Tag Archives: Postpartum Support International

Sharing the Journey with Diane Ashton

Diane Ashton is the PSI Co-Coordinator for the state of Hawaii. Sasha Williams serves as the other Coordinator for the state of Hawaii. Diane is awesome. I’ve really gotten to know her via email and facebook (we’re both on Facebook WAY more than we should be). Diane is funny, honest, and a wonderful woman. I am thrilled she agreed to a very last minute interview (sorry diane! but thanks!) To learn more about the support Diane offers in Hawaii, visit her website, PPD Support Hawaii. Now here’s Diane’s story in her own words.

Tell us about Diane. Who is she when she’s not providing support to women with PPD?

Hi Lauren!  It’s kind of funny how self-identified with postpartum issues a person can become!  I know I’m singing to the choir here to say that PPD advocates are a passionate bunch!  Along with my obsession, avocation, I am the mom to two older children–they’re 15 & 20 now, although I have no idea how they grew up so fast.  You know how that is.  And all my cherished skills I learned from and with the two of them. We grew up together, in many ways. We’re all a bunch of computer nuts, and are sitting in a 10 x 10 room on our own computers right this minute.  It’s more fun than housework.


You’ve experienced PPD and describe it at the PSI website as a mystery/horror movie. Share with us your journey through this strange place.

It’s been over 14 years, so I tend to be a bit removed from the experience now.  Maybe that’s encouraging to moms going through it now–knowing that eventually PPD won’t feel like something you live and breathe every. single. day.  Why I described it as a mystery/horror movie was that, even though I’d probably been depressed in the past, I’d never been to the depths like I was with PPD.  I’d also never been so sleep deprived.  It was a sleep deprivation due to depression, not because my kids weren’t sleeping through the night.  They were.  I was too anxious to sleep; it was that kind of anxious/depression.  And that was part of why it made it so hard to figure out what was going on with me.  I didn’t feel “depressed”.  I felt, like so many other moms have described, like I was “going crazy”.  It was a mystery to me what was wrong.  With all that came intrusive thoughts that were very gory.  And they weren’t thoughts so much as very vivid images.  They scared me and made me think someone would take my kids away from me, and me away from society forever–pretty much a horror.

What made you realize your moods after giving birth were not quite right? How were you treated when you sought help?

I…actually, …I waited until my daughter was around eight months old before I started sliding into that PPD pit.  It was partly due to her big brother going off to kindergarten with all his little friends we’d seen every week for …4+ years.  But kindergarten is somehow a big shift anyway, and can put moms off-balance for a bit.  Or maybe it’s just us moms who’ve been on the PPD ride are more sensitive to changes.  Anyway, by mid-October (6, 7 weeks into kindergarten) I was losing it.  But no way was I admitting to it.  Although I tried to look stuff up (1994–not much of an internet to surf then) I couldn’t find anything that described what I was experiencing.

Finally my husband took me for “a Sunday drive” to the ER, where they kept and observed me for a while.  I stayed at the hospital for a bit and, well, my peers there were very interesting.  The main thing was though that I finally got on a medication (Zoloft) and it started working.  I began to feel a lot like myself again within a couple of weeks.


How did your family help you during this difficult time?

They were great.  My in-laws had dd while I was in the hospital.  Dh had ds at home, and took him to school each day.  Afterwards, I stayed with my in-laws for more support and to get up to some kind of speed again.  There were other times they stepped in in BIG ways over the next year too–I don’t know what we would have done without them.


Name three things that made you laugh today.

  • A video the kids pointed me to, on youtube had us all cracking up.  A bit on the potty humor side, but we laughed.
  • Talking with a couple of my girlfriends about calling, texting, to American Idol–like we’re a bunch of tweenagers–how many phones each person uses to vote.
  • Swapping stories with my fellow former classmates tonight at dinner.
What do you find the most challenging about parenting? The least?

Still occasionally wondering if we bonded well, if I messed the kids up for life, etc.  But I imagine other moms who didn’t go through PPD wonder this as well.  Also challenging… the age of 13.  EEYuh…challenging.  The least challenging–the easiest–is loving my beautiful, vibrant kids every day!


As fellow PSI Coordinators, we’ve had the concept of self-care proven to us time and again. What do YOU do for yourself that is not a need and soothes your soul?

The beach soothes me.  Body boarding especially, but just getting in the ocean water balances me in emotional and visceral ways.

You work with women struggling with PPD all the time. Tell us a bit about what made you decide to turn your experience into advocacy and support. How empowering is it to do what you do?

