Depression, Family, Mother and daughter

The Real Life Gilmore Girls

Mum and I are like the real life Gilmore Girls. Mum and I are incredibly close and she is my best friend; I honestly wouldn’t know what to do with myself if I didn’t have mum in my life and she wasn’t my mum.

Like I said before she is my best friend but also my sister, father, aunt, grandma, daughter and all round the greatest person ever.
Although mum is a lot like Lorelai I don’t think I’m that much like Rory because to be honest I think Rory is rude, spoilt, selfish and not very respective to her mum.

I love my mum more than anything on this earth. She is the most resilient, strong, loyal, caring, smart, beautiful, loving, empathetic, compassionate, generous, funny, witty, angelic, kind, ambitious, amusing, brave, conscientious, courageous, easygoing, friendly, gentle, helpful, and honest person I know and will ever meet.
Mum has been through so much in her life and the fact that she is still living and this amazing after all that she’s been through is astounding. She really is my role model and inspiration.

Mum and I have always gotten along, we don’t really fight about anything and if we do we get over it pretty quickly.
When we were living at Michael’s we were close but definitely¬†not as close as we are now. ¬†We couldn’t be as close as we are now because Michael was such a jealous freak and would try to come between us all the time. I think the trauma that we’ve gone through has definitely made us closer.

Mum and I have a lot of mutual respect for each other and we’re equals so I think that’s partly why we get along so well. Don’t get me wrong, ¬†I listen to her when she tells me ‘off’ but from day to day we’re equals. The other reasons we get along so well is because we also have a lot of¬†love, loyalty and honesty towards each other.¬†Mum respects me as a person and my decisions and I respect her as a person and her decisions.

Mum and I have an incredibly special bond, it’s a bond like no other. She is one of my soul mates and I am thankful every day that I get to spend my whole life with her.
Mum and I have so many laughs because we have a similar sense of humour so we laugh at things that are pretty inappropriate and that others wouldn’t find funnyūüėā.

My mum is my rock and I know she will always be there for me and I will always be there for her. We have supported each other throughout these 4 years of hardship and there is no way I could have gotten through it without my Mumma Bear.

Mum is a cool mum, she’s the type of mum that all your friends love because she gives great advice and is more like part of the group than the adult of that friend.

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Here’s the letter I wrote to her a few posts ago:
https://depresssedmesswithanxietyandgrief.wordpress.com/2017/03/06/a-letter-to-my-mumma-bear/

I don’t think there is much else I can say about our relationship except that it’s incredibly special and no one will ever be able to come between us and the friendship that we have.

Love you Mum!!!

Keep safe everyone and I hope that you have your own Lorelai in your life.
Maddy xoxo

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Feel free to follow me on Twitter: https://twitter.com/Its_me_MaddyO

 

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Body image, Chronic health condition, Depression, Doctors, Gastroparesis, gluten free, Misdiagnosing, Uncategorized, Vegan

Misdiagnosing

Misdiagnosing a patient isn’t something a doctor wants to do but sadly it happens. Doctors are only human after all; even if they do act like they’re better than everyone and everything.¬†

I myself have been misdiagnosed a couple of times in the 3 years it’s taken me to finally get an accurate diagnosis. My chronic fatigue was easily diagnosed but diagnosing my gastroparesis hasn’t gone well at all!¬†

3 years ago I started getting really bad stomach aches and would alternate between diarrhoea and then constipation with a lot of blood in my stool. I was also bloated and looked pregnant (I still do but the doesn’t matter at the moment). Anyway, mum and I went to the emergency room at the Royal Childrens Hospital 4 times because of my double over stomach pains and the blood in my stool and every time they would do a blood test and then send me home. They never did anything more than take my bloods and get me to talk to a doctor. They referred me to one of their gastroenterologists and got me to talk to a social worker. They really weren’t any help at all. Well, I saw the gastroenterologist and he put me on the waiting list for a colonoscopy and endoscopy; that was meant to happen in April and I finally got in in November (even though I was on the category 2 list). I got the scopes done and the gastroenterologist told me that nothing was wrong and to come back in a couple of months.
Of course mum and I weren’t happy with that so we got a referral from my GP to see a paediatrician and to see if he could help. We went and saw the paediatrician and he straight away diagnosed me with the chronic fatigue which was great because now I had an answer to that and also to my heart problems but we originally went there for the stomach issues so we told him all about it and what had happened. I think it’s important that I also tell you that I was in the psych ward at this time. Anyway, so he basically told me that I was obese and needed to lose weight and then all my stomach issues would go away. He also made me get an X-ray which he told me was normal but when I went to my new gastroenterologist he told me that it WASN’T normal and that I needed to fix the issue ASAP. So after telling me that I was obese, grabbing my fat, telling me there was nothing was wrong with me and making me get an X-ray and then saying it was fine when it wasn’t he sent me on my merry way and told me to come back in a year or never if I didn’t need to see him.

