Debunking Common Myths About Therapy

Therapy is a powerful tool that anyone can benefit from – it can help with personal growth, healing, self-discovery and compassion towards both yourself and others. Yet, despite more and more people speaking about therapy and what it entails, there are still myths surrounding it which can cause hesitation and doubts about whether it is something to consider.

Therapy is only for people with ‘serious’ mental health issues:

Therapy isn’t just for those with severe mental health issues or those in crisis. It is a resource that can be used by anyone facing life challenges, seeking personal growth, or wanting to understand themselves better. I had a Psychology teacher when I was studying for my A Levels who told me that she really strongly believed that everyone, mental health conditions or not, should have to have therapy at some point in their life – and looking back, I absolutely agree!

Talking to friends and family is just as effective as therapy:

I am absolutely NOT wanting to dismiss the invaluable support that friends and family can offer you – I have incredible support from my family and friends and I wouldn’t be able to do life without them by my side. Therapy, however, offers something different. Therapists are trained professionals who are there in a neutral, non-judgemental capacity. They use evidence-based techniques to help you process emotions, identify patterns, and develop coping strategies.

Therapy takes forever to work:

How long therapy takes to work is entirely dependent on your goals and needs. Some people find huge benefits within a few weeks, whereas others benefit more from long-term work. It’s something to discuss with your therapist as they are in the best position to help you determine what is best for you.

The therapist will judge me or think that I am broken beyond repair:

Therapists are there to provide empathy and understanding, not to judge you. They aren’t there because they think you are broken and need fixing – they just want to help you work towards your goals in a partnership with you.

Therapy is all about your childhood experiences:

For some people, talking about their childhood is absolutely necessary. And for most people, looking at past experiences can be helpful, but therapy isn’t solely focused on the past/your childhood. The therapeutic process should be tailored to address your current concerns, whether they stem from past or present experiences.

My therapist will solve my problems for me:

As nice as this would be, it’s simply not possible for the therapist to do the work for you. Ultimately, change has to come from you – the therapist can help you and give suggestions and guidance, but you have to be the one to make those changes. One of my most commonly used phrases in my therapy sessions used to be “but I’m paying you to agree with me” which would inevitably result in an eye roll and being reminded that she definitely is NOT there to agree with me – it would be nice if she did, but then no progress would be made and therefore it would be a huge waste of time – for me and for her.

Believing myths like the ones discussed here can prevent people from seeking therapy when they need it most. So it’s important to challenge these misconceptions so that people are informed and have an accurate depiction about what therapy is like. If you’ve been hesitant about therapy, remember: it is a tool for everyone! Taking that first step could be the start of the rest of your life and provide the transformation and growth that will turn your life around.

All my love,

Anna x

Loneliness in Chronic Illness

Living with chronic illness is a journey that is full of challenges – physical, emotional, social – you name it, it can be a challenge. Among these, loneliness is something that is incredibly common but is also underestimated by a lot of people. Chronic illness fundamentally reshapes your entire life – activities that one brought you joy may no longer be possible due to pain or fatigue, friends and family may struggle to understand your limitations which also leaves you vulnerable to feelings of loneliness.

Social events often require energy and effort that a lot of people with chronic illness are unable to participate in. Spoon theory is a good way to describe the energy limitations that are imposed on someone with a chronic health condition, and often we simply lack the ‘spoons’ needed. This can lead to feelings of isolation as being around friends and family is how we feel connected and is something that people need – we use solitary confinement in prisons as a punishment because it removes that connection that all humans need.

As well as this, when people misunderstand our illness or limits that we have, it can lead to a lack of empathy or patience. It’s understandable that, unless you’ve got a chronic health condition yourself, you can’t fully comprehend what life is like. And as chronic illnesses are so unique and symptoms vary drastically from person to person there can be misunderstanding between individuals with the same condition. It often feels like no one understands what life can be like, and this is a lonely place to be!

Loneliness doesn’t just stem from chronic illness either – it can actually worsen it. Social isolation can exacerbate feelings of depression, anxiety, and hopelessness, which can, in turn, amplify physical symptoms. It can feel like a never-ending cycle that is impossible to break.

But despite the loneliness that you may feel, there are other ways to connect with people. I have found communities online that have allowed me to connect with and speak to other people with chronic illness who understand what life can be like. For me, social media is my connection to the outside world – if I didn’t have access to it then life would feel even more isolating for me. I sometimes take breaks from social media as it can feel overwhelming at times, but I do miss the sense of community and understanding when I am away from those groups.

If you know someone who is living with a chronic illness, remember that your understanding and patience can make all the difference. Reach out, listen without judgement, and offer support in whatever way your loved one needs. Offer to pop round for a cup of tea or to go to drop off some shopping. Ask if they want to chat on the phone or over facetime. Find out if they need help with jobs around the house and offer to go over and help them get some bits done. Whatever is needed at the time – knowing that they have people who love and care about them will undoubtedly make the person struggling with chronic illness feel valued and connected to you!

