I slightly disagree. Sometimes Sara offers a common sense opinion, but often she delivers a long word salad, in which she takes forever to get to her point, which is a bland, non-offensive (to anyone) opinion that adds nothing to the conversation. I find her rather boring.
You are correct about Sara. She adds nothing and only wastes time. She seems nice, but I wish they would replace her with someone who would make an impact.
Heat is the worst for me. The dishes and laundry may be a reaction to the soap, or just the clothes and dishes still being warm if they are. I feel you though.
@dgappl y’all should look into erythromelalgia. It causes burning & redness & neuropathy in hands and feet and elsewhere for some people. I have MCAS and I have erythromelalgia. It’s awful. My dermatologist gave me some topical lidocaine to use but I haven’t tried it yet.
Did investors have to sign up years ago to be a part of the lawsuit / settlement or is the fact that they bought (and still have) Aurora stock enough to get the settlement? I bought a lot of ACB and am totally screwed and should be compensated.
That’s right about Whoopi. She has conned herself and other gullible people into thinking she’s brilliant and profound and she isn’t, and when you add her attention seeking narcissism to the mix it makes her insufferable to watch. It’s frustrating because she wastes time with her incoherent thoughts and the weird unclear vague way she voices those thoughts. She has bad takes that are often just from her wanting to be a contrarian and it adds nothing to the conversation and takes time away from someone who should speak more, like Joy. I always love it when Joy is the moderator and Whoopi is out on Fridays because things run so much better without Whoopi.
whoopi often talks in a dramatic way to get an applause. it doesn't matter what she's saying but the WAY she's saying it is the audiences queue to applaud as if she's some guru that just said something to embroider on a pillow. I roll my eyes so hard so often when she talks and they all enable her by clapping. ugh
100%. Also, I may be in the minority, but Sara Haines does nothing for me. I don’t think she adds much to the show. Sometimes, I’m frustrated by her naïveté on some topics. She seems like a nice person but if she were absent from the show it wouldn’t change the dynamics much.
I had a very bad reaction to high quality, no filler colostrum powder and not only that, it caused terrible liver problems. I developed a very enlarged, fatty liver when I had a perfect liver beforehand. It also gave me eosinophilia due to my body’s reaction.
Gosh. I suspect I may have had some liver involvement too. Glad you are almost back to normal now. This whole thing has really taught me to be careful with supplements. How long did it take for you to feel better after you stopped taking the colostrum?
Xolair almost killed me. I was on it monthly for 7 months, and about two weeks after each injection I would have severe anaphylaxis and terribly burning skin, my lungs stopped working, throat swelling, cardiac problems, neurological problems, and all the rest, which warranted seven ER visits and subsequent hospitalizations.
I forgot to add that Xolair caused the blood marker for Drug-Induced Lupus called Anti-histone to be positive while I was on it and for a while after. It’s negative now.
I have MCAS and Xolair nearly killed me due to the severe allergic reactions and anaphylaxis (7 times to the ER) it gave me for the 7 months I was on it. My reactions were delayed so I didn’t put it together right away. Xolair has a black box warning for anaphylaxis. It even caused me to have a high Antihistone blood test which is the marker for drug induced lupus whike I was in it but it have returned to normal after being off of it for months. Do you think the Xolair is responsible for your terrible reactions?
I have bad MCAS and very hot burning skin all over is one of my worst symptoms. The skin temperature increases which can be felt by touching the skin and I feel like I am doused in gasoline and set aflame. It can go on for weeks.
I’ve considered MCS as well! It’s so hard to figure out but I’m hoping the tests come back with more information. Maybe I have deficiencies from the MTHFR gene causing certain issues. I will say I’m also reacting to makeup right now too. I forgot to mention that. Doesn’t hurt my skin, just mouth itchies and wheezing. I’ve quit the salon now and no more weed and I’m resting at home trying to detox and maybe get better🥹🙏🏻we shall see
I think some of his relationships aren’t real and are just for publicity. This is a strange match and it has a lot of similarities to how he spoke about his recent relationship with Tiffany Haddish. Strange couple. I doubt it will last.
Oh wait, he’s promoting his new book, so my hunch was right about his faux relationship with JHud. This “relationship” is indeed for publicity for his new book.