It is partly because I didn’t get the name for the exciting journey I had until five or so years later–Oprah had Marie Osmond on, talking about her book about some illness called “postpartum depression”.  I sat there pointing at the TV again and again. “That was ME! That was ME!!”  I finally had a name for it.  I Googled and found online information and bulletin boards where I then made myself at home.  It was because I could find nothing here to help with PPD, and with my experience on the boards that I decided to become an Area Coordinator with Postpartum Support International.  Might as well make some lemonade from the PPD lemons.

How empowering is doing what I do?  What I’ve done for 5 years now is telephone support, email support, a weekly support group, and some speaking.  –the support calls, email and the group empower the parents and are validating for both of us.  Speaking to groups still feels empowering; our recovered moms/volunteers get a chance to speak at various events. I remember my first time too–it was empowering.  People, providers, wanted to know what it is like, what could be done, how would you know.  And they listened.  There’s a threshold you cross when you speak publicly about your experience.  What a great question Lauren.  I have to tell my therapist how much it meant to me that she asked me to speak a number of times. It allowed me to step out of my shame and into myself.


Now that your children are older, have you spoken with them about your experience? If so, how did they handle the information? How do they feel about your current work with women?

They are around when I’ve been on phone calls with moms or providers, so they do hear my end of conversations occasionally.  It’s just a part of our lives.  I weave information in to our conversations when opportunities arrive, much like I have with sex education.  Dd just had one of those “pretend baby” exercises where she had to care for a hard-boiled egg for 2 weeks as if it were her baby.  Of course I wove in some PPD talk!


Last but not least, let’s say you have an opportunity to speak with an expectant mother (new or experienced) about Postpartum Mood Disorders. What would your advice be?

It would really depend on the situation.  I used to be tempted to pass out information to every new parent I saw, just so they could avoid the journey I endured.  Barring accosting new parents in the grocery aisles, what I would say though is that you’re not alone if you have a PMD, they are very treatable, they are not your fault and that honestly, I found a gift in my experience, eventually.  Maybe it was my biggest experience of “whatever doesn’t kill you outright makes you stronger.”  And in the case of PPD, as many mothers say, it loosens your judgments, revealing compassion.

Aloha!

Devastating Illness needs our attention

The Meadville Tribune published a local opinion column today by Carla J. Behr. In this article, she examines Postpartum Depression’s need for attention. You can read it by clicking here.

My favorite part of the article?

When Carla writes, “There is no room for ignorance because making a difference in the lives of women suffering postpartum depression involves a whole community.”

She is so right.

Sharing the Journey with Teresa Twomey

Teresa Twomey is a fellow Coordinator with Postpartum Support International. Over the past couple of years we’ve emailed back and forth about a few various issues and I’ve really enjoyed my exchanges with her. More often than not, we’ve shared our mutual frustration regarding the mis-conceptions about Postpartum Psychosis vs. Postpartum Depression.

This past Tuesday, her book, Understanding Postpartum Psychosis: A Temporary Madness, released. I immediately scooped her up for an interview this week. Teresa is a survivor of Postpartum Psychosis and other PMD’s as well. In her book she hopes to present a realistic portrait of PPP and aid in removing the stigma so often associated with this misunderstood condition. With no further ado, here is Teresa’s interview. I am honored to share the journey with her!


Click here to purchase Teresa's book

Click here to purchase Teresa's book

Tell us about yourself – who is Teresa when she’s not a mom or a Postpartum Advocate?

Before I had children I was a litigation attorney and a professional mediator. I am now beginning to re-enter the workforce as a professional mediator. I also do some business consulting. I am currently working on a turnaround project for a packaging company.

I also enjoy writing – I have several writing projects going at any given time. Right now I have three children’s stories finished and another two I’m working on. I also am doing some more non-fiction writing that I plan to develop into a book. (In addition to my postpartum book, I co-wrote a chapter on mediation in a newly-released textbook on Employment Law and have had several academic articles accepted as proceedings or for publication in journals.)

I am active in our PTA, our Newcomers Group, our church and I co-lead two Girl Scout troops.

I enjoy doing new things and my latest “hobby” is working with stained glass (the soldered with lead type). I enjoy designing and creating a variety of pieces.

Sometimes I teach as an adjunct at a local university. I’ve taught Business Law, Business Communication, and Introduction to Women and Gender Studies.

As many of the moms who visit this blog, you’ve traveled down the dark road of Postpartum Mood Disorders. Share your experience with us.

