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Bounce movie clips: 🤍 BUY THE MOVIE: 🤍 Don't miss the HOTTEST NEW TRAILERS: 🤍 CLIP DESCRIPTION: Abby (Gwyneth Paltrow) opens up to Buddy (Ben Affleck) about the loss of her husband and then they make love. FILM DESCRIPTION: In this romantic comedy-drama, two people whose lives were touched by the same tragedy find love. Buddy Amaral (Ben Affleck) is a successful L.A. advertising executive who has a way with the ladies, but inside he longs for a meaningful long-term relationship. One day Buddy sells his seat on a sold-out airline flight to a stranger; he's shocked when the jet crashes and the man is killed. A year later, still haunted by the incident, Buddy looks up Abby Janello (Gwyneth Paltrow), the victim's widow, who is now selling real estate to support her children. Buddy soon finds himself attracted to Abby, and the feeling is mutual, but while he's interested in marriage, he isn't sure how (or if) he should tell her that he was indirectly responsible for her husband's death. Bounce was written and directed by Don Roos, who made a splash with his independent debut The Opposite of Sex; supporting Affleck and Paltrow are Natasha Henstridge, Jennifer Grey, David Paymer, and Joe Morton. CREDITS: TM & © Miramax Films (2000) Cast: Ben Affleck, Gwyneth Paltrow Director: Don Roos Producers: Michael Besman, Alan C. Blomquist, Bobby Cohen, Steve Golin, Bob Osher, Meryl Poster, Bob Weinstein, Harvey Weinstein Screenwriter: Don Roos WHO ARE WE? The MOVIECLIPS channel is the largest collection of licensed movie clips on the web. Here you will find unforgettable moments, scenes and lines from all your favorite films. Made by movie fans, for movie fans. SUBSCRIBE TO OUR MOVIE CHANNELS: MOVIECLIPS: 🤍 ComingSoon: 🤍 Indie & Film Festivals: 🤍 Hero Central: 🤍 Extras: 🤍 Classic Trailers: 🤍 Pop-Up Trailers: 🤍 Movie News: 🤍 Movie Games: 🤍 Fandango: 🤍 Fandango FrontRunners: 🤍 HIT US UP: Facebook: 🤍 Twitter: 🤍 Pinterest: 🤍 Tumblr: 🤍
Alex is not like other girls. She is a 15-year-old with a secret, one that no other can claim. Her parents keep her hidden away at a coastal town in amongst the dunes of the shoreline, buying time before they must decide on a life-threatening operation. When old family friend and plastic surgeon Ramiro arrives with his teenage son Álvaro, Alex begins to realise that his visit could change her life forever. As the parents wrestle with the complications that will arise as Alex reaches adulthood, Alex and Alvaro become close, their relationship causing tensions amongst the locals. However, as the parents battle it out to instill a sense of open-mindedness amongst their society, it is the children who prove themselves to be flexible in understanding the sexual leanings and complexities of others. For more information, visit 🤍
Sexual exploration is a fact of life for most teenagers, but Alex has a secret to trump all others. Part girl and part boy, Alex faces danger around every corner leading to a decision that will seal her fate. Spanish w/ Eng subs. Director: Lucía Puenzo Writers: Lucía Puenzo, Sergio Bizzio Stars: Ricardo Darín, Valeria Bertuccelli, Germán Palacios
