Disability in SIGHTS SEMINAR

October is a busy month: It is not only Breast Cancer Awareness Month, but it is also International Blindness Awareness Month and National Disability Awareness Month. On October 18 my good friend, Amy Bovaird, a very talented author, is putting together a seminar called Disability inSIGHTS. There will be seven speakers on different topics like mental illness, Autism, blindness, and deafness. It will be an uplifting seminar that will encourage its attendees to work around their disabilities to inspire and touch the world.

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Amy Bovaird messaged me on instant messenger, asking if I would be willing to speak about mental illness for this very special event. I was excited and a bit scared. She wanted me to write a twenty to thirty minute lecture. I’ve never written longer then a ten minute speech. My first question was, “Can I do a speech that long, and what will I talk about?” I confided in Amy about my concerns. She was very encouraging. She is a reader of this blog and made suggestions of different topics I could write about.

Then I worried about how I would write my lecture. For a fifteen-minute speech I used index cards, but there would be is a lot of cards for a twenty to thirty minute lecture. So how will I remember everything I want to say? I asked Amy and others who speak. They suggested I do an outline of the different things I want to say. It is my story, so what can go wrong? So I am working hard on my outline.

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The title of my talk will be “Recovery from Mental Illness is Possible.” I decided I will share my story about how I suffered with mental illness and struggled to reach for recovery. I will give some examples of coping techniques I used to reach recovery and the steps to take toward recovery. I hope to inspire other attendees to also reach for recovery from mental illness. Just as the seminar states, I want to give insights into living with mental illness and becoming capable of reaching recovery and becoming an important part of society.

I urge you to come and listen to not only me, but the other six speakers. First, I want to tell you about the one putting the seminar together, my friend, Amy Bovaird. She is legally blind and is also losing her hearing. Despite her disabilities, she is an author of three wonderful books, and she is a powerful speaker and a blogger. She is a very determined person who doesn’t let any obstacles get in her way. She has been working tirelessly on making this seminar a success. I find her to be a very inspiring woman who is living her life to the fullest despite her disabilities. Let’s help her make this seminar a success.

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Here is some information about the other speakers. Maxwell Ivey, Jr., aka the Blind Blogger, speak about, “Life is like a River: Overcoming Adversity and Moving Forward.” He has a rare, incurable hereditary eye condition that results in blindness. He will have an inspiring lecture about his struggles and how he overcame his disability to become a successful author, speaker, online media coach, and podcast host.

Emmanuel Lee’s topic is, “The Life of a Deaf–Blind Adult.” He will share stories about his life, like facing abuse at home and bullying at school. He’ll tell how the Helen Keller National Center for Deaf–Blind Youths and Adults taught him to adapt to his newfound abilities.

Stephanae McCoy’s topic is “How Losing My Sight Expanded My Vision.” She will share three tips about what she learned to help you also navigate the road to social entrepreneurship.

Chelsea C. Nguyen will have a table center for “Blindness and Adaptive Hands–On Makeup, Hair Styling, and Shaving Demos.” She will give demonstrations on adaptive styling and shaving tools a person with limited or no vision can use. She will give others the opportunities to touch, feel, and practice on a mannequin head.

There will also be an expert panel on Autism, starting with Erica Ploski, MA, LPC, a licensed professional counselor and mother of three children. Casey Ireson is a college senior and public speaker sharing autism awareness and insights from his personal journey. Dr. Paul A. Bensur Jr., who is a published author of Autistic Spectrum Disorder A New Outlook, will also be on the panel.

This will be an inspiring seminar not just for people with disabilities, but for anyone. So come hear me and the others on October 18 at the Tomridge Center, Erie, PA from 10 am to 3 pm. Register now at the site below. Space is limited, so register right away. You can also find out more about the speakers and the conference at this site. Let’s all reach beyond our disabilities and challenges to dance in the light of success.

https://amybovaird.com/disabilityinsights

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EULOGY TO MY GRANDMA

God worked really hard when he made my grandmother. He put extra love in her heart, warm arms to hug with, and strength that could endure the toughest hardships. I don’t have the right words to completely describe how wonderful my grandma was. She made a big impact, not only on my life, but on the lives of everyone she met. Even while she was sick in the nursing home, struggling, she touched the people around her. She had a glow about her. It shone from the inside out. The glow was God’s light. God placed it within her soul, and it shone so bright that it radiated in her smile, her warm eyes, and in the things she did.

