posts in
health
CARROT HUMMUS | R E C I P E
7/04/2019
My husband's aunt recently offered us some carrot hummus during a visit and it was overly delicious. We instantly asked for the recipe and have made it multiple times since. I adore hummus with a side of some pita chips and veggies, both as a snack and a meal. So I thought in the case of you having similar taste, I'd share the recipe. Thank you to Debbie for sharing with us, and thus me with you.
I N G R E D I E N T S
- 1 lbs boiled carrots (I use an average bag)
- 2 tsp harrisa paste
- 2 tsp white wine vinegar (or apple cider vinegar)
- 2 cloves of garlic, minced
- 2 tsp honey (could substitute to make vegan)
- 1 tsp ground cumin
- 1 tbsp extra virgin olive oil
- Pinch of kosher salt (to taste)
P R E P
Peel and boil your carrots until fork tender.
M E T HO D
Add all your ingredients to a blender, and blend to your desired texture.*
S T O R E T I M E
Keep refrigerated for up to 4 days.
*Alternatively you could use a hand masher and mix well with a fork.
P I T A CH I P S
I N G R E D I E N T S
Preheat your oven to Gas Mark 5/350°F.
M E T H O D
Spread your triangles evenly on a baking tray, bake for 10 minutes, turning the chips after 5 minutes.
P I T A CH I P S
I N G R E D I E N T S
- 1 wholewheat pita bread per person, cut into triangles
- Pinch of kosher salt
Preheat your oven to Gas Mark 5/350°F.
M E T H O D
Spread your triangles evenly on a baking tray, bake for 10 minutes, turning the chips after 5 minutes.
This is so long overdue that it's almost laughable. I haven't really written anything personal on my blog for over a year, maybe even longer. Part of that was due to my break from anything social media, which sadly goes hand-in-hand with blogging. I wrote up my To All The Social Medias I've Loved Before post, but that was written down in physical form long before I even thought of posting it on here. It's been an internal struggle for me to decide whether I even wanted to continue with this part of the Internet, purely because my love for the interacting part of the blogging world went away. I wanted to hide, and posting seemed nonsensical if I wasn't willing to socialise for it. But I'm trying to rediscover my passion for this one thing that is purely mine in my world (this blog), so.. hi, again. And let's catch up. (I'm choosing to sip on some wine during this one-sided ramble but please, order whatever drink you want, it's on me.)
The last time I properly checked in, me and my long distance boyfriend got engaged. Yay, that would totally last, right? Ha! Jokes on anyone that thought otherwise, we're now married and I have, in theory, moved to California while we go through the dreary process that is immigration. *Insert in Chandler Bing voice* Could we of chosen a more better time to do this? Well.. probably, but it's seemingly going smoothly so far. Want me to summarise how we got here? Oh, okay. Promise to try and do it in as little words as possible.
I came for another 3 month visit back in January of 2018, and after a few appointments with various lawyers to discuss our options, we decided to do the one that was me outstaying my visa and getting married before we even applied for a green card. Sounds highly illegal, I know, but it's actually quite a common method of doing this whole immigration process and one of the more faster ways that didn't require me being either unable to see my better half or my mother for too long a period. Well, that was initially the case but as it's now been close to a year since we married and only received the letter regarding my final interview a few weeks ago. The government, am I right? Nevertheless, we're getting there and I'm as excited as I am nervous. I'm desperate to go home and see my family, and yet I am equally happy in the little life me and my husband have created. This is single-handedly the most selfish thing I have done in my life, but I think it was the best decision given the circumstances.
Since getting married we have moved into our own space that is purely thanks to his family, people I will never be more thankful for knowing. He was off work to a work injury for close to a year, which really helped in our life building. And you know, as cliche as it may sound, it was really good for us. We spent almost an entire year in each others company, rarely doing anything apart, and it didn't affect us negatively in any way. We still missed each other after he'd go out for a few hours, and we found new things to do with each other that wasn't just watching TV or going out for day trips. I think it helped us see how a future would be, and that really did aid in our decision making process. The beginning of our relationship was defined by the small chunks of the year that we got to physically be together, and it made us crave these days we now probably take for granted.. the days of chores, household duties, and just doing simple things like reading. My point being.. I think we're now just your average couple and I probably can't call us a LDR anymore. What a wonderful thing to write.
Now time for the most important part of this entire post.. We adopted two kittens! Right? That's what you were waiting for. My main little kitty Bruno is still in the UK living with my mum, and though I hope it's still a decision we need to make one day, he is now probably better undisturbed. I miss him like a chunk of my heart has been ripped out, but it is what it is and he's doing okay. That's all that matters. The kittens have helped, but they'll never take up his place.
About them.. They're siblings, a girl and a boy. And both are as bonkers as each other. They were roughly 8-12 weeks old when we brought them home, and now they're nearing 11 months. We adopted them from the Santa Cruz Animal Centre which I highly recommend if you're in the area and looking to adopt. The volunteers there were all so friendly and helpful. The girl cat, Lea (she's the less fluffy one) is a little rascal who demands attention like it's going out of kitty style. Dresden (the fluffy one) on the other hand, only really likes attention if it involves giving him loves or food. He definitely found it the hardest to adjust when we brought him home, but looking to his sister helped and now we rarely get any room on the bed thanks to his space hogging. He also thinks it's okay to take snacks out of my hand as I'm eating them. Safe to say, he's no longer nervous around us. They're happy and we're honoured to be their parents.
Health wise, I've been doing okay. Fibromyalgia will always be something that dominates aspects of my life, but I'm learning to manage it better. I've definitely gained perspective on the theory that getting a better handle on ones mental health will aid in coping with physical pain, and that's something I'm grateful for. It's all a journey, but one I'm starting to not hate myself for having to go on.
Writing it all down like this makes me realise just how much my life has changed during the past 12 months. It's crazy, but wonderful. I'm thinking of doing a series going through the entire immigration process once we've finished surviving experiencing ours, so do let me know if that would be something that'd interest you. And of course, expect a post all about the cats because I'm Anne and Cat Lady syndrome is my life description.
