Guest guest Posted December 19, 2003 Report Share Posted December 19, 2003 I am so sorry you are feeling so terrible. I fought taking any meds (except for NSAIDS) since 2000 and finally started Enbrel over the Summer. What I can tell you: -the " thought " is worse than the needles...it really doesn't hurt... -You will have to see what ins. covers ...it is VERY expensive... -It took about 1 & 1/2 months to kick in...i could finally " move " again...like a miracle! -I experienced no side affects at all -They just changed to a new mixing method and smaller needle and it's great -You now have the choice (up to your Dr.) on injecting 2 times a week or just take the 2 injections the same day to get it over with....I still stick (no pun intended!) to the 2 times a week. Hope this helps you and I will remember you in my prayers, Carole >From: " DeafEskie " <DeafEskie@...> >Reply- >< > >Subject: [ ] Re: Enbrel & PA & Flares >Date: Thu, 18 Dec 2003 18:02:11 -0600 > > >Hello all, > ><SIGH>. The worst flare of my life has arrived. Even though I am on >Soriatane I am in excruitating pain. It hurt to even lay on the bed last >night. Anything touches me it hurts. I have just gotten over a bladder and >sinus infection. My hands are an angry red, raw and swollen. My skin >alternates between too pale and red in all different places. To top that >off, my hands/fingers/feet/toes are always ice cold. And I am weak. >Cannot >lift much. > >Now my favorite dermo over at OU is talking about Enbrel. She feels I need >it to get me out of this flare. I am scared. I hate needles. Isn't enbrel >a biologic? Will medicare/medicaid even cover this?!?!??! We are waiting >to >find out--I am assuming that the clinic plans to deal with both medicare >and medicaid to get it authorized. > >I know enbrel is probably an old topic, but I am too sick to care to search >through archives. If someone could share their experiences and explain how >Enbrel works, I would really appreciate it. Right now I am drugged up on >10 >days of Prednisone (back on it), Flexeril for muscle spasms, Lortabs for >pain, Naproxen for pain, Soriatane & other meds I have to take. > >I pray I can sleep tonite! Please keep me in your prayers--I am flying to >Denver tomorrow. I hope the pain will have allievated somewhat by then.... > > >LeAnn Cayer & Furbrats Blossom & Meriko >Heart Bandits American Eskimo Dog Rescue >Railroad Coordinator www.heartbandits.com > > >---------------------------------------------------------------------------- >---- > > > > _________________________________________________________________ It’s our best dial-up Internet access offer: 6 months @$9.95/month. Get it now! http://join.msn.com/?page=dept/dialup Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 21, 2003 Report Share Posted December 21, 2003 My heart goes out to you. I hope that you will get some relief soon. There is no reson to be afraid of the Enbrel needles. The new system is just about painless. Of course you will have to wait until your infections clear up. Personally I have not even had as much as a cold while on Enbrel. Enbrel started working for me the first evening I took it. However, for me, I think that the good effect is starting to wear off after 2 1/2 years. I will say a prayer, or two, for you. Hope things are better especially for the holidays. Peggy B. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 22, 2003 Report Share Posted December 22, 2003 Your flare sounds a lot like my first one. I ended up in the hospital for several days while they pumped me full of cortisone, antiviral, and antibiotics...It was pretty scary. I know that Medicare in my state pays for Remicade infusions, but not Enbril [except maybe for RA...don't know about that] The difference is that Remicade has to be administered at a clinic or hospital while Enbril can be taken care of in the home...dumb, but Medicare has some dumb rules. Sylvia DeafEskie <DeafEskie@...> wrote: Hello all, .. The worst flare of my life has arrived. Even though I am on Soriatane I am in excruitating pain. It hurt to even lay on the bed last night. Anything touches me it hurts. I have just gotten over a bladder and sinus infection. My hands are an angry red, raw and swollen. My skin alternates between too pale and red in all different places. To top that off, my hands/fingers/feet/toes are always ice cold. And I am weak. Cannot lift much. Now my favorite dermo over at OU is talking about Enbrel. She feels I need it to get me out of this flare. I am scared. I hate needles. Isn't enbrel a biologic? Will medicare/medicaid even cover this?!?!??! We are waiting to find out--I am assuming that the clinic plans to deal with both medicare and medicaid to get it authorized. I know enbrel is probably an old topic, but I am too sick to care to search through archives. If someone could share their experiences and explain how Enbrel works, I would really appreciate it. Right now I am drugged up on 10 days of Prednisone (back on it), Flexeril for muscle spasms, Lortabs for pain, Naproxen for pain, Soriatane & other meds I have to take. I pray I can sleep tonite! Please keep me in your prayers--I am flying to Denver tomorrow. I hope the pain will have allievated somewhat by then.... LeAnn Cayer & Furbrats Blossom & Meriko Heart Bandits American Eskimo Dog Rescue Railroad Coordinator www.heartbandits.com ---------------------------------------------------------------------------- ---- Please visit our Psoriatic Arthritis Group's informational web page at: http://www.wpunj.edu/pa/ -- created and edited by list member aka(raharris@...). Also,in August 2001,list member Jack aka Cornishpro@... began to conduct extensive research which he publishes as the " Psoriatic Arthritis Research Newsletter " , monthly in our email and digest format. Many thanks to Jack. Back issues of the newsletter are stored on our PA webpage as well as the archives of the list. Don't forget that the list archives comprise a tremendous amount of information (Over three years of messages and answers).Feel free to browse them at your convenience. LET'S HEAR FROM SOME OF YOU LURKERS out there! If you have a comment or question, chances are there is a person who has been around a while who can help you out with AT LEAST an educated guess for an answer! If not,we can steer you in the right direction with a good website to go to, Blessings and Peace, Atwood-Stack, Founder Alan , Web & List Editor Jack , Newsletter Editor Pat Bias, List Editor Ron Dotson, List Editor Orin, List Editor , List Editor and any others who help in any way (thank you!) Quote Link to comment Share on other sites More sharing options...
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