Late 2017, Paige gets approved for the Sad Walrus Tube Combo. On realizing that the NJ tube will prevent her from purging everything, Paige admits it was all a lie for attention but mom, now convinced Paige is really sick, dismisses this.
I caught Paige on my tiktok fyp but forgot to note the username so I could go back and archive the video - she's started another septic arthritis saga, this time in her foot. She's working hard to catch up to Kelly.
Apologies for not having the video. Looking for it.
I caught Paige on my tiktok fyp but forgot to note the username so I could go back and archive the video - she's started another septic arthritis saga, this time in her foot. She's working hard to catch up to Kelly.
Apologies for not having the video. Looking for it.
View attachment 2347524Does anyone remember when Beefany COULDNT leave the house because she was allergic to everything? Her poor dog could only go outside once a week and play in the grass and get a bath right after or else Bethany would have to stab herself with 50 epi’s just to survive?
Seems like that all goes out the window when fat ass gets a motorized wheelchair, where she doesn’t have to use any energy to move around. Now she’s complaining that she can’t get a new free van or ramp for her precious motorized legs. And the color of that mask on her face is almost as bad as looking at a picture of her without pants.
Beefy has got to be the most self righteous person who expects to get everything handed to her while she lays in her bed surrounded by bunnies and baby chicks while claiming she’s allergic to EVERYTHING.
She looks like one of those old crusty turtle-like creatures from The Dark Crystal with that mask on- and I’m super grateful to not have to be confronted with her pant less body in this pic.
View attachment 2347524Does anyone remember when Beefany COULDNT leave the house because she was allergic to everything? Her poor dog could only go outside once a week and play in the grass and get a bath right after or else Bethany would have to stab herself with 50 epi’s just to survive?
Seems like that all goes out the window when fat ass gets a motorized wheelchair, where she doesn’t have to use any energy to move around. Now she’s complaining that she can’t get a new free van or ramp for her precious motorized legs. And the color of that mask on her face is almost as bad as looking at a picture of her without pants.
Beefy has got to be the most self righteous person who expects to get everything handed to her while she lays in her bed surrounded by bunnies and baby chicks while claiming she’s allergic to EVERYTHING.
Have you seen the old claims of her being allergic to regular size M and M’s, but not the minis? And mcflurries are one of her safe foods. She is also able to hatch baby chicks beside her bed and have a rabbit and all it’s allergen filled bedding in her small ass hoarded room. Her whole house actually seems pretty hoarded for someone who claims to be allergic to everything.
except when she’s pulled off all her drugs and forced to walk by competent medical professionals.
HEY YOU, HEY YOU ALL! Time for some more Chelsea. I read through the trash fire that is her Caring Bridge journal and jfc her writing is as annoying as her TikTok. Fortunately, I stocked up on energy drinks so I managed to push through. I may go back through and add more to her earlier timeline, but for now I'll just continue on with the added information.
She was very busy in fall 2020, so there's a lot.
Chelsea starts off September by announcing her YouTube channel, saying that she's going to start posting medical vlogs. Interestingly, her YT channel has actually existed since 2011 and contains some real zombie-themed gems that aren't particularly relevant to her medical bullshit but are cringey as hell. The actual medical vlogs apparently started back in August 2020 (oops) and are really fucking boring because this girl does not know how to get to the damn point.
Also, in the beginning of September, Chelsea gets her labs back, and most of them are normal. Negative labs don't completely rule out SPS (Stiff Person Syndrome), so, of course, Chelsea is continuing to push for that and is getting an EMG. Additionally, according to Chelsea, her aldolase came back low, though she doesn't mention the specific value, but talks about muscle wasting disease, which she googled, and how scary it is. Chelsea, being Chelsea, managed to annoy at least two nurses with her "big juicy brain."
Chelsea gets a heart monitor in the mail to wear to help diagnose her POTS. She can't take it off.
