Cystic Fibrosis Foundation - Southern California Los Angeles Chapter

Cystic Fibrosis Foundation - Southern California Los Angeles Chapter The Los Angeles Chapter is helping to advance the Cystic Fibrosis Foundation’s mission to cure cystic fibrosis and to provide all people with CF the opportunity to lead long, fulfilling lives.

The Cystic Fibrosis Foundation is committed to finding new therapies and ultimately a cure for CF. Cystic Fibrosis Foundation - Los Angeles Chapter
4929 Wilshire Blvd. Suite 760
Los Angeles, CA, 90010

The Cystic Fibrosis Foundation is committed to finding new therapies and ultimately a cure for CF. Cystic Fibrosis Foundation - Los Angeles Chapter
4929 Wilshire Blvd. Suite 760
Los Angeles, CA, 90010

With temperatures going up, what are you doing to stay cool? 😎Here is a throwback of Team Ashlee from Bakersfield stayin...
07/09/2021

With temperatures going up, what are you doing to stay cool? 😎

Here is a throwback of Team Ashlee from Bakersfield staying cool while fundraising for their Great Strides team!

Use this time during summer to raise extra funds for CF. Register for Great Strides, CF Cycle or 65 Roses Climb. 🌹

https://www.cff.org/LosAngeles/

With temperatures going up, what are you doing to stay cool? 😎

Here is a throwback of Team Ashlee from Bakersfield staying cool while fundraising for their Great Strides team!

Use this time during summer to raise extra funds for CF. Register for Great Strides, CF Cycle or 65 Roses Climb. 🌹

https://www.cff.org/LosAngeles/

What does it mean to be a Finest honoree? Hear from some of our past honorees as nominations are open for 2021!We are lo...
07/08/2021

What does it mean to be a Finest honoree? Hear from some of our past honorees as nominations are open for 2021!

We are looking for outstanding young professionals that have made an impact in their community and career.

🌟Who will you nominate in 2021? https://afasignup.formstack.com/forms/la_to_dallas_finest_2021

What does it mean to be a Finest honoree? Hear from some of our past honorees as nominations are open for 2021!

We are looking for outstanding young professionals that have made an impact in their community and career.

🌟Who will you nominate in 2021? https://afasignup.formstack.com/forms/la_to_dallas_finest_2021

🎉LA's Finest nominations are now open! We are excited to share that LA's Finest will be held in-person at FIVE On The Hi...
07/01/2021

🎉LA's Finest nominations are now open! We are excited to share that LA's Finest will be held in-person at FIVE On The Hill on Thursday, November 4th.

We are looking for outstanding young professionals that have made an impact in their community and career.

🌟Who will we honor in 2021?

https://afasignup.formstack.com/forms/la_to_dallas_finest_2021

🎉LA's Finest nominations are now open! We are excited to share that LA's Finest will be held in-person at FIVE On The Hill on Thursday, November 4th.

We are looking for outstanding young professionals that have made an impact in their community and career.

🌟Who will we honor in 2021?

https://afasignup.formstack.com/forms/la_to_dallas_finest_2021

🌞Can you believe it? Summer is back for in-person events! 🌹You are invited to join us this summer for the 2nd Annual 65 ...
06/24/2021

🌞Can you believe it? Summer is back for in-person events!

🌹You are invited to join us this summer for the 2nd Annual 65 Roses Challenge: Summer of Wellness happening NOW through August 11th! Register for Great Strides, 65 Roses Climb or Cycle and help us raise money for CF this summer!

🧘Finally heading out to your favorite vacation spot, local museum or workout class? Bring a CF shirt and tag us on social media while you are out and about spreading awareness!

🌞Can you believe it? Summer is back for in-person events!

🌹You are invited to join us this summer for the 2nd Annual 65 Roses Challenge: Summer of Wellness happening NOW through August 11th! Register for Great Strides, 65 Roses Climb or Cycle and help us raise money for CF this summer!

🧘Finally heading out to your favorite vacation spot, local museum or workout class? Bring a CF shirt and tag us on social media while you are out and about spreading awareness!

Today is Teen Advocacy Day!Teens from across the country, including Cassidy and Andi from the Los Angeles chapter, will ...
06/23/2021

Today is Teen Advocacy Day!

Teens from across the country, including Cassidy and Andi from the Los Angeles chapter, will share content directly to members of congress and advocating for CF on social media.

