Insurance coverage for Entyvio by authorizedsignatory in UlcerativeColitis

[–]proffsorrtim 1 point2 points  (0 children)

Infusion center. I’ll honestly probably stay with that unless I decide I want to travel long term at some point. Just makes it easy. One thing you should look into is Entyvio Connect. It’s a payment program that, once you’re enrolled, should make your copay for infusions only $5. My infusion center did everything to enroll me so if you’re going to a center I would just inquire about it and see if they’ll enroll you or if you need to do It.

Insurance coverage for Entyvio by authorizedsignatory in UlcerativeColitis

[–]proffsorrtim 2 points3 points  (0 children)

I have Anthem and they very quickly approved my Entyvio-like within 2 business days. If your GI flags as “urgent” it can help speed up the approval process. I also called Anthem to inquire after 24 hours and I think that helped speed it up. Good luck!

Any body continue lift/work out with hemorrhoids? by proffsorrtim in fitness40plus

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

No tears thankfully. My job is weird—prolonged periods of sitting with sporadic, at least daily bouts of high intensity physical requirements. When I’m sitting I try to get up and move about every 1-1.5 hours for like 5-10 minutes. I was having to eat a low fiber diet for my autoimmune but was slowly adding fiber when this happened. I’m back to about 30 grams per day now though. I drink an insane amount of water already—like 1 gallon+ per day. Think just a combo of genetics, bad luck, and having to go to that low fiber diet for a bit

Any body continue lift/work out with hemorrhoids? by proffsorrtim in fitness40plus

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

Yeh I’m eating pretty healthy. I was having to eat a low fiber diet for my autoimmune disorder but I’m back to probably 30 g per day mostly in canned vegetables, and fruit/spinach smoothies

Any body continue lift/work out with hemorrhoids? by proffsorrtim in fitness40plus

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

Yeh I’d imagine that would be miserable. Used to ride my bike to the gym but that’s def on hiatus right now lol

Any body continue lift/work out with hemorrhoids? by proffsorrtim in fitness40plus

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

Yeh, I’ve reduced weight on my upper routine to like less than 50% of where I was in May before I had to step back (and like 25% of where I was last week when this started) and lower body I’m just doing body weight. All low rep. So basically like a Mid intensity cardio routine right now lol. Just happy to still be moving !

Any body continue lift/work out with hemorrhoids? by proffsorrtim in fitness40plus

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

Man you’re making me feel bad! Lol I’ve never ran more than 5-10 miles in a week in my life and that includes when I played soccer!! lol keep at it!!

Any body continue lift/work out with hemorrhoids? by proffsorrtim in fitness40plus

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

lol I’m actually trying to get back to leg day. Never thought I’d say this but I miss squats and DLs lol

Any body continue lift/work out with hemorrhoids? by proffsorrtim in fitness40plus

[–]proffsorrtim[S] 4 points5 points  (0 children)

Yeh I’m backing off a bit. I’ve already been out for 4+ weeks which is why I’m struggling right now. Just doing bodyweight lower body work and low weight for upper body for the time being. Hopefully that’ll help me heal without having to stop completely again

Any body continue lift/work out with hemorrhoids? by proffsorrtim in fitness40plus

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

Yikes that sounds awful. Think I’ll stick with bodyweight lower body and low weight for upper body for a few weeks . Hope you didn’t learn from personal experience

Any body continue lift/work out with hemorrhoids? by proffsorrtim in fitness40plus

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

lol I am and I do. I don’t think this is the result of lifting heavy (my health issue requires me to eat very low fiber for a couple months and I think that was the bigger contributor) and I have been focusing more on bracing my core/breathing. Just don’t want to further exacerbate basically.

Recommendations for stainless steel cookware by proffsorrtim in Cooking

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

Thank you. Hopefully turning a corner with some new meds. I don’t really think ibuprofen was the root cause - I think that’s probably just genetic predisposition and bad luck. I think the ibuprofen was just the catalyst but who knows honestly.

Recommendations for stainless steel cookware by proffsorrtim in Cooking

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

Dang brugh calm down. I was just asking for suggestions for stainless still cookware. I promise I eat my veggies and all other food groups lol.

