How to prepare for returning to work after illness

How to prepare for returning to work after illness

Prepare for returning to work after illness or injury. Is that a thing? You’ve been through a serious illness, perhaps life-changing for you in some ways, treatment has ended, your recovery is going pretty well and returning to work is now on the horizon. Hurrah!

You just want to get back to work. Back to normality! Your regular salary and not sick pay. Being with other people again. Making a contribution. There may be concerns and worries of course. But getting back to normality like work is a key milestone.

Then you get back to work, you go for it, and you crash. Hard. Your body isn’t coping. You have to go back on sick leave. You’re thinking, ‘What the… *insert fruity language*?!?! You feel so disappointed.

 

Pic of someone returning to work after illness and it doesn't go well

When the return to work doesn’t go to plan.

 

I totally understand how that can happen. It’s pretty common actually. If you’ve haven’t been seriously ill before, how would you know how to prepare for returning to work after illness or injury? You don’t necessarily know that stuff. It’s not like your doctor gives you an info sheet on it.

I’m going to share a few tips to help you avoid that. I split them into four categories – Mind, Heart, Body and your Role at work. This is about taking a holistic approach to prepare for returning to work after illness or injury.

Click here on how to prepare your mind, heart and body to return to work after a serious illness or injury. #returntowork #seriousillness #chronicillness tell a friend

 

How to prepare for returning to work – Your mind

 

Manage your expectations of yourself.

We often expect our return to work after illness to go like this.

Person returning to work after illness expecting a smooth return to work

People’s expectations for returning to work can often look like this

 

It’s more often like this.

Pic of a graph demonstrating that the return to work after illness is not smooth

A return to work after illness often looks like this.

 

Be gentle with yourself.

It’s very easy for your pre-illness expectations of yourself to come to the fore when you start returning to every day normal activities. It’s normal for this to happen because your pre-illness expectations of yourself are all you know. But I often see clients battle to live up to those expectations. And I use that word ‘battle’ on purpose. It’s like a fight, ‘I will not let this illness and these symptoms beat me. I will WIN! I WILL last the whole day at work!’

This kind of fight is a negative fight as you have actually handed over control to your pre-illness expectations. You have become their slave. It can be a very unhappy and frustrating place to be in when you find that no matter what you do, you can’t live up to those expectations.

The thing is, your pre-illness expectations may no longer match your body’s capabilities. Your body has changed. Therefore, your expectations of what your body can do also need to change. They need to align with your new capabilities.

Being able to adapt is key for this to happen. But with adaptation comes acknowledgement of what has happened to you. For some, this process of acknowledging the change can be hard.

This brings us to your Heart.

 

How to prepare for returning to work – Your heart

 

Losing valued levels of physical and/or mental functioning can be hard. Your body and/or mind no longer do what it used to do. What you need it to do. What you want it to do. It can feel like your body has betrayed you. And that you are at war with it. You may be feeling very angry.

You feel like you are no longer you. But you also know you are you. You can feel so contradictory. Your heart hurts.

It’s important to acknowledge how you are feeling. To give your feelings some expression, to spend some time with them. As I’ve said previously, you don’t have to unpack and live in those feelings forever and ever. You just visit. And the length of that visit is up to you. If how you feel can feel overwhelming, get support from someone who can help you spend a little time with the feelings to understand what they want to tell you.

Picture of person coping with unpleasant feelings

You don’t have to unpack and live with overwhelming feelings.

 

Also, speak gently and compassionately to yourself. You’ve been through a lot. It’s ok to move more slowly, to do less, to not do things as perfectly, to not achieve as much. Focus your energies on the things that matter to you.

Your heart will thank you for this. And you will feel better.

 

How to prepare for returning to work – Your body

 

Finally, it’s important to gently prepare your body to return to work. Returning to work after an extended period of probably not being very physically active can be very draining physically and mentally.

Think through your typical work activities and ways you can simulate them at home. The purpose of doing this is to really feel how you your body copes with them and learn where your limits are.

If you are returning to work gradually, for example, 3 days a week for 2 hours each day at the start, set up that routine at home.