Do let me know what you were drinking!
PS: I started a Book Instagram account, to hopefully aid in rediscovering my love for social media. Want to interact on there? Give me a follow and let's chat >> @BranchingPages
We can always afford to add more veggies into our diets, they fuel our body with goodness and often lead to us feeling a little better about ourselves. I think we're all guilty of eating a salad and suddenly feeling like you could compete for America's Next Top Model. Because... logic. These are some easy ways I've found to up my veggie intake. Warning: I may or may not have titled each paragraph with a 'song title'. I create my own amusement.
Cold As Ice
Frozen vegetables. They aren't the best, but they're a super easy and affordable way to add extra veg to your dishes and they help bulk out a meal which in the long run helps out with expenses. I always add frozen corn to fried rice and Shepard's Pie, even if we're having a veggie side. Same with Spaghetti Bologonase, it may not seem logical to find some carrot pieces in your tomato sauce, but it actually doesn't really taste of much and as mentioned above, bulks it out for a low cost.
Blanche It Real Good
If you personally find frozen veggies to hold too much water and make your dishes get sloppy, do what I do and pour out the portion you want into a bowl. Add hot water, strain, and voila. It doesn't seem like it'd do anything spectacular, but I've noticed it does make a huge difference in it's issue of retaining water. I haven't had to drain out unwanted liquid from my pan since doing this.
How To Save A Veggie
If you're a person who hates wasting food so is reluctant to buy fresh produce in fear of it going bad too quickly, look no further than your freezer. Grab yourself one of those large food bags, chop up your soiling veggies and store for emergency meals. The same goes for fruit, freeze and either use for smoothies or simply pop some hot water over the pieces and it'll almost be a self-made fruit salad. (Side-note: As a child did you ever actually like those cheap cans of fruit salad that would act as dessert after a Sunday roast? I only wanted it because of the cherries and the whipped cream my Grandma would insist on topping it with.)
Don't Stop Blendin'
Cold As Ice
Frozen vegetables. They aren't the best, but they're a super easy and affordable way to add extra veg to your dishes and they help bulk out a meal which in the long run helps out with expenses. I always add frozen corn to fried rice and Shepard's Pie, even if we're having a veggie side. Same with Spaghetti Bologonase, it may not seem logical to find some carrot pieces in your tomato sauce, but it actually doesn't really taste of much and as mentioned above, bulks it out for a low cost.
Blanche It Real Good
If you personally find frozen veggies to hold too much water and make your dishes get sloppy, do what I do and pour out the portion you want into a bowl. Add hot water, strain, and voila. It doesn't seem like it'd do anything spectacular, but I've noticed it does make a huge difference in it's issue of retaining water. I haven't had to drain out unwanted liquid from my pan since doing this.
How To Save A Veggie
If you're a person who hates wasting food so is reluctant to buy fresh produce in fear of it going bad too quickly, look no further than your freezer. Grab yourself one of those large food bags, chop up your soiling veggies and store for emergency meals. The same goes for fruit, freeze and either use for smoothies or simply pop some hot water over the pieces and it'll almost be a self-made fruit salad. (Side-note: As a child did you ever actually like those cheap cans of fruit salad that would act as dessert after a Sunday roast? I only wanted it because of the cherries and the whipped cream my Grandma would insist on topping it with.)
All You Need Is Variety
Variety is key when trying to eat a lot of veg. Things like broccoli have a very vivid taste and it can get tiring especially if you don't especially love the taste. Maybe decide to try one new vegetable a fortnight, or just keep rotating at least three to keep your plate interesting.
Variety is key when trying to eat a lot of veg. Things like broccoli have a very vivid taste and it can get tiring especially if you don't especially love the taste. Maybe decide to try one new vegetable a fortnight, or just keep rotating at least three to keep your plate interesting.
Don't Stop Blendin'
Soup is the key to packing a ton of veggies in one dish without you feeling like a rabbit when you sit down for your dinner. There are a million different soup recipes online, so get googling and you're bound to discover one that peeks your interest. My personal favourite is a Veggie and Cannellini Bean soup, click HERE to find the recipe.
Just Can't Get Enough
It's obvious, I know, but making sure that you have at least one vegetable with every meal is a really easy way to introduce more produce into your diet. Of course, if you prefer to have something sweet for breakfast, this won't apply. But I'm personally a fan of having a bagel with either cream cheese or avocado, and I try to load it up with either spinach or some other green. You'd throw some spinach into eggs without a second thought to kick off your day, so why not on a bagel?
Just Can't Get Enough
It's obvious, I know, but making sure that you have at least one vegetable with every meal is a really easy way to introduce more produce into your diet. Of course, if you prefer to have something sweet for breakfast, this won't apply. But I'm personally a fan of having a bagel with either cream cheese or avocado, and I try to load it up with either spinach or some other green. You'd throw some spinach into eggs without a second thought to kick off your day, so why not on a bagel?
What are some ways you include vegetables into your diet? Let me know!
Since I was 16 years old and officially got my diagnosis of Fibromyalgia, I knew that getting a placement in the pain clinic was on the cards for me. It was mentioned at every appointment and we constantly hoped the waiting list would hurry up. Nevertheless, when I received the appointment letter through the post I resembled any startled cat GIF on the Internet. I was absolutely terrified as I didn't know what the expect. I don't do well with mysteries. I'm a girl of facts and I like to know exactly what is going on around me. (Maybe I'm a little bit of a control freak. But let's keep that between us, okay?) I'll be honest, I was so anxious about the unknown that I almost backed out of going. How silly is that? My own worries were trying to get in the way of my health. Turns out, I was stressed about nothing. If you're like me, I'd like to give you piece of mind by going through the steps with you so you know what to expect on the first day of class.