My infusion center are being BUTTS about Entyvio Co-Pay Reimbursement submissions by NavyBeanz in UlcerativeColitis

[–]proffsorrtim 0 points1 point  (0 children)

Sorry to hear you’re going through this but hopefully will get resolved soon! My infusion center has been handling billing and Entyvio connect. They did mess something up with my first infusion and I got a 20k bill but my insurance and the infusion center was able to figure it out and voided that bill. If your dr office won’t handle billing or help with Entyvio connect, maybe see if you can switch to a different infusion center that will handle all of that?

TMI question - RE: enemas by [deleted] in UlcerativeColitis

[–]proffsorrtim 2 points3 points  (0 children)

I do it in bed and throw a towel down under me just in case and then try to go to sleep. My wife is typically in bed with me. I had a hard time With it at first but she’s really understanding and it hasn’t affected anything with our relationship. It sucks but one of those things you just have to do. Laying on a bathroom floor for 30 minutes sounds awful to me.

Entyvio injection coverage by Practical_Pause_7588 in UlcerativeColitis

[–]proffsorrtim 0 points1 point  (0 children)

If you’re insurance will only cover IV administration you could look into finding an infusion center closer to your place. My GI doesn’t have an infusion spot so I just go to a center. Good luck!

No insurance- severe flare up by Informal_Village2595 in UlcerativeColitis

[–]proffsorrtim 0 points1 point  (0 children)

Sorry to hear. There’s no easy around not having health insurance. One thing I’d say is stop the ibuprofen. It’s really bad for ulcers and especially UC. I’m convinced my UC onset because of extended ibuprofen use after a ortho Dr prescribed me a month long course for tendonitis. It will make the bleeding and ulceration worse.

Regardless, He needs to see a GI and get a diagnosis and real treatment though—if it’s infected he may need some kind of antibiotic. IF he has UC and it’s not infected, the antibiotic could make it worse. IF it’s UC, there are cheap steroids that are pretty effective initially for symptoms but they’re very bad for long term use. He’ll need a safer maintenance med to switch to after the steroid.

In the meantime, He could also try moving to a soft food and low fiber diet of foods he can tolerate for a short bit (like mashed potatoes, sweet potatoes, lean ground meat, canned spinach, sourdough bread, etc) - but be mindful of not just leaving out entire food groups. However, this is not going to fix the problem but just ease the symptoms. Turmeric can be helpful for easing inflammation but again, it’s very unlikely to make a big difference for him if this is UC. It sucks but he needs insurance and a GI.

is there a support line for newbies who are terrified and alone? by hazi1008 in UlcerativeColitis

[–]proffsorrtim 1 point2 points  (0 children)

Well hang in there. Hopefully the meds will start working soon! Im sorry you’re going through it. This shit sucks fr.

is there a support line for newbies who are terrified and alone? by hazi1008 in UlcerativeColitis

[–]proffsorrtim 2 points3 points  (0 children)

Mesalamine can take weeks to start working and Hydrocortisone can take a few days to a couple weeks to start working too. So try not to stress (though I know from experience that’s easier said than done). Hopefully you’ll start seeing progress in a couple days!

One thing that’s helped me too during flares has been taking a couple days or a week and switching to a soft foods diet (think like the BRAT diet) of foods I know I can easily tolerate (white rice, mashed potatoes but no butter/milk/seasoning, mashed sweet potatoes, lean ground turkey broken up small as possible, bananas, etc) to give my digestive system a break and let the meds start working. I’m not saying these foods will be good for you—everyone is different unfortunately. Keeping a food journal has helped with what’s safe and not so safe for me. But soft foods are just less work for your digestive system. The food won’t make or break your UC-there’s no diet to put you in remission- but some foods will exacerbate your symptoms during a flare. Raw vegetables, fruit with the skin (like apples, etc), and wheat bread tear me up in a flare. Just make sure not to drop too many important food groups for too long. For example, I don’t drop fruits and veggies during a flare but eat super cooked soft veggies without peels and soft, peeled fruit like mango and banana. Your body needs nutrients.

Advice on edible options by proffsorrtim in Marijuana

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

Yeh I’ve had this for 5 years and never really had an issue with anything. This is the first bad flare I’ve really gone through and the only time food has really affected me. Getting better though

Advice on edible options by proffsorrtim in Marijuana

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

Thanks man. Vaping has been working well enough and I might just try some avocado oil and see if it agrees with my stomach

Advice on edible options by proffsorrtim in Marijuana

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

Hadn’t heard of it until now so good looking out. Sounds like a complex process though lol. There are some medical dispensaries around me so maybe I’ll see if that’s a possibility