September 13, Chelsea posts a TikTok outlining the new plan. She's going to stop all her meds for 36 hours. So scary, guys. She might become a board because of her SPS. Remember, she's been claiming her attacks are so severe she can't breathe. (Spoiler: She lives.) On the 14th, she'll meet with a hematologist about her iron levels and on the 15th, she gets her EMG, which will, in theory, confirm SPS. (Spoiler: It doesn't.)
9/15/2020 Hematology: Chelsea finally gets into hematology. Miraculously, this doctor knows all about MCAS and her other "zebra issues" but this appointment will still waste 3 hours. Long story short, Chelsea's low iron is probably due to her very heavy periods so now she gets infusions and an OB/GYN referral. Now, Chelsea has been mentioning low iron since at least June and, in females, period related issues are usually one of the first things doctors will investigate. So, somehow, Chelsea's doctors had her sit around for two and half months without asking about her periods. She also has to wait a month before she gets to start the infusions because COVID and scheduling.
She also posts a video where no meds=wired. Almost as if her usual meds sedate her or something...
9/16 EMG: So Chelsea's EMG came back negative. But guess what? Chelsea only stopped her meds 36 hours before the test when you're supposed to stop them 3 days before. (Google says certain meds should be stopped 3-6 days prior to testing, so that would be maybe accurate, depending on what meds Chelsea was on.) She said pushed to stop her meds even though her doctor said it was fine so she met him halfway and stopped for 36 hours. She said he doesn't know what he's talking about. He throws "that awful label" at her. She doesn't mention which awful label, but presumably either FND or psychosomatic illness. (Back in May, a nursing home doctor allegedly said her issues were psychosomatic. It's in her CB journal.) So, Chelsea is calling in her favor and going to the promised land of Mayo.
End of the month, Chelsea gets her iron infusion, where she, of course, has 'slight complications' because nothing can go smoothly for Chelsea. Then complains about feeling like shit for several days after.
Finally, it's October. Chelsea has a meeting with her complex care doctor. In summary, she's going to start the process of getting insurance approval for IVIG, to help with her MCAS and SPS, which she doesn't have a diagnosis for because of her negative test results. They talk about how her MCAS is "out of control" and so they up some of her med doses. Chelsea worries about the OB/GYN visit because she doesn't want to be put on hormones because hormones will make her MCAS flare. Since she had her infusion, several days ago, she's been having "PVCs, arrhythmias, and tachycardia like nonstop" and so they call her hematologist and her cardiologist. Hematologist says it's the iron fusions; cardiologist says it's not. Also, the heart monitor stopped working so now Chelsea has to wait for a new one. Also, Chelsea will be getting a new wheelchair for in the house. She currently does not have one in the house.
Slightly later in October, Chelsea hears back from her Mayo favor. The doctors does not think she has SPS, due to her negative labs. Naturally, Chelsea says that her labs don't really matter. The doctor also wants to reevaluate all her other diagnoses. Chelsea claims that's unnecessary and whines about this doctor creating roadblocks. She claims her Cleveland Clinic and John Hopkins referrals never went in, so she can't use those. She does find a local specialist and gets a referral there.
She finally gets an endoscopy and gets a gastritis diagnosis. They also biopsy a few different sites, but those all come back normal. She then gets another infusion, but has an anaphylactoid reaction to the infusion and that triggers a stiff person attack. Don't worry, the Benadryl works.
Now, at the end of October, Chelsea gets her tilt table test. She warns them about her stiff attacks. When they raise the table up, Chelsea gets her attack. Chelsea can't breathe. They do it again. Chelsea has dysautonomia.
And now it is, again, time for my ass to go to sleep.
Whats the need for Chelsea's neckbrace? Surely if she required one long term it wouldn't be what looks like a foam brace, and instead be one made out of proper bracing hardware?
She may as well just wear a ruff from the Renaissance.
January 2014 Chelsea was in the hospital for undisclosed reasons. Of course, she ate this shit up.
Lol the clown makeup.
Chelsea shared her dad's obit.
Someone used her pictures for a fake account so Chelsea got her followers to mass report the account.
