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Well the prescription went to the mail order thingamabob...but needed a tb test and insurance approval. Now I'm just waitin on have approval I guess
 
Just did my loading doses last night. (took 2 days to build up the courage to do the shots) I had an oops an wasted one of them, so I only did 3. I am waiting on a call back to see what I need to do about the 4th one.
I already feel better. I got up from a squatting position without cringing or yelping in pain and my back doesn't hurt nearly as much. I am sure its helping Crohn's as well, but my flare has been very silent and I hardly every notice that I am flaring, so its hard to tell.
 
I just wanted to say thank you for all the input.
I have a bad cold from one of my kids, we are all sick in the house.lol.
just the thing I didn't want to happen right after my loading dose shots. Lol
I'm not sure but I would guess this is just bad luck really, or maybe good luck. If I get sick now maybe it'll be better later.
Is it unusual to catch a chest cold three days after the loading doses?
 
Aw! Of course that would happen. :p

I would say it's unusual to catch a chest cold, but you've said you were exposed to your kids and everyone else is sick. So I don't think it's just because of the medication or anything.

Don't worry about it, and just take care of yourself. Do watch your lungs and sinuses, though, and if it gets worse see if you need antibiotics. People on Humira can be prone to sinus problems.

Hope you feel better soon!
 
Just watch the bugs. It only takes me a few hours to move from a cold, to throat, larynx, chest infection. My doc says if I get two symptoms ie runny nose and sore throat then make an appointment. I've been on humira two years now and I get real tired post *** day.
 
Your very sweet. Thanks for caring. Yes I have a 20yo ellie, 17yo lannie, and my youngest 14yo gravey, well thats my nickname for him, and my wife is not near as bad but we all have the flu or cold. Blllaaahhhhh. Lol.
I'll be keeping an eye on all of us here, especially myself with taking humira.
I also keep a journal every single day of how I feel, pain level. That kind of stuff, but only about my health. I guess you could call it a medical journal. Lol. Well I do write in the last line something romantic to my wife, so if she ever reads it she'll have a nice surprise. I guess I'm just a romantic at heart. Anyways I like talking to everyone on here. I also love the fact that people here care.
And thank you. It's late and I'm going to hit the hay. Good night all, and god bless. :)
 
That's wonderful that you have such a large family! Even if you're all sick right now, it must make things so lively at home. Hopefully you can all recover soon!

And that's so, so sweet that you'd do something like that for your wife! I actually kept a journal after I first started dating my SO, and would write little things about him that made me happy every day or how he's affected me. I gave it to him as a gift for our first anniversary. I'm a huge romantic too, and what you said reminded me of that. I'm sure your wife would be so pleasantly surprised if she ever read your journal, too!

I'm glad you like talking to people here. I'm so grateful I've joined this forum because it just has such a sense of community behind it, and everyone is so supportive. It's really wonderful.

Goodnight! Get a good rest. :D
 
That's the sweetest thing ever, writing something to her in the last line!

My dr called for pre-auth and was told it has to be board approved and could take 7 days. Today was a super-awful day symptom-wise so I'm really down about not starting yet since I basically feel untreated at this point now that the steroids are over and Imuran hasn't even kicked in.
 
I'm sorry to hear that Nancy, I'm hoping that they will do a good job and get your humira out to you soon.
I've noticed a very nice improvement in my crohns. I've only taken the 4 shots loading dose, but WOW I am feeling much much better. Sometimes these insurance companies can be troublesome. Then they have to find a preferred pharmacy. It really makes me mad. Because you know it's all about the money to them, and here we sit without the help we need because of some ridiculous rule or regulation.
We will be thinking and praying for you,, that you get it soon and it works well for you.
Well once again I'm up too late.lol.. good night all, and god bless!!
 
Hello everyone. Well good news. My surgeon removed the seton yesterday after saying it appears the Humira has been effective in my peri-anal manifestation of the Crohn's. I have blood work today. Because of my other symptoms, diarrhea and stomach pain, my GI is considering adding Methotrexate. Anyone with any experience with this drug? Any advice would be much appreciated.