I have fibromyalgia. If you're a regular reader, found me through #MentalMovement or know me personally, you may know this. If you're new and simply stumbled across my blog due to this post being published (first hi, welcome, take a seat. Coffee? Tea? OJ? Hug?) you can read my story HERE. If you're just another suffer of an invisible illness and hope to find clarity in the way of someone else understanding the words that frustrate you, I hope to do you justice. If you're someone who knows somebody with an invisible illness and want a better understanding of the right things to say, fair play to you for giving it the thought. We all too often throw around words, assuming that they're fly away comments and will be forgotten. But here's the thing, when you're stuck in bed or resting for a good portion of your current life, you have the time to over analyse every word that was said to you - because when most of your day is filled with silence, those words matter.When loved ones cease to amaze you with their thoughtless words, it grows to be a root of sadness inside of your heart. It's a sad truth. To you, your words may seem caring enough, but to us it can be extremely frustrating to repeatedly hear things that feel like a stab to the heart.
Here is my list of throwaway sentences that I've heard all too many times.
"You're looking better."
Guess what? Invisible illnesses are invisible, shock horror, right? When you say that to us, we feel unable to disagree with you. You're backing us into a corner and we have no other option than to go along with it - true or not. If we disagree and say "Actually I still feel like death." we're going to feel moany and like we're crying out for attention. Instead, why not ask "Are you feeling any better?"? Chances are, we aren't, but it gives us the freedom to answer with what we want to.
"Whats wrong?"
If we tell you that we're in pain, don't ask stupid questions like this. I mean, really? Widespread pain is simply that. Widespread pain. We can't pinpoint exactly whats wrong as it's all consuming. It's taking over our entire body and you have to understand that words cannot accurately describe the pain. Our body barely understands it and that is why it sometimes shuts down.
"This'll help you."
We've all seen the articles offering a miracle cure to our illnesses. No matter what you have, chronic or not, adverts and online forums are packed with things that will help you. They're "guaranteed" after all. No. It's horse crap. And over time, we learn to take everything we read/see with a pinch of salt. But when our loved ones come to us, adamant that their particular "miracle" will work, it's a harder pill to swallow. On one hand, it's incredibly sweet that you're looking into things that may help us. The thought is wonderful. But don't say things like a statement, and learn to not believe them yourself. If something seems plausible, don't state it as a fact to us, instead simply say "Do you think this might help you in anyway?" Let us decide, and don't make us feel bad if we're not as fast to jump on the hope train. We've been let down multiple times in the past and it's near impossible to think that there is a light down these dark tunnels. (There normally is, but it takes time. It's all dependant on the person and where they are on their journey.)
"Can I do anything to help?"
This is a kind question, of course it is. But we're going to say no. Unless we're really open with our needs and aren't mortified at having to constantly ask for help, we're going to decline because we don't want to be a nuisance. That's one of our greatest fears, after all. Isn't it everyone's? This isn't so much the question, but the wording. Try "What can I do to help?" instead. There's still a 75% chance we're going to say "Nothing, but thank you.", but it's an open ended question. It feels kinder. Sounds illogical, but it's true.
"I wish I could sleep that long."
I'm sorry, but seriously? This one grinds my gears. We're sleeping because our body literally gave up on us for an unreasonable amount of hours. We're constantly exhausted because we're in pain. And you're trying to make us feel lucky for being stuck in bed, most likely in the fetal position, wishing for just a second of normality? We all lead different paths in this life, and I understand that people are tired and sore after a day of hard graft at work. I tip my hat to you, it's respectable. But.. we as people with invisible illnesses do not choose to be unwell. We don't want to spend days on end - sometimes weeks - stuck in the house, our four walls feeling more and more like a prison.
A Notable Mention: Lastly, unless you're in a large amount of pain - I'm talking the kind that makes it hard for you to do anything that one would class as "easy" - please don't drone on and on about how sore you are after you merely slept funny. This is probably a taboo thing to say, but we hate it. We hate to hear you groan and moan about a little stiff arm or a headache caused by your choice to stay up until stupid o'clock in the morning when we can lead the most healthiest of lifestyles and still find it tremendously difficult to stand up without support. Whats more annoying? When you moan that you're in pain but say "nah" to doing things that could help. Do you realise how much we wish that we could have something that'd ease our pain? You're lucky. I'm sorry that you have to feel a smidge of pain, but you're lucky to be able to heat up a hot water bottle/heat pack, have a hot bath, a massage, or pop a simple aspirin and get relief. If you don't want to do any of those things, you aren't in proper pain. Talk to us, of course, we're your loved ones. But think about your words. Please.
- Anne x
Fibromyalgia || My Story
5/21/2016
Fibromyalgia is found under the category of "invisible illnesses". It's something that sounds made-up when you list the symptoms, as it seems unlikely that so many things can affect one human being without driving them insane. I was officially diagnosed at 16, but had been to countless appointments about my odd variety of complaints since I was 12. Three years I have "officially" had this illness and the doctors have offered therapy, physiotherapy, hydrotherapy, pain clinics, short term medications.. but they can't offer a long term solution. They can instead only offer temporary band aids to cover the parts that are screaming at that particular moment in time. Barring the pain clinic - which I'll be starting at the beginning of next month, I have done them all. So far, nothing has helped or offered relief.
Like most illnesses, each individual's symptoms differ. Mine include widespread pain after what my body classes as strenuous activity (grocery shopping, walking the dog, cleaning my bedroom, sleeping too long), inflammation of the joints, joint stiffness, skin sensitivity, insomnia, migraines, fatigue, nausea, loss of eye-sight, muscle spasms, bruising, inability to concentrate, and low blood pressure. Sounds made up, right? You can't see it show up on any medical chart, nor can you get a 100% accurate diagnosis from blood work. It's instead like a game of Tetris. All the symptoms acting as the colourful blocks until ding, ding, ding you've reached the top and are officially a Fibro victim. Much like the game, reaching the top means you lost. That's a terrible analogy and I'm pretty sure there aren't any dings in Tetris, but I hope you see what I meant.