Interrogating Fatty Acid Metabolism Impairment and Clinical Correlates in Males with Klinefelter Syndrome This research study is being done to learn more about how fat is used as a source of energy in males with 47,XXY / Klinefelter syndrome (KS) compared to typical males. The eXtraordinarY Kids team wants you to know about a new research study to learn about energy metabolism in boys and men with 47,XXY / Klinefelter syndrome. Some guys with KS do not seem to be able to use fat as an energy source, as well as others. This can lead to being more tired and storing fat. For this research, we are looking for guys with and without KS who are 15-30 years old and are not on any cholesterol medication. The study includes 2-3 study visits at Anschutz Medical Campus (Aurora, CO) over 1-2 months. Compensation is provided. We would love to talk to you more about this study opportunity! For more information, please contact: Lte_XXY🤍ucdenver.edu Screening visit: blood draw, exam, bone density scan, maximal exercise test Study visit (1 for controls, 2 for KS): -Exercise test on treadmill, blood draw x 2, muscle biopsy from leg Monitoring diet, sleep, and activity at home before the visits KS only: fenofibrate medication for 1 month Males with or without Klinefelter syndrome who are 15-30 years of age ~1 month for healthy controls ~2 months for KS 1) "Compensation Provided" 2) For studies involving healthy subjects only, if desired- Compensation amount wording: Up to $375 for healthy controls and up to $700 for KS For more information, please contact: Lte_XXY🤍ucdenver.edu
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At the age of 31, Seamus was given a diagnosis that changed his life – for the better. Subscribe to ABC Science YouTube 👉 🤍 Klinefelter Syndrome (also known as 47,XXY) is a common genetic condition, affecting one in 550 men. Despite the prevalence, it’s rarely diagnosed. Small testicles are often a sign, but other symptoms can include reduced muscle mass, reduced body and facial hair, enlarged breasts, low sex drive and low energy. Speak to your GP with any concerns. Thank you to 🤍LivingWithXXY for introducing us to Seamus. #ListenUp #ABCScience Subscribe: 🤍 Like: 🤍 Follow: 🤍 // 🤍 - This is an official Australian Broadcasting Corporation YouTube channel. Contributions may be removed if they violate ABC's Online Conditions of Use 🤍 (Section 3).
Directed by : Clotilde Produced by : Tzig'Art Genre: Experimental - Runtime: 6 min 12 seconds Production year: 2018 "I am like a tulip in the desert. I die before I open. And the desert breeze scatters my petals."—Anonymous Afghan woman Her perpetual quest to achieve fulfillment through the union of the feminine and masculine in a harmonious whole makes a woman a hostage of her inner male forces that are thirsting for power. She, the subject of internal struggles, who despite herself arouses jealousy and resentment. She, a weapon of war, is attacked and silenced. She, who loses an inner male guardian with each male warrior. Despite her creative power, She is the inner female force who weeps. More info: 🤍
At the age of 31, Seamus was given a diagnosis that changed his life – for the better. Subscribe to ABC Science YouTube 👉 🤍 Klinefelter Syndrome (also known as 47,XXY) is a common genetic condition, affecting one in 550 men. Despite the prevalence, it’s rarely diagnosed. Small testicles are often a sign, but other symptoms can include reduced muscle mass, reduced body and facial hair, enlarged breasts, low sex drive and low energy. Speak to your GP with any concerns. Thank you to 🤍LivingWithXXY for introducing us to Seamus: 🤍 #ListenUp #ABCScience Subscribe: 🤍 Like: 🤍 Follow: 🤍 - This is an official Australian Broadcasting Corporation YouTube channel. Contributions may be removed if they violate ABC's Online Conditions of Use 🤍 (Section 3).
Alex is a 15-year old with a secret. To protect her sexual identity, the family has moved to Uruguay. Her father wants what is best for her, yet he knows she cannot continue living the life she leads. When an old family friend visits their cabin along with his son Alvaro, Alex realises the disturbing ramifications of the visit and develops a relationship with Alvaro that is far from conventional.
