When we hear the phrase 9 months we think of pregnancy. Baby bumps, baby showers and of course, babies! I have 2 adorable kids who spent 9 months growing in my womb until they were ready to make their way in this world. I realised today that I have been sick for 9 months. Shocked to reliaze that 9 months had past. At the same time felt like I have lived years inside 9 months.
I am sure I have been sick for longer than 9 months but last August was when I first visited a doctor for my symptoms. These last 9 months have been a roller coaster. 9 months of hell. Of slowly feeling myself getting worse and worse. 9 months of feeling helpless. 9 months of anger & despair. 9 months of pain. 9 months in which I am slowly finding myself. Finding who I am and what is important has been a huge part of my journey so far.
In January I was finally diagnosed with gastroparesis. I finally found a doctor who did not want to just throw some medications at me and tell me to come back if they don't work. I have spent 9 months learning how to push the doctors to get them to diagnose me. If I wrote down all the details of my journey it would take up a few pages. Some of it seems like a bad dream. Like being lost in a foggy field. After months of endless tests and food trials and WAITING. I finally had a answer. The end of this is near. I cried tears of joy that I finally knew what was WRONG with me. Because I thought that is the answer to fixing it....if you know the problem then you will know the solution.
Being in a medical field (veterinary) I researched every test, symptom and result through my journey. So even before I was diagnosed I started researching. As I researched gastroparesis my heart dropped. When I read some doctor's quote that most cancer patients have a better quality of life than a gastroparesis patient I began to cry. My mom has been fighting cancer for over 4 years now...watching her strength through surgery, radiation and endless chemo is awe inspiring. I do not have her strength....how can I handle worse than her.
During my 9 months I have had my own "trimesters" or stages of grief. I call it stages of grief because people who get diagnosed with a chronic illness are grieving the loss of their old life and their health. Sadness and despair seemed to be the first. How can I be a good mom to my kids? How can I be a wife to my husband? Watching the people I love look at me with sadness was even worse than what I was feeling. I also was in denial. I tried to keep pace with my life before sickness. I went out with friends, continued to exercise and did my volunteer work. I got mono and then spent 2 months sleeping every minute I could,
My second stage was anger and selfishness. I hated. Plain and simple hated everything. Also a total pity party. Everywhere you turn is food. Commercials, movies, dining out, fundraisers, etc. Everything is food especially to someone who cannot eat. I hated watching people eat. Listening to talk about diets and losing weight made me want to scream "Just be happy you can eat". I also started medications during this time and started trading symptoms for side effects. I developed pain and bloating. During my first part of my illness I did not have any pain. As the medications have helped my nausea and vomiting my pain and bloating have gotten worse.
I believe I am now in a third stage. I am not sure what to call it except maybe acceptance. This doesn't mean I do not struggle daily with ups and downs. I have decided that this is who I am. The girl who stomach stopped working. I think of how much worse it could be. This illness could kill me someday. But right now I can eat some foods. Right now I do not have a tube in me. I can work even if it's the only thing I do during the day. I am still sad and angry at times. But I have learned to step back and smell the roses as they say. I find joy in the simple act of my daughter putting her hand into mine. To hear my son laugh deeply is at times amazing. I have lost and gained important people. Saying no when asked to participate still makes me cringe at times. Other times I do not feel any regrets.
I am still sick. I spend sleepless night because of pain. I still hate food. I still vomit about once a week. My stomach bloats after eating so I look pregnant. I do not lose weight because my starved body holds onto any nutrients it gets. My doctor is still running tests to figure out if there is a cause for my gastroparesis or if I have an additional illness. Some of my symptoms are not adding up and he wants to make sure he isn't missing anything. But last night I went out for a girls night. It was only for a couple hours. I could not have a drink or eat any "fun" food. Today I am paying for it. But it was worth it. Spending time with friends who come in the bathroom to check on me is worth it. Today at least I feel blessed to find out who is important in my life. It took me 9 months to get it.
Things WILL get better! They may not seem like they will at first, but you've taken the first important step in helping you deal with this illness - you've started a blog! I did this too, last year after I was diagnosed. My blog somehow morphed into my personal journey weaved in with advice for others based on my experiences. I hope blogging will be as therapeutic for you as it is for me.
ReplyDeleteI wanted to include one of my blog entries that may help you to cope with GP a bit better. You've probably seen through your research that there's not a whole lot about GP out there. I've compiled a list of online resources that may be useful for you: http://emilysstomach.blogspot.com/2012/12/gastroparesis-resources-online-support.html
I wish you good luck and stay strong in the fight! <3
Thanks Emily. I have read some of your blog and the facebook support groups have been a wonderful support group. Thank you for taking precious time to put that out there to help others.
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