Wednesday, June 10, 2009

In Memory of My Friend and her Daughter...I will continue to honour their light!

*****
This is The Smiling Mask's first interview, and it definitely demonstrates the need for empathy and education surrounding Postpartum Mood Disorders. As co-authors of “The Smiling Mask,” our mission is to encourage women to forgive themselves and reach out for assistance. We want to express our deepest gratitude for Terra Brockett for sharing her story and in turn honouring her dear friend, Jen and Jen's daughter.


*****

In memory of your friend, what can you tell us about her before the illness? What sparked your friendship, what are some beautiful things you remember about her?

It’s funny because Jen really amazed me in so many ways. She was a positive, open minded, energetic woman. She had a strong ethics and refused to do anything that went against her sense of right. As an academic, she graduated at the top of her class with a psychology degree from Ehwa Women’s University, one of the top universities in South Korea. As an ESL teacher, she loved being around children and her students loved her because of the relationships she developed with them. She could dance and sing like Jennifer Lopez and was naturally athletic which meant she’d play any sport someone would invite her to play. She was not afraid to try anything. She had her own sense of fashion and somehow really pulled off outfits that I am not sure you could find on any runway. I remember last summer when she spent a few weeks with us, how she was with my baby girl. There was a moment when I thought to myself that she was just a whole different level of parent as my daughter, who was always hard to settle, just cooed and laid there relaxed in her arms. She also had this effect on me. She was comforting.

How did the illness change her, and what did her symptoms look like?

I only know bits and pieces but my impression is that anxiety and fear literally ran her life. She was anxious about a lot of things, but mostly about her daughter’s health. She really thought there was something wrong with her daughter. This anxiety dictated everything she did from multiple visits to the doctor to isolating herself by not leaving the “safety” of the house or letting people in to visit. Her fears made her feel like she could not trust anyone else to take care of her daughter. Her husband was not able to step in for any of the everyday parenting things like feedings or diaper changes. This of course meant greater struggle for Jen because she was doing even more work on less sleep. It was also a struggle for her husband who did his best to be involved and really wanted to take care of the baby and help her through this.

Was she aware of the illness, and was she able to share this with you?

Her husband had done a lot of research when she started to show signs of serious depression and they talked a lot about it, but she was not able to share the illness with most people including the medical community. She didn’t want her husband to tell anyone so he became her main support. He took her to the doctor three times and she would minimize her struggle. She was afraid of what might happen. She was afraid of being away from her daughter and about being hospitalized long term in a scary place (the mental health hospital). In terms of the illness, I think she was afraid it would never end, especially when the anti-depressants she was prescribed did not work.

Were the symptoms recognizable to you as an outsider, what were some warning signs that you witnessed, or were they masked?

The warning signs, in retrospect, were the absence of phone calls, pictures and sharing stories about her baby. I assumed that this lack of contact was because she was really busy being the “perfect” mother that I always imagined her to be. She was so involved and connected with the children in her life that I always imagined motherhood as something that came “naturally” or easily for her. I never imagined that her silence was really masking the excruciating reality of living with PPD. It’s painful to think about how becoming a mother, something she had been looking forward to for so long, turned out to be such a struggle – how she struggled in silence, not allowing herself support – how those of us who knew her didn’t offer support because we assumed that this woman who always amazed us could never be vulnerable to something like PPD.

If you could have a dialogue with her during the struggle and now knowing more about PPD, what would you have said to help her?

I would have been honest about my own struggle with PPD before she even gave birth. I would have tried to open a safe space for any future discussions on PPD by being understanding and sympathetic not only to my own struggle, but to the struggles of so many others. This is so important-the need to make it OK for her to share her pain. Honestly, I would have handed The Smiling Mask over to her and even gone over the book together, sharing thoughts and listening to what was going on for her. In this particular case, Carla’s experience may have offered her hope or a different way to look at things when her meds didn’t work. I would have legitimated her struggle while talking about possible options and resources that might help. The big thing is I guess is that I would have initiated a conversation that did not take place while she was alive.

