As a result of a recent slip and fall, I have had to take more pain medication for my spine. Come Friday, I was hunched over my toilet, continually throwing up (this medication can interfere with the nausea centre of the brain). As a result, I missed seeing my daughter sing at her Highschool’s talent quest. It was the end to a stellar week, which saw us being notified that our darling little home was being sold. We are hoping with all our hearts that an investor buys it, and we are able to stay. Saturday was spent eating dry toast and apple to settle my stomach, and resting in bed. That evening, my girl and I watched a very silly movie, and laughed until tears streamed down our faces.
We had arranged to meet friends on Sunday in the city, and there was no way that I was going to cancel. We all did IVF together, ending up with daughters. We hadn’t seen each other for the longest time, life getting in the way. It were as though no time had passed, as we hugged and caught up. IVF had taken a lot out of us, but it had also given us an inner resilience. Boy, have we needed it!
Strolling along, we came across a very sweet man, who was walking his three dogs and his Eclectus parrot. The girls were invited to hold him, much to their delight!
This gorgeous boy is named Apollo, and you can follow him and his family on Instagram.
Light exuded from Apollo’s dad; he was one of those people of whom you leave lighter and much happier.
We had Italian ice-cream for brunch, then indulged in a gorgeous Earl Grey and rose donut, baked fresh. A long walk was in order afterward, and we found an eatery, where I ordered a zucchini flower and plate of Brussels sprouts, pan-fried in balsamic vinegar. Surprisingly, my friends asked that the surplus be put in a container for me to take home, and were more than a little reluctant to finish them off!
The girls paddled in the harbour, and as we reclined at a nearby park, we were surprised to have the Naked Bike Ride, Sydney, stream past! A helpful fellow at the front, announced to the gawkers that they were indeed nude riders, as if we couldn’t figure it out for ourselves! I admired their chutzpah, and the whimsy of it all. Such a random event to come across! It certainly made everyone smile!
At the end of the day, I was tired and sore, but no more than I would have been had I stayed home. In fact, I would have been worse off. I wouldn’t have seen my lifelong friends, watched my daughter have fun, met a very kind man with his canine and bird family, eaten glorious food and seen the naked bike ride. I wouldn’t have been embraced by my glorious city. I love that I can go into the city depleted, and come back retrieved.
I recently lost a young friend, unexpectedly and in the most shocking of ways. It shook everyone to their core, including those whom never had the pleasure of knowing her. There seemed to be a collective sigh as masks fell, revealing the truth behind the smiling Instagram pics and depictions of lives filled to the brim. Life is part joy, and part sorrow. Social media accounts don’t necessarily lie, but rather they tell the polished version of lives. We don’t want to burden others with the challenges and pain. Throughout the past month, I have had many people apologize for telling me that they are doing it tough, and I have insisted that ‘burden’ be reframed as ‘sharing.’ We have to share. Spells are broken when we speak aloud, and we hear our voice speaking that which was hidden. I came into December feeling that I knew more about my friends. Even strangers on the bus have become more than acquaintances through the act of sharing. What people had once kept hidden astounded me. No wonder the smile slipped on occasion, and indications of anxiety peeped through!
People have told of the challenges of having two separate Christmas celebrations for children, of estranged family members whom they have to see separately. They have told of poverty and housing stress, ill-health and exhaustion. Trying to hold it together when inside, everything is falling apart. I was diagnosed with a neurological condition a short while ago, an extraordinarily painful chronic illness. I can’t even pretend to have it together at the moment, and the relief is palpable! My daughter is in WA with dear friends of mine. The mum and I did IVF together, and we ended up with daughters, who have been best friends since they were babes. I minded this little girl earlier this year, and I had tears when I heard the girls discussing how they knew they were wanted because their mums went through so much to have them. The understanding of how we longed for them shall hold them in good stead, even when the world tries to beat them down. It is a wondrous foundation to have!
My little girl has climbed the tallest tree in Australia; she has been snorkelling and visited Quokkas. In case you don’t know what a quokka is, here is a picture.
Cute, aren’t they?!