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My grandmother never had a lot of money, yet she would give her last pennies to help another in need. I remember holiday meals at my grandparents’ home where Grandma would invite a lonely elderly lady to join us. My dad told us stories where Grandma would give food to strangers when she barely had enough food to feed her eight children. She gave endless love and compassion when she had nothing else to give. While she was in the nursing home, my husband and I brought her cookies we made, and she offered them to some of the other residents. She lost her independence, her home, and almost everything, and yet she was still giving.

As a child, I always felt abundance of love from my grandmother. She didn’t spoil me with gifts, but with love. No matter how bad I felt after being bullied at school, I would always feel better after a hug from Grandma. Grandma was a good listener, and I could talk to her about anything. She always had comforting words to share, and she knew how to make me feel special and important. When I felt rejected at school, I felt accepted at my grandparents. She always believed in me, even when I didn’t believe in myself.

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Grandma could write the most beautiful letters that brought tears to my eyes, and she loved to write them. I believe it is from her I got my writing talent. She beamed with pride each time I read her a story I wrote. Each time I got published, she had to have a copy. She loved my writing, and I was more than excited to share with her my accomplishments. Even while she lay dying, I read her a chapter from my memoir, and in a very weak and low voice, she told me she liked it. Even while life was fading from her, she loved the words I read to her. I believe they gave her comfort.

I never left my grandma’s home without a hug. She hugged everyone, even strangers. Her arms were always warm and gentle. When I brought my friends to my grandma’s, they too had to have a hug, even though she didn’t know them well. I looked forward to her hugs. Her hugs were more than just two arms wrapped around me; they were magical. They lifted me up when I felt down, they filled me with strength, they brought light into my dark soul, and they helped me face a harsh world with courage.

Grandma said that she loved all her grandchildren the same, but in my soul, I felt like her favorite. Ever since I was a child, people said I looked like a younger version of her. I believed that made me extra special. Before I went to writing conferences, Grandma would pick a day to take me shopping. She would buy me two nice outfits for the conference and take me to lunch. She even bought me a suitcase set I still have.

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I lived with my grandparents for a bit while I was in college. At church and on the phone, Grandma bragged about my good grades to friends and family. She wouldn’t let me help her around the house. She said my college work was more important. She bought me my favorite foods, and when I got sick she nursed me until I was well again. I just wish I hadn’t been so sick and could have lived with them longer.

Even though I was at the deepest depth of my mental illness, I couldn’t let my grandparents know how sick I was. They enjoyed having me live with them, and I couldn’t crush their hearts with the knowledge I was trying to take my life. Even though she didn’t know, it was her endless gifts of love that kept me from succeeding with suicide. She was the one light I had to hold onto in my darkest times.

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Grandma had a deep love for God. She didn’t have to preach the word of God, because she lived in his light. She spread her passion for the Heavenly Father by the life she lived. She gave kindness to everyone around her, she gave endlessly, she never judged anyone, and she touched people with a smile. Her faith is what got her through some very rough times in her life. When her son was killed by a drunk driver, she got on her knees and prayed. When she got in an accident that left a mother childless, she prayed for strength. When she had little money to feed her children, she prayed. God was her strength and guiding light. Her love for the Heavenly Father was so great that you could see it in her eyes and smile. She was the most faithful and religious person I’ve ever known.

My grandma has always been a huge part of my life and will forever remain in my heart. She watched me take my first steps and from heaven she’ll watch me take my exciting steps into publication when I publish my memoir. I believe she will continue to watch me with each new step I will take in my life.

Grandma always said, “Never say goodbye, because I will see you again.” So when I went to see my grandma lying in bed, skin and bones, her glow fading and death calling her, I didn’t say my goodbyes, but instead I told her, “I will see you again.” Some day when it’s my time to go to heaven, I will be reunited with my grandma and I will give her a big hug.

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Today, the day this post goes out, I will be sitting at Grandma’s funeral whispering, “I will see you again someday.” No matter how long it takes, I will see her again. Until then, I will live my life to the fullest and use my writing the way God wants me to, to help others. I’ll give from my heart and I will live in God’s light, like Grandma did.

See you again Grandma. You live in my heart and I will always be thankful to be your granddaughter.

 

 

FINDING THE RIGHT MEDICATION

Many resist going on medication when they find out they have mental illness. The idea of being on an antidepressant for life can be frightening. Some medications also have a bad reputation. There are stories of people going on them and becoming like zombies. The person just sleeps, can’t function or even think. This scares people. They want to get better, not become a zombie. So many turn to alternatives like medicating with drugs and alcohol, natural remedies, or just go untreated.

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Finding the right antidepressant that works for you is not an easy process. What works for one person doesn’t mean it will work for everyone. You have to keep trying different types until one works for you. Plus, antidepressants are not an automatic cure. You can’t take the medication and suddenly everything is better. It doesn’t work that way. An antidepressant treats symptoms of your illness, but the rest is hard work through therapy to undo years of misguided thinking and self-loathing. You have to change your way of thinking completely and that is not easy.