I mentioned before that I was in the psych ward and that I thought that that was important to mention because what doctor who knows that you’re in the psychiatric unit at the hospital and knows that you have problems with your weight tells you that you’re obese and that you need to lose all the weight and then you’ll be fine? I was obviously in the psych unit because I wasn’t doing well and I had told him that part of the reason I was in there was because of my weight gain. Safe to say that I never went back to him!¬†

After that failure with the paediatrician¬†mum and I went back to my GP to get another referral to see a different gastroenterologist (Lets call him Bob) ¬†because nothing with my stomach had improved and it was actually getting worse and not better. So off we went to see another gastroenterologist; this time it was privately and hella expensive. Bob thought I had ulcerative colitis at first and put me on steroids and another medication he also booked me into hospital for another colonoscopy and MRI. I ended up staying in hospital for a week while we tried to figure out what was wrong with me. I had the colonoscopy done and once again nothing showed up and nothing showed up on my MRI either. I was so frustrated when nothing showed up, I didn’t want ulcerative colitis but I also didn’t want to not have an answer. I was tired of seeing doctors and getting told there was nothing wrong with me when I KNEW there was something wrong with me. I got discharged from hospital and went back to see Bob. He told me that he didn’t know what was wrong with me and then sent me home and told me that I had to do a bowel flush out every month. If you’ve ever had to do a bowel flush out to get ready for a colonoscopy or just because like me, then you know how disgusting it is. I mixed it with apple juice and now I can’t drink apple juice, I also used a certain glass for the flush out liquid and now I can’t even drink from that glass because it reminds me of the flush out and how disgusting is. Yuuuck.
So I did that and it didn’t help with the symptoms at all so I went back and he told me to try this medication which I did and it didn’t help at all; it made me feel really sick. Sent me back home. I went back to Bob a few months later and he said that I should do a gastric emptying study. So I did that test and… FINALLY an answer! My stomach empties 1.5 to 2 hours slower than the normal stomach. I asked him if it was gastropareis as I had been doing my research and he said yes. So there you go, after 3 years I finally got diagnosed with a rare and horrible disease called gastroparesis. Bob hasn’t told me anything about it so I’ve had to learn what I can on the internet and through Facebook groups. He also said that I need to see a pelvic physio who I’ve been seeing and has given my exercises to help me relax my pelvic floor and to help my bowel motions come out a bit easer and for other stuff…¬†

Bob put me on a new medications and it has really helped. I can now eat most meals without getting double over stomach aches and horrible nausea. The medication doesn’t work all the time so I still get the stomach aches and nausea but it’s not every meal I eat. I’m still bloated all the time and look pregnant which really gets me down. I pretend with mum to have maternity shoots and pose in funny positions because it’s easier to laugh about the way I look than to remember and think about the fact that I’m 18 and look pregnant even though I’m not and that I will always look pregnant and be bloated. Since Iv’e lost weight the bloating has become a bit smaller so I’m hoping that the more weight I lose the smaller the bloating will get. But that’s another thing, gastroparesis can cause either weight loss or weight gain and I suffer from the weight gain aspect of it so it is so ridiculously hard to lose the weight that I’ve gained. It takes me months just to lose 500 grams and that’s with walking every day. I also eat pretty well. I’m vegan and gluten free and I don’t eat much junk food at all. It’s so discouraging and annoying to try so hard and to not see results.¬†

Since Bob hasn’t told me anything about gastroparesis and I’ve had to google it, I’ve come across some scary facts about it. I never knew it was such a serious illness! People die from it and it’s scary. I’m not saying that I’m going to die from it but I am worried that I will get worse and I’ll end up with a feeding tube in hospital not being able to eat or drink… Gastroparesis is scary and I’m scared.¬†

So, here I am! Finally got my stomach issues diagnosed along with my chronic fatigue. Now I just have to get my fibromyalgia verifed and diagnosed. 