I am trying to manage my pain, in the midst of writing a book and organizing Christmas. There is much I have had to let go of for the sake of my sanity. I have ordered a few gifts online, but for the most part, have had to go easy on myself. I won’t be up until midnight, writing out cards for everyone, as much as I would love to. I simply can’t. Events have been planned in advance, and preparations for everything from travel to what I need to bring have been arranged into bullet points on a notepad. Christmas to me is all about connections rather than gifts, and I am hoping to be up to visiting people next week to check in on them. I had been planning to catch up with a group of ladies whom I haven’t managed to see all year, and invited them around for afternoon tea. I bought some fresh fruit and a little platter of cheeses and mineral water. We had a lovely time, and it cost less than $20. Christmas doesn’t have to mean expense and maxed-out credit cards. I have known many homeless folks, and those without family connections, and believe me, being invited to a Christmas lunch is worth more than gold. The best gift is being seen and heard.
One lady apologized for how harried she felt, for complaining about the stress leading up to the main event, and felt bad for her anger. I told her to stop apologizing! “Anger; unadulterated rage, kept me going in the early years after my fall,” I told her. “It can be a way of saying that a situation isn’t right, nor is it fair. It spurred me on, to work hard on my rehabilitation.” We are allowed to be angry, particularly when too much is expected of us. I love the saying, ‘If you present as strong and together all the time, much is expected of you, and then you have nowhere to go.’ People assume you will say yes to their demands, not realizing that you too have a breaking point. We may want to retreat and that is okay too. I know many folks who take themselves away at Christmas time, to avoid unnecessary stress. We have this notion that the Christmas season should see us morph into someone larger than life; a version of us on steroids, where we need to find more money, time and energy than in the other eleven months of the year. Not only is this unrealistic, but impossible, without burning ourselves out.
My daughter and I have a tradition of going into Sydney on the last day of November. We walk around, taking in the decorations and sights. We hardly spend anything, just take festive pictures, talk to strangers and listen to pianist’s play on the Grand Piano in the Queen Victoria Building. We come home feeling as though the veil has been lifted between the hum drum of the rest of the year and the heralding of the festive season. We walk around neighbourhoods admiring light shows at night. We sing along to Christmas carols and watch Christmas movies. It is a wonderful season, when you turn down the volume on expectations and what you should do and feel. Open calls to the beach and swimming pools, taking along a picnic hamper and catching up with friends. Reviewing the year past and planning for the fresh year ahead. Allow yourself to feel what is brewing inside your mind and soul. Allow yourself at least five minutes of peace each day. If we are open and honest with one another, we will find it easier to cope. Look for the beauty around at Christmas time. It costs nothing, and brings such joy.
I am honest about the challenges I face regarding this season. There is grief for those lost, sorrow for what has come to pass, and pain for expectations unfulfilled. There is also light; a belief that the best is yet to come. There are friendships and invitations to sit at people’s tables. There is tinsel and pool parties, hugs and carols. There is reflection and gratitude. I own each in equal measure. My fervent wish is that you have a blessed Christmas, and please, be kind to yourself!
I once rejected the idea of putting up the Christmas tree and decorations before December 1st. That was until I met a group of ladies in an IVF support group twelve years ago. We went through it all, from pregnancy loss, and losing much-loved babies to enduring cycle after cycle with no result. Christmas felt like a mockery, a sneering group event that we weren’t invited to, and we dreaded the lead-in to the festive season. Somebody suggested emblazoning our environments early (starting in October), as a way of cheering ourselves and also to state that we were all still here, surviving. To ensure we did as promised, we sent pictures to the group. The joy was contagious, and a tradition was born. Through the ensuing years, some have had a bub, others have adopted and some have reimagined their lives, bringing new dreams forth. We still all put our trees up early. My daughter loves hearing about my friends, and how we supported one another. She also loves this tradition! Hey, the earlier we start celebrating the better to a kid! Each decoration is symbolic of a time and place. Some baubles were made for us, and hold a special place in our hearts. We played Christmas carols and did karaoke. As we switched on the lights, it felt like Christmas had really begun. The frenetic energy of shopping centres and the demands and exhaustion (only adults feel), was replaced with the truth that life is to be celebrated, here and now. No matter what my friend’s endured, they made sure those trees were up, and the house wrapped in tinsel and fairy lights. I think of each and every one as we fulfil this tradition, and I still post photos as evidence that we are celebrating early.