Fibromyalgia is supposedly triggered by some life changing tragic event - whether on your body or in your life. I wouldn't say I have had either so I cannot relate to that, but know of many who have connected an event to their diagnosis. I simply began to experience abnormal pains at a young age.
I haven't found a magical cure yet, nor have I found anything that really soothes the pain. My mother continues to push a hot water bottle at me when my back is aching, but it doesn't help. Just makes me sweaty. It's rather bitter-sweet - family and friends. I spent the first half of today, or rather, yesterday, running a temperature in my bed with a banging headache, sick at the back of my throat, and pain shooting up and down my spine. I took some painkillers and lay there for 2 hours until eventually drifting back off. My mother was in the next room and my boyfriend was a phone call away, but I didn't see the point in telling anyone. They can't do anything and in honesty, I'm sick of telling people what hurts when I'm unable to show them evidence of it. I sometimes wish there was a thick gash on my arm with blood pooling around my bed, as I would then feel better in going "Hey, hi, yeah. I'm in pain here. Mind keeping me company until it stops?" It isn't even a matter of feeling as though I'm burdening them, or feeling like they don't care. As neither of those are true. It's simply a matter of feeling as though it would be pointless. A waste of breath when I can lay there and wait for it to ease all by myself.
As you may of seen from my previous (and future, it's coming, I promise) Scotland post, I went on a little vacation with my partner. And my body didn't react well to it at all. I spent one night in Edinburgh literally shaking for a solid 3 hours - making me wish I was spineless in the process, and unable to stand without falling right back down. It was the first time this illness has terrified me. When I could barely muster the strength to grip the edge of the bed to pull myself up, and to then experience the sensation of my knees and ankles giving out from under me.. It was indescribable. I'm a 19 year old girl and my joints felt as though they were those of a 90 year old. My partner had to help me to the bathroom (which he thankfully doesn't remember. Let's all take a moment of gratitude for sleepy brains.), and I spilt water down my front as I couldn't hold the glass steady enough to bring it to my lips. The following day I felt as though I was hit by a bus. We took it easy and did a small walk down the town, which was torture. Every breath hurt like hell, my sides and back felt as though they were covered in dark ugly bruises. The pain was close to unbearable. I fell asleep at 07:30pm. I'm a young adult, I was in a city I had never been to, and I was fast asleep by 8pm because my body didn't have the strength to hold it together for a couple more hours. I was ashamed of my health, and still am.
There is no direction for this post, nor is there a reason for my writing it. It's 06:19am and I'm at a loss. I've spent half the night worrying over the future - my future. My back is throbbing like it has been for the past few days, and my leg continues to give me a good ol' sharp pain when I straighten it, all because I was stupid and did some yoga as a Instagram post made me feel like crap for not working out. (Social Media is a wonderful thing, but acts as the devil for anyone who is either lonely or stuck in the house.)
I'm, ironically, a carer for my mum. I don't study as I haven't the funds for online education, and my health wouldn't handle going to an actual college. I can't get a part-time job due to Fibro. I'm uncertain as to whether I can will myself to have children, knowing that they may inherit this and/or the Porphyria gene - the kidney disease that is the reason behind my being a carer. As mentioned above, I volunteer when I can but that is becoming increasingly less due to the pain. I write for fun, but struggle as my wrists begin to ache and creak. It feels like every good thing has a flip side - that side constantly being pain.
I take Circadin to help me sleep, Dihydrocodeine on the bad days, Cyclizine for the nausea, Ibroprofen in hopes that they might miraculously help, and something for the inflammation (which also doubles as a stronger painkiller when mixed with Ibroprofen), but I can't find the box and haven't the faintest chance of knowing what they're called. I've tried the bath salts, oils, gels, creams, but alas, I sit here today with no recommendations to you on what could help anyone who is going through this. I'd like to say I've come to terms with that, but I haven't, I still have those days where it gets a little too much. I'm a part of this lovely little community on Facebook that was made for people with these types of illnesses and although I act more as a bystander and watch/read what others have to say without contributing much - I find it interesting how most are upset by their stories (though I entirely understand why). I'm more fearful. Of what I'll be feeling in another 5 years time, - how I'll cope. I can't concentrate on the now as I fear I'll implode at the situation I'm in.
People look at me with disgust when they see my Grandma carrying two shopping bags and my hands are empty. People expect me to able to lift boxes or move things as I'm "a strong young woman". People don't understand and I can't expect them to, as I barely understand myself - both theoretically and literally speaking. It's consuming but sometimes too easy to forget. It's my life but isn't what should dominate it. I struggle to find a balance, and I imagine many who walk in similar shoes will understand that. You can't allow an illness to control you, but it's difficult to follow that rule when every move you make in life will trigger said illness. Mind boggling.
I'm just a girl and the world I have at my feet is seeming smaller by the day. I have it better than most, I don't doubt that and I'm thankful for the life I have been given, even during the bad days. My life will be okay, no matter where it leads. I'll aim for great but am willing to settle for okay. The bad days pass, whether after 24 hours or a longer period of time. We all find our good days again. Much like a storm, you just have to wait somewhere safe until it passes. Thankfully I'm also the type of person who finds rain beautiful.
- Anne x
#MentalMovement
3/18/2016
"When we deny the story, it define us.
When we own the story, we can write a brave new ending."
My debut post was released today into the big wide world of the Internet, but that isn't necessarily why I wanted to quickly write up this post (although it is somewhat of a shameless plug). The platform #MentalMovement hopes to tarnish the stigma around mental health and hope to offer a safe haven for those of us who are finding it hard to wake up in the morning and are crippled with the fear that we're going through our battles alone.
It's a varied site with something that could help each and every single one of you, so I'd truly appreciate it if you went over there and gave it a look through. The writers are all incredible humans who have first hand experience in the topics they discuss, which I'd personally find comforting as a reader. They know what they're talking about, and they will not make you feel silly or inadequate for having problems that aren't what class as "visible". They will help you.