Chelsea started getting deals modelling for book covers.
She used to be a much bigger girl.
She then started modelling for some Minnesota QVC rip-off.
More book covers
Modelling for some website.
Started getting acting roles.
And then suddenly she was hospitalized for herniated discs.
Chelsea then had a vague spinal surgery. She had lots of visitors. After her hospital stay, she was sent to a rehab facility.
After Chelsea was released from her rehab facility, she was ready to put her sick-girl life in the past.
She went back to work and got more acting roles.
Talked about her dad again.
More modelling and acting.
She was excited to no longer need her handicap parking placard.
Commercial work.
Ran for her town's Snow Queen or something.
Celebrated her 30th birthday.
Her Leo bday cake.
I'm pretty sure Chelsea claims her constant violent "seizures" started on September 13, 2019, and yet here she was working fashion week just seven days later.
Whats the need for Chelsea's neckbrace? Surely if she required one long term it wouldn't be what looks like a foam brace, and instead be one made out of proper bracing hardware?
She may as well just wear a ruff from the Renaissance.
It literally isn’t doing anything. Those types of braces are used for short periods of time for soft tissue injuries (e.g. whiplash) to give the neck muscles an opportunity to relax and heal.
Whats the need for Chelsea's neckbrace? Surely if she required one long term it wouldn't be what looks like a foam brace, and instead be one made out of proper bracing hardware?
She may as well just wear a ruff from the Renaissance.
She claims CCI from her hEDS. She actually switches between the foam brace, the hard brace, and no brace in her videos and pictures, so the whole thing is very sketchy. In one Instagram post, the caption says something along the lines of "Had to take my brace off because this is so important" as if having something important to say is relevant to your need of a neck brace.
This girl’s story will never be anything other than former-weight problem, felt she hit the modeling/acting wall at 30 (correction: the industry felt she hit the wall), gained some weight back after lumbar surgery, regained some weight and the industry liked her even less for it, and then decided to munch.
To this day, her Instagram account just looks like a college theater performance.
Lots of people struggle when they realize they can no longer function in the industry, there’s no shame in that. She just picked the most unique route to handle that reality that I’ve ever seen.
I went to high school with Chelsea. I had one class with her and she was by far the worst student in that class (German). She also falsely accused another classmate of sexual assault and got him kicked out of school and deported (he was an international student). Years later she drunkenly admitted at a party that she had made it up.
So in all honesty it’s not a huge surprise to see that she’s turned to something like this to get attention. She’s legitimately a terrible person. I’ll answer any questions you might have.
I went to high school with Chelsea. I had one class with her and she was by far the worst student in that class (German). She also falsely accused another classmate of sexual assault and got him kicked out of school and deported (he was an international student). Years later she drunkenly admitted at a party that she had made it up.
So in all honesty it’s not a huge surprise to see that she’s turned to something like this to get attention. She’s legitimately a terrible person. I’ll answer any questions you might have.
Someone commented on her TikTok account that they were with Chelsea on a trip, and she disappeared and claimed that she gave a guy (stranger) oral sex in a bathroom at the airport, lying about it, when she did not. Something along the lines of “you were a liar then, and you are a liar now.”
Chelsea called her a bully and told her that her TikTok was for chronic illness awareness only, and then made her comment section approved-commenters only.
While I have no idea if you really went to school with her, the comment is in line with other similar comments made about her, and common with cluster Bs.
Someone commented on her TikTok account that they were with Chelsea on a trip, and she disappeared and claimed that she gave a guy (stranger) oral sex in a bathroom at the airport, lying about it, when she did not. Something along the lines of “you were a liar then, and you are a liar now.”
Chelsea called her a bully and told her that her TikTok was for chronic illness awareness only, and then made her comment section approved-commenters only.
While I have no idea if you really went to school with her, the comment is in line with other similar comments made about her, and common with cluster Bs.