When I started on antidepressants for my mental illness, I wanted the medicine to take away all the bad thoughts, to make me love myself, and to make me feel like I was worth something. I wanted it to work right away. Unfortunately, they didn’t work that way. The psychiatrist told me it could take up to two weeks for my medication to start working, and if it wasn’t working in that time, he would try me on another one.

My first thoughts were: You mean I have to wait? It doesn’t work right away? I want to feel better now.

The psychiatrist just handed me a prescription and sent me on my way. Two weeks later I was feeling the same. The psychiatrist put me on another one. With the new one I was constantly tired. I needed lots of naps. I would go to college and fall asleep in class, and when I went home for the day all I could do was sleep. It seemed like I was spending lots of money on antidepressants that weren’t working. It seemed hopeless. Would I find any relief from my illness?

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I told my therapist how hopeless it seemed and how expensive it was to keep buying medication that didn’t work. She helped me find programs to pay for the antidepressant and encouraged me not to give up. She told me to never take myself off an antidepressant. Why? Because automatically being taken off of antidepressants can cause withdrawal and other complications. She said if I was having any problems with my medication to call my psychiatrist right away.

A good psychiatrist knows medications well and knows that a person must be weaned off of an antidepressant before a new one is started. I had psychiatrists take me off medication without weaning. I had sweats, shaking, nausea, and sleeplessness and became very sick. I couldn’t eat for days. It was awful. After that I found a new psychiatrist. I went through several until I found Doctor Lance Besner and he knew his medications well. I will never leave him because he is the best psychiatrist I ever had.

Before I saw Doctor Besner, I was seeing a psychiatrist who had me on high doses of three antidepressants. After being on that much medication for several years, I began to lose my memory and I had a tremor. I couldn’t remember what day it was and the simplest things. I have a bad memory to begin with, but this was worse. I felt like I was losing my mind. On top of that I couldn’t even hold a pen without shaking. I couldn’t hold my hands still no matter what.

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I told my psychiatrist and he sent me for neurological tests. When those came back normal, he took me off all my medication. I started making mistakes at work, I went days without sleep, I went from hot to cold within minutes, and I couldn’t eat. Just the thought of food made me sick. I got suspended from work for a mistake and my whole body began to shake. My husband took me to the emergency room. They said I was dehydrated and going through withdrawal.

A friend suggested I go see doctor Besner and I did. He started the game of trying to find what medication worked for me. It is a rough game, but this time he gave me samples of the antidepressants. That way I wasn’t losing a lot of money when the prescription didn’t work. When one antidepressant didn’t work, he cut the dosage while slowly starting me on a new one. Once I was completely off the old antidepressant, he increased the new one. He did this process until I found one that took away many of my symptoms. I could finally sleep, I had more energy, I could think more clearly, and my depression wasn’t so horrible. I took control of the rest of my depression by going to therapy and working hard to change my thought processes.

If your antidepressant isn’t working or you’re having bad side effects, tell your psychiatrist. Don’t take yourself off the medication on your own. Be patient; there is one that will work for you. Don’t expect the medicine to be an automatic fix. Remember, you have to put work into your recovery. You must go to therapy and do any homework the therapist gives you. Remember, it takes time for antidepressants to work, so don’t expect to feel relief right away.

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I have found the right combination of medication that works for me. With medication and hard work I am enjoying the light of recovery.

THE GRIEVING SOUL

Many ask, “Which is harder, having someone die suddenly or watching someone die slowly?” In my experience, both are equally hard. Death, no matter how it happens, is extremely painful and heartbreaking. We can never prepare ourselves to lose someone we love, no matter how short or long the loved one’s life was. Grief is hard either way and could send anyone into a depression. For those who have depression or who are in recovery from depression, grief can be especially cruel.

Last week my grief was just too overpowering for me to be able to release it on paper. I just couldn’t put it into words. In a way, I have been grieving for my grandma over a period of several years. It first started when she got sick about six years ago and had to go into a nursing home. Slowly, over the years, I watched my grandma’s health deteriorate. I missed visiting her at her home. I missed her inviting my husband and me over for lunch for a feast and then sending us home with a bag of groceries from her cupboard, and having her at family events, and so on.

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Even though her health has faded, God’s glow shone in her. During some visits we sat silently at her side holding her hand while she slept, and during other visits we filled her in on what was going on in our lives. One time we helped her play bingo and she won. She insisted we take her prizes home. It was her way of still giving, even when she had nothing left to give. Even though she was stuck in a nursing home, unable to give what little she had, she still had endless love to give.

