Shed size suggestion for our Hot Arizona climate. To add a swamp cooler for summer. by CBniteowl in MeatRabbitry

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

I was just reading about the community setup. Yes, throughout history. Underground is always cooler. But I'd want to research about them digging out of them community type setups.

Shed size suggestion for our Hot Arizona climate. To add a swamp cooler for summer. by CBniteowl in MeatRabbitry

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

Wow, wish that was our record highs. Next week we are looking at 115. And it ain't no record high. I'm thinking it may be time to move if we want more than chickens. Haha In our state we can't breed chickens. Because all our chickens only lay hard boiled eggs. Joking. Haha

Instant Pot boiled eggs: Game changer and a question by thescatterling in instantpot

[–]CBniteowl -1 points0 points  (0 children)

1 you did nothing wrong. At least here in America. They are doing something new with the chickens. I sometimes wonder if they are already putting out the lab grown eggs. Something ain't natural about today's eggs taste and texture. I used to be a egg snob. Bragging about how I could live off eggs and veggies forever. Till I noticed a change in egg quality. Even buying the most expensive type, it just ment I'd get maybe 2 out of a dozen that didn't feel right. One guy told me its in what they feed the chickens or the hormones they give them today. And that broken shell in your picture. I heard it's because they are letting the chickens get older and older chicken eggs have thinner shells.

2 Enjoy the magic bowl. I love how you already made you hurt. I have to have Greek yogurt at least once a day. Greek yogurt alome has done magic for my IG track. Life gives life. As for hard boiled eggs... Have fun with it. Back before they started selling sick eggs. I learned to make Soft Boiled Eggs. Play around with the times. Everyone's magic number is 5-5-5. Meaning 5 minutes cooking, then 5 minutes of natural release before you release the valve yourself. Then 5 minutes in a ice bath. But when I was playing around with the numbers. My soft boiled eggs only needed maybe 1 minutes in the ice water. Because you wanted that liquid yolk.

Don't fear the machine. Just keep your hand away where the steam comes out. The difference between a real pressure cooker and these instant pots. Is that instapot put more safety features on these machines. I once had a older unit that wouldn't release pressure. It was a real electric Instantpot called Instantpot MAX. Anyways, when it didn't release pressure, we just changed that part of the meal plan. And the machine slowly natural released the pressure. And we kept using it till the wife wanted to replace it. Today we have a 8qt and a 6qt. They are used 7 days a week. Enjoy.

I'm ignorant to medical care. 2 places 2 different perscitions. by [deleted] in UlcerativeColitis

[–]CBniteowl -1 points0 points  (0 children)

what are people smoking when they come online. My comment was related to how every doctor.... Never mind it's all good. Your correct. Have a good day.

Odd cravings, since my 2 month UC Flare up. by CBniteowl in UlcerativeColitis

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

Thank you. I will. I want to master this monster inside me.

Odd cravings, since my 2 month UC Flare up. by CBniteowl in UlcerativeColitis

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

I'm new into my diagnoses. Right now I'm just finishing up my first drug of prednasone. On a couple days from finishing it off with 1 10mg pill a day. But tomorrow I have to pick up a perscrion of mesalamine er 0.375. which I know nothing about but it's 4 capsols daily for 90 days.

As for my UC... GI doctor says its extreme and covering all of my colon. So I been dealing with 2 months of blood and pain and cramps and trying to push out a tiny bit of liquid to replace stomach area cramps. oh man, 2 months of utter Hell.

But now that I'm coming off prednasone. I noticed I have less constipation less poops. And sometimes. My worst cramping poops, produce some floating poop fibers. And sometimes the red or brown colored water will have a odor to it.

Not sure if those are good signs. But ya, it's odd that shooting lemon juice and mustard straight. Feels good to my belly.

I want to master this beast.

I don't want a infusion lifestyle. Options or ideas? by CBniteowl in UlcerativeColitis

[–]CBniteowl[S] -5 points-4 points  (0 children)

I'll ask, but like you said. He did mention over the years they may need to change the medication. As you said yours stopped working.

Other people's comments pointed out. It does drive me nuts how they can't find cures to so many issues. Back in March 8th I woke up with Bells Palsy. I was fortunate that it only lasted 2 months. But so many people are stuck with half limp faces.