After the birth of my first daughter I began to experience many strange things – I had nightmares, hallucinations, I could not read, I was paranoid. I did not know something like that could happen to someone like me – I was totally blindsided. I did not get treatment at the time, although I told everyone who would listen that I could not cope. I had physical complications and I think those around me thought that was the basis for my frustration and complaints. And I think that even the medical professionals did not understand that something like postpartum psychosis could happen to someone like me (educated, smart, capable, personable, and dynamic). After the psychosis I went into a depression. But still I did not identify it and did not receive help. I did not learn the name for my experience until I was on bed rest during my second pregnancy (with twins!) I was frustrated about the lack of information and misinformation. But I was fortunate – I did not have postpartum psychosis following the birth of my twins. Then when Andrea Yates killed her children and I heard many hurtful and ignorant comments, I decided to do this book. (The more detailed version of my story is in the book.)

At what point in your journey did you realize you needed professional help?

I knew I needed some kind of help almost immediately – but I did not know there was help for what I was experiencing. I did not know there was a name for it. I thought maybe I was going crazy. I did keep telling people I could not cope – that I was a terrible mom – that I wanted someone there to help me all the time – but I was afraid (and paranoid) so I didn’t actually describe in detail what I was experiencing. I just remember telling myself “just hold on – just hold on.”

What roles did your husband and family members play in your recovery? How did they handle your diagnosis?

I was better by the time my family learned of it. They expressed shock, dismay, some denial, and concern — all in a loving way.

My husband, mom, dad and brothers have all been very supportive of my work with Postpartum Support International.

You’re now a Coordinator with Postpartum Support International. What made you decide to become an advocate?

I recognized a need. Plus I was profoundly grateful that we had not suffered any loss of life. It felt right to express my gratitude for that by turning around and helping others. Plus, Jane Honikman asked me to be a coordinator. (I sometimes joke that she roped me in – and am usually met with a response like “you and everyone else at PSI,” or “join the club!”) I am honored to be a part of such an amazing organization.

Earlier this week your book, Understanding Postpartum Psychosis: A Temporary Madness, released. Tell us about this book and the concept behind it. What is your hope for this book?

I was dismayed about how little information there is about the actual experience of women with postpartum psychosis and the amount of misinformation most of us have. I believe those contribute to the ongoing mental anguish many women have as a result of this disorder as well as the occasional loss of life. I passionately believe that professionals and the general public need to know more about this disorder. It strikes so seemingly randomly that if people do not become informed until faced with this disorder it may be too late.

Public ignorance and mis-perceptions lead to:

  • Failure to identify and warn women (and their families) who are at high risk of having this disorder
  • Failure to take measures to prevent the illness
  • Failure to properly identify the illness
  • Failure to provide adequate care
  • Failure to take the steps necessary to prevent tragic outcomes
  • Mistreatment at the hands of police and other law enforcement professionals
  • Inequitable treatment by the legal system based on discredited science and societal myths
  • Misinformation and inaccurate portrayals in the media
  • Oppressive social stigma even for those who do not do any harm

In the short term my hope is twofold: First, I hope that this book will educate medical and legal professionals and the public to effect change regarding how we approach this illness. That this change will lead to aggressive steps to identify those at risk, to prevent the illness and when prevention fails, to adequately treat it and protect the woman and those around her. In the long term I hope this book helps to eradicate postpartum psychosis. I believe that could happen in my lifetime.

Secondly, I hope this book helps women (and their families and friends) who have had PPP to heal. I always say there are two levels of healing from this illness: There is the recovery from the psychosis and then there is the recovery from having had this illness — the learning to trust yourself again, dealing with the fear of a recurrence, being tormented by questions of “why me?” and so on. The illness is temporary – women recover from it relatively quickly. However, the emotional pain from having had this illness can last a lifetime. Just as these stories helped me to heal, to know I was not alone, to believe I could be completely well, I want them to be available to help others heal as well.

Name three things that made you smile today.

My girls singing.

Joking with the ladies in my aqua-aerobics class.

Seeing the sunshine.

I know my advocacy has affected those around me and increased their knowledge and understanding of Postpartum Mood Disorders. Have you found the same to be true about your loved ones?

Oh my, yes!

What do you find the most challenging about parenting? The least?

Most challenging: consistency and discipline.

Least challenging: loving, enjoying and genuinely liking my children.

If you had one chance to speak with an expectant mother (new or experienced) about Postpartum Mood Disorders, what would you tell her?

I would tell her that, unless she has a medical history that would indicate otherwise, it is unlikely that she will have a PPMD. But if she does, there is NOTHING she could experience that other women have not thought or felt and that ALL postpartum mood disorders are treatable. So if she does not feel right in any way, she should tell her doctor and contact me OR someone else through www.postpartum.net for peer support and information.