Use your Internet time to make your heart lay softer.
Here are the links to everything surrounding the site:
And lastly, my post:
We are living in the age of the Internet - where it is possible to connect with someone halfway around the world by typing a few words. There is no longer any reason why someone should go through a mental illness alone.
- Anne x
Living With Body Dysmorphia : My Story.
1/18/2016
I've wanted to write this post since I made this blog over a year ago. I wanted to use whatever platform I have for good. I wanted to help at least one person who might be going through something vaguely similar to me. I wanted.. I wanted a lot. Turns out, it isn't always that easy. I found myself constantly putting this post off by finding something else to write about, procrastinating until I "didn't have the time", but no more. This was a resolution, and I stick to those things. This will be a long one, and I apologize if you aren't the least bit interested in reading about me and my life. I'm not sure whether there is even a point to this post just yet, but I know I need to write it and that ought to be enough. Perhaps we'll figure it out together. Grab a tea (Or coffee. Go with coffee.), and I hope you make sense of my rambles.
According to the NHS website, Body Dysmorphic Disorder (also known as BDD) affects 1 in every 100 people in the UK alone. It's an anxiety based condition, and my own likely stemmed from social anxiety and a low period in my teenage years. Now, I'm not a doctor nor am I trained in the medical field. I can just about put a plaster on a cut. So how much insight I can offer into the condition itself is based solely on my own experience. I have yet to seek medical help, although I did have a batch of therapy late last Autumn that was initially meant for discussing my health but happened to stumble onto this topic a whole bunch. Turns out, I kind of suck at discussing things that affect me to strangers. Or friends. Or the boyfriend. My issue is, I feel like I will annoy them by burdening them with such information, which is beyond idiotic as I'd likely be offended if they felt they couldn't come to me with their own worries or problems. Anne's brain, ladies and folks.
For this to make an ounce of sense, we'll have to start at the beginning. I had just turned 12 when I started to dislike my appearance. I would look in the mirror and hate the girl staring back at me, I often still do that. You can't say I'm not a young lady of habit, heh. Yes, I mask my awkwardness with humour. I was chubbier than most girls my age back then, due to various reasons that really don't matter in this blog post. One could argue that it was just that stage of chubbiness that most girls go through,, hormones and physical changes playing a big part in it. I was a young developer. I had lumps of fat on my chest before anyone I knew, and my hips swelled outward. It was just a part of growing up, but I couldn't see past my own reflection to realise that. Or listen to what my mother was yammering on in my ear.
The following year was what I'd call my turning point. For the better? Probably not. But it was the year that moulded me into the person I am today. Home life changed a whole lot and because of that I gained a hefty amount of free time, which I chose to use by becoming obsessed with that reflection I keep referring to. I became aware of what a calorie was, and discovered the likes of Wii Fit and stomach crunches. I lost just under 2 stone in a matter of months. It was unhealthy and I don't want to properly delve into what I put my body through as I don't want to give impressionable readers any ridiculous ideas (you never know with the Internet.), but it was an obsession. I've already used that term to describe the situation and I usually hate repeating myself, but there isn't another word that does it justice. My work outs went from 30 minutes to over 7 hours. I would find myself pulling an all nighter to continue working out when the other people in the household were asleep. I pushed myself above and beyond, all while restricting myself to a mere third of one's usual calorie intake when on a diet. It was.. messy. I was a mess. I don't want to label myself as having an eating disorder, as I find it too big of a word to put on what I went through. So many other girls in the world have it far, far, far worse and my story isn't as important as theirs. So I don't feel like I have a right to include myself on that list, if that makes any sense. Therefore, I will just say that I was a troubled teen. I thought that being thin would result in being happy. Alas, it did not.
Because of all this, I grew up to find it ridiculously hard to eat in front of people. I found it difficult to talk about food with people I didn't know extremely well. I still do, and I still find it difficult to stop working out after 15 minutes, despite the fact that I know it will cause me a great deal of pain. Oh, yes. Fibromyalgia. I ought to probably explain that little dent in my story. It is what doctors describe as a 'chronic pain condition' that affects people in a various ways. I, myself, get widespread pain and skin sensitivity after prolonged activity or stress, followed by fatigue, migraines, and patches of insomnia. I was officially diagnosed shortly after I turned seventeen, but the signs had been there from when I was 13 years old. Yeah, the strain that I put on my body could of brought forth the condition sooner than it would have if I had not, but that is something we can never know for certain. It's just a thing. It's there and I'm still in the process of easing it. But anywho, this is besides the point.. Exercise was my escape, and I lost that the second pain became it's following act. This is undoubtedly the main reason why I have such an unhealthy relationship with food. It's my only source of control. I can't choose when to work up a sweat any more, nor can I choose where my life is leading.. But food? I can choose what goes in my mouth and I get the choice of how much gets eaten. It's terrible to write such a thing, but I can't hide from the abundant truth. I lack a sense of leadership in my own life, so my mind naturally takes advantage of it when I find some.
This is the part of the story where facts get blurred and the timeline gets muddled. All I know is, I never felt like I lost a pound in spite of those years. I'm 19 years old as I write this, and I still don't. I wake up everyday and feel embarrassed when I look into that shiny thing we call a mirror. That may be too honest, but that's the point of writing this. Honesty. I often feel sickened when I'm getting dressed and I can feel the skin of my body being tugged and squishing together, when I walk and can feel the way my thighs and stomach wobble and I'm adamant others can see it through the layers that I'm wearing. It hit me the hardest around a week ago, when I was shopping for clothes and tried on three items that were all a size 8 (that's an American size 4 and a European size 36, just FYI), and they were all loose on me, to the point of being unwearable. Loose. A size 8. I didn't and still don't understand. When I looked into that changing room mirror, my body looked at least three sizes larger than that. Not that there is anything wrong with that size, or any size for that matter, so please don't take my words the wrong way. It's just a difficult one to explain. It's hard to voice your thoughts when you never have done before. When I was that 12 year old girl, I envisioned myself being a certain size and being happy because of it, that I would feel confident in my skin if I were what society classes as "small". But I'm not. I can't see it and keep making excuses as to why a shop would make those size 8's in my size. Bad manufacturing, perhaps. And the second store's clothing was meant to be real baggy, that's why it was a little big on me. My brain constantly does this and perhaps because of these pathetic excuses, I can't see what ought to be right in front of me.
