Wednesday, March 9, 2022

March 9, 2022 Cervical Cancer Updates and Global Impact

The #gyncsm community was pleased to have Morgan Newman, MSW, Community Engagement Liaison for Cervivor (@IamCervivor) join us to chat about Cervical Cancer Updates and Global Impact. We had eighteen participants join us for the informative discussion.

Below are samples of the responses to our chat topic questions. You may view the complete transcript here. You may also find links to resources at the end of the post.

T1: What are the current HPV vaccination guidelines? What have been some of the main changes and how do these affect different age groups?
  • T1: HPV vaccine works best when given before any exposure to HPV. Currently recommended are: - 2 doses for Age 9-14 (routinely 11-12) - 3 doses for Age 15-26 - Shared-Decision-Making w/ patient on whether to vaccinate Age 27-46. More via @CDCgov: cdc.gov/vaccines/vpd/h…
  • A1: You'll see the ages have changed recently for the HPV vaccine to start early at 9 and 10. We love this resource from @HPVRoundtable that maps it out: 


T2: What are the current cervical cancer screening guidelines? What are some concerns around the updates?
T3: What are some of the recent treatment advances for cervical cancer? How can patients stay up-to-date and also learn about clinical trials?
  • A3: There have been more options for #clinicaltrials for metastatic/recurrent #cervicalcancer being approved: immunotherapy treatments, including activated T-cells (that can recognize and kill cancer cells), therapeutic vaccines, and immune checkpoint inhibitors. 
  •  The latest #CervicalCancer Treatment guidelines (Jan2022) from @NCCN are available: https://t.co/d7OdABRFLg NCCN Guidelines are a good place to start so you can ask questions about your doctor's plan for your care and discuss any variations from the guidelines.
  • A3: We know finding information on #clinicaltrials can be daunting so we put this together: https://t.co/aAid1v4Luw. We are also fortunate to have great community partners like doctors at @NIH volunteering their time to navigate options and organizations like @Ancora_AI
  • T3: Patient groups like @IamCervivor @StopHPVCancer and others can help with information on the latest #cervicalcancer treatments and provide guidance of finding clinical trials.
  • A3: immunotherapy in cervical cancer nejm.org/doi/full/10.10…
  • @ASCO guidelines for management of invasive Cervical cancer were updated in 2021 https://t.co/Yd1l5bRfGO #gyncsm "Clinicians may offer upfront pembrolizumab and chemotherapy with or without bevacizumab"
  • A3: Ask your healthcare team about clinical trials. Get a second opinion even you like your healthcare team and want to stay with them. There is always something to learn. 
T4: How has HPV vaccination and cervical cancer screening and treatment been impacted by the pandemic?
T5: What is the research showing about disparities in prevention, screening, diagnosis and treatment for cervical cancer? 
T6: Yesterday was #InternationalWomensDay. What new initiatives are WHO and others bringing to global efforts to reduce disparities and eradicate cervical cancer?
  • @WHO is committed to eliminating #cervicalcancer by attaining: *90% of girls fully vaccinated by 15 *70% of women screened using a high-performance test by the age of 35 (again by 45) *90% of women with pre-cancer treated & 90% of women with invasive cancer managed 
  • T6: Cervical cancer presents an amazing opportunity because we actually have the science to, in many cases, prevent it plus catch and treat it in the pre-cancerous stage.
  • T6: In 2018, the WHO Director-General announced a global call for action to eliminate cervical cancer and in 2020 the World Health Assembly adopted the Global Strategy for cervical cancer elimination https://www.who.int/initiatives/cervical-cancer-elimination-initiative
  • We were shining a light on cervical cancer with @WHO as they formally launched a global strategy to eliminate #cervicalcancer. We continue to advocate in solidarity by sharing our stories: https://www.youtube.com/watch?v=0HPcWZSSrCo . #GYNCSM #GlowTeal
  • @ASCO has put out and recently updated Resource-Stratified Guidelines for the treatment of cervical cancer - with tiers to match guidelines with available resources in different areas.

    We will not be chatting in April but we look forward to having you join us on Wednesday, May 11, 2022 for out 2nd Annual Digital Health Fair. If your organization would like to join us please DM us on Twitter (@gyncsm) or email us at gyncsm@gmail.com .

    Thank you to all those who shared info about our chat. 

