- Joined
- Nov 29, 2018
Warning: The content in this thread is graphic and disturbing, proceed with that in mind.
Because of the nature of this thread, reactions may cause some exceptional people to feel they need to intervene.
DON'T
Thank you.
Update:
The girls no longer have to wear the neck braces and only Avee still has an NG that Krissy changes weekly, as she has for over a year.
__________________________________________________________________
This is either the worst case scenario nightmare of surgical complications when you take doctor's advice, or it is an extremely well crafted tale of MBP that has left two young girls a nightmarish life of surgeries, infections, complications and permanent, life long damage to their bodies.
(she made sure those tubes showed because awareness)
If people are calling it "the Klein Girl Nightmare", it's got to be bad ... and it is.
Krissy Klein, mother of 4 living children (as of now), seems to absolutely love the attention she gets from being a martyr to both her girls. She posts and reposts and shares the memories of their surgeries and complications and calls them her "warriors". Children shouldn't have to be warriors. Her 10 year old is on palliative care because of permanent brain stem damage, her 11 year old is already severely depressed and suicidal because of the medical trauma. The two girls have been through nearly a dozen brain and spine surgeries and Krissy says they have bone/hardware infections as a result of the 2017 surgeries that require lifelong antibiotics.
Krissy has a long online history of asking for money. To date there have been 3 gofundme's made by Krissy, at least one current gofundme for the family, local fundraisers dating back to 2011 and Krissy drops her paypal in nearly every post she makes to the group.
The most recent gofundme has a $10,000 goal. The need is for a car.
They got a car and the money to repair the transmission on the other, and the gofundme was not taken down.
In Nov 2018, it appears the EDS dx was obtained without genetic testing, and the geneticist thinks Krissy's kids are "too complex" for a simple EDS dx. wow
The news is "dreaded" because it DID NOT confirm EDS. The Klein family does not have EDS. Krissy still continues the narrative that they all have some sort of connective tissue disorder that causes the myriad of constant medical issues in herself and the children.
Krissy says the new doc thinks it's Loey Dietz
After the news in July that the new doctors think the kids need less medical care and tubes, Krissy shifted the focus back to herself, first with a mysterious reaction to a new medication and an unexpected and mysterious allergic reaction from the MRI contrast, then most recently a vague revelation that she now had breast cancer. She rarely answers any questions or gives details about her own health, but posts about every medical procedure or medical issue her children have.
Let's go ahead and start with the image that made me suspicious in the first place, special thanks to Gwen Shank of 8crazyshanks/8crazygrifters (archive) for trying to emulate Krissy, had I not caught the Krissy post Gwen shared and decided to click on her name, none of this would have been possible.
Full post:
What was suspicious?
This post is all about Krissy. She completely neglects her girls to take a photo and make this post.
Krissy mentions herself 30 times through the use of I - I'm - I've - me
OTT pics of the girls in matching outfits, matching neckbraces, matching feeding tubes.
Krissy does not show relief when her children's test results show they are healthy or do not need intervention, she does not post when test results are benign, negative, She posts things like "we had an awesome appointment" when there are diagnosis and talk of surgeries. She will post that there is testing being done, then not post the expected follow-up or share the results - unless it's a new diagnosis or health problem. Not much is posted when there's good news.
The post from July showing doctors were not cooperating with Krissy's requests anymore:
"Expert" Kiwi analysis of the above post from @Kate Farms Shill
Now for her history:
In this 2012 blog (archive),
Aveahna was 3, almost 4 and had been diagnosed with Celiac and mom says doing well on the gluten free diet. Then she gets into her own health issues vaguely:
link: Rangely Christmasfest (archive) Some of the Christmasfest events included a fundraiser for Avee.
In a blog post from the end of 2014 (archive):
Summer 2013, Aveahna (then age 4) fell ill with symptoms like: migraines, fatigue and sleeping all day, pain that Krissy says kept the young girl from walking. When taken in for an exam, Krissy says the doctor noted an enlarged, sore liver. Bloodwork, Krissy says, showed elevated liver enzymes and nutrient deficiency. The girl had already been diagnosed with Celiac and mom says she follows a strict diet. Yet the bloodwork was "puzzling" and there seemed to be no cause why the girl was not absorbing nutrients.