I had been given very little hope of ever having a child with IVF (after three attempts). Despondent, I went for a walk in a local park. I was standing under a tree, brushing away my tears, when an empty bird’s nest fell at my feet. I took it as an omen, and cradled the precious gift. I still have it- behind glass in my cabinet-eleven years later.Just the other day, I was walking with my daughter, and the nest pictured above landed at my feet! I marvelled at the time and effort that went into building it; a perfect home and refuge. Of course, it came home with me, and my little bird was just as enchanted as I, coming close to inspect the handiwork. Nests and eggshells from newborn chicks are items I tend to find regularly. What are yours?
Sooo, I saw the above headline regarding Serena Williams last Sunday. I was so astonished that I doubted what I had just read. I had to read the quote a few times. I winced as though I had just been kicked in the gut. Surely, the media have grown up and are past such archaic statements? Apparently not! I am quite sure Ms Williams would recoil in horror if she saw her words twisted to make a point as to what constitutes being a real woman. I felt for women struggling with infertility when I saw the headline. I was one of those women. I look back on those years as the most achingly painful and lonely of my life. Opinions such as that above seared my soul, and made me doubt my worth on more than one occasion. When I came to the point of IVF being an absolute necessity, it was in some ways a relief. By then I had come to know myself. By then I knew that being a complete and functioning woman had nothing to do with fertility. It had to do with my biology, and the fact that I coped with constant agony courtesy of endometriosis. I was a woman because I had survived the un-survivable. I was a woman because I supported my sisters, both younger and older, providing counsel and comfort. I was a woman because I sought to rise to the status of survivor, and steer my destiny without interference. It would have been unfair to expect that a baby might gift me the label of woman. If anything, having a baby takes your autonomy for a time, and you need to grip on to retain your identity. Thousands of women read that headline, and winced last Sunday. Know that you are already a woman, and having a pregnancy neither heightens nor completes that status. It is time the media steered toward inclusivity and created less blanket statements which end in exclusion.
The Handmaid’s Tale, a series based on Margaret Atwood’s 1985 book, has just been released in Australia. Last night I streamed it, determined to watch only the first episode and have an early night. Of course, that didn’t happen. What ended up occurring was I watched all ten episodes. It was confronting and terrifying, yet it somehow made my resolve stronger. As a survivor of sexual assault, physical violence and fundamentalist religion disguised as faith and obedience, I am acutely aware that the depiction isn’t a grim warning about what may happen. For survivors it is a remembrance of what has already been, and what we must guard against.
The order decreed in Gilead is the ultimate submission by women. Not having access to money and property nor control of their bodies. It is a world I don’t want to live in. It is a world I have lived in. Having scriptures spouted to suit whatever situation befalls, and to claim it as evidence that the perpetrator is in the right. Women and girls being told that they are here to be pleasing and pleasant, first and foremost. The exquisite rebellion encapsulated by reading, driving a car or etching words of encouragement for those who come after you in your cell.
I vowed that if I survived, I would fight for my daughter to not have to endure a speck of what myself and my contemporaries endured. I was fourteen when I uncovered that grown men were placing bets on who would obtain this child, far away from home. My mental fortitude kept me alive, even as they sought to destroy me, discarded as collateral damage in a war I knew nothing of. I hadn’t been taught the rules, so how could I be expected to play? We must arm our daughters with knowledge, fill their hearts with empathy and love, and make damned sure that no part of The HandMaid’s Tale is a part of their future. I know of too many incidents of women who are infertile sitting in far-right churches, and left crushed after it is announced that yes, it is indeed a fertile church, and one of its members is pregnant with her fifth child. Everybody applauding, amid laughter that God has rewarded this place with ripe fruit. The women who can’t have children or who are undergoing IVF feel as though a sword has pierced their soul upon such occasions. Worth is down to how fertile you are, and home-making lessons are offered and encouraged. The women are kept ‘accountable’ to each other. How exhausting and depressing. Freedom is found when you can be whomever you want in this world. It is not found in your dress, your submission, nor your fertility.
I visited a friend on the other side of Sydney recently,after receiving a message. She had been suffering excruciating pelvic pains, and tests had revealed that she has extensive endometriosis. I made a massage blend to provide comfort to her abdomen and lower back, and grabbed my folder filled with reams of information- gathered from a decade of research-to give to her. Her story is sadly common amongst endometriosis sufferers. She started her periods early, and from the start, they were excruciating. She was misdiagnosed as having IBS, and the resulting diet and medication did nothing to alleviate her symptoms. To make matters worse, she had extensive adhesions, as a result of a burst appendix at eleven. A laparascopy had been ordered, and though they found a mass of endometriosis, they failed to tackle it. As a busy mum, it had now gotten to the point where her quality of life was massively impacted, and something had to be done. She has endured twenty years of seeing doctors, being prescribed the pill to alleviate the cramps, been misdiagnosed, having nothing show up on ultrasounds, and then diagnosed without treatment. She is facing huge costs in order for a gynacologist who doesnt specifically specialize in endometriosis to have “a go” at operating.