Thank you!

Today is Teen Advocacy Day!

Teens from across the country, including Cassidy and Andi from the Los Angeles chapter, will share content directly to members of congress and advocating for CF on social media.

Thank you!

🎉It's our BIG week of announcements! We are very excited to announce that 65 Roses Climb will be IN-PERSON this December...
06/22/2021

🎉It's our BIG week of announcements!

We are very excited to announce that 65 Roses Climb will be IN-PERSON this December!

🌹Thank you for your past participation and support of the 65 Roses Climb, we cannot wait to see you face-to-face this Winter. Get your team registered today!

🌟Link to register your team TODAY: https://fightcf.cff.org/site/TR/Climb/120_Southern_California_Los_Angeles?pg=entry&fr_id=8785

🎉It's our BIG week of announcements!

We are very excited to announce that 65 Roses Climb will be IN-PERSON this December!

🌹Thank you for your past participation and support of the 65 Roses Climb, we cannot wait to see you face-to-face this Winter. Get your team registered today!

🌟Link to register your team TODAY: https://fightcf.cff.org/site/TR/Climb/120_Southern_California_Los_Angeles?pg=entry&fr_id=8785

We are excited to share that LA to Dallas Finest nomination will be live in July! We can't wait to honor our amazing you...
06/21/2021

We are excited to share that LA to Dallas Finest nomination will be live in July! We can't wait to honor our amazing young professionals in-person this fall at FIVE On The Hill in Los Angeles! 🌿
Stay tuned and check your email for more details. Who will you nominate this year? 🏆

We are excited to share that LA to Dallas Finest nomination will be live in July! We can't wait to honor our amazing young professionals in-person this fall at FIVE On The Hill in Los Angeles! 🌿
Stay tuned and check your email for more details. Who will you nominate this year? 🏆

🎓Are you a college student? Join us for the Tomorrow’s Leaders College Program! 🌟This four-week, virtual program on Tues...
06/18/2021

🎓Are you a college student? Join us for the Tomorrow’s Leaders College Program!

🌟This four-week, virtual program on Tuesday and Thursday evenings from July 8 through 29 at 8 p.m. ET is intended for college students to build leadership, advocacy, and fundraising skills to make a difference on campus and beyond.

Apply today before the June 27 deadline: https://cff.swoogo.com/collegeprogram

🎓Are you a college student? Join us for the Tomorrow’s Leaders College Program!

🌟This four-week, virtual program on Tuesday and Thursday evenings from July 8 through 29 at 8 p.m. ET is intended for college students to build leadership, advocacy, and fundraising skills to make a difference on campus and beyond.

Apply today before the June 27 deadline: https://cff.swoogo.com/collegeprogram

La FDA recientemente amplió el acceso a Trikafta a niños de 6 a 11 años que tienen Fibrosis Quística y que tienen al men...
06/17/2021

La FDA recientemente amplió el acceso a Trikafta a niños de 6 a 11 años que tienen Fibrosis Quística y que tienen al menos una copia de la mutación F508del o ciertas mutaciones en el gen CFTR. Si es padre/madre o cuidador de un niño con FQ, únase a nosotros al webinar en ESPAÑOL 21 de Junio a las 7 p.m. ET, para obtener las respuestas a sus preguntas sobre lo que significa esta aprobación para su familia.
¿No puedes atender en vivo? Regístrese y le enviaremos la grabación después del evento.

https://cff.zoom.us/webinar/register/WN_lWlbkKzXQIS749ubrpJCIA

La FDA recientemente amplió el acceso a Trikafta a niños de 6 a 11 años que tienen Fibrosis Quística y que tienen al menos una copia de la mutación F508del o ciertas mutaciones en el gen CFTR. Si es padre/madre o cuidador de un niño con FQ, únase a nosotros al webinar en ESPAÑOL 21 de Junio a las 7 p.m. ET, para obtener las respuestas a sus preguntas sobre lo que significa esta aprobación para su familia.
¿No puedes atender en vivo? Regístrese y le enviaremos la grabación después del evento.

https://cff.zoom.us/webinar/register/WN_lWlbkKzXQIS749ubrpJCIA

06/17/2021

🎉🎉We are thrilled to announce the news that CF Cycle is back! We are teaming up with other CFF chapters from across the west to offer a virtual Tour de West, taking place August 1 - August 14.