I enjoy reading about each of you. I'm a little shy and don't post too often, but appreciate those that do. You all offer a great amount of encouragement. I'm 36, and didn't not have manifestations of this disease until October of this past year. It has been difficult on me, and incredibly difficult on my marriage. However, we've made it through a pretty tough time and appear to be doing better on this side of the diagnosis. Thank you all for your thoughtful and supportive posts.
 
ey218, It is amazing the parts of your life Crohn's puts a strain on. I feel like this is the only community that really gets it. I wish you all the luck and support. When I was in such constant pain and unable to eat for so long I really learned who my friends were (i'm single). Not every one got the fact that I could simply work and that was it. I'm not even sure how I did that to be honest, being a single mom leaves you no choice I guess.
 
I have a question about the loading dose for Humira. Do I just do all four in one sitting? Or do I space them out over the day?
 
Saw my doctor this morning and hopefully I will be starting Humira within the next week. Hope it goes well with my insurance company to get approved or whatever the case is. Im a bit nervous about starting this, as I've only been diagnosed for a few weeks and its been pretty rough so far...can't wait to finally know what it feels like to have normal energy! Any tips for a newbie? Ive seen to maybe ice the area before the shots...I get pretty nervous with any kind of needle so any advice helps...
 
Nancye50 said:
I have a question about the loading dose for Humira. Do I just do all four in one sitting? Or do I space them out over the day?
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You can take them in one sitting, not exactly same spot... this is the time to try out where it feels best on your body. Important to squeeze your skin good before you set in needle.
Good luck!
 
Just realized after reading through more of this that my doctor never gave me instruction on how to actually do the shots....nor did he say I was going to have help from a nurse my first time. Luckily I'm married to a nurse (fresh out of school last month) so he might be able to help me figure it out. This doctor has never been great communication-wise, so I am not suprised that he fell short telling me about Humira. He never even mentioned that it would suppress my immune system and that I might be more likely to get sick. He did mention 3 times that I have an increased risk for cancer though...
 
Oh no! That's unfortunate. There's actually an instructional video on my provider's site... can you maybe look up yours? It often requires the DIN number on the Humira box.

Also: there was actually a study that just came out that says biologics like Remicade (so that includes Humira) don't actually increase your chance of cancer!
 
My dr gave me an educational kit with a DVD and practice pen and all. Can you call and see of yours might have one? If not, I can post the instruction pages.

I got approval but now can't get the starter pack till tomorrow. Come ON! Today works better to be exhausted ;)
 
Mrsday, good to have a nurse at home!
I got a bit info leaflet with good pictures, even though the daycarenurse at the hospital helped me with the first load, it was good to have it at home, with two weeks between doses!!

my doctor forgot to tell me about the immune part of it, so always important to do your own research, without getting scared away by it.. (They really need to list al the risks... but they are often rare...)
 
Thanks pusheen, I should finally get it in-hand tomorrow afternoon!

MrsDay I wish I could give you this educational kit. The practice pen is a little over the top but the "click" definitely startled me the first time I heard it. I'd have jerked if a needle had gone in for sure.
 
Did the loading doses this afternoon. Just waiting for the tireds to kick in but feeling fine so far. Hoping to feel good tomorrow bc I'm hosting friends for the evening!
 
Nancye50 said:
Did the loading doses this afternoon. Just waiting for the tireds to kick in but feeling fine so far. Hoping to feel good tomorrow bc I'm hosting friends for the evening!
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A lady I know gets really hyper on her humira days, she gets lots done.. so we all respond in our own different ways!
 