All my love,

Anna x

Managing Guilt – When Chronic Illness Impacts Relationships

Chronic illness doesn’t just affect you, the person experiencing it – it has a ripple effect that spreads out to family, friends, colleagues. Something that I know a lot of people struggle with is the feelings of guilt that can arise because of this. Guilt can stem from feeling like a burden, missing out on social or work related events, or needing additional help from others. While this is a natural way to feel, it can have a long-lasting impact on mental health and relationships.

There are numerous reasons that you might feel guilty when struggling with chronic illness. Often people describe feeling like a burden as they require more support with things like shopping, cooking, cleaning or even washing yourself. This leads people to feel badly about the amount of time and energy that is being spent on your care. The nature of chronic illness is that they are unpredictable. This can mean that you have to cancel plans last minute and therefore feel like you are letting others down. It can also impact family dynamics and impose limitations on what you can do in terms of work – both of these can cause guilt as you feel like you are disrupting people from living their life or not pulling your weight.

I think it’s important to remind yourself regularly that needing help from others doesn’t mean that you are weak or less valuable. Relationships are mutual and those closest to you want to help you in any way they can. It can help to talk about your feelings of guilt – it may not be obvious to others that you are feeling this way, and talking to them means that they can reassure you that they are happy to help. They say a problem shared is a problem halved, right?

Even if you can’t contribute to things in the same way that you did pre-illness, you can find other ways to show your support, care and appreciation for those around you. Chronic illness is not your fault, and guilt won’t change your circumstances. Think of all the brain space you might free up if you’re not constantly berating yourself for what you can’t do!

Having healthy boundaries can help prevent resentment and allow your relationships to blossom and thrive. Remind yourself frequently that letting other people help isn’t weakness or a sign that you are no longer independent – you can be independent and still ask for help.

Remember this: guilt is a natural response to the challenges of living with chronic illness, but it doesn’t have to define your relationships or self-worth.

All my love,

Anna x

Mourning the Life You Expected

I’ve written about the grief that accompanies chronic illness before, but it’s a topic that I often come back to because it is something that has been so prevalent in my life.

Living with chronic illness often comes with a deep sense of loss. It isn’t just the physical symptoms that affect your day-to-day life, but also the realisation that the life you imagined for yourself might never come to fruition. This feeling of loss can manifest as grief, a complex emotional process that many people with chronic illness experience.

Grief isn’t just something that is limited to the death of a loved one. People often grieve the loss of:

Physical abilities – the things you once took for granted like running, dancing, walking, might now feel or become impossible.

Independence – it’s hard when you have to suddenly rely on other people for help doing tasks that you would have previously handled independently with no problems. This is something that can feel incredibly vulnerable.

Future plans – you might have to give up on career goals, travel plans, or family aspirations, or at the very least, adjust your expectations of what you can realistically manage.

Sense of identity – chronic illness can force you to redefine who you are and how you see yourself. This is something that I have struggled with a lot – who am I without the things that I can no longer do. Who am I if I’m not studying or working?

Grief doesn’t follow a linear pattern at all. There are stages of grief that people go through but the order and time it takes varies massively from person to person. The five stages that people are said to experience are as follows:

Denial – “This can’t be happening to me.” You might ignore symptoms or resist a diagnosis.

Anger – “Why me?” It is completely natural to feel frustration and resentment about your situation!

Bargaining – “If I do everything that the doctors are telling me to do, maybe I’ll get better.” This stage also often involves clinging on to the possibility of a cure or treatment that will make life bearable.

Depression – “What’s the point?” Sadness and hopelessness can feel incredibly overwhelming.

Acceptance – “This is my reality but it doesn’t have to define me.” Accepting your situation doesn’t mean that you like your situation, rather that you are finding ways to move forward despite your diagnosis and struggles.

So, what can you do help cope with these feelings of grief?

You should allow yourself to feel your feelings. Don’t try to bury them because this isn’t going to help and will likely make things more difficult in the long run. It can also help to connect with other people who understand what life with chronic illness is like – I’m very lucky to have found communities on Facebook and Instagram that have allowed me to meet other people in similar situations to myself.

Therapy can also be a very helpful tool. I have been seeing a counsellor for 4 years and she has been my lifeline, offering me a safe space to explore my feelings around my illness. Through therapy I have learned how to be more compassionate towards myself and to respect my body’s limitations. I now respond with kindness when I’m having bad days as I’ve learned that punishing myself is not going to be beneficial.

Grief doesn’t mean giving up – it means making space to acknowledge your losses but also the new opportunities that might arise as a result. Chronic illness may alter your life dramatically, yes, but it doesn’t erase who you are as a person. And it doesn’t have to get rid of your potential for growth, connection, and happiness.

All my love,

Anna x