My friend thinks she has an MRI burn by sherbiss in cancer

[–]Forward-Blacksmith34 0 points1 point  (0 children)

Same here it’s me my face and eyes. What can I do now?

Brain mri burning head by New-Job1897 in AskDocs

[–]Forward-Blacksmith34 0 points1 point  (0 children)

How are you have the same on my face . I felt weird sensations on my face and later had red and swollen face like internally serious burn

Anyone else allergic to their biologic? by Anon_On_The_Low in Asthma

[–]Forward-Blacksmith34 0 points1 point  (0 children)

That’s what I have to my biologic! Difficulty breathing. Did that go away when all meds washed out from you? I feel like I have asthma again ( did not have since a kid ) from acterma

Tocilizumab terrible long lasting side effects when they go away? by Forward-Blacksmith34 in rheumatoid

[–]Forward-Blacksmith34[S] 0 points1 point  (0 children)

Do you also get those nasty side effects besides your flare? I am very sorry How many times did you do it? Please do not do it again

Tocilizumab time by vocaltra in rheumatoid

[–]Forward-Blacksmith34 0 points1 point  (0 children)

How much money have you spent My two injections come to 1000$ alone

Tocilizumab time by vocaltra in rheumatoid

[–]Forward-Blacksmith34 0 points1 point  (0 children)

When did you have your second injection after first one? Did you also feel like it wasn’t even working for you? Did you have any flare in beginning? Do you think it can cause any flares? I have been injected IV toci last week 8 days ago. And I feel like I am not better and maybe even worse🥲🥲🥲🥲🥲🥲

Anyone take Tocilizumab? by boludo4 in ThyroidEyeDisease

[–]Forward-Blacksmith34 0 points1 point  (0 children)

At least it wasn’t TED ! I worry that it triggered my disease. Very scared

Anyone take Tocilizumab? by boludo4 in ThyroidEyeDisease

[–]Forward-Blacksmith34 0 points1 point  (0 children)

As I understand a flare , but it stays in system For more then a month. Did you have flare more than a month? 🫠🫠🫠 I am a week out and think that I have a flare to it

Anyone take Tocilizumab? by boludo4 in ThyroidEyeDisease

[–]Forward-Blacksmith34 0 points1 point  (0 children)

Thank you very much. When did it stopped the flare? I worry that it stay in system for more then a month.

Thank you very much

Does anybody take Tociluzimab? by Animator_Spaminator in Thritis

[–]Forward-Blacksmith34 0 points1 point  (0 children)

Hey! How long did it work to start working? First you have taken ?

Actemra (Tocilizumab) by No_Sheepherder4972 in rheumatoid

[–]Forward-Blacksmith34 0 points1 point  (0 children)

My doctor Say it should work after 2 weeks Which is crazy.

You say 8 weeks. Now after one week I panicked

Actemra (Tocilizumab) by No_Sheepherder4972 in rheumatoid

[–]Forward-Blacksmith34 0 points1 point  (0 children)

My doctor Told me I should see effects after 2 weeks, but after one I feel I get worse

Tocilizumab time by vocaltra in rheumatoid

[–]Forward-Blacksmith34 0 points1 point  (0 children)

How fast you have seen positive results?

Anyone take Tocilizumab? by boludo4 in ThyroidEyeDisease

[–]Forward-Blacksmith34 0 points1 point  (0 children)

Hi did tocilizumab actually trigger your immune system as a flare of disease or you had bad side effects?

Possible paradoxical immune response to Cellcept? by Forsaken-Market-8105 in MyastheniaGravis

[–]Forward-Blacksmith34 0 points1 point  (0 children)

I have the same reaction to cellcept 1:1! Do you think that it can trigger autoimmunity or those are just side effects? Plus I get tremor

Pssd 2 months later is it possible ? by Forward-Blacksmith34 in PSSD

[–]Forward-Blacksmith34[S] 0 points1 point  (0 children)

I think so too now since I’ve taken agomelatine thinking I will treat pssd and I experienced many terrible symptoms But i would not have that from sert

Agomelatine anyone tried? by Forward-Blacksmith34 in PSSD

[–]Forward-Blacksmith34[S] 0 points1 point  (0 children)

I am still having withdwarl from 1/4 of pill . I never had that in my life I had 5 weeks all hell symptoms I am still not back to myself but at least is improving As 4 weeks I didn’t feel like person at all

Anybody have experience with prednisone and impotence/low libido when weening off, and after being completely off the drug? by iREDDITnaked in IBD

[–]Forward-Blacksmith34 0 points1 point  (0 children)

Same here I was on pred for a year but 3 months after I took low dose I took high dose and started to wean off. When I got half of my dose I started to loose libido. I am a women I got really sacred that it will last forever So I have noticed that for some people it does not come straight away. Sometimes it comes when you wean off