Yet no mention of how Celiac, untreated, can cause all of these mysterious symptoms. Could it be that mom was not feeding her a gluten-free diet? Or was there a real medical condition that doctors could not explain? There never was an explanation for that, it turned into EDS and Chiari and now GI issues.
Articles claim by age 4, Avee had broken both legs. But there are no photos of the Avee in casts - as you would expect Krissy to do, with her propensity for oversharing graphic medical photos of her children. This could be explained by the toddler having had weaker bones or even stress fractures that were exaggerated for sympathy.
Dec 23, 2016 Moffat County Locals: Klein family trusts in God to see them through difficult times (archive)
By age 5, Krissy had been successful getting Avee into modeling and it seemed to be going very well.
Among the modeling links for Avee, a very unsettling YouTube channel (archive)
By the beginning of 2015, a Facebook page for baby and children's gifts posted a fundraiser for the Klein family, the first of many. In this post, it says Aveahna has "formally" been diagnosed with Juvenile Osteoporosis, Hypermobility Syndrome and Celiac Disease, and doctors suspect a metabolic syndrome. Costs were for the 5 hour trip to the clinic in Denver where they could treat her.
Krissy started a GoFundMe (archive) to help get money for the travel expenses and brain surgery for Avee. If this surgery was so life-saving and necessary, why was it not urgent? The surgery was scheduled several months out. (medical kiwis feel free to help explain Chiari)
Posted Oct 22, 2015 - Surgery was Dec 31, 2015
An important update from May 2016 reveals genetic testing DID NOT show EDS.
This was not the first time Krissy sought surgery for her children. Aaron and Haleigh had already both undergone Nissen Fundoplication surgery, which is a major abdominal surgery.
She claims many allergies for her children, and other health issues such as asthma, sometimes resulting in trips to the ER, which Krissy gleefully shared.
The ridiculous over dramatization of asthma care and pneumonia vaccine.
The video is gross:
"Our wonderful pediatrician"
She got the scans.
Avee suffered severe complications (according to Krissy) after her decompression surgery in Colorado. The second surgery for Avee might actually have been life-saving. But why did Krissy fight to get Haleigh surgery after the horrific complications Avee suffered?
Sadly, the complications post surgery were nothing short of horrific for both girls, and even worse for Haleigh, who spent 5 months old her life with an open would on the back of her head. Despite how painful and traumatic these surgeries and complications were for her children, Krissy never fails to celebrate their "zipperversary" - the day she allowed surgeons to permanently damage her children for symptoms that seem much less severe than the issues they face daily now.
Krissy celebrated Avee's 6 month, 1 year and 2 year zipperversary of this failure of a surgery that left her daughter with permanent brain stem damage and on "comfort care".
Haleigh's Zipperversary - celebrating a 5 month open wound.
Krissy says that the decompression surgery in Dec 2015 was unsuccessful and left Avee with a bony spur causing brain stem compression and permanent damage.
Watch your volume - this is in Feb, just 2 months after the first surgery. There are no videos like this before Avee's first surgery. Quite the opposite. Lots of videos of Avee being quite active.
She posts stuff like this once in a while where she says "I'm going to be completely vulnerable" - IMO this is a sneaky way to say "I'm being completely HONEST" - Lie detection 101 - when someone opens with "Let me be completely honest with you" what follows is not always the whole truth. Just speculating.
Krissy throws those parties and reposts all the graphic images in what seems like an attempt to re-live the experience and get more sympathy.
In May 2017, Krissy was successful in getting more brain surgery, this time for both girls.
Second GoFundMe (archive)
In 2018, Krissy made an awareness video that only revealed just how much life had been stolen from her daughters. These two girls "miss being kids" at 8 and 9 years old. They miss dancing, running, riding bikes, jumping on the trampoline and most of all, they miss their friends. It is incredibly sad and only raises further suspicions. Why would doctors operate on children who could run, jump, ride bikes, do gymnastics, dance and both lived relatively active lives?
For someone who loves to post all the nitty gritty about surgeries and bad test results (with excitement), why was Krissy not vocal about the symptoms her children experienced that led to surgery? In this video, Haleigh starts her list of symptoms with "trouble swallowing" and continues with vagueries like "brain stuff" and "spine stuff". Why would you list trouble swallowing FIRST, before brain and spine 'stuff'? Don't forget, Haleigh has had a Nissen Fundoplication, could that be the cause for her trouble swallowing? If that's even true. Usually a person starts their list with the most concerning symptom. Was trouble swallowing worth brain surgery?