I had a terrible reaction to Botox for migraines and it sent me to the ER three times with anaphylaxis, burning skin, neurological problems, worsening MCAS. I had three rounds that were three months apart (July 2021-January 2022). My reactions were a bit delayed each time and occurred a few days after getting the injections so I didn’t realize until the third round of shots that the culprit was the Botox. That set me off with so much MCAS suffering for a long time afterwards. I’m never touching Botox again, not even for facial wrinkles.
I’m so sorry you had this experience however it’s also really nice to have someone with the same reaction. I didn’t know I had MCAS at the time and was so lost. All the doctors would not take me seriously and I thought I was dying lmao.
Yes, it’s good to trust your instincts. That’s what I have learned through dealing with MCAS. And so many doctors are just clueless so there will be times that you will know more than they do, so if your radar goes off about something there’s probably a good reason to listen to it.
Update #8. I am sorry to inform all of you that she did not make it to this morning. We aren't really sure what happened, she was weak but responsive during her 4am feeding, temp of 101.1°F, breathing sounded clear, though she was a little mucusy. It may have been dehydration, and the electrolyte was just too little too late. Or maybe she had a gut issue that we weren't aware of. But she was discovered to have passed between 4am and 6am. I know a lot of you were invested in her story, and it is with a heavy heart that I have to break this news, but you all deserve to know how the story ends.
I’m so sorry to hear the news. But thank you for trying your best to save her. She experienced love and care while she was here because of your efforts.
Primary erythromelalgia is caused by a genetic mutation of SCN9A or SCN11A genes. Mutations in the SCN9A or SCN10A gene can cause small fiber neuropathy. I know many people who don’t have those gene mutations have eruthromelalgia, but I thought I’d mention this in case yours could be genetic.
Update #3: she's spending a lot of time sleeping. Generally only waking up and being active at feeding times. The electric kettle we've been using to heat her milk up gave out entirely, so now we start a fresh pot every morning on the stove and keep it warm throughout the day, straining through a mesh first to remove any chunks that could get caught in the bottle, then fill the bottle and feed. She's getting more vocal, we've gone from the occasional bleat to consistent murmurs and grumbles. She made an honest effort to get up at her last feeding time, and seemed frustrated that she couldn't get her legs to cooperate. She's able to stand if we stand her, but quickly loses her balance and flops over. She's had a significant increase in appetite, we're up to 6 ounces at last feeding and trying for more on an empty bottle. I've been carrying her around swaddled up when I go about my household chores, talking to her, praising every accomplishment. She's officially gone from caviar-like diarrhea to more solid poops, so She's definitely absorbing nutrients from the milk. I'm considering investing in a formula prepper, as I don't intend to bottle each lamb as the seasons come, but it'll be handy in the event that I need to bottle one or two.
Do you think it’s possible once the lamb gets its strength back a while from now that it’s mother will want to be with it? I would think that would be beneficial as long as it’s mother is loving.
The mother is expressing interest, but for some reason she didn't fully drop udders with the pregnancy, and she won't be producing milk. Once the baby is big enough and healthy enough, she'll be let out to join the flock, and im sure they'll accept her as a member, even if not as a daughter
I had horrible life threatening reactions on Xolair and had to stop it. It took me 7 months to figure out my horrific symptoms like excruciating burning hot skin, and anaphylaxis that landed me in the ER then the hospital 6 six times was from Xolair, because I had delayed reactions from the shot. My first shot was 10/30/20, then I started developing burning skin then ultimately anaphylaxis on 11/17/20, and I was so very sick. I went into anaphylaxis six times with my lungs not working, chest pains, throat swelling, very hot skin, stroke like symptoms to where I couldn’t think or speak or walk, neurological & cardiovascular problems, my nurse couldn’t believe how hot my skin was and gave me ice packs but this suffering went on for months and months. Finally, I figured out it was the Xolair because my doctor saw how badly I was doing and decided to double the dose, and that shot almost killed me (all of them would have without Epipen and the ER) and the reaction happened much more quickly and that’s when I put it all together.
Wow. Thats just so awful and I’m sorry you went thru all this. Thank you for sharing even tho I’m sure it’s hard to relive that kind of experience. Since you also had chest pain and skin burning it makes me think I should probably stop right now. I’ve only had three shots and at half the normal dose, four weeks apart. My reaction lasted 24 hours and now I feel fine but I’m not sure I want to risk feeling like that again. This also reminds me to keep an EpiPen with me at all times in case it comes back.
