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My Fiancée had to switch from Humira to Hyrimoz as well. Shit ain’t the best word to use. It’s dogshit, absolute rubbish.

I didn’t get told anything about food. What can’t we eat? I’m day 3 Thank you

Thanks for the vid, helpful. I've just been started on a biosimilar - as apparently thats the current guidelines. Too early to tell if its working. Problem is - i dont have anything to compare with! And if there are issues, not sure if the specialist would put me onto Humira. Anyone else been started on a biosimilar without first having the actual one? Thanks

Oh no... Were you able to go back on Humira?

Thank you for this. I just started and this is the best testimonial so far. How is it going now?

Thank you for this video. I'm alone and scared to give myself my first injection and this really helps

I agree with your opening 100 percent..my miracle also

How are you doing in 24?

Just started Amjevita, Humira biosimilar. Your video gives me hope. Thank you!

Wondering how you’re doing now! Hope you’re in remission!

Hi Emma, are you ok?

Oh gosh you sound like me I am so scared of bad reactions

6yrs later! Are you still taking Humira? I’ve been offered it and it utterly scares me. X

Thanks for video. I have AS (ankylosing spondylitis). Flaring right now. It’s totally out of control. And it has worn me out. It’s not ache anymore. Absolute pain all the time. I’m now homebound. Lumbar spine, is a mess: all herniated and fusion of L4 and 5. Also have all the side effects, awful psoriasis; IBD, 2 types, lucky me; uveitis, I mean the whole thing. Now in my late 60s, but things began in my 20s. I desperately want to enjoy a few yrs of retirement. I’ve had surgery after surgery and the disorder always returns with a vengeance to do more damage. I haven’t gone this route bc I thought I wasn’t eligible as I have latent TB from living in Orient as kid, but rheumatologist said he doesn’t believe that would be a problem. Insurance will only pay for Humira. I’m still worried about it all. Has anyone had side effects?

I’m 24, a dental hygienist, and was just diagnosed with RA 3 months ago. We caught it very early, thankfully. This is the absolute worst career to be in with this disease because of how heavily it relies on my hands working. It has completely destroyed me mentally especially being so young I feel like I have so much longer to have more and more damage vs if I was diagnosed at 50. I am able to push through the pain to work (because i really have no other choice). But my doctor has had me on Plaquenil for 2.5 months so far. In general I am doing a bit better with pain, but the joint pain is still spreading to other fingers and I do have bad flare ups every couple weeks. My rheumatologist is going to put me on Humira with Plaquenil in hopes that it gets me to a full remission. This video has helped me feel much more hopeful about it. I am actually excited to start Humira because if it does give me my life back, I will never take opening a bottle cap, curling my hair, putting my shoes on without pain for granted again. Thank you, and please wish me the best outcome with this. I am so glad it has helped so many people.

Thank you for posting this helpful video. Best wishes to you.

Hi thanks so much. Please can you still take heavy things with AS ?

I just started that one. Here in Canada the government use to pay for Humira. But they switched those who was on Humira to Hyrimoz. If it doesn’t work I will not be able to switch back to Humira cause I can’t pay for Humira myself. So I’m hoping that this one will work.

My health insurance recently change from Humira to Hyrimoz. The needle really hurts.

Thank you for sharing your experience. My uncles are retired physicians from different disciplines - oncology, cardiology and neurology. All were against generic drugs, now called biosimilar. The formula/ingredients are different. Generic/biosimilar means less than perfect.

Im about to start my treatment with Hyrimoz after methotrexate started to impair my liver. I have psoriasis, psoriatic arthritis and mild peripheral neuropathy. Reading about Adalimumab I'm afraid of starting treatment. I have a 4-month daughter. Kids get all kind of flu, infections and so on. How is going to affect my health? Also, I read that anti-tnf biologics leave us prone to fungal infections. I really like to perform oral sex on my wife (and she likes it too, I hope you people don't feel uncomfortable as I share this). Will I have to put this practice on hold!? How imunobiologics has affected your sex life?

Hyrimoz contains Citrate, which, for many patients, causes pain while injecting. Try switching to Humira or other biosimilars which are Citrate-free.

I just got my 2 first injections today. I have Hidradenite and Rheumatoid Artrites for many years. Humira is the treatment used for the 2 conditions so, I decided to give it a try. This first injections were done this morning an its past midnight and I have no side effects or pain at all. I just hope that will continue this way and that it helps me with my 2 conditions. I took Enbrel before and it did give side effects and I had to stop. We will see, in the future if will no be the case with Humira. I wish you the best and I am sorry for the side effects that you had.

