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Amy, the practice pen only works once. The hardest thing for me at

first was getting used to the loud " pop " when you depress the plunger -

it would make me jump every time. The first few times I had a friend

do it for me because I was afraid the startle-reflex from the sound

would make me not steady-handed. Now I don't even blink.

This sounds weird, but now I LOVE to give myself the injection because

I know that it is making my life worth living again.

good luck,

sherry z

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  • 1 month later...
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Many times when using LDN psoriasis gets worst for a while and then clears up later. It just takes a while.

Aletha

[low dose naltrexone] humira

hi all,,I've been on 4.5 for about 2 months for m.s. im slowlygetting better and better, the problem,,,my psoriasis (guttate) isway out of control and i think im being approved for humira.can i take both ? joe

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  • 2 weeks later...
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My doctor told me that it may not kick in for six weeks or so. I had

surgery in December and went off Humira.

I ended up with a horrible flare (my worst yet) and started back on

MTX/Humira a month ago. It hasn't kicked in yet, but I'm hoping soon!

Patty

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, it took about 2 months for me, but that was at an every other

week dose. That was when things started to get better, but they

continued to improve for several more months. When we upped the dose

to 3 times a month, I got more improvement. When we upped to weekly,

still another bump in improvement. I never have had complete relief

from P on the soles of my feet, which cause me quite a problem with

standing and walking. And never complete joint relief, although it is

bearable between flares. But the improvement from where I was 2 years

ago is quite remarkable. I hope you have great results!

regards,

sherry z

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I am waiting for my first dose of Humira. They are delivering it

tomorrow. Thank God for their Patient Assistance Programs. There is

no way I could afford it with out that.

" tweetygodess " <tweetygodess@...>

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Hi ,

It took 2 months for the improvement to become noticeable when I was on

every other week Humira. When it stopped working 6 months later and

everything came back with a vengeance my then-rheumy put me on every

week injections. That took a month or so to start showing improvement

and it helped for a while, but then I went under extreme stress and for

all intents and purposes it stopped working altogether (or, if it was

working I'd afraid to see what I shape would have been in without it! It

was the worst flare I have ever even heard of) so my now-rheumy started

me on Remicade in April.

Hope this is helpful, and best of luck with the Humira!!! I hope it

works for you!!!! :-)

Carla

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Six weeks? Ok. Well, that means I should be seeing some improvement (I hope!)

right about the time that I go back and visit the rheumy and the derm.

Thanks for answering,

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  • 1 month later...
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I want to be a member of the club!

I've received 4 Humira shots so far, my psoriasis is almost completely

gone. I was 40% covered for the past 13 years. My PA is getting better,

slow but sure. I'm still on pain meds, but I had a 4 day stint last

week that I felt almost perfect except for a couple twinges here and

there. Then our weather changed and it started up again, that and I

reeled in a 40lb king salmon on my own. That was a blast but it took a

toll on my arms and hands.

Kari in Alaska

> >

> > OK, can I just say I LOVE MY HUMIRA!!! I have had a scalp problem

> > for about 2 years. I never knew that it might be related to my

joint

>

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Karl, personally I would be happy to take that pain for landing a 40

pound king salmon!!! So glad to hear you're doing well on Humira.

Welcome to the club.

" S. Zorzi " <szorzi_1999@...>

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:) Sounds good to me. It's been a long time snce I've been this happy with a

medication that I'm taking. If we start a club, I'll join up. I think I'd have

to take the pain to land a fish like that as well. :)

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  • 1 month later...

:  Only your rheumy can advise you as to the best course of action, but

going off your PA meds may - in the long run - prove to have a more negative

effect that the infections have.  I don't know what kinds of infections you

experienced other than the MRSA (bad enough, all by itself) but I would try and

figure out how you were exposed in each case and what you can do to avoid future

exposure.  (With the MRSA, I would guess that there was something in the

dentist's offfice, since MRSA is often spread in hospital settings.  Hard to see

how else you might have picked it up in your absessed tooth.)  Also ask your

rheumy if there are things you can do to build your resistance because PA meds

only target one portion of your immune system.  Do some reading on nutrition and

find out what foods have anti-inflammatory properties and add them to your

diet.  I just heard a speaker on topie that last night.  He's written a book

called 101 Foods that can

Save Your Life.

He also discussed foods that can reduce pain and as some of you have pointed

out, he highlighted the elimination of nightshade vegetables.  Said that his

father developed a painful skeletal condition and didn't want to go on drugs -

went off nightshades and within 2 weeks his pain was gone.  (Not sure how I

could live without tomatoes, though - they're almost a staple in our house,

especially this time of the year.  If they're not in my salads, they're often in

whatever I cook.) 

