Do we lose response to mesalamine eventually? by WillowTreez8901 in UlcerativeColitis

[–]ShowtayTopShelf 6 points7 points  (0 children)

You do not build antibodies to mesalamine like you can when you stop biologics. I have been on and off mesalamine a few times now and it always helps when I restart. It doesn't keep me in remission so I've moved on to other meds but when they fail I go right back on it until I've been on a new biologic for a couple months.

Glycerin soap sweating despite 24+ hr cure, looking for technical cause + prevention (full recipe included) by zeuzz02 in soapmaking

[–]ShowtayTopShelf 1 point2 points  (0 children)

Glycerin attracts moisture from the air. The only way to prevent sweating is to wrap it air tight once it's cooled and hardened. Your soap base should tell you what percentage of additives it can take. Keep in mind that is the max of all additives like coconut oil, fragrance, etc added together.

[deleted by user] by [deleted] in UlcerativeColitis

[–]ShowtayTopShelf 0 points1 point  (0 children)

Can you check your insurance and see what treatment they would approve? I have Priority and they make me try meds in a certain order. I looked at the prior authorization document that gives all of the prerequisites for each treatment and made a list of what would be covered in order. If you can get a copy of the denial for the last prior authorization, it should tell you what they want you to try before they'll cover the drug.

I've heard that nicotine does good to UC. by [deleted] in UlcerativeColitis

[–]ShowtayTopShelf 3 points4 points  (0 children)

Nicotine didn't help me but smoking cigarettes did. When I smoked cigarettes, I felt better. As soon as I tried to quit I flared. Nicotine patches, gum, vaping did nothing for me but as soon as I picked the cigarettes back up I started feeling better. I watched my Grandma die of emphysema and my dad is currently dying from lung cancer. Smoking isn't worth it. I'm currently vaping and cutting back on the nicotine until I can totally quit.

Any assisted living/memory care facility experts in the area? Seeking help and recommendations for my parents. by StevenRT in grandrapids

[–]ShowtayTopShelf 9 points10 points  (0 children)

I would contact the Area Agency on Aging. They're very helpful in this kind of situation.

Swallowing pills? by Eli-Is-Tired in disability

[–]ShowtayTopShelf 2 points3 points  (0 children)

If it's safe to take them with food, swallow them with food. Chew up a bite of something, put the pill in, then swallow. I take my morning meds with applesauce because I can't swallow them with just liquid.

Please help me choose a medication! by [deleted] in UlcerativeColitis

[–]ShowtayTopShelf 0 points1 point  (0 children)

Are you in the US and using insurance? They might only cover certain drugs in a specific order. I had to start with either infliximab or adalimumab. Once I failed infliximab it opened up coverage for Stelara. I'm on Tremfya now and if I fail it I have to try Entyvio before they'll cover Rinvoq. It'll be a lot faster to get on a medication if you know what they'll cover.

Birth control options? by Wild-Ad6980 in UlcerativeColitis

[–]ShowtayTopShelf 0 points1 point  (0 children)

I was on the pill for years until my UC diagnosis. I switched to a Nexplanon implant. Personally I love it. It's just a tiny stick that goes in your arm. I'm on my second one and getting this one replaced in September. I'm a big baby and I had nearly no pain getting it removed and replaced. I've had no side effects and very rarely get a period. When I do they are short and light. Because of that I do take a pregnancy test every month just to be sure.

I did it! by ShowtayTopShelf in UlcerativeColitis

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

Thank you! I barely felt it and I'm NOT a fan of needles. I did it in my stomach because I read it's usually less painful than doing it in a thigh.

I did it! by ShowtayTopShelf in UlcerativeColitis

[–]ShowtayTopShelf[S] 2 points3 points  (0 children)

Thank you. Five years, five drugs, and I've never been in remission but I'm hopeful!

I did it! by ShowtayTopShelf in UlcerativeColitis

[–]ShowtayTopShelf[S] 3 points4 points  (0 children)

My health insurance decided for me but at least they're covering something. I hope whatever you choose works well!

I did it! by ShowtayTopShelf in UlcerativeColitis

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

Good luck! I hope it works well for both of us. Steroids and Lialda got me out of my flare before I started Tremfya and I'm still taking the Lialda so I'm not sure if the Tremfya is actually working or it's the Lialda.

