Jump to content
RemedySpot.com

Sandy

Rate this topic


Guest guest

Recommended Posts

Guest guest

When I flare up I have to go to 30 mgs a day. Then I have to do the

taper down thing every 5 days till I get to the point where my flare

settles, sort of. With me it never really goes a way. My legs and

feet look like I have some dreadful disease. I haven't been able to

wear shorts for 2 years. Hate to go around looking like somebody has

beat me up. If you are already at 25 mgs you probably should have a

talk with your doctor and see what he suggests. I can well

understand why you want to get down on the pred. I do too. But when

I do, then I get " real " bad. For me, the vasculitis is the worst

part of the RP.

The bars are in the oven and BOY do they smell good. I was very

tempted to just drink the Almaretto and forget the bars and go have a

nap. Stuff sure does smell good.

You have a good weekend and give my love to Valarie. I have lost a

lot of my hair from the autoimmune disease and decided after seeing

the message about the hat party that I would get one. Found a cute

white one at Walmart and I just wear it everywhere. Love, Marilyn

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...