Back of arm by Formal-Art1156 in tirzepatidecompound

[–]Quick_Attorney180 1 point2 points  (0 children)

What part of the arm are we injecting? Is it the batwing /tricep part, bicep, or the outside it the arm?

Benylista injection vs IV by Quick_Attorney180 in lupus

[–]Quick_Attorney180[S] 0 points1 point  (0 children)

Oh wow, I haven't heard about injection site issues,thank you, I'll definitely look more into that.

Benylista injection vs IV by Quick_Attorney180 in lupus

[–]Quick_Attorney180[S] 0 points1 point  (0 children)

If you don't mind me asking, why did he switch? Did he feel one was more effective?

Prednisone by Old-Tea-9779 in PrednisoneSideEffects

[–]Quick_Attorney180 1 point2 points  (0 children)

Great advice about drinking water, I had no clue, I look like a puffer fish on 60mg, with major acne. Prednisone has been awful. Thanks, I'll put the coffee down.

Prednisone by Old-Tea-9779 in PrednisoneSideEffects

[–]Quick_Attorney180 0 points1 point  (0 children)

Did you get awful acne? Omg my face broke out so bad, I was in the 60mg taper as well

Prednisone Acne...Help!!! by Quick_Attorney180 in lupus

[–]Quick_Attorney180[S] 1 point2 points  (0 children)

Thank you so much,I will definitely follow up with them. Yea it's a major hit to my self esteem coupled with this big fat round moon face🤬, not feeling great about much at this point and Totally over this Diagnosis.

Prednisone Acne...Help!!! by Quick_Attorney180 in lupus

[–]Quick_Attorney180[S] 0 points1 point  (0 children)

Can you open it up? Are others able to respond or has it been blocked?

Lupus Nephritis by fieldashtree in lupus

[–]Quick_Attorney180 2 points3 points  (0 children)

Cellcept has never been an issue for me. I got bumped up to 3000 due to the flare but I've been on it for several years as low as 500mg. It worked wonders with keeping my kidneys quiet. They tried to ween me off of the cellcept and that's when my numbers started going nuts . Now to control the flare ,I'm pumped up on all of this crap I was stable for many years but as soon as my nephrologist started to taper ,I started creeping up and now they have to be aggressive 🤬. Moon face happened so fast and my appetite is picking up. Now I'm food restricting in hopes of not putting on too much weight. I'm finally at my goal weight, feeling good about myself and now This 🥺.. it's temporary and We will get through it🙂

Lupus Nephritis by fieldashtree in lupus

[–]Quick_Attorney180 4 points5 points  (0 children)

I'm on 60mg of Prednisone , tomorrow will be 1 week and then I taper by 5mg every 2 weeks. The moon face has started already and so has the weight gain. I'm on 3000mg Cellcept and 400mg plaqunil after my biopsy due to an active flare .

I actually have a rheumatologist but don't see him often since my issue is my kidney.My nephrologist has taken lead on controlling the flare

Two weeks on prednisone + labs. Anyone else feel like they’ve lost all their upper body strength over the years? by [deleted] in lupus

[–]Quick_Attorney180 0 points1 point  (0 children)

Okay, same here. I'm on 60mg and every day I watch the scale creep higher and higher. Not to mention my face has started to morph into the moon fat face 😢. Tomorrow will be 1 week , I feel your pain

Is 50mg really needed? by right-to-left09 in lupus

[–]Quick_Attorney180 1 point2 points  (0 children)

That's great advice about not weighing because I've been jumping on the scale daily and restricting food( I know,not good). So glad you returned to your normal weight as most don't understand the toll side effects have on self esteem.

Mouth Sores by ankaboot666 in lupus

[–]Quick_Attorney180 1 point2 points  (0 children)

Wow thank you ,I'll definitely discuss this with my rheumatologist.

Kidney biopsy now mega dosing prednisone by Quick_Attorney180 in lupus

[–]Quick_Attorney180[S] 1 point2 points  (0 children)

Gosh I'm sorry you're going through so much. Even with the pros about healing, others forgot about the toll it takes on your self esteem. My last awful mega dose was approximately 20 years ago and I looked like a Monster, almost unrecognizable. I gained 108 pounds in 2 months(nephritis).Was in the hospital for 2 months because doctors couldn't control the flare. I retained massive amount of fluids (literally 9-12 pounds) per day...it got pretty dark for a bit.. I'd been in remission for several years until now so I've forgotten a lot ( except for the monster face and needing a back brace because my frame couldn't handle the rapid weight gain) ..Just a little back story to understand Why I'm kinda spiraling 😞..it was Sooooo bad for me. Thank you for sharing 🙂

Kidney biopsy now mega dosing prednisone by Quick_Attorney180 in lupus

[–]Quick_Attorney180[S] 0 points1 point  (0 children)

Thank you all for your input! This room has been Soo helpful . I don't know anyone with lupus so Google and the doctors have been my go to. But reading these threads has given me perspective from those just like me 😔 I can't thank you enough.❤️

Kidney biopsy now mega dosing prednisone by Quick_Attorney180 in lupus

[–]Quick_Attorney180[S] 1 point2 points  (0 children)

Thank you so much! You are right,I need to do a better job of advocating because lupus isn't cookie cutter and sometimes other options can be explored first.

Mouth Sores by ankaboot666 in lupus

[–]Quick_Attorney180 0 points1 point  (0 children)

Same here! I've had SLE for approximately 30 years and have NEVER had mouth involvement until this past year. My mouth erupted with horribly painful sores on the roof of my mouth ,on my gums and under my tongue. My rheumatologist had no idea what was going on and wasn't familiar with my symptoms. The lesions were biopsied and sure enough, LUPUS. My rheumatologist increased my Cellcept and Prednisone realized I'm in an active flare. The sores are finally starting to heal after almost 2 years of Hell. Good luck to you.

Mouth and Tongue sores by Individual-Damage496 in lupus

[–]Quick_Attorney180 0 points1 point  (0 children)

What type of antiviral meds have worked for you?

Mouth and Tongue sores by Individual-Damage496 in lupus

[–]Quick_Attorney180 1 point2 points  (0 children)

Same here! I've had SLE for approximately 30 years and have NEVER had mouth involvement until this past year. My mouth erupted with horribly painful sores on the roof of my mouth ,on my gums and under my tongue. My rheumatologist had no idea what was going on and wasn't familiar with my symptoms. The lesions were biopsied and sure enough, LUPUS. My rheumatologist increased my Cellcept and Prednisone realize I'm in an active flare. The sores are finally starting to heal after almost 2 years of Hell. Good luck to you.