Jump to content
RemedySpot.com

Re: My Humira experience

Rate this topic


Guest guest

Recommended Posts

,

Thank you your response. The Humira arrived today. I will probably

start it on friday. I am glad for your honest response on this. I

am hoping this will give me some relief. I was also on Enbrel too

and it did not work well...then doc added MTX and that was a total

disaster. I am no longer taking Enbrel or MTX due to side effects.

I am taking Plaquinil, Lodine XL and Ultram as needed for pain and

nexium along with that. Humira is the new addition.

I will post once I take it which will probably be friday nite before

I go to bed.

Toni

>

> There's been so many questions I just thought I would share my

experience

> with Humira. I was on Enbrel previously and Humira has worked

better for

> me. It has always come well-refrigerated, no problem. I have mine

delivered

> at work and put it in the fridge.

>

> My Humira is covered by my Major Medical Insurance (whatever that

means!)

> and I do not have to pay a co-pay. I do believe there is a limit,

up to $5

> million, so I've got to watch it, lol!

>

> I leave it out for about a half an hour. For me, it burns like

Hell, I have not

> found a way around this. I inject it slowly (30-60 sec.) and don't

get up for a

> while. I do it in front of my computer and I put up a nice picture

or play videos

> to distract me from the pain and I find this works pretty well.

>

> Humira does hurt but it is once every 2 weeks and it is better than

the constant

> and crippling pain of RA!

>

>

>

Link to comment
Share on other sites

Hi all,

I was so glad to see this group. I started on Humira just about a year ago,

after

working my way up from " everything else. " I was dx with systemic polyarticular

jra

more than 25 years ago, I'm now 36, and I find that each time the doc promises

the

" one that will work " it stops working after a while or I develop an alergic

reaction.

I'm now using Humira in combination with 20mg of mtx tabs. The mtx is weekly

and

the Humira is every 10 days. I got really sick on the mtx when I started it

about 4

years ago, but then I got used to the side effects, and they lessened, but so

did the

ability of mtx to control my jra. Started the Humira at every 2 wks, but had to

boost

it to 10 days. Surprisingly, it has been working! I've managed in the last few

months

to finally get off predn after taking it daily (sometimes in large doses) since

I was in

6th grade. I now have osteopenia as a result of that.

I find I do have some side effects with the Humira, especially when I take it

the same

day as the mtx. I got hair loss again like I did with the mtx, but the bonus

was that

while my head hair did thin, I now have no underarm hair and almost no leg hair!

Mostly, though, it's some nausea the next day, but I seem to be building my

tolerance

to that. The injection site hurts for a day or two, but then it's ok. I was

such a

chicken to give myself the injections at first, but the needle is so small and

sharp that

I don't have a problem

Like everyone else, I get the burning with the injection. I do it at night, and

turn on

the tv to distract me while I'm doing the injection, and do it SUPER slow.

Here's

something that happened to me--even though I pull back on the syringe

like the directions say (to avoid a vessel) once I put it in all the way through

a small

skin vessel (so none showed up in the syringe) and when I pulled it out I made

kind of

a mess and panicked. I called the nurse line and she let me know that this

happens

sometimes and that it's ok.

Other side effects I'm wondering if others have? I feel like I smell funny the

couple of

days after I take it. Also, I've been having problems with serious

constipation and

hemmorhoids since beginning the Humira. Had some blood vessels break there,

too,

and panicked since I haven't had that before. But have been using lots of Tucks

products and daily fiber tabs, and that seems to keep it in check, but not all

the way.

I'd love to hear the experiences of others with Humira.

Kris

Link to comment
Share on other sites

Everyone must be different, because for me this is the opposite! If I inject

too

much at a time the pain almost makes me pass out. I guess you just have to

experiement and find out what is best for you.

>

> I've been injecting Humira for about 4 months now. I think doing the

> injection slowly makes it burn more. When I do it and a steady pace,

> it doesn't burn as much. You can't go really fast but one smooth

> motion and not too slow seems to ease the burning.

>

> susan

>

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...