You are right to be concerned but also correct in researching and making an

informed decision since this is a major issue with potential long-term

consequences whichever path you choose. 

 Joanna Hoelscher

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  • 1 month later...

Hello

I have just started on Humira and have only had 3 injections. The first one

I had an ulcerated throat, but the 2nd. And 3rd. were symptom free and my

knees are not so swollen so I am keeping my fingers crossed that it is going

to be of help.

Good luck if you decide to take it.

Best wishes

Joan U.K.

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Hello

I have just started on Humira and have only had 3 injections. The first one

I had an ulcerated throat, but the 2nd. And 3rd. were symptom free and my

knees are not so swollen so I am keeping my fingers crossed that it is going

to be of help.

Good luck if you decide to take it.

Best wishes

Joan U.K.

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Hello

I have just started on Humira and have only had 3 injections. The first one

I had an ulcerated throat, but the 2nd. And 3rd. were symptom free and my

knees are not so swollen so I am keeping my fingers crossed that it is going

to be of help.

Good luck if you decide to take it.

Best wishes

Joan U.K.

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Stillsdisease writes:

Thanks for sharing- I was felling like the lone ranger and that is pretty scary!

I just read up on it and it sounds like it may work. Kineret worked for a short

time but I am dealing with a pretty bad flare now and had to go up on Pred. I

get my Humira in a week. I'll let you know how it works.

Thanks

>Hello

>

>I have just started on Humira and have only had 3 injections. The first one

>I had an ulcerated throat, but the 2nd. And 3rd. were symptom free and my

>knees are not so swollen so I am keeping my fingers crossed that it is going

>to be of help.

>

>Good luck if you decide to take it.

>

>Best wishes

>

>Joan U.K.

>

>

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Stillsdisease writes:

Thanks for sharing- I was felling like the lone ranger and that is pretty scary!

I just read up on it and it sounds like it may work. Kineret worked for a short

time but I am dealing with a pretty bad flare now and had to go up on Pred. I

get my Humira in a week. I'll let you know how it works.

Thanks

>Hello

>

>I have just started on Humira and have only had 3 injections. The first one

>I had an ulcerated throat, but the 2nd. And 3rd. were symptom free and my

>knees are not so swollen so I am keeping my fingers crossed that it is going

>to be of help.

>

>Good luck if you decide to take it.

>

>Best wishes

>

>Joan U.K.

>

>

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  • 3 weeks later...

Oh, Yes. Very normal for me, and I've been on it for 2 years. But it WORKS!!! I

was on Enbrel for 1 1/2 years, but it quit working the last 6 months and I was

miserable. Felt relief within two weeks with Humira. I hope it works as well for

you.

Good luck

Job in CT

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I'm curious as to how many have had similar experiences with the biologics, i.e.

you go on one and it works well but all of a sudden it just doesn't work!  Do

doctors have an explanation for this?

 Joanna Hoelscher

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The burning when injecting is normal.  Every time I do my Humira injection it

feels like the longest 10-20 seconds of my life.  I must say after 3 months I am

getting used to it.  Still hurts like hell but the results are worth it.  Good

luck!

Kohler <meganleigh713@...>

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That happened to me until I learned to:

1) take the Humira out of the refrigerator about 40 minutes before

doing the injection.

2) ice the site down for 3-4 minutes before injecting.

Now I don't get the burning at all. best regards,

sherry z

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Sherry is absolutely right.  The only thing I would add (and I don't know if it

applies to Humira but it certainly does for Enbrel)  is to inject it very

slowly.  I can really feel the burn if I push the plunger too quickly. 

 Joanna Hoelscher

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Humira has been a blessing for me. Once I got over the nervousness of having to

inject myself. I have a cousin who has RA and she led me through the first

injection I did by myself. I think that I had noticeable relief within 2 - 4

weeks of the first injection. I take mine with methotrexate, which my rheumy

just lowered from 10 pills total a week to 8.

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I didn't have much of a burn with the Enbrel but do have a bad burn with the

Humira.  I inject slowly and also don't move.  I have to stay put for a few

minutes because if I move, even with the needle out, I can feel it traveling

with a burn.  The burn for me is bad and even after years on Humira makes me

dread my injections.  With Enbrel, I used to get a welt, sometimes a bruise and

it would itch. 

Gilchrist <gilchrist414@...>

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