My endometriosis journey began at age eleven, when my periods started. They were excruciating and a gynacologist put me on the pill, which did nothing to help. The disease didn’t show up in ultrasounds, and it was suggested that I had a phobia regarding my periods, and was ‘hysterical!’ For at least two weeks every month, I was in agony, and often had to go to hospital for pain relief. I was desperate for somebody to understand, and tell me what on earth was happening. I felt very alone. Endometriosis was suggested when I was twenty, and I was given a shot of a drug made with progesterone. I was told that it was one of my only options to preserve my fertility. The next year was hell. I bled profusely, my stomach swelled and I had continual pelvic pain and migraines.
Twelve years ago, I sought the opinion of an orthopaedic surgeon about my lower back pain. My spine had been severely damaged at fifteen, and I had quite a few operations on my back to keep me walking. After I explained that the back pain became unbearable the week before my period, and started to ease the week after, it was suggested that I may have endometriosis. I was referred to a gynacologist, and he booked me in for a laparoscopy. During the lap, the disease was found throughout my pelvis, in balls the size of oranges. This doctor burnt off the disease. When I went back to him for the post-op consult, I was doubled over in pain. He told me that I was fixed, and disregarded my concerns about my fertility and ongoing pain. He wrote a script for the pill and sent me on my way. I collapsed a month later, and sought out an endometriosis specialist. When he operated, he found scores of blood-filled cysts and extensive disease underneath the scarring (the aftermath of some of the disease being burnt off). He had to perform a radical excision of the endometriosis, to seperate it from my uterosacral ligaments and ureter, amongst many places.
Straight afterward, I decided to start IVF, as it was the optimal time, whilst I had a clear pelvis. Once again, I faced ignorance regarding endometriosis, and was put on drugs that encouraged it to grow at lightning speed. I had to be carried into emergency and was put in the maternity ward for two weeks, whilst they treated me. I was told that these particular drugs were like pouring fuel onto the disease and striking a match. I changed clinics, and with a different drug protocol, I flourished. Despite only getting one follicle, I fell pregnant and my daughter was born. I was so used to being in a great deal of pain, that I had no idea that I was in the late stages of labor when I finally went to hospital! Apparently, that is quite common with women suffering endometriosis.
When my daughter was a few months old, the disease came back with a vengeance, and I had extensive surgery. When she was three, I had another operation, and nearly lost my life. I was taken back to theatre after I bled out, and had life-saving surgery. As a result of the trauma, I went into early menopause. It has been an arduous, lonely journey, and I would hope that pelvic pain in girls is now taken seriously. Endometriosis should be suspected if a girl complains of severe period pain. Go straight to a gynacologist who specializes in endometriosis. The difference in outcomes can be astounding. My friend is saving to have the surgery to give her back her life. Even with being in a private health fund, the out-of-pocket costs can be in the thousands. I stored my daughter’s cord-blood when she was born, such was my terror that she may be diagnosed with the disease one day. It gives me peace of mind that her cord-blood may one day prove useful in the event of an endometriosis diagnosis. For further information, go to the Endometriosis Association of Australia Facebook Page. March is Endometriosis Awareness month, and it’s colour is yellow. Let’s paint the town this sunny hue, living in hope that our little girls never have to suffer in the manner their mothers and grandmothers did.
Softly spoken, her voice redolent with kindness. An English lady whom I only saw in scrubs and cap, highlighting her beautiful skin and soft eyes. We had three frozen sperm and one follicle, that is all. It was my last chance. I woke from egg pickup with ‘2’ written on my hand. There was a chance this follicle may contain nothing; two was beyond all expectation! This lady watched them grow and divide, and I held my breath. One divided too rapidly, and perished within days. The other burst into a blastocyst; which was terrific news! This lady wished me luck during the embryo transfer, and gave me the dish my embryo had grown in.