You would think after all that, Krissy would be eager to keep her children away from the OR...
Yet, she says. Yet. Let that sink in. After watching both her daughters suffer endlessly after those surgeries, Krissy says, "yet"
YET???
After successfully getting doctors to agree to put a feeding tube in for Avee, the plans suddenly changed the day of and both girls got one. It startled their supporters, leaving them baffled and questioning. Krissy's explanations ranged from malnutrition, problems gaining weight to gastroparesis.
Just Avee scheduled for feeding tube:
Past talk of fraud and what looks like a hospital suspecting MbP:
Our kids really are sick!
"not sick enough.... unnecessary procedures" ...
People have asked what the dad thinks, and I think this sums it up a bit, he appears to miss life before brain surgery. I would too, man.
And to end this trainwreck, here's another bizarre inconsistency and even more bizarre behavior:
The rest of the links:
Claiming allergies for Haleigh in 2012 (archive):
Claiming allergies for Aaron allergies in 2012 (archive):
Twitter for the girls: https://twitter.com/aveahnaaurorah (archive)
Instagram fan pages for them:
https://www.instagram.com/aveahnaaurorah_fan/
https://www.instagram.com/Aveahna_aurorah_official/
https://www.instagram.com/aveahna.k/
https://tabithaw.wordpress.com/tag/zavrick (archive) (Lots of healthy family photos)
April 18, 2017 Servers at JW Snack’s will donate Thursday’s tips to help Craig family (archive)
May 21, 2017 Color fun-run brightens gray day as community rallies around the Klein family of May 21, 2017 Color fun-run brightens gray day as community rallies around the Klein family of Craig (archive)
Feb 11, 2019 200 Teens to Dance to Raise Awareness for EDS and Help Support the Klein Family (archive)
Fundraiser: https://fundly.com/dance-for-the-kleins#gallery/2 (archive)
Sounds like that's what she wants. Take another look at those cheerleading pics.
"although she's not officially diagnosed"
yeah, pretty crazy. *runs*
Personal Info:
Kristina Paige Klein (Tefertiller-Robison) b 3.15.1987
Zach Klein b 7.05.1979
The two were married 7.15.2005
Four kids:
Aaron Lee 09.2006
Haleigh-Ann Aeralynn 10.2007
Aveahna Aurorah 03.2009
Zavrich Oakley 09.2010
Because of the nature of this thread, reactions may cause some exceptional people to feel they need to intervene.
DON'T
Thank you.
Update:
The girls no longer have to wear the neck braces and only Avee still has an NG that Krissy changes weekly, as she has for over a year.
__________________________________________________________________
This is either the worst case scenario nightmare of surgical complications when you take doctor's advice, or it is an extremely well crafted tale of MBP that has left two young girls a nightmarish life of surgeries, infections, complications and permanent, life long damage to their bodies.
(she made sure those tubes showed because awareness)
If people are calling it "the Klein Girl Nightmare", it's got to be bad ... and it is.
Krissy Klein, mother of 4 living children (as of now), seems to absolutely love the attention she gets from being a martyr to both her girls. She posts and reposts and shares the memories of their surgeries and complications and calls them her "warriors". Children shouldn't have to be warriors. Her 10 year old is on palliative care because of permanent brain stem damage, her 11 year old is already severely depressed and suicidal because of the medical trauma. The two girls have been through nearly a dozen brain and spine surgeries and Krissy says they have bone/hardware infections as a result of the 2017 surgeries that require lifelong antibiotics.
Krissy has a long online history of asking for money. To date there have been 3 gofundme's made by Krissy, at least one current gofundme for the family, local fundraisers dating back to 2011 and Krissy drops her paypal in nearly every post she makes to the group.
The most recent gofundme has a $10,000 goal. The need is for a car.
They got a car and the money to repair the transmission on the other, and the gofundme was not taken down.
In Nov 2018, it appears the EDS dx was obtained without genetic testing, and the geneticist thinks Krissy's kids are "too complex" for a simple EDS dx. wow
The news is "dreaded" because it DID NOT confirm EDS. The Klein family does not have EDS. Krissy still continues the narrative that they all have some sort of connective tissue disorder that causes the myriad of constant medical issues in herself and the children.