When she was put in the nursing home, a part of her died. She had always been an independent woman and suddenly she was confined to a wheelchair. She had always been a talker. I used to be able to hold a conversation with her for hours, but the conversations turned to me doing most of the talking. The strong, vibrant woman had turned into a weak, elderly woman dependent on her nurses. I grieved losing the woman she once was.

In December, my mom called me and said Grandma was dying, and I cried. We watched her body slowly going through the dying process week after week and month after month. Each time my husband and I came to visit her, she seemed frailer and she slept more. We spent most of the time sitting at her side, holding her hand while she slept. When she was awake enough to talk to us, her words were few and sometimes she was confused. Yet she still had that glow of God’s love in her soul. The glow shone in her smile and eyes, but that glow was dimming.

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Recently, Grandma became bedridden, and the dying process sped up. Hospice told us it’s only a matter of time. Each time I go to see her, I read her a chapter from my memoir. She is now skin and bones, her body dying and her smile completely gone and in its place a frown. I look into her eyes and I can see the glow slowly fading. My heart is shattered. I want to wrap her in my arms and cry, but instead I tell her how much I love her and that I’m happy she will soon be reunited with Grandpa in heaven.

It is so hard watching her die. I pray each night that God takes her home soon. I ask God why it has to be so slow. Each time I see her, the weaker she becomes. Wednesday, when I saw her, her eyes were closed. When she did open them, her breathing was ragged. I could tell she was struggling. I read her another chapter. I asked her if she liked it. Her voice was so weak that I had to get up close to her lips to hear her say, “Yes.”

Each day I wake up wondering, “Will this be the day I get the call she passed?” I find it nearly impossible to get out of bed and go to work. My heart is so broken and filled with pain I can barely breathe. I push myself to go to work and force a smile on my lips, even though a depression is blanketing my soul. I know all the signs of my sickness. I am very aware of my illness and I know that unbearable sadness all too well. I keep pushing myself to keep going because I know that’s what Grandma would want me to do.

I’m turning to my support system for comfort. My husband is very supportive. My close friend, who has been one of my biggest supporters, is dealing with her own problems and she can’t be of much help to me, and I can’t be of much help to her. So instead, I’m turning to some of my other friends. I feel bad not being able to support my friend and it seems strange not being able to confide in her, but at least we have other people to lean on.

My grieving may have put me into a depression, but I know if I keep practicing my coping techniques, leaning on my support system, and taking care of myself, in time I will once again pull myself out of this dark hole. Maybe by the time this post goes up, Grandma may have passed. It’s hard to tell when God will take her home and give her her angel wings. I just know this will get harder before it gets easier, but I will get through this. I’m too strong to let depression keep me down.

It’s easy to slip into a depression when you’re grieving. You may have never had depression in your life, and you lose someone you love, and suddenly you’re in that dark hole. While you’re going through grief, know the symptoms of depression, practice self-care, turn to counseling if you need to, build a support team, and don’t deny yourself the right to cry. Crying helps you let that pain out. Taking care of yourself and your needs is very important. If you neglect yourself, you can fall farther down that dark hole. If you need a higher dose of antidepressants to get you through or to start some medication, then talk to your psychiatrist or doctor. Do what it takes to fight the depression and climb out of that hole.

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It may take a little time to get over my depression, but I refuse to let it drag me all the way down to the darkest depth of my hole. I am a fighter, like my grandma. Grandma is fighting all the way to the end, and when she is gone I will continue to fight until I am once again dancing in the light of recovery.

 

WHAT MY DAD TAUGHT ME

Parents teach their children lessons that will be used in the future. These lessons help us grow and evolve into strong and independent adults. We use them to guide us through a rough and unpredictable world. We can also use those lessons from childhood to help us through struggles in our lives like fighting to reach recovery from mental illness. What do you remember from what your parents taught you as a child that can help you reach above your mental illness?

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The other day my husband and I were in the car going to an appointment when I saw a small child on a tricycle on the sidewalk. I asked my husband if he had one as a child. Then I recalled the one I had was passed down from my older sister to me and from me to my younger siblings. Then I asked my husband who taught him how to ride a bike and the lesson came to me. A valuable lesson I never really thought about until that moment.

I remember my dad taking the training wheels off my bike. “Okay, Aimee, get on. Start pedaling. Don’t worry I’ll be holding on to the back of the bike.”

I started pedaling and once I got moving dad let go. I suddenly wobbled from side to side and fell into a mud puddle. I stood up, wet and muddy.