Eleven months later, I brought my miracle back to meet her, and she held my child in her arms. Years passed, and the scientist moved far away. We became reacquainted on social media. She sent a message that she would be staying nearby this Christmas, and another IVF mum and I planned to meet her with our girls. When I walked in and saw her, I squeeled with joy. My daughter was overwhelmed, meeting the lady whose picture is on our fridge; who carefully watched her as a little embryo. We hugged and looked at each other in wonder. Such a long road from where we started to having a ten year old child! I showed her the dish, and she noted the ‘2’ on the plastic. We had a moment of silence and I appreciated that the women present understood the heartache behind the second number. We talked ‘IVF speak,’ and I laughed that nobody else would understand our conversation!
Our girls both love science, and this lady set up a microscope the other miracle had been gifted for Christmas. We saw extraordinary images of cross-sections of hair, blood and many other wonders. Life-when broken down into tiny segments- really is the most amazing thing! Our girls had to battle for life, and their strength is displayed in their lives today, and shall carry them into their future. We swam in the pool on this hot summer day, the girls playing together as though they are soul sisters. I know that they are. Hours passed as we hurridly relayed what we have been up to; what the girls dreams are for their wild and precious lives.
The odds were mightily against this other mum and I, but this lady helped to see us through, changing our lives forever. How can you begin to thank her for the precious gift she handed us? Humble and kind, I pray that 2017 blesses this lady beyond her wildest imaginings. I hope the same for you all. x
Throughout the years of infertility, Christmas had been a lonely time. I made the best of it, putting on a coat threaded with stoicism. However, when I was decorating the house, wrapping gifts or shopping, there was an acute sense that someone was missing. I couldn’t bear to see children posing with Santa at the shops, and the Christmas music seemed intent on mocking my friends and I. I joined an IVF support group online, and we talked of how confronting Christmas was, and how we were dreading all the reminders. “Bugger it,” said one lady, “let’s get our trees up early!” She demanded to see photographic evidence, and we dutifully complied. There was magic in the way this act lifted our spirits; we were showing that we were still holding on, to both our sanity and dreams. Some of the ladies tragically lost babies, and others didn’t end up conceiving. Still, we all held faithful to our tradition.
Late October, my daughter discovered the decorations in the garage and pleaded to be let loose with them. I held her off until November the 1st. Bless her, she counted down the days, and on the first of the month, she ran in, reminding me that it was time.
We played Christmas carols as we unpacked the tree and decorations. As I looked around at the assembled baubles, a lump gathered in my throat. Each represented a time and place, a year or a particular person. We talked of what each piece meant to us as we worked. ” I need to put all the Christmas things up early, like you did when you were pregnant with me,” my daughter laughed. Oh darling, it started way before I was pregnant, at a time when a precious group of ladies met on the internet to give comfort to each other. We still provide a photograph each year, to assure the others that our job is done.
We need sparkle to lift us up. We need to get out the china and silver, the candles and bling. We need to create beauty. It is akin to standing on a mountain top and shouting that you are here. The more personal strife befalls, the more we need to decorate. It was worth all the work to see this little girl beam with excitement. The season of hope is starting.
I can’t tell you how much the response meant to me after I posted Til it Happens to you. The support was incredible! I was too overcome to respond for a while. People have asked how I got through it all. I suffered status epilepticus at 13, meaning I had continual seizures which couldn’t be controlled. I stopped breathing and was in a coma. It took a long time to recover from this event (it was predicted I wouldn’t). The next year, I met a monster, and was abused. The finale was being thrown off a building at fifteen. My healing has taken over twenty years. There are some things that have helped.
1. I can’t handle violence of any kind. I can’t discuss literature, nor movies, let alone view them, if they are violent. At first, I didn’t want people to think I was fragile. I didn’t want them to see the distress that talking about violence (parcelled as entertainment to the masses), conjured. I would pretend that it wasn’t hurting me. Nowadays, I don’t pretend. I gracefully bow out of conversations and invitations which would bring me into this sphere.
2. I couldn’t leave the house by myself, even to go to the letterbox. It has taken many years and many small trips to gather the strength to go farther afield. I plan ahead, and the apps I have on my phone make my preparations easier. If you are agoraphobic, be kind to yourself. Every little step is a triumph. My major incentive was that I had to get to the IVF clinic early in the morning, and simply had to do it. It made me braver than I actually felt! Now I take my daughter everywhere, and the freedom is liberating!