Hi everyone.. here is my update.. humira does not seem to be doing a lot for me. My last hospital stay was close to emerg surgery. High doses of prednisone started things again. Life should be wonderful.. My last eye exam has signes of high pressure in the eyes so i am being monitored closely.. meeting with the surgeon and i am told that all of my small bowel is bad and my next hospital visit will result in surgery. Wonderful what I didnt want to hear.. this time last year it was only a small section of the small.. things are getting worse instead of better.. where to go from here.. think a visit with the GI is in order..
 
Oh jeez... it does sound like it isn't helping too much, then. Have you gotten an antibody test for it? :( Otherwise, it may be time to consider another biologic... Have you been on Remicade?
 
I was on imuran but had reactions to it.. don't think they have tried remicade. As for an antibody test don't think they have done that.. mind you they have been taking bloodwork over the last few months but I think that is just the routine bloodwork
 
Imuran isn't a biologic, just an immunosuppressant! And yeah, that's likely just routine bloodwork. Call your GI and see if you can request an antibody test next time you go for an infusion, and otherwise I think it's time to set up an appointment and talk about the possibility of another biologic if Humira is failing.
 
I'm on humira right now and have been told that my next med will be remicade. Maybe this is an option for you?
 
I'm going to be starting Humira tomorrow, guess I'm pretty worried about it since I've stressed myself into having D. I've been on prednisone since January :( now I've been weaning off in anticipation of starting Humira but I'm feeling the effects. I really hope it works for me
 
It should kick in quickly if it's effective for you, which I hope it is! If you feel like you are getting worse during your prednisone taper, call your GI and let them know because you should probably stay on prednisone a little longer.
 
I think Humira is working for me! Took my loading dose last thurs, have felt great ever since even with a crazy exhausting weekend!!
 
Just found out my insurance approved Humira, so I should start next week! Im a little nervous, but excited to see if it works for me!
 
Anyone else really tired after their loading dose? I think I've taken a nap every day since my injections, normally I can't sleep because of the prednisone so it's weird.
 
I found myself a little tired for the first two months, then it seem to go away. I have been on humira for three years with great success.
 
Hi Everyone,

I'm on Humira and have been since February. My mom came to town, and has a bad cold, so of course I am feeling absolutely miserable today. My throat hurts. I have sinus congestion, headache, and body aches. Should I see the doctor? Should I give it a few days to pass? Thanks in advance.
 
ey218, I havent started Humira yet (Going to start later this week) so I can't help you out there. Has anyone tried taking Emergen-C or Airborne? Both of those add a ton of great vitamins that usually help me when I start feeling sick, but has anyone had luck with them on Humira?
 
ey218 said:
Hi Everyone,

I'm on Humira and have been since February. My mom came to town, and has a bad cold, so of course I am feeling absolutely miserable today. My throat hurts. I have sinus congestion, headache, and body aches. Should I see the doctor? Should I give it a few days to pass? Thanks in advance.
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I'd say to go to the doctor to be on the safe side. Humira already makes you more prone to sinus issues, so you'll want to get that taken care of.

I mostly just take Advil Cold & Sinus to deal with the congestion, especially since it gives me migraines. Then I also have a steroid nasal spray to help me breathe better. The rest of it is just time, I think.
 
ey218 said:
Hi Everyone,

I'm on Humira and have been since February. My mom came to town, and has a bad cold, so of course I am feeling absolutely miserable today. My throat hurts. I have sinus congestion, headache, and body aches. Should I see the doctor? Should I give it a few days to pass? Thanks in advance.
Click to expand...

Hi-I have been on Humira since Sept. and ever since I started, I have been getting a cold/virus every 3 months or so (that is a lot for me). I actually have one right now, sounds like you do, too. My GP now puts me on antibiotics at the first sign of a virus, as a precaution. I have been told by my GI dr. that as long as I don't have a fever or other signs of infection, I am ok to take the Humira. I was due for my injection this past Friday, but waited until today to make sure the virus did not worsen into an infection. Hope this helps and I hope you feel better. Good luck!
 