I think it was on her Instagram, but I definitely saw that comment as well. I've been following her descent into this bs for the last year and a half or so on caring bridge, insta and now tik tok. I feel like she's starting to run out of gas - or at least new things to exploit or milk for sympathy. Going to be funny/interesting to see where things go from here. She's never worked an actual job (fake regional modeling doesn't count), she has no skills of any kind, she's of unbelievably low intelligence and psychologically she's (seemingly) fully committed to believing her own lies.
Time to finish 2020 with our poor friend Chelsea (@tanzchelsea) who just needs everyone validate her. She has quite a few appointments, but doesn't really manage to accomplish much because, surprise, her doctors don't see evidence of her stiff person syndrome. Poor Chelsea with her #undiagnosed #stiffpersonsyndrome
Beginning of November, Chelsea has OT to try to learn to transfer from wheelchair to car safely. (Somehow they're just getting to this?) Chelsea has a full stiff attack in front of her OT and freaks them out. #undiagnosed
Later, Chelsea has a rheumatology appointment. Her doctor won't validate her EDS and wants x-rays of her knees. Standing up for the x-rays triggers a stiff attack, Chelsea's mom gets the doctor, and now the doctor (apparently) realizes she is serious. Anyway, she gets diagnosed with joint degeneration, specified as mild osteoarthritis in her journal. Doctor also orders labs for lyme, etc.
Chelsea also claims via her Caring Bridge journal, that her stiff attacks are getting worse, her pain is a 10 (but she's not on pain meds despite having a pain doctor and 10/10 pain), and it's getting worse in her throat/lungs and they might need to call 911 at some point. Chelsea has previously repeatedly claimed that she can't breathe during these attacks but somehow no one has called 911 over them at this point.
And some more videos of Chelsea's "stiff attacks" Still #undiagnosed #stiffpersonsyndrome
Chelsea messaged her neurologist a little while back to tell them all about her awful stiff attacks and she gets the news that they've moved her appoint from February to November 19th. She plans on bringing a bunch of medical articles and wrote a speech for her doctor. (I'll bet her doctors love that shit)
Unsurprisingly, the neurologist also won't diagnose SPS. They do agree to do the GAD labs again and maybe get another EMG. According to Chelsea, the doctor says she has an undiagnosed movement disorder and tells her "this is really is really severe and clearly disabling." Her PT discontinues her PT because Chelsea can't move. Chelsea also references her 2013 hospitalization, which was apparently for her appendix that she felt before it was testable.
(Those GAD results are never mentioned as far as I've found so likely negative again. Or never done.)
Chelsea does an unboxing of her new heart monitor and addresses her neck collar for her CCI.
Chelsea finally sees the OB/GYN. Because Chelsea can't take hormones due her to MCAS, her options for getting rid of her periods are limited. She's getting a hysterectomy but she doesn't know when. She is sad. She wants kids. But she is at peace. Okay, Chelsea.
Chelsea's complex care doctor refers Chelsea to a neurosurgeon for her worsening CCI. But first, Chelsea needs to get an MRI. Because of Chelsea's issues, she has to be sedated for an MRI. Last time she had an MRI, she had 800 seizures. Alrighty then.
12/29 Chelsea gets her MRI. Complains about a pregnancy test. Everything goes well, but then complains the next day about sore throat, bruising from the blood pressure cuff, and a goose egg on her head.
Okay, you guys. The results are SHOCKING.
Based on the MRI, Chelsea's brain is fine. But that doesn't mean it's fine because Chelsea's condition is so rare that no doctors know what they're looking at so Chelsea still needs a referral to a "zebra doctor" for her brain.
Now, according to Chelsea, she had spinal surgery back in 2016 for herniated discs and Degenerative Disc Disease (DDD), but she doesn't specify what the surgery actually did. Whatever it did, she says it reversed itself.
So, anyway, Chelsea has some bone spurs on her cervical vertebrae. She also has disc bulging at L2-L5 and some related issues. She also references T2 hyperintense signal opposing, which is a brain issue, after saying that her brain looked fine on the scan, which could be nothing or MS or lyme or other things. So, she gets her referral to the east coast special neurosurgery doctor to help her poor zebra self.