Yes, I have heard about half of mast cell patients have a hard time with NSAIDs. I just recently started taking aspirin for terribly flushy burning skin and so far I haven’t had a reaction, but who knows since random delayed reactions are never out of the question with MCAS.
Just an FYI, I have found that the best non-scented body products that don’t have extra junk in them are made by Vanicream, the body wash, shampoo, conditioner, face wash, skin cream, and body lotion.
I got this before my MCAS (Mast Cell Activation Syndrome) was treated. The biggest clue for me was that taking Benadryl around the clock for 2 days (for something else) made me realize that I was Not Itchy anymore. I hadn't realized I was itchy all the time before that. It was like someone turned the static off in my brain.
I’ll try the shampoo, that’s my mom’s biggest issue with him so if I can fix that he’ll be able to stay inside more. I’ve started letting him eat inside the house when she’s away but only dry food, Ill start feeding him his wet food during these times. I’ll ask her about the vet in a week or so, if I ask now it won’t end well for me and she’ll never entertain the idea ever again. I appreciate the advice
You could apply for CareCredit at the vet’s office and make low monthly payments for the care they could provide today. Maybe look into that. The poor cat needs vet care.
I slightly disagree. Sometimes Sara offers a common sense opinion, but often she delivers a long word salad, in which she takes forever to get to her point, which is a bland, non-offensive (to anyone) opinion that adds nothing to the conversation. I find her rather boring.
You are correct about Sara. She adds nothing and only wastes time. She seems nice, but I wish they would replace her with someone who would make an impact.
NYX Line Loud Lip Liner in Global Citizen
Heat is the worst for me. The dishes and laundry may be a reaction to the soap, or just the clothes and dishes still being warm if they are. I feel you though.
@dgappl y’all should look into erythromelalgia. It causes burning & redness & neuropathy in hands and feet and elsewhere for some people. I have MCAS and I have erythromelalgia. It’s awful. My dermatologist gave me some topical lidocaine to use but I haven’t tried it yet.
Did investors have to sign up years ago to be a part of the lawsuit / settlement or is the fact that they bought (and still have) Aurora stock enough to get the settlement? I bought a lot of ACB and am totally screwed and should be compensated.
Whoopee and Meghan tie for worst.
That’s right about Whoopi. She has conned herself and other gullible people into thinking she’s brilliant and profound and she isn’t, and when you add her attention seeking narcissism to the mix it makes her insufferable to watch. It’s frustrating because she wastes time with her incoherent thoughts and the weird unclear vague way she voices those thoughts. She has bad takes that are often just from her wanting to be a contrarian and it adds nothing to the conversation and takes time away from someone who should speak more, like Joy. I always love it when Joy is the moderator and Whoopi is out on Fridays because things run so much better without Whoopi.
whoopi often talks in a dramatic way to get an applause. it doesn't matter what she's saying but the WAY she's saying it is the audiences queue to applaud as if she's some guru that just said something to embroider on a pillow. I roll my eyes so hard so often when she talks and they all enable her by clapping. ugh
100%. Also, I may be in the minority, but Sara Haines does nothing for me. I don’t think she adds much to the show. Sometimes, I’m frustrated by her naïveté on some topics. She seems like a nice person but if she were absent from the show it wouldn’t change the dynamics much.
I had a very bad reaction to high quality, no filler colostrum powder and not only that, it caused terrible liver problems. I developed a very enlarged, fatty liver when I had a perfect liver beforehand. It also gave me eosinophilia due to my body’s reaction.
Gosh. I suspect I may have had some liver involvement too. Glad you are almost back to normal now. This whole thing has really taught me to be careful with supplements. How long did it take for you to feel better after you stopped taking the colostrum?
It took a month or so for the acute symptoms to subside.
Xolair almost killed me. I was on it monthly for 7 months, and about two weeks after each injection I would have severe anaphylaxis and terribly burning skin, my lungs stopped working, throat swelling, cardiac problems, neurological problems, and all the rest, which warranted seven ER visits and subsequent hospitalizations.
What has been your treatment after Xolair? Did you try any other medication?