Thank you for sharing

Thank you for your video. My Rheumatologist just switched me over from Humira to Hulio, also a bio-similar. I haven't had my first injection yet. I went to an injection clinic for the past 4 or 5 years to get my Humira shots. So this new company, Hulio, has set me up with a different injection clinic. I have trouble injecting myself, it always leaks out the bottom, so I don't get the full dose, and I'm so nervous doing the shots. Now, with your confession, I'm nervous about this new drug, if it will hurt, if it will still keep the pain away, if it will have side effects that I never experienced with Humira. I'm 2 days late on my last injection, so hopefully this new company has me set up quickly cos I don't want any pain to start up. And yes, it's still an auto-injector pen but a different shape. I haven't got it yet. Here's hoping I have more success than you have experienced. So sorry. Humira works but it's sooooo darn expensive. Government drug plan pays for it, thank goodness. But it really stings. Hopefully the Hulio doesn't sting. And doesn't leave bruising. I get it in my stomach. Tried my leg once, and nope, it hurt too much.

Very long winded explaination

Thanks so much for this video. I start on this soon and can't wait.

I'm very scared of the side effects

I was in USA. I was on Humira for 4 years. I came to UK in Feb. They can't give me any medicine till now. First I had to get appointment to GP. It took 1 month. Then Gastroenterologist appointment took 2 months. I had big flare ups. I had to go to A&E twice. Colonoscopy team wrote Urgent in report. But the doctors in UK does not seem to care. In this way It take total 5 months. Then doctors said you have to take TB medicine before starting the Humira again. So they gave TB medicines for more then 2 months now. Last week they said they will give me Adalimumab. The Nurse called me and told that she will give me Hyrimoz instead of Humira. They are taking so much money as national insurance. And they are not giving me my medicine.

Did you get the meds on the NHS or PMI?

Wondering if this nice lady is still doing good bcz the latest video she shared is dated 3 years ago.

There is zero point to making a vid after one shot

Bugger! Sorry to hear this. I Googled and saw the NHS did this on purpose to save money. I hope there was some proper patient advocacy done and you got your Humira back. Our PBS in Oz makes us jump through many hoops before we're allowed to start Humira, but I'd rather that than have them pinch pennies at the cost of our health. Hope you're doing better now.

How many times a day do you usually have to inject or is everyone different?

I’ve had a very similar experience. The only downside for me was gaining weight, but my doctor explained that the reason my metabolism changed was because I was hypermetabolic before Humira, due to the stress of pain and illness, and I know that’s true, so I can adapt to a more “natural” metabolism.

Did you manage to get back on Humira? I have a different biosimilar called imraldi adalimumab and it's horrible.

Im pretty scared to start this, i just got off stelara now im starting hadlima(biosimilar) for my crohns. The side effects are kindve alot but my crohns is at a point where i dont have a choice lol

what happened since, please post or write something

My sister is suffering from psoriatic arthritis...and is advised by the doctor to go for adalimumab.......

Humira was horrible for me- 2 days after I took my shot I wanted to kill myself- every single time!! Every two weeks. Never again.

You should have started a fake band, like the one in the commercial.

how are you feeling now? are you still on this medication?

I've just started it a few months ago, think I've had 5 doses now, I find it extremely painful! Not the injection part but about 30 seconds later I burn. It feels similar to a bee sting, and then I'm dizzy and nauseas for at least two days after.

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do somebody feel ill after switching to hyrimoz? im feeling realy sick in the mornings meaning dizyness and cold and nausea and cold sweating

Thank you for sharing your story. I am sorry on what you are experiencing. I too was on Humira since 2012, just recently here in Canada all patients who are on Humira will need to switch over to a Biosimilar. The options we were given were Hulio, Hyrimoz, Amgevita, Hadlima and Idacio. For me I went with Hulio. So far so good, the injection is less painfull then Humira.

I have just done no3 injection Adalimumab. I had a slight advantage over this lady as I had injected Methotrexate for a few years previously. I did find the injection slightly painful but the drug seems to be working well as this is the longest period for over 9 months when I didnt have to take steroids to stop the joint pain. Have had no real side effects so far other than possibly very slight tiredness...

So as of today 6/21-How have you been? Any side effects!

Hey, I am a medic starting adalimumab this week. You can tell the difference it's made between the 2016 video and this one, very hopeful. Just a tip, you can pasteurise eggs at home, 60 Celsius for 5 minutes (you'll need a cooking thermometer), then back to the fridge. You can poach them at a later stage then. But be careful with brie, untreated eggs, etc, etc. If you catch Listeriosis, Campylobacter or Salmonella you could become septic on these medicines.