I'm now truly scared that I will never feel comfortable in my own skin.
Christ almighty, that was a tough sentence to write. I would normally distract from it with a photo of a cat, but that wouldn't be very professional given the nature of this post.
It may seem silly to some of you that a lack of confidence could be such a burden on someone's daily life. It may even seem conceded. I might agree if this was just about me, but it isn't. There are so many people outside of my story who suffer a great deal with BDD, and I would hate for them to feel big-headed for simply being unhappy. BDD is real and I'm slightly proud of myself for finally seeing that - there was a time that I never thought it to be possible.
Like many conditions, there are good and bad days. Some days I feel brave enough to take a selfie, and only feel like crap for a few hours afterwards. I may even be strong enough to snap a shot of whatever I'm eating and send it to a friend. On the bad days, I don't want to get out of bed. The thought of leaving the house for work or shopping is horrendous, and all I want to do is curl in a ball and cry. Some days I can barely look in the mirror, while the next I want to stare into it every 5 minutes and point out everything that is wrong with me. I can wear a dress and feel okay in it, only to try it on a few days later and weep at the disgusting sight. Same goes for photos. That selfie I took on a good day could be hideous to me hours later, because the many flaws of my face have somehow become louder to my mind. It's waves. Waves of emotions and thoughts. You can't know how you're going to be tomorrow, let alone in a week's time. And as easy as it seems to trust a loved one's opinion on the matter, your brain argues that you can't. Your opinion is the only one that matters to you, because you're the object of argument.
My goal this year was to post more outfit related posts on this blog as fashion is a passion of mine. I adore a good tea dress and have more heels than I could possibly (or hope to) wear. I find nothing more satisfying than a good blazer, and have a major weak spot when it comes to collars. Yet I've been too chicken to post anything resembling a OOTD on here because my body wasn't "ready" yet. 5 weeks ago I posted the first photo below on my Instagram (RootingBranches, btw), and guess what? The world didn't end. Despite the fact various people could see my arms, and I was dressed as an elf (which was arguably the best part of the photo). I'm not going to lie, I've debated deleting the post every single day that it's been up - even this morning. But I didn't and haven't. Powering through, people. So to test the waters further, I uploaded another outfit photo on the 14th of this month. 4 days ago. Which is also pictured below. And guess what? The world, once again, didn't end.
The point of doing this is not to gain attention, good or bad. Or to make people pity me and do the obligatory "you look good!" comments. It's to show how average I am. I look at both of those pictures and I hate them. I see a blob that's trying to look humanly. I see chubby spots and cheeks that are three sizes too big. I see the arms that prevent me from wearing anything sleeveless in public (I hid in a cardigan for the entirety of my career as an elf), and the thighs that make me pair tights with shorts in Summer. I see a wonky boob (yeah, that's a thing. Being a girl is fun.), and wide hips. I digress, there is a point to all of this. Right now, I pledge to try and learn that this is only my interpretation of the images. You may look at them and see something completely different, for better or worse. And that is okay. It's wonderfully human.
My story is what it is. It's messy, but tidier than most people's. Some days I manage, and others I find myself struggling through. But it's me. It's my tale to tell, and you have your own. If you relate to me in the slightest, then I'm ever so sorry that you have to go through the difficulty that is BDD. It's painful and affects your daily life in a way most won't or rather, can't, understand. It's easier to say than do, but you have to learn to accept that a rare few will belittle you for feeling the way you do as they deem it ridiculous or stupid, and there will be some people who look at you strangely in the street for whatever reason. Loved ones who don't know of the battle going on it your mind might make passing thoughtless comments that hurt your feelings. They won't remember what they said in an hours time, but you will cry at night repeating it over and over in your head. It's raw and aches in that way sadness does, but you can get through it. As - this the part you need to jot down - there will also be people in this world who find you beautiful. Who desire your body, or long to have your legs (or waist, or neck, or whatever.). You may scoff just reading this, and I can't ridicule you for that as it would be ridiculous to do so when I, myself, don't believe any compliment that's thrown my way. But you have to try. Just as I am trying by writing this post. How else are we going to get through it all?
I could write more. I could of probably written less. There are still gaps in my story, but they are for another time. For now, I think I'm going to leave it here. At the end of this post I'm going to list some options for you if you want to reach out for help. But I'm not going to preach about it, as it would be awfully hypocritical of me. Just talk to someone. Professional or not. My email is rootingbranches@outlook.com and you are more than welcome to shoot a message my way. My other links are on the sidebar. Just think about it.
If you know of someone going through this, just do one thing for me.. don't brush their feeling aside as you think it's untrue and can see their beauty. To them, tit's frighteningly real. There is no worse feeling than when you pour your heart out to someone as you feel horrendous, and they reply with a simple "But you're beautiful." or "To me you're beautiful.". They won't believe you, and will be reluctant to come back to you at the risk of you thinking they're being dumb. Listen to them. Ask questions. Don't walk on egg shells. You were given a voice, use it.
Where am I going to go from here? I haven't the faintest idea. I'm going through a rough patch and that is largely due to some complications in my private life that aren't necessarily blog appropriate. It'll get better, it's bound to. I just need to wait it out. I'll silently wait to feel sane again, and meanwhile try my darn hardest to stop comparing myself to others. Or rather, stop thinking that those around me are making comparisons between myself and others. Especially the boyfriend. I'm well aware it makes me look stupid, and I'm constantly scared that I'm pushing him away by feeling the way I do about myself. If you have BDD and a partner, then you will know what I mean. If not, then I won't properly delve into my thought train on this. As I would likely come out of it looking pathetic.The second thing I aim to do is work on my relationship with food, as that isn't at it's best right now. I need to find a balance.
