does anyone that lives near me take enbel and spondylitis | MySpondylitisTeam

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Top 10 Search Results for "does anyone that lives near me take enbel"

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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

Enbrel And Medicare
A MySpondylitisTeam Member asked a question 💭

Will be switching to Medicare in a few months and in researching my options I'm finding Enbrel will cost me about $5000 more per year than it does on my current health insurance. What have other people done when moving to Medicare?

A MySpondylitisTeam Member

Amgen works with a program called Saftynet Fondation , if you qualify you pay 0$ for your Embrel… Contact them

Why Can't We Share Our Successes?
A MySpondylitisTeam Member asked a question 💭

I love to hear the successes, even what some people think are too small for anyone to be interested. They are ALL inspirational to me. No one on this and other forums about lifelong suffering has anything easy about their life. Every day is a triumph over death. Why not share more triumph? Venting is good, but probably better and more appropriately done with a paid therapist trained at handling it. Lashing out at strangers for sharing a win over chronic disease perpetuates the misery. I don't… read more

A MySpondylitisTeam Member

I like to remain as positive as I can. And find something to be grateful and thankful for each day.

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 💪 💙 ❤️

What Treatment Are People Taking? I’d Love To Know As They Want Me To Take The Once A Week Enbrel But I’m A Bit Afraid Of That
A MySpondylitisTeam Member asked a question 💭
A MySpondylitisTeam Member

They should have a card that puts money on it that allows you to use as your copay, normally your dr will get that started for you. I chose not to take the Enbrel injections as I work in the hospital… read more

Hi All, Happy Sunday. I Started With This Awfulness About A Year Ago.
A MySpondylitisTeam Member asked a question 💭

I am curious as to whether anyone else is dealing with something called Exertional Compartment Syndrome related to their AS. Mine is compartment syndrome of the lower legs. Little by little over the last year, I noticed that every time I would squat down, my legs felt like they were going to pop. Then I started noticing a bulge in the compartments of my lower legs, right below my knees, both legs. Finally, a very astute and kind orthopedist did some pressure measurements in the compartments of… read more

A MySpondylitisTeam Member

@SherriLawler- I am going to try someone new in the next couple of weeks. My pain management doc doesn't think I need another MRI right now. My last one was in March of this year showing mild… read more

COVID-19 and Spondylitis Essential Updates Read more >
Is It Usual To Have Swelling In Foot Pads Under Toes And Toes Themselves?
A MySpondylitisTeam Member asked a question 💭

This swelling makes my pain increase to point I am having difficulty in walking at times

A MySpondylitisTeam Member

Massage and hot bath

How Do You Deal With Loneliness?
A MySpondylitisTeam Member asked a question 💭

My "friends" dropped me after my diagnosis and I couldn't be spontaneous with activities. I can't work and have no friends to even TRY to do things with. Does anyone else experience this?

A MySpondylitisTeam Member

Yes, all the time. Still havent figured out how to make things better. I walk about 2.5 miles a day. That helps some.

Has Anyone Recieved Infusions For Thier Ankylosing Spondilitis
A MySpondylitisTeam Member asked a question 💭

My Rheumatoligist has suggested that get in infusionssf Siponi Aria? I am going to get my booster next week then I have to wait 2 weeks before I start the infusions

A MySpondylitisTeam Member

My Rheumatoligist took me of Simponi because it seemed like it stopped working in am in getting injections of Cimzia, feeling better.

Humidity Vs. Heat
A MySpondylitisTeam Member asked a question 💭

Two in one...
What does humidity DO to agrivate our condition?
How is hot & humid different from dry hot regarding our condition?
I've seen people comment on here about humidity and been surprised. I've never thought about it. I thought heat was heat. What does humidity DO to agrivate our condition?

How is hot & humid different from dry hot regarding our condition?

A MySpondylitisTeam Member

I agree atmospheric pressure makes mine worse
When we recently had a Hurricane pass by and the pressure got down to the 900's I got so much worse.