    Happy Spring,

    Dee and Christina

    ADDITIONAL RESOURCES

    Think You’re Too Old to Get the HPV Vaccine to Prevent Cancer? Maybe Not 

    Nearly One-in-Five Women Diagnosed with Cervical Cancer Over Age 65

    Cervical Cancer Treatment in Rwanda

    Advancing NIH Research on the Health of Women 2021 Conference  (Click on presentation tab to access videos) 

    Previous decline in cervical cancer incidence begins to reverse in low-income U.S. counties and stall in high-income counties

    Saturday, March 5, 2022

    Cervical Cancer Updates and Global Initiatives March 9, 2022

     


    The #gyncsm Community will be chatting on Wednesday, March 9th at 8pm ET (7pm CT, 5pm PT) about Cervical Cancer Updates and Global Initiatives. We are pleased to be joined by Morgan Newman, MSW, Community Engagement Liaison for Cervivor (@IamCervivor). Cervivor is a community of advocates who empower those affected by cervical cancer through education and using their voices to raise awareness to end stigma, influence change and end cervical cancer. 

    Their manifesto is: 

    We will use the following topic questions to help guide our chat:

    T1: What are the current HPV vaccination guidelines? What have been some of the main changes and how do these affect different age groups?

    T2: What are the current cervical cancer screening guidelines? What are some concerns around the updates?

    T3: What are some of the recent treatment advances for cervical cancer? How can patients stay up-to-date and also learn about clinical trials?

    T4: How has HPV vaccination and cervical cancer screening and treatment been impacted by the pandemic?

    T5: What is the research showing about disparities in prevention, screening, diagnosis and treatment for cervical cancer? 

    T6: Yesterday was #InternationalWomensDay. What new initiatives are WHO and others bringing to global efforts to reduce disparities and eradicate cervical cancer?

    We look forward to having you join us for this important discussion.  

    Dee and Christina
    Co-founders,  #gyncsm Twitter Community

    Wednesday, February 9, 2022

    February 9, 2022 Finding Emotional Support

    We were so happy to have twenty-six participants join us for tonight's #gyncsm chat on Finding Emotional Support. See the transcript here and other analytics here

    Here are some highlights from our chat. Note that the highlights from Question 7 include links to emotional health resources. 

    T1: What are some of the emotions that come with a cancer-related diagnosis? How have yours changed over time?

    • T1 Mine ran the gamut – shock, fear, sadness, anger, grief, and also gratitude for living close to an NCI comprehensive Cancer Center. 
    • T1. I don’t know why I was so surprised now looking back! Fear has passed as well
    • T1: Is overwhelmed an emotion? When I found out I had the genetic mutation behind all the cancer in the family, it felt good to know but also terrible. I now feel like a fell into a no-mans-land in healthcare.
    • I think guilt is there too. What could I have done differently? What will this mean for my kids?

    T2: When you have needed emotional support, who did you reach out to? Was your healthcare team involved?
    • T2. Family, friends, fellow advocates, 100% healthcare team
    • T2: I ended up not reaching out a lot. Part who I am. Part because my best friend was in end stage MBC. My husband was my rock, but I know he was overwhelmed, too 
    • T2: blessed to have a friend introduce me to @stepsthrough https://stepsthrough.org/ They offer FREE counseling for OC patients and caregivers
    • When I was first dx Family was the first support then I reach out to @CancerHopeNet and spoke one-on-one volunteer after seeing a flyer in my cancer ctr. Support groups at @RutgersCancer & @Cr4Hope helped me through the years. 
    • We sometime stigmatized patients (especially women) for having mental health need including self-censorship. Your care team should be there to help you find the support you need.
    •  I sought out a psychotherapist who specialized in people with #hereditarycancersyndromes. I believe my genetic counselor referred her.

