Inactive Chelsea Lawrence / TanzChelsea - Munchie kicked out of two hospitals, home care and multiple treatment teams; Flagged and blacklisted by EPIC; Munched Herself to Death

[LonesomeDud]

Looks like shes doubling down on the shes dying shit to her sister.
View attachment 4257486

Also someone tagged her in this photo from 2019 shes the 2nd from the left.
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Would you rather believe your sister is dying or that she's so mentally ill she's shitting her pants on purpose and begging your 70 year old mother to let her sit in it because it's part of the con? I would also prefer to believe my sister was actively dying.

 

[Android raptor]

Don't forget the opioid addiction as well, which out of the stuff that's actually wrong with her has the highest risk of killing her.

Does she take pills from her mom or other family members? Since she's flagged as drug seeking I can't imagine medical workers are prescribing them to her directly.

 

[Manul Otocolobus]

Would you rather believe your sister is dying or that she's so mentally ill she's shitting her pants on purpose and begging your 70 year old mother to let her sit in it because it's part of the con? I would also prefer to believe my sister was actively dying.

Buying into someone's delusion, which reinforces said delusion and makes them that less likely to get treatment, is in no ones best interest. With regard to this particular illness, anyone who is willfully ignoring it is literally facilitating this person's slow decent into complete madness and eventually, death. People need to stop being so willing to bury their heads in the sand with their fingers in their ears humming to themselves with their eyes tightly shut just because life isn't perfect. This is why society is going to shit. Everyone needs to grab their big girl panties, or loan a pair to those that don't have a pair, pull them up, dig in, and be willing to do the hard, dirty work that is life.

 

[GenociderSyo]

She sets this up like its her goodbye.

• 1/13/2023
  • She now wakes her mother up in the middle of the night screaming in pain.
  • She can't breathe at all anymore without oxygen.
    • She has only shown the mask btw not the oxygen itself she may not even have oxygen.
    • "My brain feels like it’s stabbing my stiff attacks are instantly stuck in there very difficult to deal with when you feel like you have half the capacity of your lungs . Even when I was talking with my doctor today, he told me to stop talking and put my oxygen mask on because I was gasping for air between sentences. "
  • Her body no longer wants food or water anymore.
    • "I officially had to turn off my feeding tube because it was too painful. I can’t handle the pain of even the smallest amount. And the IV fluid we thought maybe it would help if we put a bag up but sadly it made the lungs situation even worse and I knew exactly what that meant once that happened."
  • She needs that one only pain med that was helping her pain and no others she's allergic to all others.
    • "The medication that was controlling the stomach pain is completely out and we do not know how to order it. "
    • "I’m allergic to almost all other nausea medication‘s and stomach medication‘s"
  • Wonder if these medications were supposed to be taken this way.
    • "When my medicine gets crushed up and put into my huge syringe tube, and pushed into my j-tube , it is the most excruciating pain that it puts me into a Stiff attack that sets off a mast cell attack. The difference is that a G goes into your stomach and a J goes into your intestine."
  • Now she cant swallow during attacks and is getting reflux.
    • Due to this she is going to die of suffocation and aspiration. he also now wants GJ Tube instead of the tube she got.
      • "Also, my greatest fear is a possibility. I talked with my doctor during my attacks whatever is inside of me has been being pushed up during my attacks my jaw was closed and locked the other day and I felt everything being pushed up my G.I. tract and I was swallowing whatever I had in me down, and I am scared that it’s some point this will happen again, but it will fill my mouth. My mouth will be locked shut, and if I cannot swallow and cannot push it out of my mouth or between my teeth, and I start to suffocate, I will aspirate what is ever in my stomach or G.I. tract. "
  • People need to stop telling her to go to the ER; she can't go the the ER and she doesn't have to explain why!
    • "If you’re in that much pain, why are you going to the ER? I can’t I won’t and I don’t have to explain myself. There is a major problem and my doctor is actively trying to fix it but pretty sure I said this on another caringbridge has your doctor ever told you to grab all your medication and run out of the state just think about that for a minute I attempted to get into my wheelchair this week and when I sat up, I turned into a statue. "
  • She sets this up like its her goodbye.
    • "I have tried so hard and it seems the system has failed me again and I am left with the worst scenario. I don’t know what will happen. I don’t know who will be ready in the next CaringBridge. I hope it will be me, but if not, my sister is a co-author. I love you all. And I thank you for all the support over these years for all of my chronic illness, friends, and SPS friends. "