I forgot to add that Xolair caused the blood marker for Drug-Induced Lupus called Anti-histone to be positive while I was on it and for a while after. It’s negative now.
I have MCAS and Xolair nearly killed me due to the severe allergic reactions and anaphylaxis (7 times to the ER) it gave me for the 7 months I was on it. My reactions were delayed so I didn’t put it together right away. Xolair has a black box warning for anaphylaxis. It even caused me to have a high Antihistone blood test which is the marker for drug induced lupus whike I was in it but it have returned to normal after being off of it for months. Do you think the Xolair is responsible for your terrible reactions?
I have bad MCAS and very hot burning skin all over is one of my worst symptoms. The skin temperature increases which can be felt by touching the skin and I feel like I am doused in gasoline and set aflame. It can go on for weeks.
Is there a medication that could help with the faulty sodium channel ions like a sodium channel blocker?
It could be MCAS or possibly MCS (Multiple Chemical Sensitivity).
I’ve considered MCS as well! It’s so hard to figure out but I’m hoping the tests come back with more information. Maybe I have deficiencies from the MTHFR gene causing certain issues. I will say I’m also reacting to makeup right now too. I forgot to mention that. Doesn’t hurt my skin, just mouth itchies and wheezing. I’ve quit the salon now and no more weed and I’m resting at home trying to detox and maybe get better🥹🙏🏻we shall see
I’m so glad you’re no longer at the salon and I hope you improve with rest and abstinence to chemicals!
This feels fake to me. Possibly to raise this guy’s profile. He’s not terribly funny to me and may need the boost so this is one way to do it.
I think some of his relationships aren’t real and are just for publicity. This is a strange match and it has a lot of similarities to how he spoke about his recent relationship with Tiffany Haddish. Strange couple. I doubt it will last.
Oh wait, he’s promoting his new book, so my hunch was right about his faux relationship with JHud. This “relationship” is indeed for publicity for his new book.
I had a terrible reaction to Botox for migraines and it sent me to the ER three times with anaphylaxis, burning skin, neurological problems, worsening MCAS. I had three rounds that were three months apart (July 2021-January 2022). My reactions were a bit delayed each time and occurred a few days after getting the injections so I didn’t realize until the third round of shots that the culprit was the Botox. That set me off with so much MCAS suffering for a long time afterwards. I’m never touching Botox again, not even for facial wrinkles.
I’m so sorry you had this experience however it’s also really nice to have someone with the same reaction. I didn’t know I had MCAS at the time and was so lost. All the doctors would not take me seriously and I thought I was dying lmao.
Yes, it’s good to trust your instincts. That’s what I have learned through dealing with MCAS. And so many doctors are just clueless so there will be times that you will know more than they do, so if your radar goes off about something there’s probably a good reason to listen to it.
I’d be relieved af to know Trump wouldn’t be president, just like the last election.
Update #8. I am sorry to inform all of you that she did not make it to this morning. We aren't really sure what happened, she was weak but responsive during her 4am feeding, temp of 101.1°F, breathing sounded clear, though she was a little mucusy. It may have been dehydration, and the electrolyte was just too little too late. Or maybe she had a gut issue that we weren't aware of. But she was discovered to have passed between 4am and 6am. I know a lot of you were invested in her story, and it is with a heavy heart that I have to break this news, but you all deserve to know how the story ends.
I’m so sorry to hear the news. But thank you for trying your best to save her. She experienced love and care while she was here because of your efforts.
This is such great news!! So much love to that sweet baby and to you!! Thank you for caring and thanks for the updates! We are invested!
Primary erythromelalgia is caused by a genetic mutation of SCN9A or SCN11A genes. Mutations in the SCN9A or SCN10A gene can cause small fiber neuropathy. I know many people who don’t have those gene mutations have eruthromelalgia, but I thought I’d mention this in case yours could be genetic.