Kelsey was diagnosed with Klinefelter syndrome at the age of 27 trying to start a family with his wife. He talks about the challenges and overcoming those challenges to start a family. Learn more about Klinefelter syndrome at 🤍 Follow us on Instagram 🤍Livingwithxxy
Hi, everyone. I'm Dr. Shanlee Davis. I'm a pediatric endocrinologist that works at the Children's Hospital, Colorado, and the University of Colorado Anschutz Medical Campus. Here we have the Extraordinary Kids Clinic, a specialty clinic for children with XXY and other X and Y variations. I will review some of the most common questions as a pediatric endocrinologist. I take care of many boys with Klinefelter Syndrome. So the first question is: What hormones do you need to measure? When do you need to measure them? Hypothalamic pituitary gonadal access is a big long word that we often refer to as HPG access isn't even active until true puberty starts. The brain sends signals to the testes to tell them to make testosterone. This is when the start of puberty is initiated. This can happen anywhere from age 9 to 14 in typically developing boys. And we see the exact onset of puberty in Klinefelter syndrome. However, as puberty progresses in Klinefelter syndrome, the testes can't keep up with the demand for making testosterone in the rest of the body. And so the brain starts sending out signals louder and louder. Those signals are called Gonadotropin for LH and FSH, and we can measure these hormones in the blood. So once puberty starts, the doctors should begin to evaluate the exam, how the body changes over time, and what these labs look like in the blood. So LH FSH and total testosterone. The relationship between those labs makes a difference when deciding when and how to consider starting testosterone replacement in boys with Klinefelter Syndrome. Disclaimer: The Video Content has been made available for informational and educational purposes only. Living With XXY does not make any representation or warranties concerning the video content's accuracy, applicability, fitness, or completeness. The Video Content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health providers with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read or seen on YouTube. Living With XXY at this moment disclaims any and all liability to any party for any direct, indirect, implied, punitive, special, incidental, or other consequential damages arising directly or indirectly from any use of the Video Content, which is provided as is, and without warranties. To learn more information about Klinefelter syndrome 47 XXY, please visit 🤍
Luke is 15 years old, Nick is 27 and Ryan is 35. To them, having Klinefelter syndrome is just part of everyday life, and it's not something that stands out to them as "being different". Luke did his first video with Ryan shortly after he was diagnosed at 11 years old and Nick recently did a video with Ryan about finding out he was diagnosed in utero at the age of 3. We hope this helps those in our community and others.
Since researching about Klinefelter syndrome in 2017 I have learned that metabolic syndrome is very prevalent with our diagnosis. Since advocacy and awareness is so important I wanted to touch base on some of the possible health concerns. Most of us who are diagnosed with Klinefelter syndrome don’t even understand our own syndrome. Creating more awareness will help bring more education not only to our community but to the rest of the medical community and the world.
Living With XXY Presents: "What does he have again?" Luke Greene is a tall, handsome 15-year-old from Michigan diagnosed with Klinefelter syndrome (47 ,XXY). Klinefelter syndrome is the most common chromosome condition in men, yet rarely diagnosed. Filming with Luke taught us so much about how self-acceptance at a young age can give you the tools to beat the odds stacked against you. This film shows us that Luke is breaking the stigma in a nonconventional way. Whatever life has thrown at Luke, he always finds a way to smile and be his own "normal." The results are what people see, and the hard work is what parents behind the scenes see. We all have our own "behind the scenes" people rarely see. We often don't share how hard we work because we don't want recognition or to be treated differently. Though this film does not show the "behind the scenes," it does show anything is possible and that research and medical information need to show these possibilities. We welcome you to 2022, where anything can be achievable. 🤍
. Chapters 0:00 Introduction 0:27 Causes of Klinefelter Syndrome 0:57 Symptoms of Klinefelter Syndrome 1:31 Diagnosis of Klinefelter Syndrome 1:54 Treatment of Klinefelter Syndrome Klinefelter Syndrome is a genetic condition that affects males. It occurs when a male is born with an extra X chromosome, resulting in a total of 47 chromosomes instead of the typical 46. This extra chromosome can lead to a variety of physical and developmental issues. The symptoms of Klinefelter Syndrome can vary from person to person, but typically include: Small testicles Reduced fertility Breast development Tall stature Learning and language delays Social and emotional difficulties Diagnosing Klinefelter Syndrome can be challenging, as symptoms can be subtle and may not appear until later in life. However, a blood test can confirm the presence of an extra X chromosome. While there is no cure for Klinefelter Syndrome, treatment options are available to help manage symptoms. Testosterone replacement therapy can help improve fertility, increase muscle mass, and reduce breast development. Speech therapy, occupational therapy, and educational support can also be beneficial for those with learning and language delays. It's important to note that individuals with Klinefelter Syndrome can still lead fulfilling lives. With the right support and treatment, they can thrive in many areas of life, including work, relationships, and hobbies. It's also important to spread awareness and understanding of Klinefelter Syndrome. Many people are unaware of this condition, and individuals with Klinefelter Syndrome may face stigma and discrimination. By educating ourselves and others, we can create a more inclusive and supportive society for all. In conclusion, Klinefelter Syndrome is a genetic condition that affects males and can lead to a variety of physical and developmental issues. While there is no cure, treatment options are available to help manage symptoms and improve quality of life. It's important to spread awareness and understanding of Klinefelter Syndrome to create a more inclusive and supportive society for those with this condition. Thank you for reading, and I hope you found this information helpful.
