"I have been told my by doctor that the drug company has a card (copay) program. Tell your friend to go to the humira web site and read how you apply for it. I have chosen to take the Enbrel. It has a card program too. I have to first be pre-approved…"
Paula's Discussions
Enbrel vs. Humaria
Started this discussion. Last reply by Jannie M Stickney Nov 14, 2009. 4 Replies 0 Likes
I am a new member and was advised if I post this question I may find some help. I was diagnosed with RA 2 years ago. I am HLA B27 gene positive which carries the diagnosis of Spondolitis. It can also…Continue
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Toni McGrew replied to Paula's discussion Enbrel vs. Humaria"I recently met a friend with psoriasis all over her arms. She knows about Humira but does not have any insurance and of course Humira is costly. Is there any type of program in Texas that helps with the cost or is there any type of plan that Humira…"
Paula left a comment for Ashley K"Did you use the auto inject or the Enbrel that you draw up yourself? I was tole that the auto inject you kind of sit it on you skin then push a button and the needle comes out the end "pokes" in and the med goes right in. But the other you…"
Ashley K left a comment for Paula"Needles arent fun, but giving yourself shots is not as bad as you think. I did it for two years and after the first few times its not even a big deal anymore :) Hope this helps!"
Lewis D replied to Paula's discussion Enbrel vs. Humaria"Paula the meds costed the same to me after insurance...the real cost was $1500 before insurance and after it came out to be $150 with insurance. Enbrel is a once a week shot so you will get 4 and Humira is a once every 2 weeks shot. I had used…"
Paula left a comment for Ashley K"40 years! Yikes! I bet you do have a lot of information for us newbies. I was diagnosed 2 years ago. I currently take methotrexate and use every kind of topical cream there is. My rheumatologist asked me on Friday to decide on Humira or Enbrel to my…"
Paula left a comment for Cindy Foe"Thanks. I'm thankful for people like Patsy W.,Jane L. and your self for encouraging me to do this. I have never participated in any type of online groups. Yes, not even Myspace or Facebook! Oh, my gosh."
Paula posted a discussionEnbrel vs. Humaria
I am a new member and was advised if I post this question I may find some help. I was diagnosed with RA 2 years ago. I am HLA B27 gene positive which carries the diagnosis of Spondolitis. It can also be psoriatic arthritis. My first treatment of methotrexate was keeping the joint pain under control, but has never really helped with the psoriasis on my elbows. Lately it is getting worse. I work in the dental profession and worry that the patients will fear that I "have something" that they may…See More
Jane Lacher left a comment for Paula"Hi Paula,
I would just like to give you a hug right now. Some of those questions would be great for the discussion board as there are many in your situation. I do not have PA, and just started on methotrexate. Unfortunately, I am in the same…"
Paula commented on Linda's blog post Harmful to scratch in the hot shower?"Hi, I used to do the same thing. But, I noticed that when the plaque grows back on my elbows it is thicker. So I try to pat dry out of the shower and then use the steroid spray (Clobex). I did notice that mine got soooooo much better while I was at…"
Paula left a comment for Jane Lacher"Thanks. I am new to all of this and just today went for more x rays and blood work. I was diagnosed a little over two years ago. I am HLA B27 gene positive so that carries a diagnosis of spondolitis and can also come across as psoriasis. I have been…"
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Comment Wall (5 comments)
- At 11:19am on November 4, 2009, Ashley K said…
- Needles arent fun, but giving yourself shots is not as bad as you think. I did it for two years and after the first few times its not even a big deal anymore :) Hope this helps!
- At 9:12am on October 31, 2009,
Cindy Foe said… - Hey Paula......Welcome...you will love our family.....
- At 8:55am on October 31, 2009, Jane Lacher said…
- Hi Paula,
I would just like to give you a hug right now. Some of those questions would be great for the discussion board as there are many in your situation. I do not have PA, and just started on methotrexate. Unfortunately, I am in the same situation with insurance deciding my course of treatment. My derm was using directed UVB laser treatments, and it was working. But, and this was after pre-approval, my insurance carrier decided to review the claim. They ultimately ruled it a "cosmetic" procedure and would not pay the bills. I would love to go into their offices and scratch up a "snow storm" until I bleed (which does not stop quickly). Anyway, thanks for letting me vent. Seriously, post your questions on the forum - that's what it is there for - to let everyone help you.
- At 10:14pm on October 30, 2009, Jane Lacher said…
- Hi Paula, welcome to the group!
- At 5:33pm on October 30, 2009,
Patsy Wessinger said… - Yay!! You found us. I think you will find this site very useful.
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