Perhaps I will do a follow up blog post in a couple of months, or not. Either way, thank you letting me have a blog vomit to you and I hope things get better for any fellow BDD sufferers out there.
Remember, all you have to do is try. It's enough.
According to the NHS website, Body Dysmorphic Disorder (also known as BDD) affects 1 in every 100 people in the UK alone. It's an anxiety based condition, and my own likely stemmed from social anxiety and a low period in my teenage years. Now, I'm not a doctor nor am I trained in the medical field. I can just about put a plaster on a cut. So how much insight I can offer into the condition itself is based solely on my own experience. I have yet to seek medical help, although I did have a batch of therapy late last Autumn that was initially meant for discussing my health but happened to stumble onto this topic a whole bunch. Turns out, I kind of suck at discussing things that affect me to strangers. Or friends. Or the boyfriend. My issue is, I feel like I will annoy them by burdening them with such information, which is beyond idiotic as I'd likely be offended if they felt they couldn't come to me with their own worries or problems. Anne's brain, ladies and folks.
For this to make an ounce of sense, we'll have to start at the beginning. I had just turned 12 when I started to dislike my appearance. I would look in the mirror and hate the girl staring back at me, I often still do that. You can't say I'm not a young lady of habit, heh. Yes, I mask my awkwardness with humour. I was chubbier than most girls my age back then, due to various reasons that really don't matter in this blog post. One could argue that it was just that stage of chubbiness that most girls go through,, hormones and physical changes playing a big part in it. I was a young developer. I had lumps of fat on my chest before anyone I knew, and my hips swelled outward. It was just a part of growing up, but I couldn't see past my own reflection to realise that. Or listen to what my mother was yammering on in my ear.
The following year was what I'd call my turning point. For the better? Probably not. But it was the year that moulded me into the person I am today. Home life changed a whole lot and because of that I gained a hefty amount of free time, which I chose to use by becoming obsessed with that reflection I keep referring to. I became aware of what a calorie was, and discovered the likes of Wii Fit and stomach crunches. I lost just under 2 stone in a matter of months. It was unhealthy and I don't want to properly delve into what I put my body through as I don't want to give impressionable readers any ridiculous ideas (you never know with the Internet.), but it was an obsession. I've already used that term to describe the situation and I usually hate repeating myself, but there isn't another word that does it justice. My work outs went from 30 minutes to over 7 hours. I would find myself pulling an all nighter to continue working out when the other people in the household were asleep. I pushed myself above and beyond, all while restricting myself to a mere third of one's usual calorie intake when on a diet. It was.. messy. I was a mess. I don't want to label myself as having an eating disorder, as I find it too big of a word to put on what I went through. So many other girls in the world have it far, far, far worse and my story isn't as important as theirs. So I don't feel like I have a right to include myself on that list, if that makes any sense. Therefore, I will just say that I was a troubled teen. I thought that being thin would result in being happy. Alas, it did not.
Because of all this, I grew up to find it ridiculously hard to eat in front of people. I found it difficult to talk about food with people I didn't know extremely well. I still do, and I still find it difficult to stop working out after 15 minutes, despite the fact that I know it will cause me a great deal of pain. Oh, yes. Fibromyalgia. I ought to probably explain that little dent in my story. It is what doctors describe as a 'chronic pain condition' that affects people in a various ways. I, myself, get widespread pain and skin sensitivity after prolonged activity or stress, followed by fatigue, migraines, and patches of insomnia. I was officially diagnosed shortly after I turned seventeen, but the signs had been there from when I was 13 years old. Yeah, the strain that I put on my body could of brought forth the condition sooner than it would have if I had not, but that is something we can never know for certain. It's just a thing. It's there and I'm still in the process of easing it. But anywho, this is besides the point.. Exercise was my escape, and I lost that the second pain became it's following act. This is undoubtedly the main reason why I have such an unhealthy relationship with food. It's my only source of control. I can't choose when to work up a sweat any more, nor can I choose where my life is leading.. But food? I can choose what goes in my mouth and I get the choice of how much gets eaten. It's terrible to write such a thing, but I can't hide from the abundant truth. I lack a sense of leadership in my own life, so my mind naturally takes advantage of it when I find some.
This is the part of the story where facts get blurred and the timeline gets muddled. All I know is, I never felt like I lost a pound in spite of those years. I'm 19 years old as I write this, and I still don't. I wake up everyday and feel embarrassed when I look into that shiny thing we call a mirror. That may be too honest, but that's the point of writing this. Honesty. I often feel sickened when I'm getting dressed and I can feel the skin of my body being tugged and squishing together, when I walk and can feel the way my thighs and stomach wobble and I'm adamant others can see it through the layers that I'm wearing. It hit me the hardest around a week ago, when I was shopping for clothes and tried on three items that were all a size 8 (that's an American size 4 and a European size 36, just FYI), and they were all loose on me, to the point of being unwearable. Loose. A size 8. I didn't and still don't understand. When I looked into that changing room mirror, my body looked at least three sizes larger than that. Not that there is anything wrong with that size, or any size for that matter, so please don't take my words the wrong way. It's just a difficult one to explain. It's hard to voice your thoughts when you never have done before. When I was that 12 year old girl, I envisioned myself being a certain size and being happy because of it, that I would feel confident in my skin if I were what society classes as "small". But I'm not. I can't see it and keep making excuses as to why a shop would make those size 8's in my size. Bad manufacturing, perhaps. And the second store's clothing was meant to be real baggy, that's why it was a little big on me. My brain constantly does this and perhaps because of these pathetic excuses, I can't see what ought to be right in front of me.
I'm now truly scared that I will never feel comfortable in my own skin.
Christ almighty, that was a tough sentence to write. I would normally distract from it with a photo of a cat, but that wouldn't be very professional given the nature of this post.
