Jump to content
RemedySpot.com

Re: new mewmber JO

Rate this topic


Guest guest

Recommended Posts

Hi Jo, I am also a new member, just diagnosed. My experience sounds

soumething like yours. I also have 2 other immune diseases and I was

on pred. when my ear began to swell, turn bright red and was very

painful. Felt like a nerve ending in pain. It really hurt when I

forgot and put the telephone up to that ear. They could not find

anything wrong with it, so in about a week it went away. Then it began

to hurt each day, no swelling, just pain. Finally I went to an ear

doctor and he diagnosed it RP. but with no biopsey. Seeing as I had

been on pred and still remain on it, I felt it was helping my ear not

to be so painful. So far it has not spread, except my ribs are

beginning to hurt, don't know if that is related or not. I also

belieave that the exercises are the best. I go to the gym every other

day for weights and leg exercises plus walking each day. Of courseit

is also for my " Termporal Arteritis and Polymylagia " that I have. I

feel the RP was caught very early and am thankful for that.

I hope you are feeling better and I know this support group will help.

Maybe some of the other members could give us their experience to help

both of us understand this strange disease more. Also how rare is it,

I hear not many people havae ever heard of this.

Take care of

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...