Krissy says the new doc thinks it's Loey Dietz
After the news in July that the new doctors think the kids need less medical care and tubes, Krissy shifted the focus back to herself, first with a mysterious reaction to a new medication and an unexpected and mysterious allergic reaction from the MRI contrast, then most recently a vague revelation that she now had breast cancer. She rarely answers any questions or gives details about her own health, but posts about every medical procedure or medical issue her children have.
Let's go ahead and start with the image that made me suspicious in the first place, special thanks to Gwen Shank of 8crazyshanks/8crazygrifters (archive) for trying to emulate Krissy, had I not caught the Krissy post Gwen shared and decided to click on her name, none of this would have been possible.
Full post:
What was suspicious?
This post is all about Krissy. She completely neglects her girls to take a photo and make this post.
Krissy mentions herself 30 times through the use of I - I'm - I've - me
OTT pics of the girls in matching outfits, matching neckbraces, matching feeding tubes.
Krissy does not show relief when her children's test results show they are healthy or do not need intervention, she does not post when test results are benign, negative, She posts things like "we had an awesome appointment" when there are diagnosis and talk of surgeries. She will post that there is testing being done, then not post the expected follow-up or share the results - unless it's a new diagnosis or health problem. Not much is posted when there's good news.
The post from July showing doctors were not cooperating with Krissy's requests anymore:
"Expert" Kiwi analysis of the above post from @Kate Farms Shill
(Edit to correct, it is the younger daughter on marinol for palliative care because of, and I cannot repeat this enough, the permanent damage to her brain stem from all the surgery)
Now for her history:
In this 2012 blog (archive),
Aveahna was 3, almost 4 and had been diagnosed with Celiac and mom says doing well on the gluten free diet. Then she gets into her own health issues vaguely:
link: Rangely Christmasfest (archive) Some of the Christmasfest events included a fundraiser for Avee.
(IH - or Intracranial Hypertension, or Pseudotumor Cerebri)
In a blog post from the end of 2014 (archive):
Summer 2013, Aveahna (then age 4) fell ill with symptoms like: migraines, fatigue and sleeping all day, pain that Krissy says kept the young girl from walking. When taken in for an exam, Krissy says the doctor noted an enlarged, sore liver. Bloodwork, Krissy says, showed elevated liver enzymes and nutrient deficiency. The girl had already been diagnosed with Celiac and mom says she follows a strict diet. Yet the bloodwork was "puzzling" and there seemed to be no cause why the girl was not absorbing nutrients.
Yet no mention of how Celiac, untreated, can cause all of these mysterious symptoms. Could it be that mom was not feeding her a gluten-free diet? Or was there a real medical condition that doctors could not explain? There never was an explanation for that, it turned into EDS and Chiari and now GI issues.
Articles claim by age 4, Avee had broken both legs. But there are no photos of the Avee in casts - as you would expect Krissy to do, with her propensity for oversharing graphic medical photos of her children. This could be explained by the toddler having had weaker bones or even stress fractures that were exaggerated for sympathy.
Dec 23, 2016 Moffat County Locals: Klein family trusts in God to see them through difficult times (archive)
By age 5, Krissy had been successful getting Avee into modeling and it seemed to be going very well.
Among the modeling links for Avee, a very unsettling YouTube channel (archive)
By the beginning of 2015, a Facebook page for baby and children's gifts posted a fundraiser for the Klein family, the first of many. In this post, it says Aveahna has "formally" been diagnosed with Juvenile Osteoporosis, Hypermobility Syndrome and Celiac Disease, and doctors suspect a metabolic syndrome. Costs were for the 5 hour trip to the clinic in Denver where they could treat her.
Krissy started a GoFundMe (archive) to help get money for the travel expenses and brain surgery for Avee. If this surgery was so life-saving and necessary, why was it not urgent? The surgery was scheduled several months out. (medical kiwis feel free to help explain Chiari)
Posted Oct 22, 2015 - Surgery was Dec 31, 2015
An important update from May 2016 reveals genetic testing DID NOT show EDS.
This was not the first time Krissy sought surgery for her children. Aaron and Haleigh had already both undergone Nissen Fundoplication surgery, which is a major abdominal surgery.
She claims many allergies for her children, and other health issues such as asthma, sometimes resulting in trips to the ER, which Krissy gleefully shared.