It may seem silly to some of you that a lack of confidence could be such a burden on someone's daily life. It may even seem conceded. I might agree if this was just about me, but it isn't. There are so many people outside of my story who suffer a great deal with BDD, and I would hate for them to feel big-headed for simply being unhappy. BDD is real and I'm slightly proud of myself for finally seeing that - there was a time that I never thought it to be possible.
Like many conditions, there are good and bad days. Some days I feel brave enough to take a selfie, and only feel like crap for a few hours afterwards. I may even be strong enough to snap a shot of whatever I'm eating and send it to a friend. On the bad days, I don't want to get out of bed. The thought of leaving the house for work or shopping is horrendous, and all I want to do is curl in a ball and cry. Some days I can barely look in the mirror, while the next I want to stare into it every 5 minutes and point out everything that is wrong with me. I can wear a dress and feel okay in it, only to try it on a few days later and weep at the disgusting sight. Same goes for photos. That selfie I took on a good day could be hideous to me hours later, because the many flaws of my face have somehow become louder to my mind. It's waves. Waves of emotions and thoughts. You can't know how you're going to be tomorrow, let alone in a week's time. And as easy as it seems to trust a loved one's opinion on the matter, your brain argues that you can't. Your opinion is the only one that matters to you, because you're the object of argument.
My goal this year was to post more outfit related posts on this blog as fashion is a passion of mine. I adore a good tea dress and have more heels than I could possibly (or hope to) wear. I find nothing more satisfying than a good blazer, and have a major weak spot when it comes to collars. Yet I've been too chicken to post anything resembling a OOTD on here because my body wasn't "ready" yet. 5 weeks ago I posted the first photo below on my Instagram (RootingBranches, btw), and guess what? The world didn't end. Despite the fact various people could see my arms, and I was dressed as an elf (which was arguably the best part of the photo). I'm not going to lie, I've debated deleting the post every single day that it's been up - even this morning. But I didn't and haven't. Powering through, people. So to test the waters further, I uploaded another outfit photo on the 14th of this month. 4 days ago. Which is also pictured below. And guess what? The world, once again, didn't end.
The point of doing this is not to gain attention, good or bad. Or to make people pity me and do the obligatory "you look good!" comments. It's to show how average I am. I look at both of those pictures and I hate them. I see a blob that's trying to look humanly. I see chubby spots and cheeks that are three sizes too big. I see the arms that prevent me from wearing anything sleeveless in public (I hid in a cardigan for the entirety of my career as an elf), and the thighs that make me pair tights with shorts in Summer. I see a wonky boob (yeah, that's a thing. Being a girl is fun.), and wide hips. I digress, there is a point to all of this. Right now, I pledge to try and learn that this is only my interpretation of the images. You may look at them and see something completely different, for better or worse. And that is okay. It's wonderfully human.
My story is what it is. It's messy, but tidier than most people's. Some days I manage, and others I find myself struggling through. But it's me. It's my tale to tell, and you have your own. If you relate to me in the slightest, then I'm ever so sorry that you have to go through the difficulty that is BDD. It's painful and affects your daily life in a way most won't or rather, can't, understand. It's easier to say than do, but you have to learn to accept that a rare few will belittle you for feeling the way you do as they deem it ridiculous or stupid, and there will be some people who look at you strangely in the street for whatever reason. Loved ones who don't know of the battle going on it your mind might make passing thoughtless comments that hurt your feelings. They won't remember what they said in an hours time, but you will cry at night repeating it over and over in your head. It's raw and aches in that way sadness does, but you can get through it. As - this the part you need to jot down - there will also be people in this world who find you beautiful. Who desire your body, or long to have your legs (or waist, or neck, or whatever.). You may scoff just reading this, and I can't ridicule you for that as it would be ridiculous to do so when I, myself, don't believe any compliment that's thrown my way. But you have to try. Just as I am trying by writing this post. How else are we going to get through it all?
I could write more. I could of probably written less. There are still gaps in my story, but they are for another time. For now, I think I'm going to leave it here. At the end of this post I'm going to list some options for you if you want to reach out for help. But I'm not going to preach about it, as it would be awfully hypocritical of me. Just talk to someone. Professional or not. My email is rootingbranches@outlook.com and you are more than welcome to shoot a message my way. My other links are on the sidebar. Just think about it.
If you know of someone going through this, just do one thing for me.. don't brush their feeling aside as you think it's untrue and can see their beauty. To them, tit's frighteningly real. There is no worse feeling than when you pour your heart out to someone as you feel horrendous, and they reply with a simple "But you're beautiful." or "To me you're beautiful.". They won't believe you, and will be reluctant to come back to you at the risk of you thinking they're being dumb. Listen to them. Ask questions. Don't walk on egg shells. You were given a voice, use it.
Where am I going to go from here? I haven't the faintest idea. I'm going through a rough patch and that is largely due to some complications in my private life that aren't necessarily blog appropriate. It'll get better, it's bound to. I just need to wait it out. I'll silently wait to feel sane again, and meanwhile try my darn hardest to stop comparing myself to others. Or rather, stop thinking that those around me are making comparisons between myself and others. Especially the boyfriend. I'm well aware it makes me look stupid, and I'm constantly scared that I'm pushing him away by feeling the way I do about myself. If you have BDD and a partner, then you will know what I mean. If not, then I won't properly delve into my thought train on this. As I would likely come out of it looking pathetic.The second thing I aim to do is work on my relationship with food, as that isn't at it's best right now. I need to find a balance.
Perhaps I will do a follow up blog post in a couple of months, or not. Either way, thank you letting me have a blog vomit to you and I hope things get better for any fellow BDD sufferers out there.
Remember, all you have to do is try. It's enough.
- Anne x
Anxiety UK - Helpline: 08444 775 774
Email: support@anixietyuk.org.uk
Mind - Information line: 0300 123 3393
Email: info@mind.org.uk
Subscribe to:
Posts (Atom)












Socials