Alex, une adolescente de 15 ans, a un secret : elle est hermaphrodite. Peu après sa naissance, ses parents décident de quitter Buenos Aires pour s'installer sur la côte uruguayenne, dans une maison de bois perdue dans les dunes. XXY commence avec l'arrivée d'un couple d'amis venus de Buenos Aires, accompagnés d'Alvaro, leur fils de 16 ans. Le père, un spécialiste en chirurgie esthétique, a accepté l'invitation en raison de l'intérêt médical qu'il porte à Alex. Une attirance inéluctable naît entre les deux enfants qui va les obliger à affronter leurs peurs... Des rumeurs se répandent dans la ville. On commence à dévisager Alex comme si elle était un monstre. La fascination qu'elle exerce risque désormais de devenir dangereuse.
Diferente. #xxy2007 #inesefron #luciapuenzo Álex (Inés Efron) es una singular adolescente de quince años que esconde un secreto. Poco después de su nacimiento, sus padres, Kraken (Ricardo Darín) y Suli (Valeria Bertuccelli), decidieron dejar Buenos Aires para vivir, aislados del mundo, en una cabaña de madera a orillas del mar. Lo que pretendían era que su hija creciera libre de cualquier tipo de prejuicios, protegida y feliz, hasta que llegara el momento de decidir qué camino debía seguir. Gracias por ver este vídeo, si te ha gustado el contenido de este canal, te invito a que te suscribas, dejes un comentario o me gusta. Suscribirse a CCDPA: 🤍 También puedes apoyar este canal uniéndote a la comunidad de Patreon. 🤍 #genz #millennials #cineindependiente #cinema #cine #cinedeculto #cultmovies #indiefilm #clips #movieclips #moviescenes #films #peliculas
Living With XXY Presents: PERSISTENCE with Mike Christoff. This brand new, never been done before documentary series is about real people within our community helping spread more light on what life with Klinefelter syndrome is really like. This series is filmed and produced by Daniel Milchev and Ryan Bregante who volunteer their time. Mike shares about overcoming the many hurdles he has faced in his life and despite his struggles, he climbs to the top of the mountain conquering those fears and setbacks. Please Help support future documentary series: 🤍 Our NonProfit website: 🤍
Recently Ryan Bregante and Kelsey Fuglsby had the opportunity to be guest speakers at Hunter College in NYC. The Class is called Abnormal Psychology which has roughly 100 students. This video is just a few of the highlights from our hour-long conversation. 1-500 men are born with Klinefelter syndrome, a genetic condition in which males are born with an extra X chromosome. Ryan was born with XXY and is the founder and president of Living with XXY Nonprofit. Kelsey Fuglsby is the mother of a 14-year-old boy named Elliott, diagnosed at ten years old. Only 25% of our community will receive a diagnosis. 75% will die, never knowing. The full version of this presentation is available on our podcast. 🤍 For more information, please visit: 🤍
XXY - Sortie le 26 décembre 2007 🤍 Un film de Lucia Puenzo Avec Inés Efron, Martín Piroyansky, Ricardo Darín Alex, une adolescente de 15 ans, a un secret : elle est hermaphrodite. Peu après sa naissance, ses parents décident de quitter Buenos Aires pour s'installer sur la côte uruguayenne, dans une maison de bois perdue dans les dunes. XXY commence avec l'arrivée d'un couple d'amis venus de Buenos Aires, accompagnés d'Alvaro, leur fils de 16 ans. Le père, un spécialiste en chirurgie esthétique, a accepté l'invitation en raison de l'intérêt médical qu'il porte à Alex. Une attirance inéluctable naît entre les deux enfants qui va les obliger à affronter leurs peurs... Des rumeurs se répandent dans la ville. On commence à dévisager Alex comme si elle était un monstre. La fascination qu'elle exerce risque désormais de devenir dangereuse. Vous pouvez voir ce film en : VOD : 🤍 🤍 DVD / Blu-ray : 🤍 🤍 🤍 🤍