 

[lolnah]

IS SHE FINALLY TRYING TO VSED LOL
We need a poll, because I've got money that says she's going to fake a suicide attempt next

 

[BoomerPrime]

Holy shit, I just caught up on this thread thanks to Community Happenings and the awards and such. So much has been said, I can't add much but--without power-leveling too much--I have a close friend who is an RN for many years, and I shared some tidbits about Chelsea to them. The response: "This bitch lies like a rug. She needs a shrink, not dilaudid."

 

[LonesomeDud]

Buying into someone's delusion, which reinforces said delusion and makes them that less likely to get treatment, is in no ones best interest. With regard to this particular illness, anyone who is willfully ignoring it is literally facilitating this person's slow decent into complete madness and eventually, death. People need to stop being so willing to bury their heads in the sand with their fingers in their ears humming to themselves with their eyes tightly shut just because life isn't perfect. This is why society is going to shit. Everyone needs to grab their big girl panties, or loan a pair to those that don't have a pair, pull them up, dig in, and be willing to do the hard, dirty work that is life.

Oh, feeding into someone's false reality is BAD? Glad you're here to clear that up.

 

[GenociderSyo]

THE DRUG SHE IS SEEKING AND IS TAKING IS KETAMINE!
She has been mainlining Ketamine into her hickman and other Ports.
This is definitely why they are DEMANDING she get her Feeding Tube and Hickmann removed.
​

She finally got herself posted as by the SPS Research Foundation and in the Q&A she stated the only pain med she will take is Ketamine and that she wants it to be in her IV. Bitch was mainlining Ketamine!

Here is the IG post where most commenters called them out for believing her.

Now onto the Q&A:

Spoiler: Text of Article

My SPS Story: Chelsea L.​

Describe your life at your healthiest point.​

Probably before elementary school started even though I already started to have aches and pains due to an undiagnosed genetic condition called EDS (Ehlers-Danlos Syndrome).

How many years before your diagnosis were you experiencing Stiff Person Syndrome (SPS) symptoms?​

6 years.

Describe your most debilitating symptoms.​

Being stiff as a rock and in pain. I need to be moved for my safety but any touch makes it worse. But what I really want is someone to lie next to me or pet my hair or rub my back. But that’s the cruelest thing about SPS. Any touch makes it worse.

Describe treatments you have tried, what has worked and what has not.​

Benzodiazepines (they seem to help a lot). Medical marijuana (I am allergic so that did not work out well). Painkillers (due to allergies there are only three types of painkillers I can take and ketamine usually works the best for me. Or if I am in a bad state in the hospital they’ll use intravenous ketamine).Then IVIG – WHEN IT WORKS, IT WORKS WONDERS!

Describe a time you received compassionate care.​

After my first round of IVIG they pushed it too fast and I got really really sick from midnight to morning. I couldn’t even roll my body. So the nurse just laid me on my side. I couldn’t even get my head out from underneath the pillow. My nurses know me so well – they know what I want before I want it! And of course the doctor who saved me – who finally took a chance on me – and diagnosed me.

Describe how SPS has changed you.​

I feel like I’m not living a lie anymore. I feel I’m not second-guessing anymore. I also feel like I want go to all the neurologists that have done me wrong and say, look what you missed! But in reality, I just want to raise awareness. There are too many of us suffering and that needs to change!

What brings you joy?​

I feel like I’m at peace. Because I told my family I don’t want to die not knowing. Slowly things were getting worse and worse and I was so scared that I was never going to have any answers. Everything makes so much more sense now!

What do you want people to know about you?​

Follow your dreams but sometimes those dreams change and God shows you your true calling which is advocating for others and raising awareness for rare diseases (for me, it’s on TikTok). Never give up your fight for a diagnosis!