Tears streamed down my face, but dad looked into my eyes. “You can’t give up now. Get back on and try again.”

I pouted. “I don’t want to fall again.”

Dad patted the seat. “When you fall, you dust yourself off and give it a try again until you get it right.”

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Dad’s lesson followed me through my journey to recovery. See, on the road to recovery I fell off the bike quite a few times. I took time off from college to get treatment for my mental illness. During that time I started working in a grocery store. I began to make friends, I got a social life for the first time, and I even started dating for the first time. Life was going great. I got off my antidepressants and discontinued therapy. I was in recovery.

A few years down the road, the depression began to settle in again. I felt myself falling off that bike so I looked into getting a therapist. Before I knew it I was lying in that mud puddle again. I felt like my world crumbling around me, I began injuring again, I got into an abusive relationship, and I began to feel like a close friend was abandoning me. I sent that friend notes (with blood on them) begging her not to leave me. I wasn’t thinking straight. My friend told me she couldn’t handle my illness and ended our friendship. Then my boyfriend began to hurt me physically and emotionally.

I ended up in a mental health hospital after my boyfriend packed my bags. I wanted to lie in that puddle and give up. It would have been easy to do, but that lesson my dad taught me was engraved in my mind and soul. I had to pick myself up and get on that bike again. I had to keep trying no matter how many times I crashed. So I participated in therapy, I took my medication, and began to journal my feelings. Within a week I was released from the hospital to continue treatments at home. I was back on the bike to recovery.

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In the years to follow I fell off the bike again. I got depressed and began injuring again. The abuse I received from my ex-boyfriend was hard to get over, and it seemed like I had lost all my friends. I cried my eyes out in therapy. I went to work and came home and that was all I did. I wanted to give up, but once again the lesson my father taught me kicked in. A co-worker with gave me a goal to go six months without injuring. So I got on my bike and began pedaling up a steep hill to reach that goal. I went to therapy each week and began to learn healthier coping techniques. Each time I felt myself wobbling, I pedaled harder until I succeeded. Once I reached six month my co-worker threw me a party to celebrate my accomplishment.

 

I tried to stay on that bike, but I kept falling off. On my road to recovery I kept crashing into episodes of depression. I’d pull myself up only to swerve, wobble, and tumble down again.

I met my husband and he began holding that bike for me. Like my father, he encouraged me to get up and try again. Each time I tumbled my husband told me, “Don’t give up.” In time I was riding down that road of recovery without any help. I finally got it right and I reached recovery.

If you slip up in your road to recovery, remember to pick yourself up and try again. Don’t give up because you fell a couple times. That’s part of the process. Just keep pulling yourself up and pushing forward. Never give up, just get back up, dust your pride off, and get back on that road to recovery again. Think of it as learning to ride a bike. You keep falling and getting back up again until you’re pedaling right into the light of recovery.

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I have been on the bike of recovery for a while now. I fall from time to time, but I dust off my knees and get back on again. The road can be full of hills, it can be bumpy, and it can twist in many directions, but I never give up. Because I never give up, I am riding my bike in the light of recovery.

CELEBRATING THE MAN BESIDE ME

I saw my grandfather die of cancer; I also knew of co-workers who died of the disease and heard of many others going through cancer. I told myself that if I ever got cancer I’d fall apart and sink back into the dark hole of depression. I never actually thought it would happen.

Last May when I heard the words, “You have breast cancer,” I thought it was the end of my world, I didn’t give up. I went through the steps, the appointments, and the surgeries with courage and determination. I fell apart a few times, but I still stayed strong. I didn’t give in to depression even though it threatened to throw me down that hole again, and I didn’t let cancer ruin my life. This is why celebrating one year cancer free is so important.

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I didn’t fight cancer alone. Through it all my husband stood at my side. He sat for hours in the waiting room with my mom while I was in surgery. He stayed the night with me, sleeping beside my bed in a recliner. He took twelve days off work to take care of me. Each morning, afternoon, and night he emptied my drains and measured them and what came out of the drains wasn’t pleasant. He brushed my hair when it hurt too much to reach up, and he held me when I broke down into tears. He was the strong unbending tree standing tall during the storm while I huddled beneath his branches for protection.

Celebrating one year cancer free wasn’t just for me, but also for my husband Lou. He cried with me when we found out about it, and he went through the battle with me. He never complained about taking care of me. Lou just stood strong at my side. I wanted July 17 2019, my one year cancer free, to be special for him, too. What made it special for Lou is spending a whole day with me and for him to spoil me, something he loves to do. I wanted to do more for him, but he wouldn’t let me. I am trying to think up a way to also spoil him.

