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Top 10 Search Results for "experiencing biologic side effects this video explains what to bring up to your doctor"

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Does Anyone Have Abdominal Pain With AS?
A MySpondylitisTeam Member asked a question 💭
A MySpondylitisTeam Member

@A MySpondylitisTeam Member hi! I read your post about that you have a lot of UTIs. I have that problem too. Trough my adult life I’ve been having that problem. And since my diagnosis of PSo,AS and… read more

Why Isn't Some Sort Of IV Cortisone, Ativan, And Ketamine Weekly To Help With This? So Many Are Suffering. Biologics Are $1,200-$5,000
A MySpondylitisTeam Member asked a question 💭
Managing Spondylitis Flare-Ups Read Article...
A MySpondylitisTeam Member

Cortisone can’t be used continuously because of its side effects on the body. That is why cortisone shots can only be had a few times a year (2 or 3 times a year in each joint). Ativan does nothing to… read more

What Will Life Be Like On A Biotherapy ?
A MySpondylitisTeam Member asked a question 💭

Hello everyone :)

So I’ve been diagnosed and my treatment have failed to work … my rheumatologist evoked the possibility of getting me on bio therapy . I’m kind of scared of what my life might look like during the treatment …. I’m not really looking for people explaining what a biotherapy is , but more for people telling me what life is like when on this treatment .

Here are some questions I’m wondering about :

What kind of changes should I expect from it ?

Will I still be able to go to… read more

A MySpondylitisTeam Member

Theses are all great questions! I would. Like to hang out and see the reply’s to this myself for similar concerns.

Is Anyone Else Terrified Of Trying Biological Medicine? TB,Cancer,side Effects. Thanks
A MySpondylitisTeam Member asked a question 💭
Explaining the Invisible Pain of Spondylitis Read Article...
A MySpondylitisTeam Member

I concur with @A MySpondylitisTeam Member. In my observation amongst this and a couple of other forums that I've been on, I have yet to meet anyone on meds that don't have to change their meds or who… read more

What Can I Expect From Taking The Biologic Medication? It's So Expensive Any Advice When Your In A Flare For Relief
A MySpondylitisTeam Member asked a question 💭

Hello I'm shanica from Dallas tx I was just diagnosed with AS it's a horrible disease very painful most of the time stiffness in my back headaches loss of appetite stomach pain IBS issues I could go on and on

A MySpondylitisTeam Member

Prednisone during a flare helped, but I hate the side effects. The only dude effects I've noticed from remicade has been dry mouth and mild hair thinning. I too have copay assistance that takes a lot… read more

In Accord With The Latest Research, What Is The Most Effective Biologic?
A MySpondylitisTeam Member asked a question 💭
A MySpondylitisTeam Member

The most effective biologic is the one that targets the specific cytokine(s) attacking the body of the individual taking any particular niologic. Learn what they do and you will understand the… read more

Tentative About Starting Humira
A MySpondylitisTeam Member asked a question 💭

I was recently diagnosed with AS. I had started Celebrex 3 days before meeting my rheumatologist. The rheumatologist barely read my chart or listened to anything I was saying before telling me I need to start Humira. My inflammation markers are all down to normal ranges after Celebrex. My pain levels are drastically reduced - though I still have SI joint pain. The Dr said Humira stops the disease progression- which is why I need to start. If my inflammation is down, is the disease still… read more

A MySpondylitisTeam Member

Thank you so much for sharing your story

Is There Anyone That Take A Biologic But Still Have Lots Of Fatigue?
A MySpondylitisTeam Member asked a question 💭

I am on my second biologic. I have tried Humira and 6 most later my body attacked the meds. I am now on Cosetyx. It's been about 8 weeks and I still feel so fatigued. I was thinking depression and is it still this disease?

A MySpondylitisTeam Member

Stay strong warrior 💪 💙 ❤️

My Son Is Hoping For Some Relief With His AS With His New Medicine
A MySpondylitisTeam Member asked a question 💭

My son was diagnosed with AS a few years ago. He is now 36. He is going to start Humira in a few days. I was wondering if anyone else who is currently on Humira is having good results and what side effects you may be experiencing.

A MySpondylitisTeam Member

Thank you so much Danielle. I really appreciate you sharing your experience with me. I will let my son know and I hope he has a similarly positive response. I will pray that you find something to help… read more

Are Biologic Meds In The Same Family Of Medications As Tylenol And Antinflatory. I'm New To All Of This. Trying To Figure It All Out.
A MySpondylitisTeam Member asked a question 💭
A MySpondylitisTeam Member

Thank you