Occupation/previous occupation, if disabled.​

Model, actress, director, production assistant for commercial and movie sets (if I was not in them).

Misdiagnosed? With what.​

Yes. FND (Functional Neurological Disorder).

What do you want The SPSRF to achieve?​

Help those with SPS and SPSD and their providers find information, support, and better treatment options.

 

[lolnah]

THE DRUG SHE IS SEEKING AND IS TAKING IS KETAMINE!
She has been mainling Ketamine into her hickman and other Ports.
This is definitely why they are DEMANDING she get her Feeding Tube and Hickmann removed.
​

She finally got herself posted as by the SPS Research Foundation and in the Q&A she stated the only pain med she will take is Ketamine and that she wants it to be in her IV. Bitch was mainlining Ketamine!
View attachment 4260899

Here is the IG post where most commenters called them out for believing her.
View attachment 4260932View attachment 4260947View attachment 4260966View attachment 4260970
View attachment 4260904View attachment 4260918View attachment 4260919

Now onto the Q&A:

Spoiler: Text of Article

My SPS Story: Chelsea L.​

Describe your life at your healthiest point.​

Probably before elementary school started even though I already started to have aches and pains due to an undiagnosed genetic condition called EDS (Ehlers-Danlos Syndrome).
View attachment 4260980

How many years before your diagnosis were you experiencing Stiff Person Syndrome (SPS) symptoms?​

6 years.

Describe your most debilitating symptoms.​

Being stiff as a rock and in pain. I need to be moved for my safety but any touch makes it worse. But what I really want is someone to lie next to me or pet my hair or rub my back. But that’s the cruelest thing about SPS. Any touch makes it worse.

Describe treatments you have tried, what has worked and what has not.​

Benzodiazepines (they seem to help a lot). Medical marijuana (I am allergic so that did not work out well). Painkillers (due to allergies there are only three types of painkillers I can take and ketamine usually works the best for me. Or if I am in a bad state in the hospital they’ll use intravenous ketamine).Then IVIG – WHEN IT WORKS, IT WORKS WONDERS!

Describe a time you received compassionate care.​

After my first round of IVIG they pushed it too fast and I got really really sick from midnight to morning. I couldn’t even roll my body. So the nurse just laid me on my side. I couldn’t even get my head out from underneath the pillow. My nurses know me so well – they know what I want before I want it! And of course the doctor who saved me – who finally took a chance on me – and diagnosed me.

Describe how SPS has changed you.​

I feel like I’m not living a lie anymore. I feel I’m not second-guessing anymore. I also feel like I want go to all the neurologists that have done me wrong and say, look what you missed! But in reality, I just want to raise awareness. There are too many of us suffering and that needs to change!

What brings you joy?​

View attachment 4260992
I feel like I’m at peace. Because I told my family I don’t want to die not knowing. Slowly things were getting worse and worse and I was so scared that I was never going to have any answers. Everything makes so much more sense now!

What do you want people to know about you?​

Follow your dreams but sometimes those dreams change and God shows you your true calling which is advocating for others and raising awareness for rare diseases (for me, it’s on TikTok). Never give up your fight for a diagnosis!

Occupation/previous occupation, if disabled.​

Model, actress, director, production assistant for commercial and movie sets (if I was not in them).

Misdiagnosed? With what.​

Yes. FND (Functional Neurological Disorder).

What do you want The SPSRF to achieve?​

Help those with SPS and SPSD and their providers find information, support, and better treatment options.

No wonder her pupils were always fucking huge, holy shit

 

[LonesomeDud]

It's ketamine. Well, I'll be darned. Mainlined, it would be quite the trip. You can buy shrooms all over the place now.

K will make you so nauseous, though.

 

[HarrietTubmansTittyFuckSu]

Well if the sps foundation co-signs her addiction then dr Godzilla has to play by her rules! Jesus, no wonder she’s freaking the fuck out about losing her high.

I feel like I’m at peace.

lol. Lmao.