Thank you for this opportunity Lauren.

A new project – just for DADS!

Ok, ok, so in the interest of full disclosure, I am co-partner in this project. Go check it out already!

ppd-dads-project-logo

New Support Site for Postpartum Dads Launches just in time for the Holidays

The Postpartum Dads Project plans to focus on collecting stories from Dads who have experienced depression themselves or have been with a partner who has experienced a Mood disorder after the birth of a child.

December 5, 2008 – With the goal of getting new Dads to open up about the havoc Postpartum Depression can wreak, the Postpartum Dads Project launches today. The project will also focus on developing a close knit community which would provide Dads a safe haven in which to connect with other fathers with similar experiences.

The project is an outcome of a partnership between Lauren Hale and David Klinker, both Coordinators with Postpartum Support International. Ms. Hale serves as the Co-Coordinator for the state of Georgia while Mr. Klinker serves as the Father’s Coordinator. In June, Ms. Hale featured interviews with Dads and their experiences with Postpartum Depression. Mr. Klinker was one of the Dads featured and this led to further discussion regarding the lack of resources available for Dads.
The Postpartum Dads Project will also be placing emphasis on Paternal Postnatal Depression. This can occur in up to 10% of all new dads. In fact, if a father’s partner is depressed, the father has a fifty percent chance of developing depression himself.

One of the primary goals of the Postpartum Dads Project will be to create a published volume that will include submissions collected through the website. These submissions will be categorized and designed to be read in between calming a fussy baby and watching the game. The development of the website will continue and many of the stories will be found there as well as insights from professionals, tips and hints from other dads who have been in the trenches, as well as the eventual addition of a Dads only forum.

A key addition to the website in the future will be a professionals only area in which professionals will have their own forum and other tools with which to discuss this relatively new area of support.
The Postpartum Project will begin by publishing interviews with Dads and professionals in the know such as Country Music Artist Wade Bowen, Michael Lurie, David Klinker, Dr. William Courtenay and has been granted permission to reprint the interview with Dr. Shoshanna Bennett’s husband, Henry. The Project will also be featured in an upcoming segment at The FatherLife.com.

For additional information on the Postpartum Dads Project, contact info@postpartumdadsproject.org or visit the website at www.postpartumdadsproject.org.

About the Postpartum Dads Project
Lauren Hale and David Klinker are both volunteers with Postpartum Support International. Lauren is very active in Postpartum Peer Support and moderates the iVillage Postpartum Depression Board, runs a local peer support group, writes Unexpected Blessing, a blog dedicated to pregnancy after PPD, and is a stay at home mom of three children. David is the Father’s Coordinator for Postpartum Support International and also runs www.postpartumdads.org. He is strongly dedicated to supporting Fathers throughout the Postpartum Period.

Contact:

info@postpartumdadsproject.org

Lauren Hale, Co-Founder

The Postpartum Dads Project
http://www.postpartumdadsproject.org
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Sharing the Journey with Wendy Davis

Wendy Davis is the glue that holds all of us Postpartum Support International Volunteers together. She is an amazing woman and I have come to enjoy her friendship and support. Since embarking upon my peer support journey, Wendy has been more than willing to answer any question I may have and has encouraged me the entire way. It’s almost been like having a personal cheerleader! I know that I can take anything to Wendy and she will not only listen to what’s going on but aid in coming up with a solution that will work for all involved. Wendy does absolutely amazing work each and everyday and for this, I thank her. I am honored to post her interview today and hope you enjoy reading!

Tell us a little about yourself – What makes you tick?

I am married and a mom of two children who amaze me with their wisdom and humor. I was the 4th out of five myself, and then had 4 stepbrothers. I thrive on relationship even though I am by nature an introvert.

How did you get involved in Postpartum Depression work? What drew you in?

I had postpartum depression and anxiety after the birth of our first child in 1994 and I had no idea what was happening to me. Every negative theory of depression crowded into my anxious brain, and I could only believe that I was a complete failure and that my life was ruined. I thought I had made a terrible mistake by deciding to have a child. I had already been a therapist for 14 years when that happened, and had specialized in depression, anxiety, and grief. But nothing had prepared me, no course had taught me, and I was completely ashamed and frightened. When I did start to understand that I had postpartum depression, I found very few pictures of hope and healing, and that scared me more. After I recovered I was compelled to learn everything I could and to make a real difference for other women and their families. I wanted to make it safe for them to reach out. I didn’t need to reach big numbers, I just wanted each woman and dad that to know that there was hope for them. I wanted to help them learn to see their strengths and healthy instincts.  After I had our second baby three years later, and I didn’t have a repeat PPD, I was even more motivated.

