremities. The pepper is

supposed to help circulation and warm up the fingers & toes. It didn't help

with the numbness but it did seem to aggravate the L'Hermitte's sign in my

neck.

Anyway, it seems that something like capaisin might aggravate pain.

--

Mr. Dana F. Utz

utzdana@...

https://home.comcast.net/~utzdana/

[Guest guest]

Do any of you get the feeling of chills anywhere on your body? I've had this before, and I've had it 3 days this time. Before it would start at my right thigh and go down. This time it starts from my head and goes down. It's really unpleasant. Forgive me if I've already asked this. I'm in a funk the last few days, and can't think straight.

Hugs, Trista~*~*~*~*~*~*~*~*~*~*~*April is Autism awareness monthSome disabilities are invisible.

Re: Re: Capaisin

SEE.i have wayyyy to much in common with ms.Why can they not just find something already?I really hate this.Im so sorry you have to deal with the skin sensitivity to.Theres nuthn fun about that.Big hugz,cassy[

..

[Guest guest]

You know I told ya this before that I have this, but I didn't even remember I can't use icyhot or bengay or anything like that. It burns too badAkiba wrote: I get skin

sensitivity too, sometimes it is like a hot/cold reversal...my arm might tough the wall, which I KNOW is cold, but it feels like fire and I'll jump like I've been burned. The LDN has helped, it used to be much worse...like if Robbin came up and touched my arm it HURT! Just more MonSter fun I guess... Hugs Akiba -- Re: Re: Capaisin Thanks for sharing Dana.It aggrates my skin.One of my newest symptoms has been skin sensitivity.Usually from light touch,clothing,bedding.Sends me into spasms and jerking.Well this stuff burns the crap out of my skin.For hours,then it eases up a little and burns like I just put it on.My doc had meutting it on my hips,so when I went to sleep (I can only sleep on my side) so the normal pain I have in my hips was way more then it was on top of the burning.Who knows maybe it was aggravating the nerves.hugz,cassy[utzdanacomcast (DOT) net] wrote:That is interesting that capaisin is a pain killer. A couple years ago I tried cayenne pepper to help

with numbness in the extremities. The pepper is supposed to help circulation and warm up the fingers & toes. It didn't help with the numbness but it did seem to aggravate the L'Hermitte's sign in my neck.Anyway, it seems that something like capaisin might aggravate pain.--Mr. Dana F. Utz utzdanacomcast (DOT) net https://home.comcast.net/~utzdana/ ' in Texas Courage is not being fearless, courage is facing your fears and not running for cover!

[Guest guest]

I cannot use icyhot or bengay either for this reason.About a yr.ago I was using

those OTC skin patches so much that I had scars from were they were either

burning my skin or taking the skin when i took them off.Same with my tens unit,I

used it so much that it was scared.The numbness in my back is bad and i have to

crank it up high to feel it.I had to stop both for awile.Then when I tried the

patches again it burned like hell it felt like my skin was literally on

fire.Havnt used them since.The tens hardly works anymore.If i touch it with my

finger it shocks the crap outa me.lol.then if i do my back I cant feel it.What a

life.Hugz to all,cassy

[dixmstx@...] wrote:

You know I told ya this before that I have this, but I didn't even remember I

can't use icyhot or bengay or anything like that. It burns too bad

Akiba wrote: I get skin sensitivity

too, sometimes it is like a hot/cold reversal...my arm might tough the wall,

which I KNOW is cold, but it feels like fire and I'll jump like I've been

burned. The LDN has helped, it used to be much worse...like if Robbin came up

and touched my arm it HURT!

Just more MonSter fun I guess...

Hugs

Akiba

-- Re: Re: Capaisin

Thanks for sharing Dana.It aggrates my skin.One of my newest symptoms has

been skin sensitivity.Usually from light touch,clothing,bedding.Sends me into

spasms and jerking.Well this stuff burns the crap out of my skin.For hours,then

it eases up a little and burns like I just put it on.My doc had meutting it on

my hips,so when I went to sleep (I can only sleep on my side) so the normal pain

I have in my hips was way more then it was on top of the burning.Who knows maybe

it was aggravating the nerves.hugz,cassy

[utzdana@...] wrote:

That is interesting that capaisin is a pain killer. A couple years ago I tried

cayenne pepper to help with numbness in the extremities. The pepper is supposed

to help circulation and warm up the fingers & toes. It didn't help with the

numbness but it did seem to aggravate the L'Hermitte's sign in my neck.

Anyway, it seems that something like capaisin might aggravate pain.

--

Mr. Dana F. Utz

utzdana@...

https://home.comcast.net/~utzdana/

' in Texas

Courage is not being fearless, courage is facing your fears and not running

for cover!