 

[VisceraNexus]

"Even when I was talking with my doctor today, he told me to stop talking and put my oxygen mask on because I was gasping for air between sentences. "

Obviously she is not a reliable narrator so I don't believe any of this happened exactly as stated, but does she really not consider it might be her completely sedentary lifestyle that would affect her breathing? And does she think her doctor doesn't also recognize this?

"I felt everything being pushed up my G.I. tract and I was swallowing whatever I had in me down"

Again, she seems to lay on her back a lot of the time, and she's very overweight. I know there's a whole narrative of "doctors blaming everything on weight", but this is so blatantly not due to some true medical malfunction, it's that she's fat and essentially immobile by choice. Her doctor absolutely knows this. She seems to never mention her weight at all, and that really showcases her talent for ignoring what's directly in front of her and plain to see.

Edit: Also the Ketamine. Very high doses of Ketamine are known for slowing down breathing, and makes it difficult for the body to regulate breathing in general. For the unaware, Ketamine is used in medicine legitimately, but often for anesthesia. When people talk about "horse tranquilizers", this is usually what they're referring to. Holy fuck lol.

Spoiler: I don't want to clog the thread with my sperging

As an aside, I cannot diagnose her and I won't pretend I can, but she has more going on than just substance abuse issues and malingering. Those are often comorbid with other disorders, but I'd be fascinated to see what a psych treating her would have to say. There's almost certainly something cluster B going on, and the more she speaks the more the narcissistic traits come to the surface. The way she thinks she always has a "way out" is really suspicious. She always has an answer or explanation, they're not convincing but they're there, she has a constant "endgame" card she can pull whenever it suits her (her death), she always has another "official" to turn to (new doctor, the mayor, etc) and she seems to very sincerely believe they will fix her problem, she holds her sister and mother hostage with guilt and is enabled. There's more, but I won't keep going. Usually I suspect BPD with munchies, but she doesn't check as many of those boxes in my mind. Would love to see some others' insights about this, if they'd like to share.

 

[lolnah]

It's ketamine. Well, I'll be darned. Mainlined, it would be quite the trip. You can buy shrooms all over the place now.

K will make you so nauseous, though.

You know what else K does, according to the DEA?



Lol. Lmao, even.

 

[GenociderSyo]

It's just sinking in that the drug she called a rescue med that she's been making her mother shoot into her iv almost daily to stop her attacks. With her mother being a NURSE. Was ketamine. Her mother is an idiot and a danger to the nursing profession.

She has now made a goodbye post on Facebook too:

 

[Triple Flutz]

It's just sinking in that the drug she called a resuce med that shes been making her mother shoot into her iv almost daily to stop her attacks. With her mother being a NURSE. Was ketamine. Her mother is an idiot and a danger to the nursing profession.

I'm not in the medical field in any capacity, but I swear I remember Ketamine use in humans on a long-term basis being linked to cognitive decline? She's been mushmouthing everything and her train of thought makes no sense, apparently since school so prior to her fucking mainlining it, surely this isn't helping. Lol. Lmao, even, indeed.

This is like Christmas, lol. Thank you, Syo.

 

[Troonos]

She now somehow got herself an oxygen mask with a bag attached to it.

"Non-rebreathing masks are not available for home use. A non-rebreathing mask is meant for short-term use in situations such as transporting people to a hospital. They’re rarely used outside of an emergency department and should only be used under medical supervision. If the oxygen flow is disrupted, it can lead to suffocation."

View attachment 4258495View attachment 4258507

• She can't handle tube feeds anymore.
  • Which she lost access to so does not even have.
• And now she can't breathe if they give her IV fluids.
  • The same fluids she said she no longer had access to.

LOL @ NRB outside a health care setting. 110% chance it isn't connected to anything.

Is she claiming CHF now with the pulmonary edema? That's a rare malingering diagnosis, since the diagnostic standard is so straightforward and noninvasive.

What a fucking retard. Do you guys think she's escalating this quickly because she's aware of the thread now?

 

[OK_Cogitator]

The comedy of her being a fatshit Christina Farley in a k-hole almost cancels out the selfish niggatry of her abusing IVIG.

Syo you absolutely earned your JULLAY win, big homie.