As a Mother, how important is it to remember to care for yourself? What do you do to recharge your batteries when they’re down?

I feel like it’s a continuous practice to remember to take care of myself. It’s not enough to just know I need to do it – I need strategies and reminders. And if I’m lucky, I get positive reminders like feeling good or having a friend ask me out, not negative reminders like getting sick or cranky. I recharge my batteries by taking walks in the beautiful Oregon mist, listening to music, going to visit my mom at the coast, having dinner with my sisters, brother, and their kids. And now that my kids are at the wonderful ages of 11 and 14, I really do recharge by being with them. That’s a great surprise!

What do you find the most challenging in motherhood? The Least?

The most challenging thing for me on a daily level is scheduling time for myself.  The challenges change as kids get older: when they were little, the biggest challenge was having patience when I was frustrated or angry with them. I learned a lot about conflict management and how to express my frustration and anger by working on that. Another challenge is that it’s hard to make time to have dates with my husband or my friends. The least challenging? I seem to have a lot of tolerance for their individuality and creativity and it has always brought me joy to see them express themselves even if it’s … unique.

How did you get involved with PSI?

I had started the Baby Blues Connection in Portland and of course I found PSI as the main clearinghouse for information and support. At first, to be honest, I wanted to do it myself and didn’t know if I needed PSI. (PPD Risk factor: off the chart need for self-sufficiency.)  All it took is one conversation with PSI founder Jane Honikman. I wanted to know her, to learn from her, and I felt immediately welcome and encouraged. That was in 1997, after my daughter was born. I became the Oregon Coordinator that year. In 2005 I volunteered to be the Coordinator of the State and International Coordinators and then I joined the PSI board as the Coordinator Chair. I love our PSI volunteers and I am immensely proud to be volunteering with them.

Awareness of Postpartum Mood Disorders has come a long way. In your opinion, what are some obstacles we still face in gaining even more acceptance and reliable treatment for new mothers who struggle with this?

There is less of a taboo than there used to be, but shame and fear still exist.  I think that it’s hard for people, providers and the public alike, to have positive images of healing and recovery. Our local and federal policy-makers still have the habit of ignoring the needs of new mothers. It’s the same challenge WE have! I am optimistic though, and remain undaunted. Every challenge I see is another opportunity for education and communication. I used to be angry that people didn’t get it; now I’m just busy.

How important is it to have the entire family involved in Mom’s recovery? What can family members do to create a supportive and positive environment around her during her journey towards recovery?

It is essential to have the family involved not only in Mom’s recovery but in the prevention of a crisis. Family members can first gather information for support and care before there is a crisis. Every family that is planning to bring home a new child needs to know where to turn for help if they need it. If mom is struggling, family members can be most helpful by believing in her strength and recovery, and truly listening to her when she is able to tell them how she feels and what she needs. In the beginning, most women don’t know what to ask for. At that time, family can just stay present, don’t judge her, don’t scare her, but tell her you’re there for her all the way through.

You currently serve as the Volunteer Coordinator Chairperson for Postpartum Support International. What advice would you provide to those who wish to provide support to women with Postpartum Mood Disorders? What is most important to remember when embarking on this endeavor?

If you want to provide support for other women, the first step is to check in with yourself to make sure that you are taking care of your own needs. Contact PSI to find out what is going on in your area and how you can become involved. You can contact the office or go to the support map and find your area coordinators. Learn about the great service of social support and what that means. Read through Jane Honikman’s website as well. It is not giving advice or recommendations; it is being a peer who can listen and help women learn that they are not alone, it is not their fault, and there is help.

Name three things that have made you smile today.

This question. Voters. My daughter made a necklace out of a peace sign.

Last but not least, you have a chance to share with an expectant mother (new or experienced) some advice regarding Postpartum Mood Disorders. What would you share with her?

Don’t be afraid to reach out. Know that it is a statistical risk factor to be a high-achieving, self-sufficient person and that it might not come naturally to you to look for support or help. It is a great new skill and made the biggest difference for me between my first and second postpartum experience. What we survivors have learned is that the new strength is the ability to ask for help when needed, even before it’s needed, and to take it in. If you are struggling now, know that you are not alone and that you will get better if you stick to a plan of self-care and recovery. There are many options for treatment – choose what works for you. The universal aspect of recovery is the connection with hope, coming out of isolation, and knowing that you will come through this no matter how severe your symptoms are when most acute. If you need help, we are here to help you find what you need.