[Guest guest]

Lol.but wed prbobly get dx'd.Sad but true.My moms fiance is bi-polar and has

been commited a few times.They treated him so good,and guess what they also dx'd

him,and sent him to a good back doc! I TALKED to the reumatologist.She couldnt

believe they were still trying to say fibro was a possibility so she already

sent me the letter saying its not.She asked if he took her recomendation for a

muscle biopsy for MD and others.I told her they threw that out the window and

didnt even consider it.She couldnt believe it,she said once again they just dont

want to dig.She said it is just ridiculous what im going threw and I can always

come back to her but she is sure it is a neuro problem.Its nice to know someone

is on my side.Her and my pcp is all I got,if it were up to the others I would be

severly depressed with mania or something and it would all be a figment of my

imagination.lol.Even though now they see the funky stuff my legs do I still get

noooooo answers.I can only hope and

pray for us.Big hugz, cassy

[tabeloe@...] wrote:

We'd be committed. lol.

Hugs, Trista

~*~*~*~*~*~*~*~*~*~*~*

April is Autism awareness month

Some disabilities are invisible.

Re: Re: Capaisin

OmG! They treated you on planiquil without knowing for sure?Well im sure if

you sued you'd get a dx.lol.I am currently trying to get a pt advocate,of course

my ins. Company dosnt have them so I have to search. I really am thinking

about getting a lawyer.As quickly as im progressing it scares the crap outa me.I

cant risk waiting for them to decide they should keep digging.I havnt even been

treated specifically for depression/anxiety but they still say I am.Im like WTH!

Ok you keep telling me what I am and what im not wile I get sicker and sicker.I

have kids,a family,a life,and ill be damned if I lose it due to there negligence

or failure to believe my symptoms.There has got to be more options for us.What

if we did a website do you think there would be docs out there kind enough to

help us.Just a dreamie thought.I hate that there are so many of us in the same

boat it breaks my heart to know my friends are goin threw the same BS as me.I

hope you get answers,dont give up.Big

hugz, cassy

[tabeloe@...] wrote:

All I have to say is that it seems like doctors these days are afraid to think

outside of the box, or call it like they see it. If it's written in a medical

journal that you have to have 1 sx from column A, and 2 sx's from column B,

that's all there is to it. (rolling eyes) It cracks me up, that people seem to

think we know it all, because it's 2007. If the Dr. can't figure it out, then it

must not exist, or it's all in your head, and off to psych you go! Gee, can you

tell I'm disgusted? That is why I am currently not seeking a dx. Because every

time I do, I get discouraged. I KNOW this is real.....

[Guest guest]

I'm full of wierd sensations!!!LOL Started my nerve studies today, did my hand then the computer froze. Dr. said to send me back to my room, I wasn't going anywhere soon. I like here she is keeping me here until they figure out what kind of MS it is 'cassandra workmn wrote: I have so many weird sensations,i finally gave up on telling the docs about everything cuz

half the time they act like im crazy and the other half the time they dont have a clue.lol..My pcp is pretty good even if he dosnt know he tries to give me an explanation.lol.The pt I just seen said that it has sumthn to do with the nerve impulses and when they are interupted they travel differently causing weird feeling sensations or sensitivity.One of our nurses here would probly know a lil more..CALLING ALL NURSES! HELLO...LOL.?anyone?Did you ask your doc?Hugz, cassy[tabeloecharter (DOT) net] wrote:That's interesting. I'd love to hear my doctor's explanation of what might be causing it. lol. Have you ever asked your Dr. about it? Hugs, Trista~*~*~*~*~*~*~*~*~*~*~*April is Autism awareness monthSome disabilities are invisible. Re: Re: CapaisinSEE.i have wayyyy to much in common with ms.Why can they not just find something already?I really hate this.Im so sorry you have to deal with the skin sensitivity to.Theres nuthn fun about that.Big hugz,cassy[Recent Activitya.. 3New Membersb.. 18New Photosc.. 1New FilesVisit Your Group

[Guest guest]

Oh sweetie I wish I could help! I hate that you're going through this. I'm having a few cognitive problems but nothing like what you're going through Hugs Akiba -- Re: Re: Capaisin I'm full of wierd sensations!!!LOL Started my nerve studies today, did my hand then the computer froze. Dr. said to send me back to my room, I wasn't going anywhere soon. I like here she is keeping me here until they figure out what kind of MS it is 'cassandra workmn <payngabby72> wrote: I have so many weird sensations,i finally gave up on telling the docs about everything cuz half the time they act like im crazy and the other half the time they dont have a clue.lol..My pcp is pretty good even if he dosnt know he tries to give me an explanation.lol.The pt I just seen said that it has sumthn to do with the nerve impulses and when they are interupted they travel differently causing weird feeling sensations or sensitivity.One of our nurses here would probly know a lil more..CALLING ALL NURSES! HELLO...LOL.?anyone?Did you ask your doc?Hugz, cassy[tabeloecharter (DOT) net] wrote:That's interesting. I'd love to hear my doctor's explanation of what might be causing it. lol. Have you ever asked your Dr. about it? Hugs, Trista~*~*~*~*~*~*~*~*~*~*~*April is Autism awareness monthSome disabilities are invisible. Re: Re: Capaisin! SEE. i have wayyyy to much in common with ms.Why can they not just find something already?I really hate this.Im so sorry you have to deal with the skin sensitivity to.Theres nuthn fun about that.Big hugz,cassy[Recent Activitya.. 3New Membersb.. 18New Photosc.. 1New FilesVisit Your Group