Join the Fight: Depression Awareness Month

I wrote yesterday’s post thinking it was a silly confession about overindulging in chips and ice cream. Today, as I entered hour three of being curled up in bed in my parents’ guest room watching reruns of The Big Bang Theory on my laptop (having again vacated our house for showings), my head was finally quiet enough for that little voice to be heard. The one that says, “It’s back. You’re back there.” The one that tries to brush away my cranky exterior enough to get through to me with its message that being bitchy and snapping at my husband and my kid is a sign of more than just being bitchy and snapping at my husband and my kid.

It’s the other side of the voice – the usually much louder one – that says, “Life sucks. This is too hard. I don’t want to live with this anymore.”

Today, while I deal with the battle of the voices, I’m sharing a guest post from from Help for Depression. In honor of Depression Awareness Month, they’re hosting a fundraiser for To Write Love on Her Arms (TWLOHA).

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It is so hard to take care of the house and the kids when you need a fork lift to get out of bed each morning. That is why it’s so important to spread awareness about depression during October, Depression Awareness Month. I would surely like my husband to have more awareness, although generally he is patient and sympathetic with me.

What motivates me to write about Depression Awareness Month is my daughter. She called me from her dorm and said, “Mom, I can’t sleep, I can’t eat, I can’t focus on my homework. What’s the point of all this anyway?” I had hoped none of my children would experience depression. I’ll have to revise my hope.

While searching for information on depression in young adults, I learned that 44% of college students have depressive symptoms. As my daughter would say, “OMG.” How is it possible that so many young people, close to half, are depressed when they’re just out of life’s starting gate? I find it outrageous that suicide is the second leading cause of death among college students. It can’t be right to ignore these statistics.

How bad does it have to get?

Think about it: if 44% of university students had the flu all at once, it likely would be labeled an epidemic. I think if people realized how big this problem is there would be more concern, or at least the start of more concern.

The other day my ten-year-old said, “Mom, you’re such a crab,” and that was to my face. My husband calls our life boring, and my mother thinks I’m lazy. There is a little truth to the laziness part, but that’s not why the laundry is piled up.

I do not want my daughter to be afraid of people finding out she is depressed.

That is why I am thrilled about Depression Awareness Month. It won’t fix the problem, but it is a start. People need to know what the symptoms are, what resources are available, and those suffering deserve to feel accepted.

As for myself, I want people to know that I do not expect to be babied, and do not feel sorry for myself. I want people who are suffering unnecessarily to find help. I want to purchase my medication without feeling a tinge of shame.

There is an easy way to help

To Write Love On Her Arms logoThere are people doing more to spread depression awareness than just talking, like me. Help for Depression, a depression resource, and a nonprofit called To Write Love On Her Arms, have joined forces this October to raise money for depression awareness.

If you can click with a mouse, you can make a difference. Go to the Help for Depression Facebook page and click the ‘Like’ button. For each new ‘Like’ given between October 1st and the 15th, $1 is donated towards their $15,000 goal. Please take a few seconds to click and contribute.

 

About the Author 

Jacqueline is a creative writer, published poet, and has an MA in counseling psychology. Her education is backed by 12 years experience as a licensed clinical counselor. 

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When I first “liked” the Help for Depression page, there were only a handful of other likes. Now, not even two weeks later, they’re at almost 10,000. This is clearly an issue that affects a lot of people.

Please click through and click “Like” to help them towards their $15,000 goal. Depression is a horrible thing to live with.

PS You can also find me on Just.Be.Enough. today talking about my current struggles as a parent. Please come and visit me over there and tell me I’m not the only one…

I Believed Once

I believed once.

I thought I could make a difference. I followed my heart and used my voice and put it out there. I worked. Hard. I worked through lunch. I worked late, came home, had dinner, and worked some more.

I wrote. I wrote and wrote and brainstormed because I believed. And because I believed I put my whole heart in to my work.

The path my life has taken over the last five years has made me who I am now. Some of that evolution is on this blog, but so much of it is because of my work – the absolute passion and dedication I put into it, the opportunities I’ve had, and the people I’ve worked with.

My work changed who I knew I could be, but it’s the evolution chronicled here that has changed who I am. It has changed what I believe.

It has changed what I believe I can do.

