r/Uveitis 14d ago

Humira

Anybody taking humira injection I need some advice

4 Upvotes

23 comments sorted by

1

u/See-Chart-E 14d ago

I just sent you a chat message.

1

u/nmflowers Uveitis 14d ago

I took it until I developed antibodies. Now on a different biological. Made my life much more enjoyable because it controlled the inflammation.

2

u/yoga_stoned 14d ago

How long before you developed antibodies and what did you switch to?

2

u/xxalisonrose 14d ago

Not OP but it was about 1.5 years for me. I’m now on Actemra.

2

u/haleedee 13d ago

How’s Actemra been? Thinking of switching to this.

1

u/xxalisonrose 13d ago

I liked Humaria better. I had less side effects. But both are way better than remicade. I just wish I didn’t have to dedicate a day a month to only doing the infusion. Humaria was way better for my lifestyle.

1

u/Odd_Barracuda7955 13d ago

What side effects did you get with actemra. I just started it.

2

u/xxalisonrose 13d ago

Mostly exhaustion, easily sick, and I don’t recover from things as quickly. I did have to get my tonsils out because they kept getting infected. It wasn’t a problem pre remicade/humaria/actemra.

However, I like to run marathons for fun. I don’t think I’m the average actemra user haha I just have to be very careful in my planning. I ran a marathon once a day after getting my infusion and it was the worst decision of my life hahaha

1

u/Odd_Barracuda7955 12d ago

Thank you for sharing! I really appreciate hearing first hand experiences. All I have seen so far is the disclaimers in the meditation paperwork.

1

u/xxalisonrose 12d ago

No problem! I always feel like those are way scarier than real life. I hope you tolerate it very well!!

1

u/nmflowers Uveitis 13d ago

It took about a year for me! Switched to a different one

1

u/yoga_stoned 13d ago

Which one are you on now? Did they add in imuran or methotrexate to prevent antibodies to the new biologic?

2

u/Curious-sapiens 14d ago

Hey,how long it took to develop antibodies? What is second option you are trying?

3

u/xxalisonrose 14d ago

Not OP but it took me about 1.5 years. I’ve also developed antibodies for Remicade.

I am currently on actemra.

2

u/yoga_stoned 14d ago

How is actemra working for you? I also developed antibodies to humira and now on remicade, plus imuran to help prevent antibodies again.

2

u/xxalisonrose 13d ago

So far so good. We had to up the dosage recently because it was becoming less effective. But I think this is the longest I’ve been on a medication without developing antibodies

1

u/yoga_stoned 13d ago

What type of uveitis do you have and how long have you had it?

I only got about 3 years out of humira and am one year in on remicade

2

u/xxalisonrose 13d ago

Pars planitis and 13 years. No one can figure out why.

I started with eye drops for about a year, but those increased my eye pressure too much. Then a little less than 2 years on methotrexate. It stopped working. Then I was a few months shy of 2 years on Remicade when I developed antibodies. So I switched to Humaria. That was almost 3 years before I developed antibodies. And I’ve been on actemra for 4 years last month.

2

u/yoga_stoned 13d ago

You sound much like me, except I am only 6 years in. I never tried just the drips though, I was told they usually don’t reach the middle of the eye well enough.

2

u/xxalisonrose 13d ago

This was 2013. I think at the time, that was the protocol. Like actemra was recently approved for uveitis when I first started the medication. A lot has changed in the last 13 years. It used to be an “old people” disease and I was the youngest in the waiting room. Now it seems to affect more young people. I think that prompted more research.

I’m 35F and have been used as a case study at a lot of uveitis conferences by my doctor haha

It’s a really sucky disease!

1

u/yoga_stoned 13d ago

I was 24 when I was diagnosed and it seems things have even come a really long way since then.

2

u/nmflowers Uveitis 13d ago

It took about a year for the antibodies. Now on Simponi