Make sure you get up at the same time you will need to when you return to work. Wash, get dressed, eat. Go through that routine to see how your body copes. Set yourself activities to do in the time frame you will be at work – say 2 hours of paying bills, work on the computer, some errands (if you can do them), a bit of light cleaning, tidying, calling people.

You can simulate a meeting. For example, meet a friend for coffee and notice what it’s like for you to get to the coffee house, visit with your friend, deal with the noise around you and being in public, and return home.

Do these activities at different times of the day to see how your body responds.

As you do this, notice how your body feels. Do you feel really tired? Do your symptoms get worse? Or do you find the activities distract you from the symptoms? Do you find it doable? Or too much? Do you find you cope better in the morning or afternoon?

This will give you an idea of what your body is capable of and the tasks you can and may not be able to do back at work. Of course, what you can and cannot do may change the longer you simulate work activities at home and then when you are back at work.

Before returning to work, get your body ready by simulating your work routine at home. You will learn how your body copes, its limits, and what adjustments you may need back at work. Read more about it here. #returntowork… tell a friend

 

What does this all mean for your role at work?

 

After having simulated your work routine at home, think of your work environment. First, think about the physical environment: how furniture is arranged, is it open plan, do you not have a desk, the lights, getting to the different areas within the office you will need to go, etc. Is there anything there which may be an obstacle? Do you need to make a request for a reasonable adjustment? I wrote about what reasonable adjustments are last week and you can read more about that topic here.

Also think of the non-physical aspects of the environment. Does your work have a recommended time frame by which they expect you to return to work full-time? How flexible can that time frame be? (The after effects of illness and injury don’t often work to others’ time frames including your expected time frame.)

What is the culture like? Are your teammates helpful? Is your line manager understanding, and their line manager? And HR? Do you have people at work who can help you look after your interests, whether formally or informally? What support will you need? How will you manage the pressure?

I appreciate these are a lot of questions so take your time in thinking them through. I have just a few more questions about your role at work

What tasks can you currently do, cannot do at the moment, or you may no longer be able to do ever? This is important to consider because if you have an idea on this, you can communicate this to your employer at the appropriate time to help them help you return to work. Also, if you cannot do the significant tasks in your role, then you may need to consider doing a different role.

Let me give you an example. I once knew someone who worked in a department store arranging their displays. They were affected by an illness which affected their balance and mobility. So they were no longer able to climb up a ladder. This significantly impacted their ability to do their role. They had to change roles in the organisation which did not require them to climb up ladders and carry heavy items.

If you think you are no longer able to do your current role, or only a part of it, are there other roles you could and would like to do in your organisation? You may not have to ask yourself this question, but I ask it just in case you do. I’ve had people say to me if they had only thought that there could be alternatives, they would have thought them through. So think through possible alternatives if that is what you feel you will need.

Prepare for returning to work

Questions to ask yourself as part of your preparation for returning to work after a serious illness or injury.

 

Those are my key tips how to prepare for returning to work after illness. All the very best with your return. And come back next week when I will be sharing what to say to whom and managing your own and others’ expectations at work.

 

What’s it like for you?

 

What key tips do you have to share with someone preparing to return to work after illness or injury? Has anything in particular worked for you? Or do you have questions about your situation? Share your thoughts in the comments below.

If you are living with a serious health issue, which may be a serious illness or injury or chronic illness, and will soon be or have returned to work and would like support to ensure it is an effective transition, have a look at how we can work together and get in touch for a free no obligation consultation.

 

Help with research on acceptance

 

If you or a loved one experienced a serious health issue in the past 2 years and are struggling or wondering if you can accept what has happened, I would love to speak with you. I am researching the concept of ‘acceptance’ within the context of a serious health issue by collecting people’s experiences with it. Click here to find out more. And in exchange, I offer you a free 1 hour coaching session.

 

Pass it forward

 

Although I wrote this blog in the context of living with a serious health issue, the ideas contained within are applicable to everyone. If you think someone you know would benefit from reading this blog, or you just want to spread the ideas, click on the icons to share.