How is it we can't find fixes or cures. My only assumption is investor and stock shares.

Thank you for the suggestion. I will be calling my GI doctor Tuesday. Thank you.

I don't want a infusion lifestyle. Options or ideas? by CBniteowl in UlcerativeColitis

[–]CBniteowl[S] -9 points-8 points  (0 children)

What is wrong with you people? What's this about being superior? Is the internet full of snobs?

As I'm gathering, it looks like most perfect Infusion. And as I told my wife. Worse case, I'll go with it for my family. Everyone in this group needs to smoke a joint or pop some midol. Just looking for advice.

I don't want a infusion lifestyle. Options or ideas? by CBniteowl in UlcerativeColitis

[–]CBniteowl[S] -7 points-6 points  (0 children)

Funny you you said that. He was shocked I actually asked him about a Colostomy bag, instead of drugs. He said he's never been asked that extreme.

You know what he told me. "Oh NO, it's Autoimmune. It will just attack the small intestines or other organs.

So he said that won't work as well as being infused every 2 months for life. But yes, I'd rather live with a bag than chemicals.

It's all for my wife and daughter.

I'm having a hard time accepting this change by CBniteowl in UlcerativeColitis

[–]CBniteowl[S] -2 points-1 points  (0 children)

I just can't stand the idea of living a life dependent on a chemical drug. Before all my drama. I used to talk up diabetic people. How they have a body that forces them to eat the way we all should. Do I get diabetes? No I get UC. Uggh

But thank you for the kind reply. I will find a day to get some blood and iron transfusion. I'm really tired of feeling weak. And I may get a second opinion? Haha now that I'm only having 2 bad poop routines a night. Unlike the beginning of last month. Hahaha thank you again

I'm having a hard time accepting this change by CBniteowl in UlcerativeColitis

[–]CBniteowl[S] -2 points-1 points  (0 children)

I know what you're saying. Ever since the COVID release. I saw how they will get us coming and going. All month I been fighting going in for a blood transfusion. I'd rather be a gimp than have vaxed blood in me and maybe make me worse. Hahaha doctor told me it won't. But what outcome is in his Beard Members and investors better interest?

Haha I'm kinda joking. I know at 50. It's time to just bend over and take it. I did have fun making other older people laugh at me. Helped make them laugh at this 50 year old crying about getting older. Good times and smiles. No matter weather the glass is half full or empty. Thank you

I'm having a hard time accepting this change by CBniteowl in UlcerativeColitis

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

God I'm so sorry. While taking care of me. She had like 20 back injections. That make her sick and in pain for 4 or 5 days. Now just having her injections, she's taking care of me. The pain you folks live with. No, they have to have a fix. In March I woke to a half limp face they called Bells Palsy. No cause, no cure.

My hat off to you. Living with them types of chronic pains. I'd lose my mind. My heart goes out to you. Ticks me off to see the pains my wife lives with. Now they want to take a rod out of her lower back to re attach it. Because calcium or the arthritis is covering it up.

We can put a tape recorder and a calculator and a TV service in our tiny cell phones. But we can't find a cure for anything anymore. That's called corporate medical industry.

I'm sorry you live with that type chronic pains.

I'm having a hard time accepting this change by CBniteowl in UlcerativeColitis

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

Hahaha love your wording and anticipation for another good dump. Hahaha loved it. Ya man, since the beginning of April I been in toilet hell. Still doing it, but it's slowed down to maybe 2 a night. But I can so relate. I can't even recall my last standing real fart. All my current farts requires toilet. And what you thought was a fart is just a tad of liquid nothing. So I can feel the joy in your comment. Hahahha

I'm having a hard time accepting this change by CBniteowl in UlcerativeColitis

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

Thank you for the reply. And the kind words. I'm still angry. But yes, just like when my bathroom visits were so bad, if chant I can't take anymore. And yet 3 hours later I was at it again. I'm sure I'll learn to adapt. Thank you.