Nancye50 said:
I was told no NSAIDs, was that only while on prednisone?
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Hi Nancye,
I made the mistake of taking advil and it caused a minor colitis flare-up. My GI specialist told me NEVER to take ibuprofen because it can, ironically, cause bowel inflammation.
Hope this helps!
 
Luthien said:
Anyone else really tired after their loading dose? I think I've taken a nap every day since my injections, normally I can't sleep because of the prednisone so it's weird.
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Hi Luthien,
The Humira made me tired for the first several months. I had terrible fatigue, and my doctors didn't really know what to do about it. In the meantime, I came down with a cold and my dr. prescribed Levaquin (antibiotic) as a precaution so that I wouldn't develop an infection.
A possible side effect of Levaquin is sleeplessness. Not only did I experience that side effect my first few days on it, but is somehow cured my fatigue permanently! I doubt your dr. would prescribe Levaquin for fatigue associated with Humira, but this is what happened to me. It was a blessing in disguise. If you are feeling fatigued, I just wanted you to know that I did also due to the Humira. It's not just you. :) Hopefully it will get better for you one way or the other. Good luck and HTH.
Nancy
 
ey218 said:
Hi Everyone,

I'm on Humira and have been since February. My mom came to town, and has a bad cold, so of course I am feeling absolutely miserable today. My throat hurts. I have sinus congestion, headache, and body aches. Should I see the doctor? Should I give it a few days to pass? Thanks in advance.
Click to expand...

My doctor said not to wait too long, and always go when having a fever.
 
Well my fever went up to 102.4. I saw the GP on Tuesday. She did a strep test, which was negative. She doesn't want me to take too much Tylenol as my liver panels were elevated because of the Humira. I am still feeling pretty miserable, but my fever broke and I'm back at work. I see the GI tomorrow about everything. This is just the worst.
 
Oh gosh, I'm sorry to hear you're still not feeling well. :( At least the fever finally broke... I know those are so miserable. You rest up as much as you can and take care of yourself, and good luck with your appointment!
 
I have a nurse coming over to my house in 2 hours to start my Humira! I'm pretty nervous :( hopefully I start feeling better soon. Does anyone know if it helps with the fatigue? Unlike most people, I have gained weight since my Crohn's symptoms started. I wonder if it will help my weight to go back down
 
You can do it! :D And depending on what your symptoms manifested as, it could help with the weight you gained -- if you were on prednisone and are able to get off of it, that would make a huge difference, too.

The fatigue it kind of depends. It may be caused by malabsorption, low iron/hemoglobin/ferritin, or low B12. Have you gotten a blood test to check for any deficiencies lately? If it is caused by your IBD causing malabsorption, it would definitely help with that.
 
ey218 said:
Well my fever went up to 102.4. I saw the GP on Tuesday. She did a strep test, which was negative. She doesn't want me to take too much Tylenol as my liver panels were elevated because of the Humira. I am still feeling pretty miserable, but my fever broke and I'm back at work. I see the GI tomorrow about everything. This is just the worst.
Click to expand...

It is miserable, but it's positive that your fever broke. Really watch and keep your doctor on top of your liver panels! Unfortunately, three weeks ago I was diagnosed with Autoimmune Hepatitis, and have been unable to take my Humira until my LFTs normalize/plan of attack. Humira and almost ever single other drug is hard on the liver, and us with Crohns/UC also are more likely to have concurrent liver autoimmune issues, like Autoimmune Hepatitis, Primary Sclerosing cholangitis, and primary biliary cirrhosis (not saying or inferring you have these issues, just something to be cognizant of as an IBD patient).
 
I have low iron and low b12, and I am on supplements for both. I've still been pretty tired though. Haven't noticed that they have helped a ton, but a little. I know different people react differently to humira, but I hope I feel the results soob
 
...my humira came yesterday...loading dose...it's in the fridge and I have to wait till wed for the humira nurse...
 