I believe I’ve done what I can do in my current job, especially because recent changes have taken the work in a different direction. Despite knowing this is what I must do, I do it with a heavy heart. I played a big part in building something bold, and because that something will inevitably change – partly because the organization has changed but also because that’s what things do – I feel as though I’m saying goodbye not only to a job and a team but to a piece of myself. When I pack up my desk the box containing my pictures will also contain the shadow of my contribution, exiting the building with me dressed in both regret that things must change and an attempt at preserving something that meant something to me.

It’s time for me to move on.

We’ve spent the better part of the last month sprucing up our house and on Friday a For Sale sign will appear on our lawn.

On a date in the not-too-distant future I will write a letter to my boss and sign a piece of paper giving my house over to someone else.

I’m leaving the work and the people and the organization that changed how I think about what work is.

I’m leaving the first house we owned, and the house I brought my son home to.

I’m leaving the city I grew up in, where my parents – and my son’s grandparents – are six minutes away.

I’m leaving who I used to be in order to find out who I can become.

Who I think I am now.

I believed once.

And I’m choosing to believe again.

Sunrise. A new day in the Canadian Rockies.

 

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Building Stronger Families, One Mom at a Time

I remember the exact day I found Postpartum Progress. November 10, 2010. It was a Wednesday.

I can’t remember exactly how I found it, but I think the site actually found me. That was before I started this blog. It was before I discovered #PPDChat. It was before I really started talking about my experience with PPD. But someone – one of my Facebook friends – posted a link and I clicked on it.

All of a sudden everything seemed a little better. I looked at the definition of postpartum depression and the 6-things series and I noticed, throughout, the tone of acceptance and support and hope. Finding that site turned me around and pointed me in the right direction, and at the time I had only a glimpse of how totally amazing it is.

That day, I sent an email to the site’s founder, Katherine Stone:

Katherine,

Just a quick message to say that I came across your site this morning via a link on Facebook. I immediately grabbed it and sent it to myself to read later, and I’m so glad I saw that one message pop up before I missed the chance to really notice it.

Your site is incredible, and it’s found its way to me at a very opportune time. My perfectionist personality (oh, how that is a factor for me!) has made it very hard to reach out for help. I finally did that nearly a year ago and overall am much better, but this has been a rough week and I’m realizing that I’m not quite there yet.

I’m not sure where this journey will continue to take me, but I’m very grateful to have found your site as I think it will be a good resource for both me and my family.

Robin Farr

Katherine sent this to me in response:

I’m so glad you found Postpartum Progress, and that it has been helpful.  It is so normal to have rough weeks in the process of recovery.  Just keep doing what you are doing – I am so happy that you reached out for help.  Just keep putting one foot in front of the other!!

The content of that short reply sums up everything that is amazing about Katherine and the work she does.

When I created my mama Twitter account and started blogging, I came across Katherine again and have come to know her as a totally supportive, incredibly dedicated woman. When she started her Daily Hope emails earlier this year, I signed up immediately. For months they gave me what I needed to face each day and while I no longer need them, I still get them. A dose of love and support every day – how could I not want that?

I get a lot from Postpartum Progress, and today I’m hoping to give back.

October 5th is the day when more children are born each year than any other day. Today is Strong Start Day

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I’m going to quote directly from Postpartum Progress to explain the significance:

Only 15% of all women with perinatal mood and anxiety disorders ever receive professional treatment. This means that each year hundreds of thousands more women and their children may suffer from the negative effects of untreated PPD and related illnesses for the rest of their lives.

Postpartum Progress will change that with your help. We are developing a compelling national awareness campaign for postpartum depression, as well as new and improved patient education materials (the kind new moms won’t throw away!), and new uses of technology to reach suffering moms no matter where they are.

On October 5th, the day when more children are born each year than any other day, I am asking you to do one of three things:

1)   Make a donation to Postpartum Progress.  Any amount is welcome.

2)   Ask at least 2 other people who love you and know what you went through – people who’ve come to know that postpartum depression is real and that all women deserve to have access to the best information and help – to make a donation today in your name.

3)   Refer us to contacts at organizations that can help us with our work.

If you are financially unable to donate, send us your prayers or moral support so that we may find the right people to help us make major change.

Today’s the day.  Please help us build stronger families, one mom at a time.

 

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Sail Away, Sail Away

Thought of the day:

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Beating Cancer With Love

September is Ovarian Cancer Awareness month. This disease barely registered with me until my mom showed up on my doorstep the day after I got home from my honeymoon and told me she had a tumour the size of a grapefruit. She’s here today to tell her cancer story. 