🚴There will be virtual mission stops throughout the region along with fundraising and cycling challenges to promote some friendly competition! So, to get started, register for Cycle for Life through the following link and get your team together too! And the best part, you can participate from anywhere.

We hope you are looking forward to some fun on your bike this summer!🌞

Register today! https://fightcf.cff.org/site/TR/Cycle/General?fr_id=8861&pg=entry

🌟Natalie for the CFF LA Chapter has accepted the challenge! She is walking a mile each day to raise funds and awareness ...
06/16/2021

🌟Natalie for the CFF LA Chapter has accepted the challenge! She is walking a mile each day to raise funds and awareness for CF this summer.

💜Tell us what you plan to do this summer in the comments below and you can be featured on our page!

#UntilItsDone #SummerofWellness

🌟Natalie for the CFF LA Chapter has accepted the challenge! She is walking a mile each day to raise funds and awareness for CF this summer.

💜Tell us what you plan to do this summer in the comments below and you can be featured on our page!

#UntilItsDone #SummerofWellness

Photos from Cystic Fibrosis Foundation - Southern California Los Angeles Chapter's post
06/15/2021

Photos from Cystic Fibrosis Foundation - Southern California Los Angeles Chapter's post

🌟It's week two of our 65 Roses Challenge: Summer of Wellness! What activity have you decided on completing for 65 days? ...
06/15/2021

🌟It's week two of our 65 Roses Challenge: Summer of Wellness! What activity have you decided on completing for 65 days? Tell us by using one of our frames!

🚴Don't forget to register for Great Strides, 65 Roses Climb or CF Cycle for Life this summer!

🚶‍♀️Great Strides - https://fightcf.cff.org/site/SPageServer...
🌹65 Roses CF Climb- https://fightcf.cff.org/site/TR?fr_id=8785&pg=entry
🚴 Cycle for Life: Tour de West: https://fightcf.cff.org/site/TR?fr_id=8861&pg=entry...

“I was diagnosed with cystic fibrosis on my first birthday. I recently turned 25, and I am working as a wildlife field r...
06/11/2021

“I was diagnosed with cystic fibrosis on my first birthday. I recently turned 25, and I am working as a wildlife field research technician while I am in school getting my master’s degree in biology.

I have always been comfortable telling friends, family, and strangers about my CF, so when I was questioning my sexuality, it was never something I considered hiding. I enjoy speaking out and advocating for cystic fibrosis, so my sexual orientation was something that followed suit. I am fortunate to connect online with the CF and LGBTQ+ communities. Sometimes they overlap, and I get to connect with q***r people with CF! Meeting people like me gives me the drive to continue to advocate for both communities.

The LGBTQ+ community fights for love, equality, and kindness, and that has made it so easy to find my place in this world as a gay woman. Similarly, the CF community and supporters join together to fight for a cure for me and thousands of others, making it easy to find my place in the world with a chronic illness.

Unfortunately, people with CF and the LGBTQ+ community both face discrimination. The ‘Ew, gross’ look I get from strangers when I am having a coughing fit is the same look I get when non-accepting people see me kiss a woman or my pride flag. The judgmental eyes are something I’ve experienced my whole life, so although CF has taken a lot from me, it has also given me the strength to be fearless and unapologetically myself.” -Natalie Park, an adult with #cysticfibrosis #happypride #pride #lgbtq🌈 #loveislove

“I was diagnosed with cystic fibrosis on my first birthday. I recently turned 25, and I am working as a wildlife field research technician while I am in school getting my master’s degree in biology.

I have always been comfortable telling friends, family, and strangers about my CF, so when I was questioning my sexuality, it was never something I considered hiding. I enjoy speaking out and advocating for cystic fibrosis, so my sexual orientation was something that followed suit. I am fortunate to connect online with the CF and LGBTQ+ communities. Sometimes they overlap, and I get to connect with q***r people with CF! Meeting people like me gives me the drive to continue to advocate for both communities.

The LGBTQ+ community fights for love, equality, and kindness, and that has made it so easy to find my place in this world as a gay woman. Similarly, the CF community and supporters join together to fight for a cure for me and thousands of others, making it easy to find my place in the world with a chronic illness.