Having suffered the loss of your friend what would tell others who may encounter PPD with their own friends or family?

Share your stories, experience, and knowledge about PPD. Others may feel differently about this, but I truly feel like being educated and prepared is important so that she can identify when something is not “normal.” Don’t assume anything. Don’t assume that a completely resilient capable woman can’t suffer PPD. Don’t assume that silence is only a sign of being a busy mom. Don’t assume that someone who appears happy is OK. Don’t assume that she will let you know when she needs help-even if that was the case before having the baby…just don’t assume.

Having the courage to share your story is very brave, what are your hopes for this interview?

I hope that this will speak to the serious potential of this illness and how it affects many different kinds of women. It is everyday women, our sisters, our daughters, and our friends who suffer from this illness. It is not something to be taken lightly or passed over as something that “women just need to get over” or “suck it up” (both comments of which I have heard in the past). Women themselves need to know that this is not a matter of being strong enough to handle it yourself, but being able to ask for help because this illness in its most severe form, has taken other women’s lives. It is a serious, real illness that can hit anyone – including my friend, one of the most brilliant, selfless, loving women I knew.

*****

If you feel compelled to become an Ambassador by telling your story on our website www.thesmilingmask.com, PLEASE feel free to contact us, we would be most honoured to showcase your truth. If you have more ideas on how the message of hope and healing can get around our world…contact us at info@thesmilingmask.com! Make a difference, today, by speaking out loud the valuable lessons you just learned. Even print and share this interview for others to read!

Sunday, June 7, 2009

THE BIG APPLE EXPERIENCE!

The Smiling Mask Team travelled to New York for its first academic conference. The bright lights, billboards and big city adventure was surreal.

The conference, “Mothers Gone Mad,” opened our eyes to the shared experiences of many women surrounding Postpartum Depression and Mothering.

Personally listening to the ideas presented by the various speakers was interesting on many levels, these women touched on so many aspects of mothering and their own experiences. The knowledge we received spoke about the respect for our own mothers and generations past.

There was no judgment of mental illness but rather a deep admiration for the strength and suffering of past and present mothers. The experience of congregating with such spirited, passionate and intelligent women was poetic. Our differences in age, education, social class and ethnicity were lost as we entered and spoke about women as a whole; mind, body and spirit. We encouraged, educated and empowered each other!

Our hope is that with more education and awareness future mothers will be free of the mask and move towards the original beauty of creation. Finally beginning with the universal thread: If we nurture the mother we nurture humanity.

Thursday, May 21, 2009

Connections, connections, connections!

Tania and I were able to showcase our project at the Canadian Counsellor's Conference held in Saskatoon, SK yesterday...and what a day of connecting with like-minded people...WOWSA! I would like to mention the people that truly will make a difference to us and the people we connect with...

two fabulous women Darlene Ouimet and Tammy Morales of Face to Face who want to help us to create a platform on our website in which we can connect with all of you...face to face, online!!

Suzane Proulx of SUMAE who has expertise in non-verbal communication (body language) and symobolism. An incredible process that optimizes individual thinking processes and decision making through the use of focusing and the recognition of symbolism! Suzane is such a spark!

Liz Coben of Turner Coben Event Marketing Inc. who gave us the opportunity to attend this conference in their Trade Show at such a pivotal location because the call for papers were already chosen last year, yet!

Joelle Emond of Ecole St-Germain and a member and website manager of the Manitoba School Counsellor's Association who will post our site as a resource for families - thank you!!

We sat beside Ivy Armstrong of the University of Saskatchewan who works in Recruitment & Admissions, who is a bright and bold 24-year old woman who has a lot of life figured out, already...so impressive! She touches families lives so beautifully by teaching music and mentoring teenagers in Air Cadets, as well.

Leah Deans of the Adoption Support Centre of Saskatchewan Inc. who says we may be asked to speak so that these parents will know that it is actually quite common that parents of adoptive children ALSO experience Postpartum Depression!

