Tag Archives: peer support

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.

Hey Dads – PPND Online Forum Just for you!

If you’re suffering from Paternal Postnatal Depression and are feeling all alone then I have some AMAZING news for you.

Dr. Will Courtenay has a forum at his website, www.postpartummen.com where you can post your concerns and get advice from other dads who have been where you are or still struggling. A great solace lies in finding others on the same journey.

Click here to go directly to the forum.

(and guys – if you’re interested, Dr. Courtenay has just posted at the forum about the possibility of doing a FREE support conference call if there’s enough interest. If this is something you think you’d benefit from, let him know!)

A Closer Look at Charlotte Perkins Gilman

Charlotte Perkins Gilman

 

Why write about Charlotte Perkins Gilman at a blog about Postpartum Depression you might ask. She suffered a near nervous breakdown after the birth of her first child, leading her to author The Yellow Wallpaper, an intense short story about a woman’s treatment during a nervous breakdown, a story that one led a Boston Physician to state in The Transcript that “Such a story ought not to be written, he said; it was enough to drive anyone mad to read it.” Possibly so, but a physician from Kansas also wrote that “it was the best description of incipient insanity he had ever seen, and–begging my pardon–had I been there?” (Perkins Gilman)

Sadly, her nervous breakdown led to divorce and leaving her daughter in the custody of her ex-husband. Turning to writing as a way of earning money,  Gilman eventually found herself as a spokesperson regarding “women’s perspectives on work and family.” Perkins Gilman believed that men and women should share household duties and particularly that women should be taught to be economically independent from a very early age (DeGrazia, Jodi), a topic she focused on in her work, Women and Economics, penned in 1898.

The Yellow Wallpaper has been a favorite story of mine since first read, love at first words. I identified with the main character well before experiencing motherhood and my own brush with insanity shortly thereafter. Perkins Gilman did an exquisite job of breathing a realistic insanity into her main character as well as exposing the mental health diagnoses and “cures” of the day for what they truly were – sadly insufficient and ignorant of treating the illness and instead closeting away those who suffered in hopes of recovery or at least not be part of mainstream society and  therefore remain to be a “figment” of one’s imagination, the dark family secret.

In 1887, Perkins Gilman sought treatment for continuous nervous breakdown from the best kThe Yellow Wallpapernown nervous specialist in the country. The rest cure applied and she responded well physically; however, the physician then declared all was well; sending her home with “solemn advice to ‘live as domestic a life as far as possible,’ to ‘have but two hours’ intellectual life a day,’ and ‘never to touch pen, brush, or pencil again’ ” for the remainder of her days. Gilman then writes regarding the effectiveness of this advice, saying “I went home and obeyed those directions for some three months, and came so near the borderline of utter mental ruin that I could see over.” (Perkins Gilman)

Engaging the help of a close friend and gathering what strength she had left, Perkins Gilman picked up her artistic work again and began to recover, finding strength within her work and “ultimately recovering some measure of power.” This experience is what led her to write The Yellow Wallpaper. Perkins Gilman admits to embellishments, stating she “never had hallucinations or objections to my mural decorations”. Written as a celebration of return to her success, her true motivation behind sharing her story, albeit in a fictional world, lay within the hope of saving others from her fate of mistreatment and the nearly paralyzing insanity following soon after.

In Perkin Gilman’s own words regarding her authorship of The Yellow Wallpaper, she states:

It has, to my knowledge, saved one woman from a similar fate–so terrifying her family that they let her out into normal activity and she recovered.

 But the best result is this. Many years later I was told that the great specialist had admitted to friends of his that he had altered his treatment of neurasthenia since reading The Yellow Wallpaper.

 It was not intended to drive people crazy, but to save people from being driven crazy, and it worked.

The number one reason I hear when women have chosen to share their experience with a Postpartum Mood Disorder is the hope that it will provide comfort to another as she travels down the same road. It is with the same spirit Perkins Gilman penned The Yellow Wallpaper that I share my story. Recovery is a hard road and sometimes a lonely road. I said from the very beginning of reaching out to others with a helping hand that if I could help even one woman, it would all be worth it.

The screaming, the agony, the tears, the lifting of the fog – it would all begin to somehow make sense and instead of continuing to drag me down, it would lift me up. The fog did not begin to lift until I reached out for help and found it – drenching myself in the stories of others who had been where I no longer wanted to be and read with new understanding and an intensity I had never known before just how they were able to escape the depths of depression and reach the light, breathing in sweet fresh air again.

Determined to shine a light on the path for those behind me and around me, I dove full force into sharing my story. Every time I shared my experiences with a woman who believed she had no hope left and found herself ashamed of her condition and witnessed what an impact my openness and vulnerability had on her, I knew supporting Mothers was my calling.

So I write about Charlotte Perkins Gilman in order to better explain my mission here at this blog and in life. I refuse to let another woman suffer alone and in silence. Not on my watch.