Unfortunately, people with CF and the LGBTQ+ community both face discrimination. The ‘Ew, gross’ look I get from strangers when I am having a coughing fit is the same look I get when non-accepting people see me kiss a woman or my pride flag. The judgmental eyes are something I’ve experienced my whole life, so although CF has taken a lot from me, it has also given me the strength to be fearless and unapologetically myself.” -Natalie Park, an adult with #cysticfibrosis #happypride #pride #lgbtq🌈 #loveislove

🧘‍♀️How can you create a well-rounded life?Join us as we tackle the pillars of emotional intelligence and how they can h...
06/10/2021

🧘‍♀️How can you create a well-rounded life?

Join us as we tackle the pillars of emotional intelligence and how they can help your life at work and home. The “Emotional Intelligence 101” session, part of the Tomorrow’s Leaders track, “Self-Improvement; Creating A Well Rounded Life,” starts on June 15 at 11 A.M PST.

🌟We are excited to share that Stacey Armato, our Board Advocacy Chair will moderate the event and share her CF story.

📍Register today: https://tomorrowsleaders.cff.org/track3

🧘‍♀️How can you create a well-rounded life?

Join us as we tackle the pillars of emotional intelligence and how they can help your life at work and home. The “Emotional Intelligence 101” session, part of the Tomorrow’s Leaders track, “Self-Improvement; Creating A Well Rounded Life,” starts on June 15 at 11 A.M PST.

🌟We are excited to share that Stacey Armato, our Board Advocacy Chair will moderate the event and share her CF story.

📍Register today: https://tomorrowsleaders.cff.org/track3

👨‍👩‍👧‍👧 If you’re a parent or caregiver to a child with CF, join us for a community webinar from 4-5 p.m. PST TOMORROW o...
06/09/2021

👨‍👩‍👧‍👧 If you’re a parent or caregiver to a child with CF, join us for a community webinar from 4-5 p.m. PST TOMORROW on Thursday, June 10, to have your top questions answered by experts from the Cystic Fibrosis Foundation. All those who register will receive a recording of the event.

📍Register to save your seat: https://cff.zoom.us/webinar/register/WN_7zJwrDRsRJqusnF9zeO7CA

👨‍👩‍👧‍👧 If you’re a parent or caregiver to a child with CF, join us for a community webinar from 4-5 p.m. PST TOMORROW on Thursday, June 10, to have your top questions answered by experts from the Cystic Fibrosis Foundation. All those who register will receive a recording of the event.

📍Register to save your seat: https://cff.zoom.us/webinar/register/WN_7zJwrDRsRJqusnF9zeO7CA

🌟BREAKING NEWS! The U.S. Food and Drug Administration has approved the use of Trikafta for children with cystic fibrosis...
06/09/2021

🌟BREAKING NEWS! The U.S. Food and Drug Administration has approved the use of Trikafta for children with cystic fibrosis ages 6 through 11 who have at least one copy of the F508del mutation or one copy of certain mutations. With this approval, approximately 1,500 children will be eligible for a CFTR modulator for the first time.
“We have seen the transformative effect that Trikafta can have on older children and adults, and we are excited by the prospect that this medicine may slow or prevent the progression of the disease at an early age and stave off the most common complications of CF before they start,” said Michael P. Boyle, MD, president and CEO of the Foundation.

Learn more: https://www.cff.org/News/News-Archive/2021/FDA-Approves-Trikafta-for-Children-Ages-6-Through-11-With-Certain-Mutations/?sf145466435=1&fbclid=IwAR1Bc-tO_z1VHw6HphPJUC597wiAK3AKzIF7roRNMhsY73yZ6Pm-Z8tIXfI

🌟BREAKING NEWS! The U.S. Food and Drug Administration has approved the use of Trikafta for children with cystic fibrosis ages 6 through 11 who have at least one copy of the F508del mutation or one copy of certain mutations. With this approval, approximately 1,500 children will be eligible for a CFTR modulator for the first time.
“We have seen the transformative effect that Trikafta can have on older children and adults, and we are excited by the prospect that this medicine may slow or prevent the progression of the disease at an early age and stave off the most common complications of CF before they start,” said Michael P. Boyle, MD, president and CEO of the Foundation.