We also connected with the organizer of this incredible event, Barbara MacCallum, and were asked to submit a proposal to speak in next year's conference in Charlottetown, PEI!

Finally, a large thank you to Christine M. Gatzke, a Clinical Psychotherapist www.clc-apathtohealing.ca and friend, who introduced us to this conference in the first place!!

What a day filled with synchronicities! We are so grateful for each and every one of you for your support for us and the families we have and will be connecting with! We are immensely grateful we had the opportunity to show you our thanks for all the awareness you helped bring to our own families :)

Tuesday, May 5, 2009

A woman and her mission that I would like to bring your attention to...

Natalie Dombrowski, the author of "Back to You," founder of S.P.E.A.K. (Spread Postpartum Education & Awareness Kinship) and writer of
http://nataliedombrowski.blogspot.com. She will be having her first radio interview that is going to be aired on May 8, 2009 at 9:00 am central time in honour of Mother's Day and Mothers everywhere. Tune in on Thursday it will be broadcast from Chicago, May 7th at 9:00 am on 91.5FM; Anyone, anywhere can listen on-line at www.wbez.org/848 So spread the word!! We are such kindred spirits ;)

Happy Early Mother's Day!!

Here's a link on our website of Mothers' Stories ~ Mothers who have chosen to share their stories of hope and healing! Our one and only, Tania Bird, has also included her story that was written by her friend Colleen Opseth for one of her university courses! Sharing the awareness happens in a myriad ways and we thank each and every one of you who have chosen to embrace their experiences and share with the rest of the world! Enjoy...http://www.thesmilingmask.com/page/women_using_their_voices.

Monday, May 4, 2009

The Canadian Press is also spreading the awareness around Postpartum Mood Disorders!!

Check out the latest article that our Carla O'Reilly had a HUGE hand in http://www.cbc.ca/canada/montreal/story/2009/05/04/montreal-cp-perinatal-obsessive-compulsive-disorder-0504.html!! Here's to health, wealth and awareness! Thank you Dominique Jarry-Shore of "The Canadian Press!"

The Smiling Mask has exploded!

We have connected with women across Canada and all over the world! The mask has been destroyed and mothers are speaking their minds and unveiling their own truths! Check out our website to read “Women using their voices,” the more we connect, we realize the world is a small place and we can heal each other by education and validation!

When I was suffering alone and looking for more information I came across a website with information about Postpartum Psychosis. http://www.melaniesbattle.org/. The heartbreaking realization was it was brought forth with a tragic ending. Carol Blocker of Chicago lost her Daughter Melanie Stokes to Postpartum Psychosis and she is also on a mission to create awareness in the United States. I was shocked when a number was listed on the site and I called Carol thinking a voicemail would pick up my message. Instead a real voice answered and it was Carol! As I cried on the phone, I thanked her for the information that helped me so long ago and shared my story.

As we move forward in our journey I would like to remember the women that have suffered needlessly and encourage our followers to look to the future. Excerpt from “The Smiling Mask-Truths about Postpartum Depression and Parenthood”...

I believe that the initial first step of admitting that I had a problem and asking for medical help was what saved me. Going to the hospital on that grim day when I could not bear it any longer saved my life. I believe that finding a Postpartum Depression support group gave me the best coping skills and helped me to heal at a deeper level. Feeling validation from others and that I wasn't the only one dealing with this illness was also very important. The friends I made at the support group guided me to new ways of thinking about life and eventually encouraged me to be a survivor and not a victim. We were united together and we realized our full potential. We survived by using many tools and skills, and it is now our mission to spread the word and give hope to other women and families that are suffering. I have now accepted my illness as a gift that will create awareness and give hope to other people living in this inner “Hell.” Women need to ask for help, to find a support group or start a support group, to stop blaming themselves, and stop being a victim to this illness. Being a mother and creating life is the most important thing in the world. We are creating the children of the future. We need to take hold of our power, and remember our strengths.


I made a choice to survive and not be a victim to this illness ~ Carla