Hey everyone. We are excited to announce two brand new sections to our website. "The voices of adults living with XXY" are written biographies from adults around the world who have been diagnosed with Klinefelter syndrome. They talk in-depth about what life is like from their perspectives. This is something we recommend you spend the time to read. 🤍 We also have created "early intervention programs for XXY" which is a list of all 50 states here in the USA, the eligibility, and the state website for early intervention services. This will help all families navigate services for their child from birth to 3 years old. 🤍 Please consider donating to allow us to continue to provide for our community and establish resources for everyone. Thank you 🤍
Jen was faced with a horrifying decision her doctor placed on her when she found out her NIPT test returned positive for Klinefelter syndrome. Over 70% of boys diagnosed in utero with Klinefelter syndrome are terminated. Klinefelter syndrome is males' most common chromosome condition, yet rarely diagnosed. Misinformation is killing these boys, and we need your help to update this information. 🤍
Klinefelter sendromu sperm üretim bozukluğuna bağlı azospermik erkeklerin %10'unda görülen bir genetik hastalıktır. Bir X kromozomunun erkekte fazladan olması nedeniyle erkeğin kromozom analizinde 47,XXY tespit edilir. Klinefelter sendromu olan erkeklerde mikroTESE yöntemi ile testis dokusundan sperm elde edilerek ICSI yöntemi ile eşlerinin yumurtalarına aktarılarak baba olmalarını sağlayabiliyoruz. 2011 yılında Fertility and Sterility dergisinde 106 Klinefelter sendromlu erkeklerde mikroTESE ile sperm elde etme ve ICSI sonrası gebelik sonuçlarımızı makale olarak yayınladık. Detaylı bilgi için: 🤍
Available on VOD on Vimeo: 🤍 Listen to the original soundtrack: 🤍 Website : 🤍 "XXY [ɛks/ɛks/wʌɪ] by Clotilde is a transgender film; a sensitive, multidisciplinary experiment; an equation with several unknowns; a poetic work open to interpretation that overwhelms the senses and urges reflection." MEDIAPART XXY [ɛks/ɛks/wʌɪ] is the result of Clotilde’s reflections on the feminine, taking a holistic approach and using multiple media, including music, dance, and images. It takes the form of seven portraits, involving seven films and seven original soundtracks, which combine to form a feminine archetype. Entitled Rhéa, Ruby, Juliette, Ishtar, Magda, Hannah, and Enk'aï, they embody in turn the child, the working woman, the mother, the artist, and the warrior woman, all heroines, both famous and anonymous. Short texts by Maya Angelou, James Joyce, Gloria Steinem, and Paul Auster echo behind the androgynous bodies of the dancers (France, United States, China) seeking harmony between their masculine and their feminine halves, as they progress through landscapes stretching out in all their beauty, whether horizontally (Iceland) or vertically (the American city). There are no songs, but murmurs and chants, cries and laughter, over resonating trumpet, oud, piano, brass, and didgeridoo. Clotilde adopts a universal language, opting for the neutrality of bodies, the impressionism of contexts, and the emotional over the analytical. The cast and crew - Written and directed by Clotilde Produced by Tzig’Art With the support of the French Ministry of the Women’s Rights, the SPEDIDAM, the SACEM, the French National Audiovisual Institute, the Simone de Beauvoir Centre Cinematographer : Florent Bourgeais Editor : Clotilde Rullaud Additional editor : Violeta Fernandez Compositing and calibration : Stéphane Jarreau / Donc Voilà Titles animation and direction: Bérangère Lallemant Composers : Fred ‘Parker’ Aliotti, Adèle Blanchin, Emmanuel Bex, Grégory Dargent, Tristan Macé, Clotilde Rullaud, Alexandre Saada Musicians : Fred ‘Parker’ Aliotti, Adèle B., Nicolas Beck, Boris Cacciaguerra, Médéric Collignon, Anne-Lise Clément, Yann Clery, Grégory Dargent, Angelique Debay, Justin Faulkner, Jean-Baptiste Goraieb, Etienne Gruel, Cyril Hernandez, Marie Kuchinski, Albin Lebosse, Jean-Louis Marchand, Antoine Paganotti, Vincent Posty, Laurent Salzard, Clotilde Rullaud, Alexandre Saada Dancers : BANDALOOP, Marina Chojnowska, Keiko Sato, Shanghai Jin Xing Dance Theatre Choreography in collaboration with the performers. Painter : StayReo Sound engineers : Jean-Paul Gonnod, Thomas Pégorier, Bruno Gueraçague / Tabaskko Documentalist : Laurent Sternbach Filmed in Iceland, in San Francisco and Chicago (USA), and in Picardie and Montreuil (France) ℗ & © Tzig'Art and Clotilde - 2018