    T3: What do you see as some of the impacts that the global pandemic is having on the emotional needs of those facing a cancer-related diagnosis? How has the pandemic impacted your need for emotional support?
    • T3: Can't image how hard it must be to go through treatment now during the pandemic, being immunosuppressed, having visitor restrictions. I miss having my husband with me during routine followups
    • T3: Cancer is super isolating to begin with! I guess I think every emotion has got to be more intense when people are already stressed and stretched emotionally.
    • Agree. Also, people are afraid of being in groups which make it more isolating when seeking help 

    T4: Based on your experience and perspective, what types of emotional support do patients need most and what areas do you see as lacking adequate resources?
    • T4. It’s comforting to talk to survivors of your specific cancer. They totally understand what you are going through & are a good resource for hope & info
    • T4: As someone mentioned, it is important that doctors make referrals and be the one to bring it up. Open the door for that conversation. I see the “we saved your life, now you are on your own” kind of experience changing but a ways to go re: whole-person healthcare
    • T4 For me I needed more help after I finished treatment handling the emotions - not seeing my gyn onc as frequently I admit freaked me out a bit. I needed a way to handle the fear of recurrence.
    • T4: Yes, this right here. My cancer center was great that first year post treatment, with referral to therapist. Now I sense they are impatient with me.
    • T4. #gyncsm I think many woman do seek out some sort of support -- it's the men who have #hereditarycancersyndromes that concern me the most. They just don't want to talk about it or deal with it. #Lynchsyndrome
    • 4. Support at different stages - early dx, active treatment, survivorship - matters. Long-term survivors like @womenofteal provide such comfort to women facing challenges when "normal life" is actually "new normal."
     
    T5: What have you found to be most helpful in providing emotional support? In-person or virtual support groups, other online platforms, one-on-one peer support, friends/family, counseling, other?
    • T5: As an introvert, I think I could definitely handle a Zoom meeting better than in-person. Nice that the options are increasing. 
    • T5: Reading books about #Hereditarycancer and connecting on Twitter with other advocates like @BRCAresponder has been super helpful to me. Meeting someone who truly understands what you're feeling and experiencing makes all the difference in the world. You feel less alone.
    • ...it takes a village of support options to provide emotional support when, where, and in the way that's best for each individual. 
    • I prefer online platforms like @smart_patients and @FacingOurRisk discussion boards. I do better in written formats like Twitter :)
    • There is no one size fits all. This is why it is so important to have multiple choices for emotional support. We need a healthcare system that can point you to the resource options. Including different types of technology
    • Having so many resources is great. And also overwhelming at first. Be sure to offer resources all along the way and not just in the beginning when processing info is difficult and needs not yet known. #gyncsm :)

    T6: How do you think disparities in care and access to care impact emotional support needs following a cancer-related diagnosis?
    • #gyncsm disparities in care can make it difficult to get that initial diagnosis!! It was a challenge for me and I have access and knowledge. #SystemicRacism is prevalent in this area. Advocacy & awareness a needed.
    • T6: We know Black women's physical pain tends to be dismissed more than white women's, so I can imagine their emotional pain is, too 
    • #SystemicRacisim and the health disparities it causes runs the spectrum of your #gyncsm journey from diagnosis to emotional support.
    • Let alone those who are transgender 
    • https://ascopubs.org/doi/full/10.1200/JCO.21.01249 This was a very powerful piece. @JCO_ASCO
    • #gyncsm The #healthdisparities amongst minorities are enormous and disconcerting. Minorities often to not get the basic care they need, require and deserve, let alone the emotional support. It's sad and we must do better on this front. #MinorityHealth

    T7: What resources, organizations, groups, and/or people have offered you the best emotional support? What resources do you recommend for those looking for emotional support?

    T8: As patients, advocates, and healthcare professionals, burn-out is a problem that has for many only intensified in recent years. Where do you find emotional support for interacting with the healthcare system?
    • T8: I think it is important as advocates to give ourselves permission to step back from time to time. And also to give yourself a healthcare/cancer-land break when you can. 
    • T8: #gyncsm: Limiting interaction -- social media detox is always helpful.
    • T8 Some oncology organizations like @ASCO are addressing provider burn-out and offering support . 
    • T8: I’d have to say colleagues, friends, family, counselors. People with an open ear and a willingness to listen and provide support and help with resiliency.

    We invite you to join us for our next #gyncsm chat on Wednesday March 9th at 8pmET as we discuss “Cervical Cancer Updates and Global Initiatives”.

    Have a good month! 

    Dee and Christina



     


    Thursday, February 3, 2022

    Finding Emotional Support - February 9, 2022 #gyncsm chat


    When you receive a cancer-related diagnosis, there are many areas of your life in which you may need support. Sometimes we need help cleaning our homes. Sometimes we need help with food shopping or preparing meals. Sometimes we need help getting to treatments, doctor visits, blood draws and scans. When these issues occur, there are many who want to jump in and help us or we can find organizations that will help us complete some of these tasks.

