humirasideeffects stelara ulcerativecolitis cdiff coconutoil crohn crohnsflare crohnsnomeds glutenfree pregnantcrohnie remicadeinfusion steleraweds stoma stomachsurgery vegan sepsis remicadecollage colitissurgery ibdrecovery howtobesick ensureplus modulen crohnssurgery humira ostomybag probioticsyall hernia stelera giappointment modulen
I guess Monday’s are going to be Humira shot days
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Got my Humira delivery today!! A nurse is going to come out on Monday for my loading dose. Definitely not looking forward to these 4 injections on Monday but if it is going to help my Crohn’s symptoms and put me in remission I’m up for staying positive and trying anything right now.
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Once every two weeks I will be injecting myself with one humira pen if this means it will help put my crohn’s into remission then I’m up for it. One step closer to getting back to normality! To start off with the first week i will be injecting myself with 4 pens and then two weeks after it will be two pens, this is to kickstart the medication. From then on after it will be once every two weeks with one pen.
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Would anyone like to see a video of me injecting myself with Humira?
Would this help anyone?
Or would you just like to see what Humira is all about and to see my reaction?
Scoprire di avere una malattia autoimmune che colpisce le articolazioni non è piacevole , svegliarmi e non riuscire a camminare oppure piegarmi per infilarmi i calzini e non arrivarci o stirare con dolore alle mani .... tutto diventa un impresa .... ritrovarsi con le ginocchia gonfie calde doloranti non è una bella sensazione.... correre , nuotare andare in bici e sentirsi imprigionata nel corpo di Pinocchio diciamo che non è quello che avrei immaginato per me a 41 anni ....ma non mollo e insieme alle mie medicine Metotrexato e Humira alla corsa al nuoto alla bici allo stretching , all alimentazione celiaca senza nichel e lattosio e grazie a mio marito tassello fondamentale nella mia vita , cerco di andare avanti ma soprattutto ogni giorno immagino di tornare ad essere quella che ero : una persona sana .... amate la vita è trattatela sempre con i guanti bianchi ❤️se state vivendo la mia stessa esperienza contattatemi insieme siamo più forti #nonmollaremai #lovetriathlon #loveironman #juvenilearthritis #artritereumatoide #artritereumatóide #artritepsoriasica #blogartritereumatoide #humira #humirapen #metotrexato #metotrexate #malattiereumaticheautoimmuni #malattiereumatiche #doloriarticolari #sport #triathlon #swimbikerun #fabiodiniccola #gonfiore #blogartritereumatoide #artritepsoriatica #artritepsoriásica #pamelamancini❤️ #humirainjection #humirasideeffects #rheumatoidarthritiswarrior #reumatologo #blogartritereumatoide #artritepsoriasica #nonmollaremai #donne #donnetoste #fabiodiniccola #
Well the good news is the #humira is working really well for #RA symptoms, but the bad news is I have started getting these big injection site reactions . Not painful, just itches and very swollen. Lasts about 4 days. Any other Humira pen users dealing with this Well I know it is the most common side effect so that is kind of a stupid question . Started after my 5th injection.
#rheumatoidarthritis #humirapen #humirasideeffects
#ibdawareness #ibdawarenessweek #crohnsdisease #crohns #crohnsgirl #crohnswarrior #humira #humirasideeffects Raising Awareness for IBD Awareness Week 2018. Humira is my magic drug but I get awful side effects including Fatigue, Joint Pain, Hair Loss and Thrush. My immune suppressants make it hard to fight off infections so I need a yearly flu jab, plus monthly blood tests and regular colonoscopies. Not nice but the drugs are bloody lovely lol.
Today’s affirmation: I will stay healthy.
Due to being on immune system suppressors, last time I was on a commercial airline, I caught a nasty cold. So now I get to be that weird person with the face mask when traveling. Honestly it feels super weird. I’m hoping it gets less awkward for me over time. For now, I’m just pretending I’m at burning man and keeping my goals in mind: DO NOT GET SICK. maybe more people should wear these normally ♀️ •
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#crohnsdisease #crohns #crohnswarrior #crohnsfighter #crohnsawareness #humira #humirasideeffects #sick #lookingfly #crohnsiscray #colitis #ibd #travel #traveling #travelforwork #travelblogger #stayhealthy #health #facemask #mask #respirator #falife #crew #crewlife #southwestairlines #blogger #burningman
1 year ago today...what a journey. Since I take humira for Crohn's, my immune system is low.
On the left is my impetigo outbreak that appeared 3 months after I started a strict diet and supplement protocol. I removed so many common foods that it shocked my body (my immune system in particular.) I was so focused on removing food allergens in hopes of repairing Crohn's, I did more harm than good.
My body didn't know how to cope with missing foods I had been eating my whole life. I didn't realize how sensitive my body was. In 1 month I noticed I had a swollen lymph gland on my throat, which scared me, I never had swollen lymph glands, ever, no matter how sick I was. I didn't want to think that my diet changes were the cause so I continued doing what I was doing (under the supervision of a naturopathic doctor, which clearly, this one was no help.) I also had a reoccurring sore throat that developed the same time I got the swollen lymph gland. I didn't really think much of it, it was during cold season in November so I assumed I was fighting off the common cold.
When my impetigo broke out, it first looked like acne so I treated it like acne, but it only made things worse. I tried everything....oils and tea compresses, rosehip seed oil, seabuthorn oil, zinc oxide, she butter and lavender, raw honey, I can't even remember it all but it was A LOT. It was so itchy and cracked, so uncomfortable, and so embarrassing to go out in public.
After a few months of the impetigo outbreak, I went to see a doctor and got a topical antibiotic with corticosteroid. It worked instantly to relieve the itch and redness, but I didn't feel comfortable using it. Luckily, I only needed to use it for a few months, 3 times a day, and also seabuthorn oil in between.
It took 3 months for my skin to repair, but the impetigo disappeared. I also realized that my swollen lymph gland also disappeared when the impetigo got better...which makes sense since the immune system was so stressed. *So after all this, the biggest lesson was to take things slow to recover my Crohn's. The body requires balance and is so sensitive. Patience and respect. That is what the body deserves.
So, I’m taking my Tamiflu, despite my test being negative. It felt like the flu yesterday, for sure. However, I’m starting to think it could have been a really bad RA flare. I lost my appetite, stuffy, my hand joints were hurting, and then my head, neck, and entire body were killing me. I was in tears and barely had the energy to drive to the clinic and home. Now, I’m still stuffy. I think that these continuous sinus issues are related to my Humira injections. Plus... both my hands are super swollen! Is it flu or just RA? Anyone else experience anything similar? Btw, I’ve not had a fever. #humirasideeffects #ra #rawarrior #raawareness #rheumatoidarthritis #rheumatoidarthritiswarrior #rheumatoidarthritisawareness #rheumatoidarthritisproblems #rheumatoiddisease