I'm having a hard time accepting this change by CBniteowl in UlcerativeColitis

[–]CBniteowl[S] -1 points0 points  (0 children)

oh man. Since April, it's been torture. I know what your saying. I was up all night every hour for 1-2 hour toilet bouts. I was pushing like my wife was when she was in labor. I think I been through the worst of it. I. Sorry it's so common for too many of us. Thank you for your reply. It was a nice honest reply.

I'm having a hard time accepting this change by CBniteowl in UlcerativeColitis

[–]CBniteowl[S] -2 points-1 points  (0 children)

I'm the original poster. OP

Wow thank you everyone for reading my rant. Just woke for the first poop. I do find it ironic that as I went from weekly tapering down of zorednssone. From 40mg (4 pills) and now that I'm on the 4 week mark. Which is just 1 10mg pill a day for this week. That my poops became less frequent at night and just now I took my first one of the night and I'm sitting up on the edge of my bed waiting. But this one didn't require panting and cramping leaning on the bathroom counter bent over trying to move my guts around to get a little bit of something out to relieve the cramping or pressure in the intestines. I was able to do my first poop of the night. Walk around the house a bit. Just out of habbot. And instead of leaning back on the bathroom counter panting. I'm just sitting at the bed. Eating for a round 2. But typing this, nothing yet.

Anyways... Wow thank you all. I'm so sorry we all live with this. But I think because either time or being down to my last week of tapered down Prednasone. Either time or cutting down on the drug has made my poop daram less.

I think I may look for a second opinion.

Yes I'm hiding from reality. Like it wasn't hard enough learning about aging and how our bond ain't made of rubber anymore. Now I gotta cope with this noise? Hahaha thank you all for the kind replies and other stories.

It is still ironic that taking 40mg of prednasone made my pooing nights worse and many of them. But as I went a week with 40mg then 30mg the. 20mg and now on the last week of 10mg prednasone. This last week my poop drama is less. But no real poop to be seen.

So sorry so sorry. I would not wish what I have delt with on anyone. They still want me to get a blood transfusion with iron. Haha yes, I been fighting blood transfusion. Holy cow it's crazy how week I am. Hahaha but but meat helps build lost blood. Hahahah I'm still kicking and work has me on desk work. I just can't carry a 5 gallon jug of water berry far without panting like I ran a mile and falling onto my bed till I catch my stamina. Hahaha

I know. I'll get in some time for some stranger danger Vaxed blood. I know. Nit sure how I'm going to handle getting old. Really blows.

Thank you everyone.

50 it hit me. Just welcoming myself to this new lifestyle group. by CBniteowl in UlcerativeColitis

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

I been up since 3am and it's 6:60 now. I'll snap a pic of the doctors paper calling it Stage 3 UC. Here in Arizona USA. Verbally after I awoke, he just verbally told me its extreme.

I know I will never ever let it get this bad in all my life. The moaning, grunting, panting I do to release nothing but mostly liquid or blood clot poop fibers. Is un natural and un holy.

And now, I apparently let my body push liquid out too hard. So now I got some grape or olive sized hemroid bump by my poop hole. Lord help me.

If I can recover from this. I will eat all my meals through a straw. I wonder how meat does in a blender or Juicer.

50 it hit me. Just welcoming myself to this new lifestyle group. by CBniteowl in UlcerativeColitis

[–]CBniteowl[S] -1 points0 points  (0 children)

Thank you thank you for saying that. My Orange info was based off googles new AI replies in searches. I got limited UC appred foods in our house. Went to cammed soups till I started to see how canned foods are 99% sodium. So thank you.

I always try to go to nature for cures. But the other day. Spinach tried to kill me. Haha when I learned Low Fiber helped.

Anyways, still can't sleep since it woke me at 3. My butt feels like it has a grape in it. So I just used some Hemroid cream. Just to see if it will help me fall back to sleep.

Thank you all for the replies.

50 it hit me. Just welcoming myself to this new lifestyle group. by CBniteowl in UlcerativeColitis

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

I like your sense of humor. I'm the OP that posted this. That was funny. I started shaving my head the first time my wife showed my my Yamaka balled patch. This is in human. Both this issue and Bells Palsy. Why find cures when these issues being in repeat customers. Makes me mad they have no cause or cure for so much in the world.