The Power of XXY Do you want to know what bravery looks like? It looks like a 13 year old boy Owning who he is Right here, Right now, On this stage. I was born special. I mean, all babies are special, They’re cute and they’re funny when they talk, But, I was extra special I was born with an extra chromosome Most babies are born with 23 pairs of chromosomes, But that wasn’t enough for me I’ve got 23 + 1 You might call that extra chromosome A random genetic event The source of my superpowers If my parents had a gender reveal party The cake would’ve been blue But that doesn’t tell the whole story See, Most boys are born with an X and a Y And most girls are born with two Xs. But, I, being a super hero, Have both. Klinefelter Syndrome, or XXY Signs vary widely And often aren’t diagnosed until adulthood But, it’s part of who I am What makes me me It changes how I see the world Superpowers like empathy And kindness I will be likely be tall and youthfully handsome for most of my life, Have a photographic memory, Be a hands-on learning specialist, and able to pick up learning a musical instrument quickly This is part of who I am It makes me special And I am proud of who I am The differences that make me me: Worthy of respect Honest Kind Generous Helpful Joyous A creative problem solver Fair A loving brother to Oliver and Louie A thoughtful son to Jason and Kelsey A friend Brave a 13 year old boy Owning who he is Right here, Right now, On this stage. 🤍
Mathew Fasone created this power point presentation when he was going to college. This presentations was for the teachers and staff to understand his abilities, strengths and the things he struggled with. Since Klinefelter syndrome can be an invisible disability for some in our community Mathew wanted them to understand that his diagnosis isn't just about what he cant do but also what he was capable of doing. You can learn more about XXY and the community by visiting 🤍
Andy, Kelsey, and Ryan all have Klinefelter syndrome. Andy, who is 52, talks about his life and overcoming challenges. Andy is a commercial beekeeper and has a Hazlenut farm. Stay up to date with the latest from living with XXY and subscribe. 🤍 Weird video distortion, we are not gumbas I promise. haha
La directora Lucía Puenzo recoge el Premio Goya 2008 a la Mejor Película Iberoamericana por la cinta argentina XXY. Entregan Goya Toledo y Juan Diego Botto. La 22 edición de los Goya se celebró el 3 de febrero de 2008 en el Palacio Municipal de Congresos de Madrid, y fue presentada por José Corbacho.
As my solo road trip continues I get to explore USA civil war history around the south. People might wonder what its like having low testosterone in your body as I break down what its like. 🤍
Brandon who was born with Klinefelter syndrome 47 XXY decided he wanted to take me out for a spin in his off-roading side by side machine! This was filmed up in Washington state on some old fire roads. You can listen to Brandon's Podcast here 🤍
HOSENTASCHENHELDEN feat. XXY Wenn das Herz geht… Jetzt überall streamen MUSIK: HTH TEXT & GESANG: XXY Facebook: 🤍 Instagram: 🤍 Produktion, Regie, Animation & Schnitt: EMBE-ILLUSTRATION Website: 🤍 Facebook: 🤍 Instagram: 🤍 Kamera: Jochen Haussecker 🤍 & JLB © 2021 HOSENTASCHENHELDEN © 2021 EMBE-ILLUSTRATION #hth #hosentaschenhelden #wenndasherzgeht #xxy
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