Update #3: she's spending a lot of time sleeping. Generally only waking up and being active at feeding times. The electric kettle we've been using to heat her milk up gave out entirely, so now we start a fresh pot every morning on the stove and keep it warm throughout the day, straining through a mesh first to remove any chunks that could get caught in the bottle, then fill the bottle and feed. She's getting more vocal, we've gone from the occasional bleat to consistent murmurs and grumbles. She made an honest effort to get up at her last feeding time, and seemed frustrated that she couldn't get her legs to cooperate. She's able to stand if we stand her, but quickly loses her balance and flops over. She's had a significant increase in appetite, we're up to 6 ounces at last feeding and trying for more on an empty bottle. I've been carrying her around swaddled up when I go about my household chores, talking to her, praising every accomplishment. She's officially gone from caviar-like diarrhea to more solid poops, so She's definitely absorbing nutrients from the milk. I'm considering investing in a formula prepper, as I don't intend to bottle each lamb as the seasons come, but it'll be handy in the event that I need to bottle one or two.
Do you think it’s possible once the lamb gets its strength back a while from now that it’s mother will want to be with it? I would think that would be beneficial as long as it’s mother is loving.
The mother is expressing interest, but for some reason she didn't fully drop udders with the pregnancy, and she won't be producing milk. Once the baby is big enough and healthy enough, she'll be let out to join the flock, and im sure they'll accept her as a member, even if not as a daughter
Thank you for loving and caring for this sweet lamb.
I had horrible life threatening reactions on Xolair and had to stop it. It took me 7 months to figure out my horrific symptoms like excruciating burning hot skin, and anaphylaxis that landed me in the ER then the hospital 6 six times was from Xolair, because I had delayed reactions from the shot. My first shot was 10/30/20, then I started developing burning skin then ultimately anaphylaxis on 11/17/20, and I was so very sick. I went into anaphylaxis six times with my lungs not working, chest pains, throat swelling, very hot skin, stroke like symptoms to where I couldn’t think or speak or walk, neurological & cardiovascular problems, my nurse couldn’t believe how hot my skin was and gave me ice packs but this suffering went on for months and months. Finally, I figured out it was the Xolair because my doctor saw how badly I was doing and decided to double the dose, and that shot almost killed me (all of them would have without Epipen and the ER) and the reaction happened much more quickly and that’s when I put it all together.
Wow. Thats just so awful and I’m sorry you went thru all this. Thank you for sharing even tho I’m sure it’s hard to relive that kind of experience. Since you also had chest pain and skin burning it makes me think I should probably stop right now. I’ve only had three shots and at half the normal dose, four weeks apart. My reaction lasted 24 hours and now I feel fine but I’m not sure I want to risk feeling like that again. This also reminds me to keep an EpiPen with me at all times in case it comes back.
Thank you, I’m so glad I could help with my experience. Whatever you choose, I hope it goes very well.
Also, it made my MCAS explode and so much worse. I’m still dealing with the fallout and I took Xolair from 10/20-5/21.
Bummer I'm not allowed nsaids bc of stomach issues. Always hitting roadblocks to treatment with these problems. *sigh
Yes, I have heard about half of mast cell patients have a hard time with NSAIDs. I just recently started taking aspirin for terribly flushy burning skin and so far I haven’t had a reaction, but who knows since random delayed reactions are never out of the question with MCAS.
Thank you for your kindness love.
❤️
Occult tethered cord.
Thanks
No problem. If you have any questions you can pm too happy to help
That’s kind of you. Thanks again!
Just an FYI, I have found that the best non-scented body products that don’t have extra junk in them are made by Vanicream, the body wash, shampoo, conditioner, face wash, skin cream, and body lotion.
I have suspect MCAS and I reacted to Vanicream, it made my face itchy and burny :(
I’m sorry to hear that. :( I hope you can find something that works for you.
The paytreeyarkeigh
You can really class it up even more with additional letters: Paightrēyahrkeigh!
I got this before my MCAS (Mast Cell Activation Syndrome) was treated. The biggest clue for me was that taking Benadryl around the clock for 2 days (for something else) made me realize that I was Not Itchy anymore. I hadn't realized I was itchy all the time before that. It was like someone turned the static off in my brain.
That’s great to know your MCAS is under control. What things specifically did you do to get it under control?
I’ll try the shampoo, that’s my mom’s biggest issue with him so if I can fix that he’ll be able to stay inside more. I’ve started letting him eat inside the house when she’s away but only dry food, Ill start feeding him his wet food during these times. I’ll ask her about the vet in a week or so, if I ask now it won’t end well for me and she’ll never entertain the idea ever again. I appreciate the advice
You could apply for CareCredit at the vet’s office and make low monthly payments for the care they could provide today. Maybe look into that. The poor cat needs vet care.