Chelsea also gets her ultrasound, which we won't get the results of until 2021.
Time to finish 2020 with our poor friend Chelsea (@tanzchelsea) who just needs everyone validate her. She has quite a few appointments, but doesn't really manage to accomplish much because, surprise, her doctors don't see evidence of her stiff person syndrome. Poor Chelsea with her #undiagnosed #stiffpersonsyndrome
Beginning of November, Chelsea has OT to try to learn to transfer from wheelchair to car safely. (Somehow they're just getting to this?) Chelsea has a full stiff attack in front of her OT and freaks them out. #undiagnosed 2020_11_03.mp4
Later, Chelsea has a rheumatology appointment. Her doctor won't validate her EDS and wants x-rays of her knees. Standing up for the x-rays triggers a stiff attack, Chelsea's mom gets the doctor, and now the doctor (apparently) realizes she is serious. Anyway, she gets diagnosed with joint degeneration, specified as mild osteoarthritis in her journal. Doctor also orders labs for lyme, etc. 2020_11_04b.mp4
Chelsea also claims via her Caring Bridge journal, that her stiff attacks are getting worse, her pain is a 10 (but she's not on pain meds despite having a pain doctor and 10/10 pain), and it's getting worse in her throat/lungs and they might need to call 911 at some point. Chelsea has previously repeatedly claimed that she can't breathe during these attacks but somehow no one has called 911 over them at this point.
And some more videos of Chelsea's "stiff attacks" Still #undiagnosed #stiffpersonsyndrome 2020_11_06.mp4 2020_11_06b.mp4
Chelsea messaged her neurologist a little while back to tell them all about her awful stiff attacks and she gets the news that they've moved her appoint from February to November 19th. She plans on bringing a bunch of medical articles and wrote a speech for her doctor. (I'll bet her doctors love that shit)
Unsurprisingly, the neurologist also won't diagnose SPS. They do agree to do the GAD labs again and maybe get another EMG. According to Chelsea, the doctor says she has an undiagnosed movement disorder and tells her "this is really is really severe and clearly disabling." Her PT discontinues her PT because Chelsea can't move. Chelsea also references her 2013 hospitalization, which was apparently for her appendix that she felt before it was testable.
(Those GAD results are never mentioned as far as I've found so likely negative again. Or never done.)
Chelsea does an unboxing of her new heart monitor and addresses her neck collar for her CCI. 2020_11_20.mp4 2020_12_03.mp4
Chelsea finally sees the OB/GYN. Because Chelsea can't take hormones due her to MCAS, her options for getting rid of her periods are limited. She's getting a hysterectomy but she doesn't know when. She is sad. She wants kids. But she is at peace. Okay, Chelsea.
Chelsea's complex care doctor refers Chelsea to a neurosurgeon for her worsening CCI. But first, Chelsea needs to get an MRI. Because of Chelsea's issues, she has to be sedated for an MRI. Last time she had an MRI, she had 800 seizures. Alrighty then.
12/29 Chelsea gets her MRI. Complains about a pregnancy test. Everything goes well, but then complains the next day about sore throat, bruising from the blood pressure cuff, and a goose egg on her head.
Based on the MRI, Chelsea's brain is fine. But that doesn't mean it's fine because Chelsea's condition is so rare that no doctors know what they're looking at so Chelsea still needs a referral to a "zebra doctor" for her brain.
Now, according to Chelsea, she had spinal surgery back in 2016 for herniated discs and Degenerative Disc Disease (DDD), but she doesn't specify what the surgery actually did. Whatever it did, she says it reversed itself.
So, anyway, Chelsea has some bone spurs on her cervical vertebrae. She also has disc bulging at L2-L5 and some related issues. She also references T2 hyperintense signal opposing, which is a brain issue, after saying that her brain looked fine on the scan, which could be nothing or MS or lyme or other things. So, she gets her referral to the east coast special neurosurgery doctor to help her poor zebra self.
