I was diagnosed in 2012 with UC. Since then I have tried Sulfasalazine, 5-ASA, steroids, and currently am using Humira. Nothing has ever made any difference in my symptoms and now my GI is recommending Entyvio. I am hesitant though as I have read many horror stories about side effects with this drug. Does anyone have personal experience with Entyvio they wouldn't mind sharing with me? I feel like I don't have many options left and would like to feel more confident in my choice.
Thanks!
Reply posted for louisebelle.
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Reply posted for louisebelle.
Hey there!
I have been on entyvio for a year now. It has worked however, every infusion I suffer from many many side effects including the infections or colds that follow since it weakens your immune system. Just make sure you wash and sanitize your hands vigorously and I wear a surgical mask in places I know I will be a while in. Especially when im at work but only because I work in retail and we have tons of sick customers that come in. I am however working with a holistic doctor to eventually get off this medicine. I do not feel it is healthy and has increased my quality of life. Yes it has stopped the symptoms but it has created a million other symptoms so I want off of it not to mention the potential risk of getting PML or cancer no thank you. I am doing bone broth daily (heals your immune system) enzymes(gives me energy and non addictive) artichoke extract (helps my gallbladder function properly again) I swear that I have felt 100 times better doing this. Plus regular exercise and proper eating meaning protein based foods, water, and gluten free foods have enhanced my life so much! I hope this helps :) if you decide to do entyvio just remember there are other options too.
Reply posted for louisebelle.
I just started this medication and I am feeling better. No side effects thus far.
Reply posted for louisebelle.
I have been on Entyvio for a year and according to my doctor I am now in remission. I have had no issues or side affects from Entyvio. I hope you have the same outcome from taking this drug.
Reply posted for louisebelle.
I haven’t had any problems with entyvio other than psoriasis, which is not listed in the possible side effects, but is for remicade which I used to be on. They are similar drugs so i’ll blame the entyvio. I’ve had psoriasis for years but this is much worse. It started in my feet and worked its way up my legs, plus on my forearms.
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