The ridiculous over dramatization of asthma care and pneumonia vaccine.
The video is gross:
"Our wonderful pediatrician"
She got the scans.
Avee suffered severe complications (according to Krissy) after her decompression surgery in Colorado. The second surgery for Avee might actually have been life-saving. But why did Krissy fight to get Haleigh surgery after the horrific complications Avee suffered?
Sadly, the complications post surgery were nothing short of horrific for both girls, and even worse for Haleigh, who spent 5 months old her life with an open would on the back of her head. Despite how painful and traumatic these surgeries and complications were for her children, Krissy never fails to celebrate their "zipperversary" - the day she allowed surgeons to permanently damage her children for symptoms that seem much less severe than the issues they face daily now.
Krissy celebrated Avee's 6 month, 1 year and 2 year zipperversary of this failure of a surgery that left her daughter with permanent brain stem damage and on "comfort care".
Haleigh's Zipperversary - celebrating a 5 month open wound.
Krissy says that the decompression surgery in Dec 2015 was unsuccessful and left Avee with a bony spur causing brain stem compression and permanent damage.
Watch your volume - this is in Feb, just 2 months after the first surgery. There are no videos like this before Avee's first surgery. Quite the opposite. Lots of videos of Avee being quite active.
Krissy throws those parties and reposts all the graphic images in what seems like an attempt to re-live the experience and get more sympathy.
In May 2017, Krissy was successful in getting more brain surgery, this time for both girls.
Second GoFundMe (archive)
Krissy can't complain?
Trouble swallowing appears to be the only concern and driving factor behind surgery for Haleigh
The NS who performed Avee's 2015 decompression apparently didn't want to operate on her again. Why would he refuse if it was so medically urgent?
In September, it appears Avee got a staph infection from surgery, it destroyed enough bone that a screw came loose and Avee had to have more surgeries.
She reminds me of Gwen Hartley here -
And she sure does get excited about surgery!
After the surgery, Haleigh suffered with severe wound healing issues.
Haleigh complications, warning: gross
Avee with supposed CSF leak:
Haleigh's complications didn't have an end in sight... She had multiple brain surgeries in 2019.
"Not sure how you can help" ... *drops paypal*
Trouble swallowing appears to be the only concern and driving factor behind surgery for Haleigh
The NS who performed Avee's 2015 decompression apparently didn't want to operate on her again. Why would he refuse if it was so medically urgent?
In September, it appears Avee got a staph infection from surgery, it destroyed enough bone that a screw came loose and Avee had to have more surgeries.
She reminds me of Gwen Hartley here -
And she sure does get excited about surgery!
After the surgery, Haleigh suffered with severe wound healing issues.
Haleigh complications, warning: gross
Avee with supposed CSF leak:
Haleigh's complications didn't have an end in sight... She had multiple brain surgeries in 2019.
"Not sure how you can help" ... *drops paypal*
For someone who loves to post all the nitty gritty about surgeries and bad test results (with excitement), why was Krissy not vocal about the symptoms her children experienced that led to surgery? In this video, Haleigh starts her list of symptoms with "trouble swallowing" and continues with vagueries like "brain stuff" and "spine stuff". Why would you list trouble swallowing FIRST, before brain and spine 'stuff'? Don't forget, Haleigh has had a Nissen Fundoplication, could that be the cause for her trouble swallowing? If that's even true. Usually a person starts their list with the most concerning symptom. Was trouble swallowing worth brain surgery?
You would think after all that, Krissy would be eager to keep her children away from the OR...
Yet, she says. Yet. Let that sink in. After watching both her daughters suffer endlessly after those surgeries, Krissy says, "yet"
YET???
After successfully getting doctors to agree to put a feeding tube in for Avee, the plans suddenly changed the day of and both girls got one. It startled their supporters, leaving them baffled and questioning. Krissy's explanations ranged from malnutrition, problems gaining weight to gastroparesis.
Just Avee scheduled for feeding tube:
Looks like she really wanted a GJ tube instead of NJ
"not just because" ?
This Thanksgiving dinner in a bottle looks so delicious and savory, what a treat.
The reality of the tubes was overwhelming.
But Krissy still wants a g-tube for avee
"not just because" ?
This Thanksgiving dinner in a bottle looks so delicious and savory, what a treat.
The reality of the tubes was overwhelming.