Learn more: https://www.cff.org/News/News-Archive/2021/FDA-Approves-Trikafta-for-Children-Ages-6-Through-11-With-Certain-Mutations/?sf145466435=1&fbclid=IwAR1Bc-tO_z1VHw6HphPJUC597wiAK3AKzIF7roRNMhsY73yZ6Pm-Z8tIXfI

🎉Calling all Grampions!💜Join us on Tuesday, June 22nd, at 1 PM for a virtual care center tour with DJ Kaley, Nurse Coord...
06/08/2021

🎉Calling all Grampions!

💜Join us on Tuesday, June 22nd, at 1 PM for a virtual care center tour with DJ Kaley, Nurse Coordinator at Lucile Packard Children's Hospital Stanford!

📍To attend, please register: https://cff.zoom.us/meeting/register/tJcqduCuqDwiG9VWWpylHbjiXIhxXsXt5Ci

🎉Calling all Grampions!

💜Join us on Tuesday, June 22nd, at 1 PM for a virtual care center tour with DJ Kaley, Nurse Coordinator at Lucile Packard Children's Hospital Stanford!

📍To attend, please register: https://cff.zoom.us/meeting/register/tJcqduCuqDwiG9VWWpylHbjiXIhxXsXt5Ci

🎨How does your creativity encourage or inspire you to connect with the cystic fibrosis community? 💜If you’re an adult wi...
06/08/2021

🎨How does your creativity encourage or inspire you to connect with the cystic fibrosis community?

💜If you’re an adult with CF, you’re invited to submit an original design for our BreatheCon swag contest that illustrates the healing power of connecting, creativity, and integrating well-being practices into your life.

Follow the link for more details on submitting your art work! http://on.cff.org/BreatheConswag2021

🎨How does your creativity encourage or inspire you to connect with the cystic fibrosis community?

💜If you’re an adult with CF, you’re invited to submit an original design for our BreatheCon swag contest that illustrates the healing power of connecting, creativity, and integrating well-being practices into your life.

Follow the link for more details on submitting your art work! http://on.cff.org/BreatheConswag2021

💪Do you have what it takes? The 65 Roses Challenge, Summer of Wellness kicks off today!Challenge yourself for 65 days to...
06/07/2021

💪Do you have what it takes? The 65 Roses Challenge, Summer of Wellness kicks off today!

Challenge yourself for 65 days to get active and fundraise for CF!

Register for any of our CF events:
🌟Great Strides - https://fightcf.cff.org/site/SPageServer?pagename=143_gs_landing_page
🌹65 Roses CF Climb- https://fightcf.cff.org/site/TR?fr_id=8785&pg=entry
🚴 Cycle for Life: Tour de West: https://fightcf.cff.org/site/TR?fr_id=8861&pg=entry&_ga=2.265514694.832382192.1622666548-874306621.1548188956

💪Do you have what it takes? The 65 Roses Challenge, Summer of Wellness kicks off today!

Challenge yourself for 65 days to get active and fundraise for CF!

Register for any of our CF events:
🌟Great Strides - https://fightcf.cff.org/site/SPageServer?pagename=143_gs_landing_page
🌹65 Roses CF Climb- https://fightcf.cff.org/site/TR?fr_id=8785&pg=entry
🚴 Cycle for Life: Tour de West: https://fightcf.cff.org/site/TR?fr_id=8861&pg=entry&_ga=2.265514694.832382192.1622666548-874306621.1548188956

Address

4929 Wilshire Blvd Ste 760
Los Angeles, CA
90038

General information

Posting Policy for the Cystic Fibrosis Foundation The Cystic Fibrosis Foundation – Los Angeles Chapter welcomes participation on our page and we encourage you to interact with us often. It is our goal to provide those in the CF community an opportunity to learn more about the local events and activities of our chapter. Individual medical questions are best answered by your CF doctor. Please use caution when searching for health information online, and always consult your doctor before making changes to your or your child’s treatment regimen. You should not rely on information posted on Facebook to suggest a course of treatment for any medical condition nor should you disregard medical advice from your doctor or deviate from any prescribed treatment program because of what you read on Facebook. Please note: giving away, sharing or selling medication or medical equipment that requires a prescription is against the law. To protect your own privacy and the privacy of others, please do not include phone numbers, mailing addresses or e-mail addresses in your posting. You participate at your own risk, taking personal responsibility for your comments, your username and any information provided. This is a public site and visitors do not have to be a member of Facebook to view comments posted to this page. In accordance with Facebook’s rules, users must be 13 years of age or older to participate on this page. Posts made by those identifying themselves as younger than 13 will be deleted. Please note that posts containing personal attacks, profanity, or illegal material are prohibited. In addition, multiple postings of the same content may be construed as spam and will be deleted. We reserve the right, at our discretion, to remove any post that is deemed unintelligible or irrelevant, or to block a user's privilege to post to our page. The appearance of external links on this page does not constitute official endorsement on behalf of the Cystic Fibrosis Foundation. All content posted by the Cystic Fibrosis Foundation is the property of the Cystic Fibrosis Foundation and is subject to copyright laws. For more information, please visit http://www.cff.org/legal_terms_and_conditions/#Policy_on_Intellectual_Property. The Cystic Fibrosis Foundation is a 501(c)(3) tax-exempt organization and therefore prohibited from directly or indirectly participating in any political campaign. In accordance with the Internal Revenue Service regulations, any posts determined to be political activity will be removed.