LCATC945 said:
The being able to drink again is the best part.
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I haven't started Humira yet & I was wondering about Humira & alcohol consumption. Can you still consume alcohol while on Humira? I am having difficulty finding documentation on Humira & alcohol consumption.
 
BayAreaChronie said:
I went straight from prednisone to Humira with a dose every other week. No Imuran and I hope it stays that way. 1 Biologic was already tough to accept.
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My GI has recommended Humira treatment immediately. I have skipped over everything : ) I have not started Humira yet. Due to a positive TB test I have to treat latent TB before starting the Biologic.
 
Man that stinks about the TB. Hopefully it clears up soon. I will have to go look up Humira and alcohol. I remember it wasn't as much of an issue like if taking Imuran, but don't quote me.
 
Jay Woodman said:
I haven't started Humira yet & I was wondering about Humira & alcohol consumption. Can you still consume alcohol while on Humira? I am having difficulty finding documentation on Humira & alcohol consumption.
Click to expand...


I drink and there don't seem to be any problems with it. I think antibiotics/antidepressants/etc are the only medications where that's a problem. Biologics and immunosuppressants should be fine.
 
Scaryman said:
MTX on humira is prudent if tolerable.
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I had no idea your body produced antibodies against Humira. Nor was I aware you could use Methotrexate in combination with Humira to reduce these antibodies. I am reading as much as possible to understand Humira before starting the drug. The more I read the more confused I become : )
 
Jay Woodman said:
I had no idea your body produced antibodies against Humira. Nor was I aware you could use Methotrexate in combination with Humira to reduce these antibodies. I am reading as much as possible to understand Humira before starting the drug. The more I read the more confused I become : )
Click to expand...

It happens with any of these biologics, unfortunately! There are tests to see if you've developed antibodies to the medication or not, and using immunosuppressants in combination with biologics often help.

Remicade is a biologic that people are more likely to develop antibodies to, since it's made from mouse protein. Humira and other biologics are made from humanized ones instead so they don't run quite the same risk. I instantly developed antibodies to Remicade and had to stop because of that, whereas even without an immunosuppressant I haven't developed any to Humira. :)
 
Start Humira in the morning, feeling very anxious about the side effects. However looking forward to it working and getting off steroids. I have very bad cognitive issues at the moment and pains on the inside of my legs and arms. Arthritis?? So I'm trying to be positive that this Humira will help of these as well.
 
farm296163 said:
Start Humira in the morning, feeling very anxious about the side effects. However looking forward to it working and getting off steroids. I have very bad cognitive issues at the moment and pains on the inside of my legs and arms. Arthritis?? So I'm trying to be positive that this Humira will help of these as well.
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Stop worrying about the side-effects, most people do really well on Humira!!!And so will you!!
help your body with positive thinking, My GI said about 1-3% have side effects on Humira, all the others are perfectly fine!
 
If you worry about side effects they'll A.) actually get them because you think you will get them. B.) psych yourself out of taking the medication all together and go longer untreated. I had a friend that didn't want to take the steriods that were prescribed to her (rehmatoid arthritus) and waited a year to try it because she was so worried about sued effects. After a few days taking it she wasn't in pain and she kept kickin herself cause she didn't try it sooner
 
I haven't had problems with side effects & I've been on it 3 weeks now. I have drank a few times too without problems except I think it causes some inflammation or dehydration that leads to mild constipation.
I have been wondering about thigh and back soreness/stiffness. Maybe I've just been overdoing it while I'm so out of shape!
 
Are we not supposed to drink on humira? I don't even remember reading/being told that. I know I have to go easier on it anyway, tho, learned when I was on Remicade that different types of alcohol may give me more inflammation.
 
