Part 5 – What I wish you knew…

“Brain Injury is misunderstood by many people. You don’t just ‘get over’ Brain Injury. It affects your whole life, your relationships, who you are as a person. Nothing is the same anymore. Brain Injury is a lifelong battle with very good days and very bad days. If you know someone living with a Brain Injury, be patient and compassionate. They need your support more than you know. Especially on those very bad days. Be kind.

-Traumatic Brain Injury Support Group

This blog post could go on for so long, and I could bore you all to tears with how much I wish you knew.

When you tell me “You look great”, I wish you could see how messed up and disjointed I feel on the inside, or the fact I probably just had about 5 hot flushes before you saw me. I wish people saw me at 3am when I wake up with chronic pain in my head and my jaw, or that I desperately need to ice and heat bag my neck at least twice a day to be able to get through. I wish people saw me five minutes before my carefully planned and timed appropriate shower verses 5 minutes after I’ve been stripped of all the energy I had left in me, or when people say “You’re so strong and have such a positive outlook”, I wish you saw every single one of my breakdowns where I tell myself I’m done.

But then I think to myself, the only reason why I’d want anyone to see all those parts of my recovery would be because I feel like I have to somehow justify or validate how I’m feeling and my diagnosis to some people, and why the hell do I feel like that?!? Why do we all get so caught up in worrying and wondering about what other people think, and why on earth, in the position that I’m in, am I making myself feel this way?

I just want to say, both to myself and to some people that may be reading this, to go back and compare my blog to how I might present myself in person or photos….

My injury is real, my feelings are real, my symptoms and limitations are real, and most of these experiences and setbacks happen behind closed doors. I know my body, I know what I can do, I know what I can’t do, and I also know that activities on both of those lists can swap and change very easily depending on the day I’m having. The only person that I’m going to worry about when I think about how my body will react to different settings and tasks from now on, is me, and I am sooo okay with that! I’m okay with that, because I know that the people closest to me make an effort to understand as much as they can, and would never judge any of my decisions throughout this whole process. Every decision I make is carefully planned down to the very last detail, for me.

So that’s enough of what I wish people knew! Because in all honesty, I believe that the people truly interested will ask questions, and I will be100% honest and open with every single question people have for me. The rest of this post I want to talk about how people can support not only me, but others living with a Brain Injury. I have been so lucky to belong to a supportive group of individuals across the world living with all forms of Brain Injury, and I asked them all this question….

“What would you like people to know about how to best support you?”

And this is what they said…..

From our perspective….

“I’ve found a big thing for others to try to understand is that they need to be patient. As do we, for our brains to heal, and for us to learn how to work with our new brains.”

“Educate yourself about what is happening if you don’t understand. Talk to people, join a group, google. Or fake it, even if you don’t believe the person or you’re frustrated, just make me feel like you believe I’m not going crazy.”

 “I would say to support a TBI survivor, accept them how they are now and don’t expect them to be their old self. The TBI survivor is kicking their own ass hard enough comparing themselves to the person they were before, they don’t need others contributing.”

“This is an uninvited change. We didn’t want to change our personalities, we are not being dramatic or lazy, and we don’t want to complain all the time. We also never fake it! When I say I can’t do something today, I am not being lazy trying to get out of activities or tasks, I’m saying that I honestly cannot perform or go to that social outing today.”

 “I wish I had a scar on my head. The invisible signs of a TBI (memory and concentration problems, fatigue, insomnia, chronic pain, depression or anxiety) can be more difficult to live with than a visible injury. If I had a scar on my head, it would help me feel validated or better understood. We may look normal, but shrugging off the invisible signs of brain injury is just belittling. Please don’t do that.”

Raw, honest and heartfelt responses above from individuals living with the diagnosis of Brain Injury every day for the rest of their lives. I know I’m not the person that I was before my accident. I live a “new normal” life, adapting the best way I know how. As the months go by I do get glimpses of her coming back, my personality, my sense of humour, and all the things that made me who I am. Not going entirely back to the “old me” is not all negative. I have found joy in new activities and strength I didn’t even know I had. To be honest, I feel like I’m becoming a better version of the person I use to be, fresh outlooks and all 🙂

It is so unbelievably frustrating living with an injury that the majority of the time is so invisible to others around you, but for me personally, I don’t need 100 text messages or calls a week from people asking how I am. To have people in your life that do genuinely care and make an effort to show you they’re trying to understand is the most amazing feeling. It’s sort of like okay wow, they’re hearing what I’m saying, not judging me, but rather taking it on board and trying to find out more information to help me. I have one friend that will google all the things I’ve been talking to her about over text message before she sees me, so that she can acknowledge and talk to me about them in person, BEST FEELING! I actual feel like an absolute crazy person most of the time when I talk about some of the things I’m feeling or what’s happened lately, and if I feel that way, in my head I can’t imagine what other people are thinking right now, so it does really calm me down to know that my friends aren’t brushing off my difficulties, but acknowledging how I’m feeling in such a comforting way. 🙂

