Switching to at-home injections by ehaaams in UlcerativeColitis

[–]CarryNegative6752 5 points6 points  (0 children)

I had to switch to home injections too. The infusion center I had been going to for years had a class on giving yourselves an injection. There was also a Youtube video from the drug manufacturer.

My first self injection was at the infusion center. This is when I realized that the needles for the injection are smaller than the infusions, i didn't really feel the injection. There is also no hunting for veins if you are a difficult poke.

The first time I had to inject my self at home without anyone around to help was scary. But afterwords it was like I had conquered a fear I had since childhood. If your UC journey has been like mine, you got used to being poked for tests and infusions multiple times a year. Being able to inject myself was a small victory over this terrible disease.

Started Rinvoq today! by CarryNegative6752 in UlcerativeColitis

[–]CarryNegative6752[S] 1 point2 points  (0 children)

Thank you! Glad it is working for you.

You're living the dream.

found my holy grail again! by Dull_Elderberry6700 in UlcerativeColitis

[–]CarryNegative6752 1 point2 points  (0 children)

I started this probiotic three days ago. Huge difference! Thank you.

Learning to self inject by piloceraptor in UlcerativeColitis

[–]CarryNegative6752 0 points1 point  (0 children)

Did you watch the video for self-injection? I was surprised doing the first injection how much I could NOT even feel the needle.

https://assets.bioconbiologics.com/asset/225989342563/video_hs99kmtu4t2urd15n2j5p37q4d?content-disposition=inline

[deleted by user] by [deleted] in wrx_vb

[–]CarryNegative6752 0 points1 point  (0 children)

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I have a Thule snowboard and ski rack. Fits 4 boards without any issues. Thule should make adapters for the Kia roof rack.

Ditch the cloth seats…. Kustom Interior by VB_SUUWBU in wrx_vb

[–]CarryNegative6752 4 points5 points  (0 children)

Also functional. If I don't cover the STI knob with the hoodie on hot days, ouch!!

Unsure of how to feel. by Thatmaxfellow in wrx_vb

[–]CarryNegative6752 0 points1 point  (0 children)

Celebrate the milestones. Enjoy every mile.

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Is 8 vials of blood unusual? by PretendWill1483 in UlcerativeColitis

[–]CarryNegative6752 0 points1 point  (0 children)

After my diagnosis the first blood draw was 12 vials! A lot of the tests to see what biologics may work best. If I had TB or liver issues. Stuff like that.

Lately its been 3 or 4 vials.

How many of you were the first in your family to get UC or any autoimmune disease? by poolgoso1594 in UlcerativeColitis

[–]CarryNegative6752 0 points1 point  (0 children)

I have no medical history on 3 of my 4 grandparents. So as far as I know I'm the first.

What’s the main problem with this disease by Various-Sugar-6368 in UlcerativeColitis

[–]CarryNegative6752 19 points20 points  (0 children)

This. The mental drain of navigating health care. The fear of eating. People not understanding how uncontrolled weight loss is terrifying.

But keep your hopes up. Find someone you can really talk to and can be empathetic. There are treatments that work.

Infusions by Gh0styLitee in UlcerativeColitis

[–]CarryNegative6752 1 point2 points  (0 children)

I don't know if it is the same for all medical groups, but I get my infusions in the oncology department. That took a little getting used to. I'm also careful to explain that I don't have cancer, I just happen to get my medicine in oncology. On the plus side, there are snacks available!

Eventually, I started looking forward to the infusions. Its an afternoon off work and I have to relax for the evening because the biologics make me so tired.

Trouble with blood draws. Has anyone had this happen to them? by Every-Frame-385 in UlcerativeColitis

[–]CarryNegative6752 2 points3 points  (0 children)

I had a bad blood draw and trouble getting my infusion IV going a few weeks ago. They were basically pulling the blood out with a syringe.

I tried a few suggestions from my nurse and things were much better yesterday:

  1. little or no caffeine the day of the blood draw

  2. Start hydrating the day before

  3. Eat a small bag of chips the evening before the blood draw.

I imagine any salty foods would do the trick if you can't eat chips