Time to finish 2020 with our poor friend Chelsea (@tanzchelsea) who just needs everyone validate her. She has quite a few appointments, but doesn't really manage to accomplish much because, surprise, her doctors don't see evidence of her stiff person syndrome. Poor Chelsea with her #undiagnosed #stiffpersonsyndrome
Beginning of November, Chelsea has OT to try to learn to transfer from wheelchair to car safely. (Somehow they're just getting to this?) Chelsea has a full stiff attack in front of her OT and freaks them out. #undiagnosed 2020_11_03.mp4
Later, Chelsea has a rheumatology appointment. Her doctor won't validate her EDS and wants x-rays of her knees. Standing up for the x-rays triggers a stiff attack, Chelsea's mom gets the doctor, and now the doctor (apparently) realizes she is serious. Anyway, she gets diagnosed with joint degeneration, specified as mild osteoarthritis in her journal. Doctor also orders labs for lyme, etc. 2020_11_04b.mp4
Chelsea also claims via her Caring Bridge journal, that her stiff attacks are getting worse, her pain is a 10 (but she's not on pain meds despite having a pain doctor and 10/10 pain), and it's getting worse in her throat/lungs and they might need to call 911 at some point. Chelsea has previously repeatedly claimed that she can't breathe during these attacks but somehow no one has called 911 over them at this point.
And some more videos of Chelsea's "stiff attacks" Still #undiagnosed #stiffpersonsyndrome 2020_11_06.mp4 2020_11_06b.mp4
Chelsea messaged her neurologist a little while back to tell them all about her awful stiff attacks and she gets the news that they've moved her appoint from February to November 19th. She plans on bringing a bunch of medical articles and wrote a speech for her doctor. (I'll bet her doctors love that shit)
Unsurprisingly, the neurologist also won't diagnose SPS. They do agree to do the GAD labs again and maybe get another EMG. According to Chelsea, the doctor says she has an undiagnosed movement disorder and tells her "this is really is really severe and clearly disabling." Her PT discontinues her PT because Chelsea can't move. Chelsea also references her 2013 hospitalization, which was apparently for her appendix that she felt before it was testable.
(Those GAD results are never mentioned as far as I've found so likely negative again. Or never done.)
Chelsea does an unboxing of her new heart monitor and addresses her neck collar for her CCI. 2020_11_20.mp4 2020_12_03.mp4
Chelsea finally sees the OB/GYN. Because Chelsea can't take hormones due her to MCAS, her options for getting rid of her periods are limited. She's getting a hysterectomy but she doesn't know when. She is sad. She wants kids. But she is at peace. Okay, Chelsea.
Chelsea's complex care doctor refers Chelsea to a neurosurgeon for her worsening CCI. But first, Chelsea needs to get an MRI. Because of Chelsea's issues, she has to be sedated for an MRI. Last time she had an MRI, she had 800 seizures. Alrighty then.
12/29 Chelsea gets her MRI. Complains about a pregnancy test. Everything goes well, but then complains the next day about sore throat, bruising from the blood pressure cuff, and a goose egg on her head.
Based on the MRI, Chelsea's brain is fine. But that doesn't mean it's fine because Chelsea's condition is so rare that no doctors know what they're looking at so Chelsea still needs a referral to a "zebra doctor" for her brain.
Now, according to Chelsea, she had spinal surgery back in 2016 for herniated discs and Degenerative Disc Disease (DDD), but she doesn't specify what the surgery actually did. Whatever it did, she says it reversed itself.
So, anyway, Chelsea has some bone spurs on her cervical vertebrae. She also has disc bulging at L2-L5 and some related issues. She also references T2 hyperintense signal opposing, which is a brain issue, after saying that her brain looked fine on the scan, which could be nothing or MS or lyme or other things. So, she gets her referral to the east coast special neurosurgery doctor to help her poor zebra self.
I definitely believe that someone who writes that her MRI report was like "a paragraph of Sand script" is more knowledgeable about the brain than an actual neurologist.