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How do you survive a cancer that has a 30% survival rate? It’s been 7 years since my surgery and I have long since been declared free of ovarian cancer, but I’m still not sure of the secret. Truly I think my time had not come. However, in addition to good care I firmly believe positive thinking and a huge dose of support are key.

Just before our oldest daughter’s wedding – first wedding, oldest of four – we were putting the the last details of The Plan in place. The couple wanted a relaxed get together with out of town guests so we planned a buffet at our house after the rehearsal.

I was feeling not so good. Unusually for me I decided to go to the doctor; I didn’t want to be sick for the wedding. If not for that wedding I doubt I’d have made it.

teal ovarian cancer ribbon“How long have you had this growth?” my doctor asked.

“What growth?” was my response.

I’d read about the signs of ovarian cancer but there was no family history so I didn’t think it could happen to me. As it turned out I did have several of the signs.

By the Tuesday before the wedding I’d had blood tests. My CA125 score was really high, six times what it should be. An ultrasound was scheduled. The technician, looking serious, promised to have the result to my doctor by Friday. I told her to wait until after the wedding but it was there that afternoon, which seemed like a bad sign.

An MRI was scheduled for Thursday. My husband and I sneaked away saying we were picking up supplies for Friday’s dinner. By then I knew it was serious but (fortunately) didn’t have time to think. And of course we couldn’t tell anyone. How could we tell the other kids if I didn’t tell the bride? And how could they keep a secret like that? On the other hand for me not talking about it may have carried me through!

The wedding was wonderful, a huge success. I don’t remember much but do have one flash of memory, quoting an Ogden Nash poem during the speech I made on behalf of my husband and me: “To keep your marriage brimming, With love in the loving cup, Whenever you’re wrong admit it, Whenever you’re right, shut up.”

When it was done my marvellous gynaecologist oncologist suggested I do a course of chemotherapy “in case of rogue cells”. She was pretty sure she’d got it all and she would like to declare me cured before she retired. My family said I wasn’t through with life yet. (Remember that positive thinking component?)After that it was reality time. I was at the top of the surgery list and in at the first cancellation. The Universe decided it was to be right after the honeymooners got home.

My city has a terrific treatment facility due to a generous donation. The chemo room is surrounded by windows and trees. And I am truly blessed in my family. One of the kids came each time I went to my day-long chemo treatment. My husband (who had to skip the IV insertion part because of needle phobia) brought lunch. There was never nothing to do or nothing to say.

I had a few days of miserable neuralgia each time but limited nausea because of the timely invention of a good anti-nausea drug. I was bald and puffy from steroids and my energy was low but I never doubted I could make it. I even worked part of the time. What I remember now is the sea of love. That was the most important therapy.

My out of town daughter sent me a lovely journal suggesting I keep a sunshine journal, putting in only things that made me smile. (I am on the 4th one now and still smiling.) She invited me to come on a soul journey after chemo was over, to drive to the mountains for an injection of peace, hope and serenity.

A friend sent me to a wonderful alternative treatment program during the chemotherapy time.

My oldest daughter came with me and also gave me a treasured silver bell charm from her wedding to wear.

My son, who was both working and commuting to Vancouver for classes, came to one chemo treatment, supposedly for an hour and stayed 4 hours, causing him to miss his ferry and his class.

My healer daughter supported me in listening to my body rather than well meant advice and found me a wonderful cancer patient yoga CD which I still use.

People made marvellous soups and dropped them off. People sent plants and flowers. My son-in-law gave me mind-bending crossword puzzles. My husband did the cooking. My cherished colleague said, “go away and heal” and looked after my business. Another friend sent me some wonderful meditation CDs. How could I not get better?

Out of meditation came a couple of lullabies that appeared in my head for (then nonexistent) grandchildren. That was when I knew it was going to be okay for sure. I don’t know how to write music down. I had to be here to sing them myself.

Grandmother and newborn grandchild

Grandma and Connor when he was a couple of hours old

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I will be forever grateful that my mom’s cancer was caught in time for her to be treated and fully recover. Please make sure you know the symptoms. Your grandchildren will be grateful.  

PS The colour of my blog – similar to ovarian cancer teal – is a total coincidence, and one I only caught today. I think it was meant to be.