Elektrikhd said:
Are we not supposed to drink on humira? I don't even remember reading/being told that. I know I have to go easier on it anyway, tho, learned when I was on Remicade that different types of alcohol may give me more inflammation.
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I remember seeing something about that in the literature but I still drink like a fish on occasion. I just try not to do it in injection day
 
Hi all,

I was on humira from Feb 2009 until May 2013 when I asked my consultant if I could come off humira to see if my body could cope without it (worst mistake ever), my consultant simply said "yes try it." In October 2013 I had a big flare until Jan 14 when it was more under control. I have never felt like it has been put into remission completely as I was sensitive to so much food that I could eat prior to the flare - even melon. About 5 weeks ago it started flaring again but not as bad as the previous one (mostly D after eating, going around 5-6 times a day, some cramping, urgency and stomach grumbles and bubbles a lot). The consultant has put me to x1 weekly humira instead of fortnightly. I have been injecting weekly for about 4-5 weeks now and I know that it can take up to 3 months to take proper effect. The specialist nurse has said I should persevere as I'd then be put on steroids which they know I am reluctant to do.

I'm just wondering why I'd be put on steroids as my view is if the treatment is no longer working then steroids may just settle it for a short time and then it will come back when I taper and the humira isn't working? So what's the point? Why don't they look at another biologic or Methotrexate? (Remicade has failed 2/3 times with me over the years).
I will take entocort if I have to but not pred). Do you think I need to just give it more time to work before I panic and ask for steroids or resign myself to the fact the humira isn't working?

I'm no longer under the consultant's care who said I could come off humira due to poor management from them as a team. I changed trusts and consultant in November last yr.
I'm currently not in work due to the urgency I get and lack of energy and stomach discomfort like bloating etc. I am frontline nhs and my job is far too active and stressful to cope with this flare too :(

Thank you for any advice/opinion you may have.
 
I was considering coming off of Humira but after reading your story I'm having second thoughts. Were your symptoms immediate after you stop taking the medicine?
 
^^^^ yeah that
DS has been on humira for over a year
No drug issues .
The thing with biologics is the docs /drug companies keep telling you about the dreaded possible side effects over and over.

No one does this for Tylenol and it's given to infants but can cause liver damage and deadly side effects .

Nothing is risk free .

We focus on the benefits instead
 
I am immensely grateful to biologics. I know what the potential side effects are but what choice do we have eh? Don't take it = very very unwell, take it = most likely well and possibly have side effects.
In the years I have been on it the only side effects I could link is raynaurds (but then again this is common in young women so may not be humira to blame) and more susceptible to infections like viral infections and a bit of dermatitis on my left toes - I can live with all those. If it wasn't for humira I'd be in a much worse place, I am so happy how well it has worked for me and free from our wonderful NHS.

Starbynight: my symptoms started 5 months after stopping it. I thought within those first 5mths 'wow this is great, I don't even need humira or other nasties' then boom along comes a monster flare to knock me down. My personal advice to you is don't come off the treatment if it works for you. The consultant has always said my moderate/acute crohns needs nipping in the bud and humira did that and kept me well. I wish so much I never came off it as I know I wouldn't be like this now, I have probably built antibodies to it now - joy. Stay on it and be happy you're well :)
 
Sometimes meds work and you don't see it or know they are working. My daughter almost came off Humira as we aren't seeing any difference. Her symptoms weren't really changing. Its behind the scenes that we can see the results with better scopes. If I didn't see it I wouldn't believe it. I was ready to give up after 7 months but there aren't any alternatives. Adding a combo drug can help a lot and I suggest it. We just switched from methotrexate to Imuran. For the first time in 2 years my girl went to the bathroom only 6 times yesterday and today will probably be 8. It is a wonderful feeling that for the first time we see some light in her treatment. Don't give up to find what works.
 
Thanks for your input. The reason my GI put me on Humira was due to to a possible recurrence of symptoms. This was last year and since then I only had one mild flair up. Sound like I should wait before acting.
 
This Thursday will be my second dose of Humira... I have noticed that I have gotten more headaches in the last couple weeks than before...and that I seem to be extra tired (which is saying a lot, Im already tired) Has anyone else had trouble with this? Is it maybe because I just did the loading dose a couple weeks ago and my body is just getting used to it? Or should I just suffer through the headaches for a while? Its making it hard for me to be at work in the afternoons especially...
 
