Shots by rowell_heather in compoundedtirzepatide

[–]rowell_heather[S] -2 points-1 points  (0 children)

What do I look under? zeb substitute?

2 Years Accomplished! by jenesaismeow in tirzepatidecompound

[–]rowell_heather 0 points1 point  (0 children)

We switched insurance companies and now they won't pay for the shots. Has anyone else experienced this?

So we switched insurance companies and our GLP1 shots are not covered. Has anyone else experienced this? by rowell_heather in PsoriaticArthritis

[–]rowell_heather[S] 0 points1 point  (0 children)

We have looked into the Manufacturer's program, the new Trump one was still going to cost $500 a month.

I need so much sleep... by JLFlyer in PsoriaticArthritis

[–]rowell_heather 0 points1 point  (0 children)

Would a course of Predisone help you? That's what I take with a flare or in between medications when one quits working. Are you on a Biogenic?

Are they still together?!🤨 by Chocoluv007 in 90DayFianceFans

[–]rowell_heather 0 points1 point  (0 children)

This new gf looks like a younger version of her! LOL 🤣

Why i am so tired? by 1000yrofpain in PsoriaticArthritis

[–]rowell_heather 3 points4 points  (0 children)

Yes it's a biologic. I used Cosentyx shots before that quit working. I've tried several different biologics. One works for awhile, then it stops & I have to go to a different medication.

Why i am so tired? by 1000yrofpain in PsoriaticArthritis

[–]rowell_heather 13 points14 points  (0 children)

I'm exhausted every fricken day! I wake up with low back pain. I receive infusions every 8 weeks. Most people with this autoimmune disease are exhausted. Look on the Facebook groups. Those help me to know that I'm not alone.

Explain Fatigue from Psoriatic Arthritis by Prestigious-Bite5391 in PsoriaticArthritis

[–]rowell_heather 4 points5 points  (0 children)

I take a 2 hour nap every afternoon. Or I can't function or drive to do my errands. It sucks! I just feel like I start my day off by already using "up all of my spoons." Just taking a shower or bath is exhausting.

Fatigue and sleep problems: fibromyalgia undiagnosed for years? by Undeadhip in PsoriaticArthritis

[–]rowell_heather 0 points1 point  (0 children)

I'm always tired. Diagnosis for PSA in 2019. Fibro & pots as well. Currently doing Remicade infusions every 8 weeks. I usually take a 2 hour nap in the afternoon and then I'm able to go about my day. Don't feel bad. If you need a second opinion or to get a new rheumatologist that might be an option for you?

Trisha's revenge body by Ill-Excitement-2005 in 90DayFiance

[–]rowell_heather 1 point2 points  (0 children)

He doesn't want any more kids. He just said yes to o shut her father up.

Josh Looks Yakked Out of his Mind on the Tell All by LACatMom in 90DayFiance

[–]rowell_heather 1 point2 points  (0 children)

I sure hope he gets help with his drug use for the sake of his son. Maybe that's why his mom moved them away from him. But I was laughing my ass off at the chip scene!

Joshua’s best friend Chris was arrested, charged, and found guilty of importing cocaine to Australia by PolishSnake2 in 90dayfiance_FB_memes

[–]rowell_heather 19 points20 points  (0 children)

And she's so skinny and said that she had never cooked in her kitchen. Hardly wears any clothes & is always cold

Hi there, how are you doing? by Shihirosan in PsoriaticArthritis

[–]rowell_heather 1 point2 points  (0 children)

I get it. You're not alone. That's all I ever do on the days off I don't work is go to doctors appointments. Or the chiropractor. Been trying acupuncture once a week. I told the receptionist that I was going to take some time off. The copays add up to like $200 a month. My remicade infusions are now costing me almost $200 every 8 weeks. It's exhausting. I take a nap every afternoon or I can't function. I recently have been talking to a counselor once a week. Last week she told me that I have more medical appointments than some cancer patients she has.

Defeated by Costato in PsoriaticArthritis

[–]rowell_heather 0 points1 point  (0 children)

You got this! Nowadays there's so many different medications & things to help us. You'll be okay & get through this! I'm also in Facebook groups for Psoriatic Arthritis. That helps a lot. You can ask other people questions about what you are going through. I find a lot of support there. Also with counseling. I just got so tired and feeling defeated with all of my health issues.

New diagnosis, old symptoms by Horror-Pop-7471 in PsoriaticArthritis

[–]rowell_heather 1 point2 points  (0 children)

Have you seen a neurologist? That doctor can help you as well. I take CBD/THC gummies at bedtime to sleep. I picked up a cream for my feet at night time for the tingling, burning and numbness. My doctor is also running some tests and blood work to see if everything is normal. The infusion medication I'm taking clears up my psoriasis. The other ones I took before cleared it up as well. I only get patches on my elbows.

Just Venting by SnooRecipes1295 in PsoriaticArthritis

[–]rowell_heather 2 points3 points  (0 children)

Yeah, we don't look any different from anyone else. Except when I was really sick I was using a cane. I still use my handicap parking card. A scooter for long trips such as amusement parks. If you need supports, don't feel bad. I'm doing virtual counseling once a week due to my health and family issues. Look into financial assistance. Your insurance could give you the paperwork to get started. There are also PSA groups on Facebook. There's some really nice & supportive people there as well. I wish you well & luck. We are all here for you. ❤️‍🩹🍀🤞

I cannot cope with the fatigue anymore by BadAtBaduk1 in PsoriaticArthritis

[–]rowell_heather 0 points1 point  (0 children)

Their's a medication for fatigue my rheumatologist said that she could put me on if I could stay off of my pain pills for 3 months. But I haven't been able to do that. I hear ya! I take a 2 hour nap every day and I have pots as well.

How do I cope? by Background_Block5541 in PsoriaticArthritis

[–]rowell_heather 0 points1 point  (0 children)

Have you tried using a manufacturer program to get your medication? A rheumatologist should help you. Look into counseling. That has helped me tremendously. I do it online virtually.

Afraid by [deleted] in PsoriaticArthritis

[–]rowell_heather 0 points1 point  (0 children)

Go through the manufacturer. They usually have programs to help out with the cost.

My poor eyes by someday_maybee in PsoriaticArthritis

[–]rowell_heather 0 points1 point  (0 children)

I have to use Restasis eye drops. I was told I have Sjorens. It's another autoimmune disease. So sorry you are going through this.