3. I have had to confront my deepest fears. The ones I was frightened of encountering, as I would surely fall apart. My fears included rejection, loneliness, being left alone and finding out that people weren’t as they appeared. Confronting these fears has been terrifying, and it has hurt. I have uncovered that people I looked up to were abusive behind closed doors. I have been let down and let go, but I have survived. I learnt not to leave myself behind in the process. Comforting myself became of premium importance.
4. People see a smiling, functional adult when you are out and about. They don’t recollect the child kept alive in Intensive Care on a respirator. They came into my life during a different chapter. I know what it took to get to here. The hundreds of hours of physiotherapy, the scores of surgeries… I have to remind myself of my achievements and give myself a quiet pat on the back.
5. Boundaries are a big one for a survivor. I felt as vulnerable as a newborn when I started to make a life for myself. I believed anything anyone said, and believed everyone was a friend. It has taken trial and many errors to come up with boundaries, and to trust my judgement above all else. It was a revelation, to give myself the space to honour my instincts. If a person or situation doesn’t sit right, and makes me uncomfortable, I walk away. It is imperative to do so, as I have a little girl watching me. I need to display good boundaries so she knows that its okay to be in touch with her own. It has sometimes taken me being struck mute in the company of somebody who is toxic, for me to comprehend that my body is trying to protect me by producing physical symptoms. I am free, and thus I get to decide who stays in my life. It may not be anything that anyone is doing. Rather, they remind me of someone from the past. I still have to honour my discomfort.
6. Things will trigger me on a daily basis, and much of it is out of my control. It could be a song coming on in the supermarket, an aftershave I detect in passing. It might be a conversation, or visiting a friend in a hospital where I had prior surgery. Deep breaths are required, and sometimes a visit to the lady’s restroom to compose myself. I tell myself that my anxiety is a natural reaction, and I am doing fine. If I am with close friends, I will tell them that a memory has come up. If I am not, I will breath deeply, find a focal spot to concentrate on, and reassure myself quietly.
7. I will not drink to excess, nor take tablets to blot out a bad day. Sometimes, the memories hit hard, and along with the massive amount of pain I suffer, it becomes overwhelming. Alcohol is a depressant, and thus, is disastrous as an antidote. I will only have alcohol when in the company of friends at dinner, or as a toast of celebration. It only compounds the depression which inevitably comes after overworked adrenals have crashed. Instead, I go for a walk, swim or am otherwise active. It helps tremendously.
8. I will space out at times. When you hardly sleep, and are in pain, it happens naturally. When you put flashbacks or a panic attack into the mix, let’s say I am sometimes away with the fairies! Writing (and preparing for a writing task), also lends itself to spacing out. If you holler at me on the street and I don’t respond, that’s why! I am escaping into my inner world, which is expansive and magical. I nearly jump out of my skin when I am walking along and a car beeps me. I remain jittery for the rest of the day. I am hyper vigilant; always scanning a crowd for danger, even when in my own world. It’s quite a combination!
9. You are allowed to say “no” to a request. You are allowed to rest. I keep going until I can’t, and at that point, I retreat for a bit. I have to. It is a revelation, when you learn that you can keep free spaces in the calendar. Even thirty minutes to sip tea and daydream is heavenly. I need time alone to restore and reboot. Time is precious, and I try to use it wisely.
10. My survival has been an odyssey of epic proportions. I tried to run from the memories. I attempted to smother them, as one instinctively does a fire. The smoke streams from underneath the cloth, and then the flames explode forth in a cacophony of rage. It is like burning off disease, only to have damaging adhesions form underneath. Running doesn’t work, and it certainly doesn’t help. Over many years, I have visited my places of trauma. I have wept and I have released at each site. I only did so when I was ready. You have to be ready. My natural instinct is still to run when triggered, but now I have tools. They come in the form of a laptop, a paintbrush, a pastel. They come to me as bird song, my walking shoes, my friends and my music.
When I was a child, I had big dreams. I had a determined spirit and an acute awareness that what was being done to me was not only wrong, but evil. I felt as though a cannon had ripped through my psyche, smattering me into pieces. Over time, I have laid out all the pieces, and put them into place. I am glued, sewn, fused and grafted together. I was once a china doll. Now I am reinforced and can never be broken again. It takes time to heal. You will want to give up. You will consider yourself beyond repair. You will want to run and you will try to escape your own mind. You will want to give up. Please don’t. The joy of finally accessing the tools to help you cope are worth the fight.