I did notice headaches and tiredness at first, but it went away, I guess once my body got used to the medication.
 
I had horrible migraines for a day or so after my Humira injections for the first few months, then that side effect went away. I was exhausted after my loading dose, but the second dose and the subsequent doses have not made me any more tired than I already am. Give it some time; it should resolve. :)
 
MrsDay said:
This Thursday will be my second dose of Humira... I have noticed that I have gotten more headaches in the last couple weeks than before...and that I seem to be extra tired (which is saying a lot, Im already tired) Has anyone else had trouble with this? Is it maybe because I just did the loading dose a couple weeks ago and my body is just getting used to it? Or should I just suffer through the headaches for a while? Its making it hard for me to be at work in the afternoons especially...
Click to expand...

Hi MrsDay!Looks like we are on the same track! last week I had my first 4 doses and I will take 2 on June 26 then 1 every other week. I am tired also, circles under my eyes and sighing alot! -not too much energy either. I haven't had any headaches though... I DO think my pain is a little better though and I am down to 5mg of prednisone and usually I am hurting bad by now. So I am hopeful!
I know they say it can take 4 weeks and who's to say what is going on with this crazy disease? I hope you feel better soon!! :)Meg
 
I'm also on my second dose of Humira next week and so far so good. No headaches and have dropped down to 5mg of pred for 2 weeks before going off. Still have mouth ulcer so hopefully the Humira will fix that soon. Glad I haven't had any side effects like I had with aza and ap6. Does anyone find that the Humira helps other manifestations of Crohn's:.
 
After 35 years of Crohns and old meds, my doc has put me on Humira. I'm on social security and a prescription plan and scared to death about the costs. Any help there? My rep is coming to see me next week.
 
Pollie there is help directly through Humira. In Canada it is Progress that helps us with the 20% our insurance doesn't cover. I recall this in another thread. Search the forum (& I will search for the thread too). Hopefully someone in the states chimes in soon if we don't find the thread.

Good luck with Humira!
 
Humira was covered by my Medicare "silver scripts."Have to get Pre-approval though. Download application from Medicare site fill out what you can then take to doctor to complete. ( Silver Scripts is a part of my Empire Plan NY State Medical Insurance for retirees)
Good luck!
 
I will check that out. Thank you. I'm also really concerned at my age about the side effects. I've had 2 surgeries (docs advise no more than 4) but I'd almost rather face another surgery than the side effects (cancer, etc) of Humira.
 
I am going in Humira next month and I'm wondering if my ileum needs to be resected first. Ive had two blockages this year. Also, has Humira helped with artritis in spine?
 
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Ive been on humira for 4 months. Started helping me after 2 months or so. Recently been having a few issues with BM. But been a helper thus far. Have had half desending colon removed and had 2 feet of intestine split. Tried mosr every treatment and humira best so far. Waiting on SCR....
 
Question for you all i'm kind of freaking out. I have been on humira for about 6 months and now have sore muscles in the legs, the left side of my neck and shoulder. Numbness in my hand if I carry anything. The other day was a sore throat and today I lost the vision for 5 min or so in my left eye. Has anyone ever had any side effects like this? Should I be heading to the hospital?
 
I would definitely mention it to your doctor if you haven't already, but I don't think it's at the point where you need to go to the hospital. You should let your GI know right away, though.

Are you on any other medication?
 
Please help, I have put so much weight on since starting humira last summer it is getting unreasonable now I need to do something. I have a as healthy as can be lifestyle now thanks to humira but cannot stop the steady weight increase
 
I caught a GI bug from my son. So miserable. Do I take Tylenol for the fever? Just try to stay hydrated?
Trying to see it as a reset button because the last few weeks have been awful. Need to stock up on probiotics and get this under control.
 

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PARADIGM SHIFT NEEDED!!!
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