My husband is very good at going all out for me. Wednesday morning my hubby got up at ten-forty. He said he had to go somewhere and I was not allowed to go downstairs until he returned and came to get me. I lay in bed trying to figure out what he was up to. I tried to guess what he had planned, but my mind went blank.

At eleven he came upstairs to get me. He said to follow him down the stairs, but look straight. So I focused on his back. At the bottom of the stairs he directed me to close my eyes. He led me to a chair and told me to sit. Once I sat down, I was allowed to open my eyes. On the kitchen table before me was a bouquet of pink roses, sponge candy, a balloon that said, “Congrats,” and a white medium size box. I opened up the box and inside there was a small cake that said, “Happy 1 year Anniversary.” Tears fell from my eyes as I got up and wrapped my arms around him.

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He smiled. “There’s more. We have somewhere to go at five tonight, but first how about we have a piece of cake.”

We cut into the cake while I tried to guess where we were going at five. After our piece of cake and lunch we went for a ride around the Peninsula. I continued to make guesses, but Lou wouldn’t budge. When five o’clock finally arrived, we got into the car and he took me to Hoss’s for dinner. He made sure the waitress knew we were celebrating my one year cancer free. The waitress brought out a small cake for me and congratulated me.

That day Lou made me feel like I was on top of the world. That night when he went to bed I stayed up and bragged to all my friends. When I went to bed I felt so giddy that it took a while for my sleeping medication to kick in. He made my day extra special with not only the things he bought me, but with the love he put into it.

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He tells me continually, “I don’t want any pats on the back for what I do for you.”

I can’t help but pat him on the back. He is an extra special man. He puts his whole heart in everything he does for me. He is the love of my life, my soulmate. He doesn’t just spoil me with gifts, but with love. He gives me lots of attention, he kisses me every morning, and every night we snuggle before going to sleep. He’s always looking out for me and he often puts me before his own needs.

While I went through cancer he put me first. He took care of my needs and put aside his own. It was a difficult time for him, too. He has lost a lot of people to cancer, especially his grandma, the woman who raised him. I can’t imagine what he was feeling to have his wife go through the same disease. I’m sure his heart was breaking, but he wouldn’t admit to it. He gave his all to me without one complaint and I can’t love him anymore than I do for it.

If you have someone taking care of you while you’re sick or who is always at your side during the roughest times in your life, let him or her know how grateful you are. We not only need to be there for the ones struggling, but also for the caretakers. The caretakers need to know how important they are. We need to celebrate all the people out there who care for their loved ones selflessly.

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This blog post is a celebration of the man who holds me up and stands beside me no matter what. I’m in the light because of my husband, Lou. Together we slow dance in the light of recovery.

GIVING BACK

Being in recovery from mental illness doesn’t mean you’re cured, but it does mean you’re in control of your illness. Once you know how to handle your bad days and enjoy your good days, you find yourself stronger than ever. It takes strength to reach recovery and to stay in it. Things change when you’re in recovery. You take new steps, you take on new roles, and you step out of your comfort zone into new beginnings. You find yourself able to give back to those who helped you when you were at the bottom of your hole.

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Almost 19 years ago I was deep into my mental illness. The only thing I could see was how awful I felt and how awful living seemed. I couldn’t focus on anyone else’s problems but mine. During that time I leaned heavily on my friend Cheryl. She was my support and strength. I called her in the middle of night when I wanted to injure. She’d talk to me, even if it was at one am, until she got me to laugh. Sometimes we talked for hours. I cried and then I laughed. She knew what to say and what to do. She made herself available at any time.

When my ex-boyfriend couldn’t handle my illness or sudden emotional episodes, he called Cheryl. She was even there when I struggled to get through a day of work. One day I stood out in the middle of a road ready to die and Cheryl pulled me off. She has always been at my side when I needed her.

We lost contact for a few years, but once I found her again on Facebook, I was much stronger and happier. I had reached recovery, yet she picked up from where she left off. Instead of calling her to keep me from self-injuring or attempting suicide, I text her for advice on my bad days. When I started writing this blog, she began to use my post to help me, but suddenly roles have changed.

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Lou, Aimee, Cheryl and Cheryl’s boyfriend, Kieth. Peeking in from the back is Brianna Cheryl’s daughter. First time we saw each other face to face after reconnecting.

Cheryl has dipped into depression and is struggling with anxiety due to a situation in her life. Instead of me leaning on her, she is now leaning on me. Instead of her using my blog posts to chide me, I am now using them to child her. Being in recovery and going through years of therapy, I am now taking on a new role. Instead of me turning to her at my lowest, she is turning to me at her lowest. I am finally strong enough to be part of her support team. Roles have reversed. Now I am the strong one.

