Jump to content
RemedySpot.com

susan

Rate this topic


Guest guest

Recommended Posts

, thank you for the uplift i know that all off you are my angels thats why God sent me to this group.......... SHERRIE

-- Sherie, , and all/pep talk. LOL

Hi Sherie and everyone,

I just want to add my two little cents here. I've been where you are all now. In fact, I am suppose to be dead by now. I have had RP for 10 years now and when I first got online, there were exactly 3 articles on RP all outdated. The most extensive one I read claimed most RP patients were dead in 10 years. To add to my misery and suffering the first Rheumy I saw told me to write my will. This was his exact words!!!! I was a zombie for weeks........

Then I met an angel named Angie who told me the "real" facts. She was a god send to me. I know some of you are just learning to deal with RP and are finding out what damage you have and I know you are very very scared. I can relate as everyone here can, believe me, we all have been there and a lot of the members are still dealing with this. But!!!! and there is a but.........LOL Sherie, it sounds like you have excellent doctors which a lot of us never had. They know how to deal with this and it sounds like you are getting the kind of treatment for this disease early in your illness, so please girl, don't get depressed, be so happy that you have the kind of help you need. You will be OK, I just know it. Your doctors will find the right drug regiment to treat your RP and stop it and you will be just fine. The main thing is not to get discouraged and try like hell to keep your spirits up. The damage done can not be reversed, but your doctors sound dedicated to making sure no other damage is done, so you are going to live a long life. You keep your chin up and keep the faith.

, I can really relate to your body screaming in pain as I know many members in the group can.

I'm so glad you use this group as a sounding board. God knows I did when I was hurting. Most of us can relate to your pain. Do you have fibro also? I have been where you are many times. I feel for both of you so much. I can remember crying, hurting, and wondering if I was going to live another year. BUT!!!!! I am now in partial remission and doing good. This is the main thing I want you both to know. It's not hopeless and it will get better with the right drugs, exercise and positive thinking!!!!

Please just try not to let yourselves get too down and remember it will get better and one day you will both, ALL OF YOU will end up in remission. Keep the faith!!!! I know we all get depressed over this damn disease, but don't let that depression overwhelm you, keep it all in perspective and get yourself thinking that this will not defeat you.

Life will get better. Just keep that chin up and keep the faith. I'm sorry I went into a book here, just wanted you Sherrie and and everyone to know that I have felt your pain and depression many times before, but I am so much better now, it took quite a few years, but it will happen to you too. Remission is a beautiful word. Learn it!!! You will be saying it before you know it. Trust me on this............

Prayers are with you all.

w

>>>>>>>>>>>>>>>>>>>>>>>>>>

I flared up something terrible. my ear, nose, same tie and really bad. Also my lower back and neck are hurting so bad it is making me sick. i went back up on my pred. I am sick of this disease.DISCLAIMER!!WE ARE NOT MEDICAL PROFESSIONALS, THEREFORE ANY INFORMATION THAT IS RECEIVED HERE IS FROM EXPERIENCE ONLY. PLEASE CONSULT WITH YOUR DOCTOR BEFORE TRYING ANYTHING THAT IS SUGGESTED. WE ARE NOT A SUBSTITUTE FOR YOUR PHYSICIAN AND ARE NOT TRYING TO BE. REMEMBER EVERYONE IS DIFFERENT AND TREATMENT MAYBE DIFFERENT FOR MANY OF US. THANK YOU

Link to comment
Share on other sites

  • 2 years later...
Guest guest

thanks for calming me down :o) i guess i needed a shoulder to cry on

more than i thought - and a person to gently push me back into

reality. it really helped - thanks...

-becky

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...