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Hello everyone, My colleague Kim Hager and I are interested in studying the experiences and barriers to accessing mental health services for families. For the purpose of our research, we intend to compare three groups – caregivers of children with one or more mental health conditions (including developmental diagnoses), caregivers of children with mental health conditions and common medical conditions, and caregivers of children with mental health conditions and rare diseases. Caregivers include biological parents, adoptive parents, foster parents, step-parents, guardians and kinship homes with children under the age of 18. The survey is nationwide and open to families who live anywhere within the United States. The hope is the survey results will assist mental health providers in tailoring services to meet families’ needs. The study was approved by the IRB and survey is anonymous. Please help us by filling out the survey and/or sharing it. English survey: https://www.surveymonkey.com/r/PQFSMVV Spanish survey:https://es.surveymonkey.com/r/2DXD5TX Thank you and we appreciate all your help
An exciting announcement for CF parents and CF'ers: I'm a CF parent and I've created a FB page... "CF ZoomConnect"... for the purpose of connecting CF parents and CFers on a weekly Zoom call (Sunday evenings) to build strong and supportive relationships. The call will include breakout rooms of up to 6 or 8 people, to allow for effective conversation and relationship building. If you are a CF'er or a CF'er parent, I invite you to join us. :) https://www.facebook.com/groups/2863363707105877/
Thank you to CFF - Los Angeles for all you do!
My name is Danielle and I am a student attending UCLA. I was so inspired by the individuals the I met at the Cystic Fibrosis Foundation's Great Strides Santa Monica event last year that I am creating a hypothetical product for individuals with CF in my entrepreneurial class. I am looking to have individuals with CF and/or family members answer a 4-minute online survey about their experiences to better illuminate possible inventions that may help those with CF live life more comfortably. I would greatly appreciate if you would take the time to answer this quick survey: https://goo.gl/forms/kMDPAMTDcikJVwkF2 Thank you!
Is there a branch in the Coachella Valley? Palm Springs- Rancho Mirage- Palm Desert - LaQuinta - Indio
Benefitting cystic fibrosis
A fiction suspense book that just came out a month ago has a character in it with CF that really brings awareness to CF affects families. The proceeds of the book are being donated to the CF Foundation. It's called The Naked Block and can be found on Amazon or Kindle. It's receiving 4 and 5-star reviews, so hope everyone gets a chance to order the book to raise money for CF and to enjoy a comical and suspenseful book at the same time.
Susan Thau, PhD., and I are offering a 1 day workshop, 9/23, in L.A. for couples whose child has a serious medical condition. We know from experience just how stressful this is on the couple. As psychologists who practice Emotionally Focused Therapy for Couples, we can teach couples the basics about emotional connection and health, and help them strengthen their bond with each other as an antidote to dealing with their child's condition. For more info, please contact me: [email protected] or (818) 888-7923.
My colleague and I are offering a 1 day workshop on 9/23 in L.A. for couples whose child has a serious medical condition. We know from personal experience the emotional stress of this situation. As psychologists who practice Emotionally Focused Therapy for couples, we want to help couples learn communication skills that strengthen their bond as an antidote to dealing with their child's condition. For more information, contact me at: [email protected] or (818) 888 7923
Why won't you enjoy the benefits of this great ancient therapy at home? Now you can with our new AirSalter https://www.facebook.com/healovation http://www.newsmax.com/…/salt-therapy…/2017/07/21/id/803040/