Many times I texted Cheryl, “It’s not fair. You’re using my own blog post against me.”

Now Cheryl texts, “Hey, it’s not fair, now you’re using your blog posts against me.”

When I started this blog I never considered that my posts could be used to not only help others, but also for others to use it to help me. I never thought I could actively put them to use on my own friend. I never thought I could be strong enough to be Cheryl’s shoulder to lean on. It is a good feeling to be able to help a friend in distress.

Cheryl messages me in tears and when she is at her lowest. I text her back or use Marco Polo to give her words of comfort, to encourage her, and to use what I’ve learned in therapy and what I have written in these posts to help her. This time I’m able to give back to her, by being her shoulder to lean on and cry on, to talk to her until she laughs, and to encourage her to fight for recovery. I’m more than happy to be able to be there for her like she has been for me.

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Once you reach recovery, your life changes and you change. You learn to manage your illness each day and still find the strength to be the friend you couldn’t be while you were ill. You take on new roles and you make big steps into new beginnings. Instead of being the person in need you can be the rock others are leaning on and standing on. You can give back to those who gave selflessly to you while you were at the bottom of the hole. Instead of the person needing support you can be the person giving support.

I still need to lean on Cheryl from time to time, but I am so happy to be the one she can lean on right now. I’m giving back to her what she has given me so many times. I’m giving her strength like she gave me, I’m giving her support like she gave me, I’m giving her a shoulder to cry on like she gave me, and so much more. I will stand at Cheryl’s side until we both can dance in the light of recovery.

 

HAHA I DON’T HAVE BREASTS

While going through mental illness, I learned that during the saddest times I needed to look for something positive. My therapist had me keep a journal where I wrote down something positive each day. In time the list grew. I was also taught even during bad situations, there is something good. Adding humor doesn’t cure mental illness, but helps make the good things shine even more. I have also found these methods work for when you go through other illnesses. I have looked for the positive while struggling with breast cancer.

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Cancer is an awful illness and it affects its victims not only physically, but also mentally. Due to breast cancer and the BRCA gene, I had to decide to have a double mastectomy. While struggling with accepting myself as a beautiful woman without breasts, I found that looking at the positive side helps. I decided to add a little humor to my bad situation and this has lifted my spirits and helped me accept myself.

When my friends complain about their big breasts, I can now laugh at them and say, “Haha I don’t have breasts anymore.” I no longer have those giant melons hanging from my chest wreaking havoc in my life. I fought like heck to keep them, but now I am free. I no longer sit at the kitchen table in the morning to find my boob bathing in my bowl of cereal. I no longer have to worry about pulling it out to make a big splash and have cereal with milk dripping, spilling and soaking my table and me.

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I am also free of those sling shots they call bras. They never fit right, they stretched out of shape, and they came undone at the wrong moments. I can’t count how many times I tucked, squeezed, and pulled a bra over my breasts because the ones that fit perfectly don’t exist. Then suddenly I’d unintentionally pull that wandering bra strap up. In time the sling shot stretched to the point my boobs dangled like pears on a tree and at the wrong time something is poking me in the back. I could be in a crowd of people and guess what my bra came undone. Do I try to reach back and fasten it or run for the ladies room, making up some crazy excuses on the way?

I also no longer have to worry about those pesky heat rashes that taunted me every summer. I can remember the itch that drove me crazy to the point I would do anything to relieve it. I remember gently reaching under my breasts to scratch it to only realize people were standing in front of me looking at me oddly. I quickly pulled my hand away and greeted them with a smile.

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I no longer have to worry about my melon wiggling free of that contraption called a bra and my loose-fitingt shirt so it could go streaking in public. I tried hard to keep it under control, but at the worst possible time it would decide to show itself to the world. Of course having a double D made it hard to keep it from dancing out of its hiding place, especially in a swimming suit.

I am now free of bouncing bosoms threatening to give me a black eye when I run. I no longer have to worry about trying to explain to my coworker why I suddenly got a black eye running to the bus stop. Sometimes I lost track of time and found myself running to the end of my road to catch the bus. Up and down they bounced like basketballs. I had to concentrate on holding my head high so one of those wild things didn’t jump up and sock me in the eye. My husband loved to watch them bounce, but I hated how those big things thought they were made of rubber.

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I’m happy to no longer have these heavy melons dangling from my chest like someone taped fifty pound weights to me. Sometimes they were so heavy I thought I needed a walker for them. They weighed me down and pulled at my back. Carrying them around was a task of its own. So many times I wished I had something to carry them in. Unfortunately no one ever evented a walker with wheels and baskets just for the breasts.