    But there is another area that is many times overlooked during and after treatment - emotional support. In a study #gyncsm participated in and reported in the Journal of Patient-Centered Research and Reviews, many women feel vulnerable and 


    During this month's chat on Wednesday, February 9, 2022 at 8pm ET ( 7 CT, 5 PT) we will discuss ways and places to find emotional support. After a discussion of the emotions we can experience, we will discuss who to talk to about your emotional needs, what organizations support those with emotional needs, and also the impact Covid -19 is having on survivors' emotional needs. 

    Guiding our discussion will be the following topic (T#:) questions:

    T1: What are some of the emotions that come with a cancer-related diagnosis? How have yours changed over time?

    T2: When you have needed emotional support, who did you reach out to? Was your healthcare team involved?

    T3: What do you see as some of the impacts that the global pandemic is having on the emotional needs of those facing a cancer-related diagnosis? How has the pandemic impacted your need for emotional support?

    T4: Based on your experience and perspective, what types of emotional support do patients need most and what areas do you see as lacking adequate resources?

    T5: What have you found to be most helpful in providing emotional support? In-person or virtual support groups, other online platforms, one-on-one peer support, friends/family, counseling, other?

    T6: How do disparities in care and access to care impact emotional support needs following a cancer-related diagnosis?

    T7: What resources, organizations, groups, and/or people have offered you the best emotional support? What resources do you recommend for those looking for emotional support?

    T8: As patients, advocates, and healthcare professionals, burn-out is a problem that has for many only intensified in recent years. Where do you find emotional support for interacting with the healthcare system?

    We look forward to having you join us on the 9th. 

    Dee and Christina 
    #gyncsm Co-founders


    Thursday, December 30, 2021

    #SaludTues Tweetchat 1p ET 1/4/22: “Raising Awareness for Cervical Cancer”

    We are pleased to participate in the #SaludTues chat on "Raising Awareness for Cervical Cancer" with  @IamCervivor@NFIDvaccines@StopHPVCancer@latinxvocesllc@UTHealthSAMDA . 



    Via #SaludTues:

    Each year, more than 14,000 people are diagnosed with cervical cancer. The cancer is especially hurting communities of color, with Latinas at a high risk of diagnosis. But cervical cancer is preventable . 

    Stopping cervical cancer for Latinas and all communities means equitable education about the causes, prevention and treatment of HPV and cervical cancer . 

    Join #SaludTues on Jan. 4,2022 at 1:00PM EST to tweet about how we can stop cervical cancer in celebration of Cervical Cancer Awareness Month.

    We will open the floor to data, resources and your experiences as we explore: 

    • How cervical cancer is caused ,screened and treated
    • What we can do to address the stigma and misinformation around HPV and cervical cancer
    • What resources are available to cervical cancer patients and survivors
    Learn more about Salud at  https://salud-america.org/
    Learn more about #SaludTues chats at https://salud-america.org/tweetchats/

    See you in the New Year! 

    Dee and Christina











    Wednesday, December 8, 2021

    Dec. 8, 2021 Surviving Holiday Stress

    For the last chat of 2021 we discussed Surviving Holiday Stress. Online resources and advice were shared by participants to help with the challenges of celebrating holidays as a cancer patient/survivor. You may find the transcript here and the analytics here

    Below is a summary of the topic questions and answers . 

    T1: What do you look forward to during the winter holidays? What traditions bring you comfort and/or joy?

    • I continued the tradition I had growing up where each child picks out a new ornament for the tree each year. We also have 2 different advent calendars - one from my childhood - that we all enjoy. Watching ELF and the original Miracle on 34th Street are also a must. :)
    • My favorite holiday traditions are time with my people, our annual homemade gifts, baking, music, and holiday light tours.
    • I love baking cookies that I used to eat growing up. And I love decorating the tree. Every ornament has a story - a trip , event or from when my kids were growing up.
    • I also love to attend a Christmas Eve candlelight service with my husband and kids before heading off to celebrate with extended family. Some peace before the bustle. 
    T2: How can a major diagnosis impact your experience of the holidays and your traditions? Does this change over time?