Keep safe,
Maddy xoxo 

Follow me on twitter if you’d like xx

PS- I got a puppy! Her name is Asher and I’m going to train her to be a therapy dog and get her certified so she can go everywhere with me and support me out there in the scary anxiety inducing world!¬†

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Chronic health condition, Family, Mother and daughter, Uncategorized

A Letter To My Mumma Bear

 

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Dear Mum,

You are the most amazing person and mother I will ever meet. You inspire me to be a better person every day and to keep going, you are my rock for staying here and I yours. Your strength amazes me. You’ve been through so much in your life and the fact that you are still alive, especially after Chase is astonishing. 
Teachers at school used to ask us who our role model was or who’s a person that we look up to and my answer to those questions every time was you, and it still is. You truly are my role model and if I end up half as good as you I will be happy. 

You are the most amazing mum even though you don’t think so sometimes. For the past 4 years I have definitely not made your life any easier between my stints in the psych ward and all my heath issues you have stuck by me and given me the power to keep going. If I didn’t have you in my life I would be lost and most likely dead. You are my everything and I am so thankful that you haven’t given up on yourself, me and us. Thank you for loving me like you do and being not only my mum but my best friend and sister. I honestly couldn’t ask for a better mum, best friend and sister. You are my family. Me and you, just us two remember.

Here are a few words I would use to describe you:
Kind
Compassionate
Loyal 
Trustworthy 
Generous 
Loving
Funny
Strong
A survivor 
Spiritual 
Courageous 
Considerate 
Empathetic 
Sympathetic 
Intuitive 
Passionate 
Reliable 
Witty
Amazing
Angelic 
A role model 
Beautiful 
Brilliant 
Inspiring 
And there’s more but my brain isn’t working and I’ve gone a bit blank… sorry about that! 

You really are all those things I mentioned above, you’re pretty freaking amazing.
I’m sorry your life has been so hard and you have never really had a break from all your stresses, but the fact that you’re still living after everything you’ve been through really does amaze me. If I was you I would’ve died a loooong time ago.

Thank you for keeping me safe from Rohan and Michael. I know that you feel as though you could have done more about Michael sometimes but the truth is, is that you couldn’t! You did everything you could to prevent Michael from becoming worse and making Chase and Dusty suffer more also. I do not and never will resent you or blame you for what Michael’s done. You stood up for me and helped me get though the abuse the Michael did caused and you were always there for me, I’m just so sorry that you had to go through that for so long and suffer the way you did. It broke my heart to see you so depressed and sad while with him. I wish that I could’ve done more to help. 

I’m so so sorry that you lost Chase, I can’t even begin to imagine how that must feel. I’m so sorry you lost your soul mate and twin flame. So many times I wish I could trade places with Chase so you would have him back and live a life with him. I just hope I’ve been a helpful support to you and helped you through your grief a little bit. As much as the thought of you dying kills me, I’m looking forward to you finally being free and being able to be with Chase again forever. It must be so hard to have to stay here for me and Dusty when you just want to be with Chase and that is totally understandable, if I was you I’d feel the same. 

You and I have been through so much between your health conditions, my health conditions, Chase, Michael and everything else in-between you have stayed strong and kept going. I will always love you with all that I am and I will always be there for you. It’s going to be a sad and hard day for me when I move out and we won’t see each other everyday.

All I really want to say is thank you and I love you. Just thank you so much for everything that you’ve done. You are the most amazing and inspiring woman I will ever meet and you truly do inspire me everyday to be a better person and to keep going. 

I love you so much Mum and I will always fist you and tips you (this is a private joke and in no way entails what it sounds like ūüėČ )

Keep going Mum, I know you can do this and I will always be there beside you to help you and push you to keep going. 

All the love in the entire solar system and more,
your daughter Maddy. xoxo 

 

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