The most positive thing about no longer having breasts is being able to rub it in with my friends. When they complain about theirs I just laugh and say, “Haha I don’t have breasts.” I had planned on burning my entire stretched-out sling shots, but I think my neighbors would be calling the looney bin on me. So instead I resorted to putting them in a bag and doing a dance while I stood over the garbage can we have outside tossing them in one by one.

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If you are facing breast cancer, mental illness, or some other illness, find the positive hiding behind the darkness. Have fun with the positive; add humor to it. A little laughter helps lift the spirits and makes things seem less awful. Laughter is no cure, but it helps. Sometimes when we are in the hole it’s hard to laugh, but don’t give up. Keep looking for ways to find the good during the bad.

I’m in recovery from mental illness and breast cancer because I worked hard at finding the brighter side to my ordeals. I’m laughing and enjoying life within the light.

 

WRITING, LEARNING, AND GROWING

Not everyone has the ability to write, and no one starts out as the perfect writer. Writing is a God given–gift that needs lots of fine tuning and learning. Published writers have a wealth of information to share and techniques to try. No author knows everything there is to know about writing and everyone has a different technique. The learning process is endless. Writers participate in workshops and conferences to better their work. They also read books on different techniques.

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Back in seventh grade I found I had a talent to write. Writing became my therapy to deal with bullying and it became my passion. In school I bought books on writing and read them religiously. My high school English teacher signed me up for a summer program for talented writers at Chautauqua Institute. I loved it. A bus took us there and home each day for a week. I lived a half hour from the institute.

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Bell tower at  Chautauqua Institute

Then my teacher gave me information on a writing conference for high school students at Susquehanna College. My parents scrounged up the money for me to go. My science teacher took me for a weekend writers retreat in a small town called Findley Lake. In eleventh grade I raised enough money to go to Washington, DC for a journalism conference. Yet I still had a lot to learn.

Going to writing workshops helped not only my writing, but it also helped lift me up during some depressing times in my life. Every time I came back my parents and teachers said I was glowing. I was learning about what I loved and I was making friends with other people who loved the same thing. The conferences took me away from my sad, lonely world for a little while and they helped me grow as a writer. In high school I felt like a nobody, but at the conference I felt like somebody.

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Me and friends I made at Susquehanna University writing conference.

As an adult I joined a writing critique group called Pennwriters. I began to learn and improve my writing even more. Much of what I learned about writing in high school was obsolete. Learning to be a professional writer was a whole new experience. I had lots to learn.

I started going to Pennwriters writing conferences. I had made some friends at my group and I shared a room with my friend Jan. I was pretty shy and I stuck to her like glue. Then Jan introduced me to Saint Davids Christian Writers conference. Again I stuck to Jan, but in time I blossomed. I broke free of my shyness and began making new friends. When I returned home I was glowing.

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Jan and I at Pennwriters conference

Going to the conference helped me shed the chains that were holding me down since high school. It helped me break free of my silence. I made some really good friends at Saint David’s that have been my friends for years now. I met my friend Kelly who helped me invite God into my life and my friend Roberta who edits these blog posts. Now that I am married and we own a home, I no longer can afford the Pennwriters weekend conference, but I go to the one day conference. I go to Saint David’s when I can get a scholarship.

Writers never stop learning and improving their abilities. Writers have their own techniques. At the conferences I learn something new from each workshop. I take a little bit from each workshop to improve, to grow, and to develop my own technique. There is always room for improvement, for learning, and growing as a writer.

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Saint Davids Christian Writers conference attendees years ago before I was married. Can you find me?

Right now I am packing to go to Saint Davids Christian writers conference. I am very excited to see my friends and to learn. I sold copies of the book I’m published in and raised enough money to get a partial scholarship. A lot has been going on in my life with being a cancer survivor, two people I love very much having a rough time, and having my own health problems. Last week I was sick in bed with a sinus infection and not too long ago I dealt with plantar fasciitis. I need this conference. It’s my therapy.

I enjoy every minute of learning about my craft and I love meeting new people who also have the same passion as me. I also love to buy books and have the author sign them. I can’t wait to be signing my own book at Saint David’s in the future. I can’t wait to see my friends and to talk about something I love, writing.

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God gave me a wonderful talent and I will continue to work on improving it so I can use it to help others. I have noticed since I started this blog my posts have gotten better. I will continue to work on improving them. My writing is my heart and soul. I always tell people if you really want to get to know me read my writing. I pour all of me in every word. My writing keeps me in the light of recovery.

Since I am going to Saint David’s Wednesday there will be no new blog post next week.