But Krissy still wants a g-tube for avee
Krissy claims to have diabetes, IH, heart issues, hypertension, Chiari and EDS, even though they had no formal genetic testing for EDS and was told she and her kids do not have EDS. By the beginning of the year, Krissy appeared to be trying to shift the focus back to her own health issues:
We don't know who she was asking about though, the image could have been a freckle on her, her husband or any of the kids. But it didn't show up and there's no more information. Just weird.
https://www.reddit.com/r/Dermatology/comments/atcq3x/is_this_cancer/ (archive)
https://www.reddit.com/user/Zandkklein/posts (archive)
There wasn't much explanation here. And still not much explanation when she responds to the worried followers.
She gives zero details, not even what type. Comments include stuff about DCIS, but she doesn't respond.
drops that paypal again
We don't know who she was asking about though, the image could have been a freckle on her, her husband or any of the kids. But it didn't show up and there's no more information. Just weird.
https://www.reddit.com/r/Dermatology/comments/atcq3x/is_this_cancer/ (archive)
https://www.reddit.com/user/Zandkklein/posts (archive)
There wasn't much explanation here. And still not much explanation when she responds to the worried followers.
She gives zero details, not even what type. Comments include stuff about DCIS, but she doesn't respond.
drops that paypal again
Our kids really are sick!
"not sick enough.... unnecessary procedures" ...
People have asked what the dad thinks, and I think this sums it up a bit, he appears to miss life before brain surgery. I would too, man.
And to end this trainwreck, here's another bizarre inconsistency and even more bizarre behavior:
Twins?
Say happy birthday to your dead baby brother!
Only there is not really a history of a twin that could be found, from what I found on Krissy's old MySpace (archive):
]
Not a doctor, but I see one baby. I see no markings of Twin A or B. I don't see two names on her belly. So where did this male twin come from?
In the Avee birthday post from 2018 there is no mention of a twin.
Say happy birthday to your dead baby brother!
Only there is not really a history of a twin that could be found, from what I found on Krissy's old MySpace (archive):
]
Not a doctor, but I see one baby. I see no markings of Twin A or B. I don't see two names on her belly. So where did this male twin come from?
In the Avee birthday post from 2018 there is no mention of a twin.
Claiming allergies for Haleigh in 2012 (archive):
Claiming allergies for Aaron allergies in 2012 (archive):
Twitter for the girls: https://twitter.com/aveahnaaurorah (archive)
Instagram fan pages for them:
https://www.instagram.com/aveahnaaurorah_fan/
https://www.instagram.com/Aveahna_aurorah_official/
https://www.instagram.com/aveahna.k/
https://tabithaw.wordpress.com/tag/zavrick (archive) (Lots of healthy family photos)
April 18, 2017 Servers at JW Snack’s will donate Thursday’s tips to help Craig family (archive)
May 21, 2017 Color fun-run brightens gray day as community rallies around the Klein family of May 21, 2017 Color fun-run brightens gray day as community rallies around the Klein family of Craig (archive)
June 5, 2017 Family returns home to Craig after children have brain, spinal surgery in New York (archive)
Jan 23 , 2019 Basking Ridge Teen Hosts Dance-A-Thon To Raise Awareness For EDS (archive)
Feb 11, 2019 200 Teens to Dance to Raise Awareness for EDS and Help Support the Klein Family (archive)
Fundraiser: https://fundly.com/dance-for-the-kleins#gallery/2 (archive)
Sounds like that's what she wants. Take another look at those cheerleading pics.
"although she's not officially diagnosed"
yeah, pretty crazy. *runs*
Kristina Paige Klein (Tefertiller-Robison) b 3.15.1987
Zach Klein b 7.05.1979
The two were married 7.15.2005
Four kids:
Aaron Lee 09.2006
Haleigh-Ann Aeralynn 10.2007
Aveahna Aurorah 03.2009
Zavrich Oakley 09.2010
Krissy's Facebook (screenshot below)
Krissy's new Instagram (screenshot below)
Krissy's old MySpace (archive)
Zach's Facebook (screenshot below)
Couple's Twitter (archive)
Her Facebook group (screenshot below)
YouTube (archive)
Krissy's new Instagram (screenshot below)
Krissy's old MySpace (archive)
Zach's Facebook (screenshot below)
Couple's Twitter (archive)
Her Facebook group (screenshot below)
YouTube (archive)
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