THE DRUG SHE IS SEEKING AND IS TAKING IS KETAMINE!
She has been mainling Ketamine into her hickman and other Ports.
This is definitely why they are DEMANDING she get her Feeding Tube and Hickmann removed.
​

 

[ZB927]

What a fucking retard. Do you guys think she's escalating this quickly because she's aware of the thread now?

Nah, she's been complaining about us since at least July of 2021, according to this archive in the OP.

 

[LikeAStone 2.0]

THE DRUG SHE IS SEEKING AND IS TAKING IS KETAMINE!
She has been mainling Ketamine into her hickman and other Ports.
This is definitely why they are DEMANDING she get her Feeding Tube and Hickmann removed.
​

She finally got herself posted as by the SPS Research Foundation and in the Q&A she stated the only pain med she will take is Ketamine and that she wants it to be in her IV. Bitch was mainlining Ketamine!
View attachment 4260899

Here is the IG post where most commenters called them out for believing her.
View attachment 4260932View attachment 4260947View attachment 4260966View attachment 4260970
View attachment 4260904View attachment 4260918View attachment 4260919

Now onto the Q&A:

Spoiler: Text of Article

My SPS Story: Chelsea L.​

Describe your life at your healthiest point.​

Probably before elementary school started even though I already started to have aches and pains due to an undiagnosed genetic condition called EDS (Ehlers-Danlos Syndrome).
View attachment 4260980

How many years before your diagnosis were you experiencing Stiff Person Syndrome (SPS) symptoms?​

6 years.

Describe your most debilitating symptoms.​

Being stiff as a rock and in pain. I need to be moved for my safety but any touch makes it worse. But what I really want is someone to lie next to me or pet my hair or rub my back. But that’s the cruelest thing about SPS. Any touch makes it worse.

Describe treatments you have tried, what has worked and what has not.​

Benzodiazepines (they seem to help a lot). Medical marijuana (I am allergic so that did not work out well). Painkillers (due to allergies there are only three types of painkillers I can take and ketamine usually works the best for me. Or if I am in a bad state in the hospital they’ll use intravenous ketamine).Then IVIG – WHEN IT WORKS, IT WORKS WONDERS!

Describe a time you received compassionate care.​

After my first round of IVIG they pushed it too fast and I got really really sick from midnight to morning. I couldn’t even roll my body. So the nurse just laid me on my side. I couldn’t even get my head out from underneath the pillow. My nurses know me so well – they know what I want before I want it! And of course the doctor who saved me – who finally took a chance on me – and diagnosed me.

Describe how SPS has changed you.​

I feel like I’m not living a lie anymore. I feel I’m not second-guessing anymore. I also feel like I want go to all the neurologists that have done me wrong and say, look what you missed! But in reality, I just want to raise awareness. There are too many of us suffering and that needs to change!

What brings you joy?​

View attachment 4260992
I feel like I’m at peace. Because I told my family I don’t want to die not knowing. Slowly things were getting worse and worse and I was so scared that I was never going to have any answers. Everything makes so much more sense now!

What do you want people to know about you?​

Follow your dreams but sometimes those dreams change and God shows you your true calling which is advocating for others and raising awareness for rare diseases (for me, it’s on TikTok). Never give up your fight for a diagnosis!

Occupation/previous occupation, if disabled.​

Model, actress, director, production assistant for commercial and movie sets (if I was not in them).

Misdiagnosed? With what.​

Yes. FND (Functional Neurological Disorder).

What do you want The SPSRF to achieve?​

Help those with SPS and SPSD and their providers find information, support, and better treatment options.

Have fun with that APS report and rehab lmao there’s no way it isn’t happening now.

CONGRATS YOU STUPID FUCKING NIGGER ADDICT!

I have absolutely zero sympathy for you and your plight! You drug addicted retard! Fuck you and your dumb enabling mother!!
May your downward spiral be hilarious and continuous!!!

 

[NoodleFucker3000]

Ketamine?!?!

Who the fuck approved this not only once, but *multiple times*, how do people even buy her shit long enough to consider listening to it. Most people have to go to a veterinarian to aquire ketamine.

Who is this gullible. Who is giving these gullible motherfuckers a license to treat patients.