    • per @SHAREing expectations of being or looking like the person you were before your diagnosis can have an impact on your decision to attend gatherings or on your interactions during gatherings. Financial strain can also make gift giving an added source of stress.
    • When getting chemotherapy treatment I didn’t have time for things or was so tired I could do the things if I wanted to. So was a tough to adjust at first.
    • I also talk with clients about giving themselves permission—and explaining to others—to need something completely different than previous years. Sometimes, it is okay to let a tradition lapse.
    • Some people may just need to have a caregiver say - It's OK to not - bake dozens of cookies or buy all the gifts or put every decoration out. 
    • per @CancerHopeNet a great strategy is to simplify - get to the core of what matters to you - but also plan for how cancer may interrupt your celebrations. They also remind us all to check on caregivers and their needs over the holidays.
    • If you have a holiday tradition you'd like to participate in please talk with you healthcare team. You may be able to reschedule to allow a short treatment break so you don't miss important times with your family. #LittleBigThings
    • And some caregivers need a support person who is reminding _them_ that it is “okay to not” as well
    T3: What are some things you changed about how you celebrated when you/your loved one were first diagnosed? What are some tips for those celebrating while in active treatment?

    • Similar to the last topic, I encourage people to focus on their top priorities, and let some of the rest fall to the side. Maybe you do less baking, fewer cards, less running. That’s all okay
    • For the holidays, @power4patients suggests: 1) Know your limits and rest when you need to. 2) Allow extra time for preparing for travel or a get together - especially med prep. 3) Be conscious of foods you don't normally consume.
    • I picked out only 2 cookies to make (instead of 5), I had family help set up and put the lights on the tree. Which left me with what I love adding ornaments. I asked my husband to do the shopping for gifts.
    • Another reality is that, if you are in active treatment and physically miserable, the traditions may need to take a backseat. If needed, give yourself permission to have Christmas in February or Hanukkah in March.
    • In 2011 I wrote this - Advice from Holidays Past https://womenofteal.blogspot.com/2011/11/advice-from-my-christmas-past.html with some tips.

    T4: How can you manage relationships when you feel like you are expected to fulfill all your "usual" roles during the holidays? What can you do ahead of time to set expectations?

    • In some ways it is so much easier to just do what we always do... but talking about things - even hard things - can end up being rewarding. Maybe someone else in the family has always wanted to help do or try something but no one's ever asked. :) 
    • I encourage patients and caregivers to be willing to set aside “usual.” To talk to one another and key family members about most important goals/priorities and to say up front that things can be both different AND good.
    • We downsized everything - room-sized tree, modified versions of activities or holiday shows to keep the spirit while recognizing my MIL’s limitations. #gyncsm #caregiver
    • In this article, @cancerhopenet suggests sending a letter/cancer update so you don't have to keep repeating yourself and to be able to just set some clear expectations about how you can celebrate and what you do/don't want to talk about. #gyncsm https://blog.cancerhopenetwork.org/2021/11/03/surviving-the-holidays/
    • I gently remind folks that it is wildly unfair to expect themselves to navigate the holidays as if they didn’t have cancer. They don’t have to like it, but the cancer is there. Holidays with different expectations can be way more fun than holidays with exhaustion.
    • It is hard to ask for help but sharing with loved ones that you might need help with things ahead of time will make it easier.Telling them which festivities are top of your list can help them let others know your situation
    • Women are notoriously bad at asking for help. Everyone who loves someone with a gynecologic cancer this holiday - please ask, offer, ask, insist on helping. #gyncsm #LittleActsofKindness
    • This is a place where family and loved ones have a role. “Let me know how I can help” may mean leading the charge to scale back or modify traditions. Or being the one to champion your loved one’s need for rest. Take the hard convos off their plate. 
    T5: How do you feel about starting new traditions and letting go of others? How will this year be different for you?

    • I love the hope and possibility of a new tradition. There are some chores that we hang on to because “we’ve always done it” not because we love them. A forced re-evaluation can make room for something beautiful to grow.
    • Even if you stopped treatment a few months before, you still might not have the energy to "do it all".
    • Traditions ground and connect us to our past, so letting go can be hard. Being sad about that is okay. Mixed feelings are to be expected. Traditions can morph and change over time and new ones can bring joy too - while still finding ways to honor the past.
    • It was hard that first year but the next year holiday season I was – “I don’t need to do that this year either” So the new traditions were OK. 
    • We stopped doing gifts for the 18+ several years back and started doing charity donations instead. Some small gifting has crept back in but, all in all, it is way less stressful. Sometimes a change of pace is just what everyone needs.
    • @americancancer has this great article Handling a Serious Illness Through the Holidays During the COVID-19 Pandemic https://www.cancer.org/latest-news/handling-a-serious-illness-during-the-holidays.html

    T6: What are some tips for being more mindful or "in-the-moment" as you celebrate? How can you re-center if things get overwhelming?