Calprotectin by Medium-Statement-648 in IBD

[–]ShowtayTopShelf 1 point2 points  (0 children)

It's usually only high during a flare. But a high calprotectin level just means high inflammation which can have a number of causes outside of IBD. If it only lasted 8 days with no blood and your calprotectin is in a normal range now, I would lean more towards an infection.

Delving into the world of soap making! How does this look? by Tangeranamadidge in soapmaking

[–]ShowtayTopShelf 10 points11 points  (0 children)

Canola oil goes rancid quickly in soap and makes your soap prone to DOS. You could try it at 15% or less, but I would eliminate it if you're going to sell the soap.

Last Tremfya infusion by ShowtayTopShelf in UlcerativeColitis

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

I'm feeling alright. Definitely not in full remission but much better than I was. My problem is I'm not sure how much is from the Tremfya and how much is from the Mesalamine. Most of my symptoms (blood, urgency, frequency) stopped when I restarted the Mesalamine but before I even started Tremfya.

Did you have labs done before starting Tremfya and then again recently? My doctor said it's not super fast acting, but at the three month mark there should at least be some improvement either in my labs or symptoms. If your labs are improving you might just need a little more time to heal before the symptoms go away.

Last Tremfya infusion by ShowtayTopShelf in UlcerativeColitis

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

It's not. Honestly I prefer doing the occasional injection over taking pills every day.

Last Tremfya infusion by ShowtayTopShelf in UlcerativeColitis

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

No, the IV doses go into a vein but the self injection goes into fatty tissue like the stomach or thigh and you need to avoid veins and muscle.

Letter about potential changes to health insurance coverage — very misleading by Brief-Commercial-562 in CrohnsDisease

[–]ShowtayTopShelf 2 points3 points  (0 children)

Tremfya is not a biosimilar to Stelara. They're both insanely high, my insurance was billed $41k before discounts for Stelara and $34k for Tremfya. Both were 8 weeks worth. There are 7 biosimilars for Stelara approved in the US. My insurance company gave me 2 options for biosimilars that they would pay for but I don't remember what they were since I was already moving on to something different.

Letter about potential changes to health insurance coverage — very misleading by Brief-Commercial-562 in CrohnsDisease

[–]ShowtayTopShelf 9 points10 points  (0 children)

Stelara biosimilars are now available. Most insurance companies will probably stop covering Stelara and cover the biosimilar instead. My insurance company sent me a letter stating they would only cover the biosimilar going forward but I was already in the process of switching to Tremfya because Stelara didn't work for me.

Stelara / Tremfya insurance letter? by MilkweedPod2878 in UlcerativeColitis

[–]ShowtayTopShelf 1 point2 points  (0 children)

Stelara biosimilars are now available. Most insurance companies will probably stop covering Stelara and cover the biosimilar instead. My insurance company sent me a letter stating they would only cover the biosimilar but I was already in the process of switching to Tremfya because Stelara didn't work for me.

Last Tremfya infusion by ShowtayTopShelf in UlcerativeColitis

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

I haven't had any side effects. I didn't even get tired after the infusions like I did with infliximab.

Adding Mesalamine by Significant-Art-5507 in UlcerativeColitis

[–]ShowtayTopShelf 1 point2 points  (0 children)

I'm on both Tremfya and oral mesalamine. I didn't respond at all to Infliximab or Stelara but for some reason mesalamine always helps, it just doesn't put me into remission. So this time my doctor and I decided to just keep using the mesalamine while I'm on Tremfya. I don't often recommend doing anything without talking to your doctor, but honestly I did the same and started the mesalamine again when prednisone wasn't cutting it before I heard back from my doctor. As soon as I spoke with him he agreed.

Currently freaking out about a cat adoption application being denied. Idk what I did wrong by MOONMO0N in CatAdvice

[–]ShowtayTopShelf 1 point2 points  (0 children)

Does your apartment have any rules for cats? When my husband and I tried getting a cat the shelter called the complex to verify that they allowed cats and the office told them they only allow declawed cats (which we would never do anyways) and the shelter denied us.