It goes both ways though, and I’m always going to be there for my friends no matter what’s going on in my life. My friends will go through my mind so many times throughout my day, I think about them constantly. It is however, the process of taking those thoughts and putting them into action by reaching out to them that is sometimes really hard for me. I honestly can’t tell you why, it sounds really silly saying sending a text message can be really difficult for my brain, but it is sometimes. When I can do it, it is the best feeling because straight away I feel more connected with the outside world, and I want my friends to know how much they truly mean to me. I didn’t want this whole post to be about us with Brain Injuries telling everyone what to do!! I know for a fact, every single one of my family members, friends and relationship have been affected dramatically this last year. I sent some of my friends a couple of questions asking them what they have found hard about this last year and my injury.

And this is what they said…..

From their perspective…

“I find it hard because I don’t feel like I’m there for you enough. I feel like some of the best support I can give you is just time to sit and chat or just someone to sit next to you in silence. Unfortunately, I know I haven’t been able to do that with you anywhere near enough.”

 “Honestly, your diagnosis is complicated and difficult to understand. Even though you look fine, you’re not and I can tell when somethings not quite right because I can see it in your eyes. I find it frustrating that there is no timeline or date when things will get better. This scares me.”

“We can’t have nights out anymore, go to the movies or stay up late, but that’s not going to stop me from hanging out with you or being there for you. I do my best to consider where we are going to eat, is there going to be too many people, is the drive too long, is it too loud or am I staying too long at your house, should I leave now?”

 “I find it incredibly hard to find the words to help make you feel better and to be supportive. I didn’t know when to message you, did I not message enough? Did I message too much and was I being annoying? If I said head up it will be okay would that actually help or was I just being annoying?

“As a friend I have felt many emotions. Sad, because why did this happen to you? Mad, because why did you just ignore me and pull away when I went to give you a hug? Why did you not talk to me? Annoyed, because no matter how hard I tried I felt what I was doing to help wasn’t helping at all and I didn’t know what else to do. Scared, that I would say the wrong thing when I didn’t want to upset you. Heartbroken, because you’ve had to go through this incredibly hard, tough journey and it all happened from a fall, while you were doing something you loved. But most of all, I’m proud of you.”

“I wish I could be in your shoes. I wish I could understand what you are going through, both the good times and tough times. I wish I knew so I could support you and be a better friend.”

“I find it hard because I don’t know as much as I would like to about brain injuries and how the brain functions. I often don’t know the right things to say and that disappoints me that I could be letting you down.”

 “This process and your diagnosis has already taught me so much about brain injuries. But I would like to know more about the type of brain exercises you do and other ways I can assist in your recovery.”

I feel like there’s a communication mismatch. Not just with myself and my friends, but with Brain Injury and the community in general. How better would individuals feel if they knew the community or the people closest to them were thinking of them, but they too were so confused about their role in the recovery process and about what to say?! We could fix this communication mismatch together!!

I’m so lucky, because I know I’m surrounded by people who care and will be there for me, just as I want to be there for them. I am, however, constantly reminded that some others are not so lucky, and don’t have such a big support team around them.

So the next time you see or reach out to your family members, friends, or some random on the street, give them a smile, open a door for them, send them a love heart or just be present with them. We have no idea what others in our lives are going through, and small random acts of love and compassion could make someone’s day!

Be kind 🙂 

“Too many people have a vision in their head of what a disability ‘looks’ like, and if you don’t fit that vision, you don’t get the appropriate response.”

-Alysha Pellizzari, Speech Therapist

10 thoughts on “Part 5 – What I wish you knew…

  1. you are trying to be sooo many things Lauren the most important is to be kind to yourself & allow those who surround you to be kind to you. Your personal hellish journey is shared but not always visible to everyone. No one would really want to be in your shoes. To some degree you do get to chose who you share your journey with & should pretend if only for a little while all is right in your world, you know how to laugh at silly things and to truly enjoy cuddles from friends. These qualities are important on your road to recovery too. I wish you nothing but the best it is what you truly deserve.xx

    Liked by 1 person

  2. Firstly, I am so sorry that you have had to have this experience.

    Secondly, thank you for sharing your story and promoting awareness of brain injury. The knock to the head is not taken a seriously as it needs to be taken and can have devastating results for the individual and their loved ones.

    I wish you all the best in your continuing recovery and may you find happiness in your new normal

    Like

  3. Firstly I’m sorry to hear about your situation but congratulations on shining the light on an often stigmatised condition. The best advice I can give you is to not be too hard on yourself with your recovery / progress. My motto has always been to just take each day as it comes. All the best with your recovery.

    Like

Leave a Reply

Fill in your details below or click an icon to log in:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out /  Change )

Google photo

You are commenting using your Google account. Log Out /  Change )

Twitter picture

You are commenting using your Twitter account. Log Out /  Change )

Facebook photo

You are commenting using your Facebook account. Log Out /  Change )

Connecting to %s