    • https://www.hopkinsmedicine.org/health/wellness-and-prevention/4-mindful-tips-to-destress-this-holiday-season 1) Accept Imperfection. Can good be good enough? 2) Where does this fit in the grand scheme? Can I use this moment of frustration as an opportunity to reflect or find a way to make it pleasant? 3) Take a deep breath and respond w/kindness, 
    • I think I've gotten better about listening to my body and asking for what I need. I can better sense my anxiety creeping in and have gotten better about speaking up.
    • For me- If we were visiting others I would ask ahead of time if they had a spot I could lay down if I needed too during the festivities. I did take advantage of it a few times and felt refreshed when I returned to the group.
    • I appreciate these tips on "Protecting Your Mental Health During the Holidays" from @afspnational: https://afsp.org/story/from-thanksgiving-to-new-year-s-protecting-your-mental-health-during-the-holidays Get outside during daylight hours. Take a risk and connect if you are feeling lonely. Do at least 1 thing to improve your sleep this season. (1/3)
    • (2/3) continued... Take breaks. Remove something from your holiday “to do” list. Find a balance between being w/ others and being alone. Find the choices w/in the obligations (assuming you can’t avoid them entirely). Prioritize activities that support your mental health
    • (3/) continued... They also suggest rehearsing a few phrases to help you answer various lines of questions that might come up like: “I’d rather not discuss that today/here.” “I don’t know how to respond to that.” “I’ll have to think about that and get back to you.”
    • @cancercare has good advice in Coping with cancer during the Holidays https://www.cancercare.org/publications/55-coping_with_cancer_during_the_holidays 
    Please see Resources below. 


    Note there will be no #gyncsm chat in January 2022. 

    Save the Date for our next chat on February 9, 2022 at 8pmET on “Finding Emotional Support”.

    In January, you can join  #gyncsm @iamcervivor and more for a #SaludTues chat during #CervicalCancer Awareness Month on Tuesday, January 4, 2022 at 1pmET .



    We hope peace and light are with you through the winter holidays. We look forward to chatting with you in 2022!

    Dee and Christina

    RESOURCES 


    From Thanksgiving to New Years Protecting Your Mental Health During the Holidays https://afsp.org/story/from-thanksgiving-to-new-year-s-protecting-your-mental-health-during-the-holidays


    Handling a Serious Illness Through the Holidays During the COVID-19 Pandemic https://www.cancer.org/latest-news/handling-a-serious-illness-during-the-holidays.html


    Let's Talk About it : Ovarian Cancer   The Power of Traditions








    Sunday, December 5, 2021

    Surviving Holiday Stress #gyncsm December 8, 2021

     


    The holidays are a busy time for everyone. There are religious celebrations, getting together with family and friends, traveling, shopping for gifts, decorating, and food preparation. Being newly diagnosed with cancer, in active treatment, or during the survivorship stage adds to an already hectic schedule. You may have to juggle family obligations with a treatment schedule, adjust how you celebrate due to treatment side effects, and/or balance gift purchases with the financial burdens of cancer treatment. Join the #gyncsm community as we discuss the impact the holidays have on those impacted by cancer this Wednesday, December 8, 2021 at 8pm ET during our Surviving Holiday Stress chat.  

    We will talk about the challenges and discuss ways to cope and make those special gatherings with family and friends more meaningful and less stressful.

    T1: What do you look forward to during the winter holidays? What traditions bring you comfort and/or joy?

    T2: How can a major diagnosis impact your experience of the holidays and your traditions? Does this change over time?

    T3: What are some things you changed about how you celebrated when you/your loved one were first diagnosed? What are some tips for those celebrating while in active treatment?

    T4: How can you manage relationships when you feel like you are expected to fulfill all your "usual" roles during the holidays? What can you do ahead of time to set expectations?

    T5: How do you feel about starting new traditions and letting go of others? How will this year be different for you?

    T6: What are some tips for being more mindful or "in-the-moment" as you celebrate? How can you re-center if things get overwhelming?

     

    We look forward to seeing you on the 8th!

    Dee and Christina
    #gyncsm Co-founders