© Copyright Barbara Babcock 2018

 

Support for carers – 4 things to consider to help you care effectively

Support for carers – 4 things to consider to help you care effectively

There is good support for carers out there, but I’ve found there are some things which aren’t always explicitly talked about. And if carers knew about them, which are often of a psychological nature, they would realise what they are experiencing is normal. This awareness would also reduce the chances of the carer operating from the dark side of helping.

So I am going to share 4 things to consider as a carer to help you in your caring role. (There is more I am sure, but this is a good enough start.) This is the last post in a blog series about the dark side of helping people whose capabilities are limited by illness or injury. It is meant to support those of you in a caring role whether you are a spouse, partner, another family member, friend, colleague.

 

But a quick recap on what the dark side of helping is

 

In the first post, I explained that the dark side of helping is when someone helps another, and the person helping hasn’t asked if it’s needed. It’s a proactive form of help, which is deemed to be a good thing in our society. But it has been assumed on the part of the helper that the person being helped needs or wants it. The person being helped hasn’t asked for it, so it may not be wanted or needed.

Pic of man insisting on helping a person who uses is sticks and is carrying a bag, the dark side of helping

 

In the second post, I wrote about the impact the dark side of helping has on the people on the receiving end of such help, their views of it and the reasons for that. The third post focused on proactive strategies you can use to manage situations where you are holding on to their anger and getting angry yourself.

So let’s move on to the four phenomena which happen but aren’t often talked about and what it means for you as the carer.

 

Support for carers 1 – Being able to withstand difference to support effectively

 

So much is required of you to enable you to support someone effectively. It can take a lot of patience on your part. It is so important that you have good support from people you trust, respite breaks when you can, and your own life. This all enables you to top of your inner-resources so you can stay with and keep going without wearing yourself out.

Pic of a carer's balance account of inner resources getting low and people offering to help

It’s important to keep your balance account of inner resources topped up.

 

If you’ve known the person you are caring for for years, it can be very hard to see them so different. This is a big test for some. Can you withstand standing before this difference that feels uncomfortable for you? Can you give yourself the time to become more comfortable with it? Support from others can help you do that.

 

Support for carers 2 – Being able to notice and sit with your discomfort and anxiety

 

Sometimes when we are very uncomfortable with a person or situation which is so different from what we once knew, it can highlight the anxieties we consciously or unconsciously hold about the difference. For example, seeing someone formerly physically active who no longer is due to an illness or injury. We can feel (even on an unconscious level), ‘That can be me one day,’ and that can be hard for some people to experience. Or you could be thinking, ‘I didn’t sign up for this. This wasn’t in my life plan!’

It can also highlight our assumptions of illness, health, disability and capabilities. For example, some in society think that if you have a disability, you are no longer capable, or being ill is somehow a bad thing. But others feel that a disability means being differently abled. (I opt for the latter as it is the realistic scenario. Just because your body doesn’t work like other people’s, it doesn’t mean you are deficient in any way. You have the same dreams, hopes and fears as everyone does. You have a difference and finding ways to adapt your approach to do what you want in life is key.)

When we help from a place of anxiety and assumptions which discount the abilities and desires of the person we are helping, we often do it to calm our anxiety and reduce our stress levels. That ends up taking precedence over the needs of the person we are helping rather than there being a reciprocal relationship where the needs of both people are met.

To help effectively we have to learn to recognise when our anxiety and unhelpful assumptions are triggered and be able to hold that whilst helping people in the way they wish to be helped.

To help effectively we have to learn to recognise when our anxiety and unhelpful assumptions are triggered and be able to hold that whilst helping people in the way they wish to be helped. tell a friend

 

Support for carers 3 – Getting to know the ‘new’ person, getting to know yourself now

 

Linked to this, you may feel that they are a different person. They are to some extent because of the all the change they are dealing with. Yet they are still the same person they were before the illness or injury. You know that too. It can feel like a contradiction and I’ll explain why.

When a loved one has a life-changing #seriousillness or injury they often feel like they don’t know themselves anymore. This is normal. Read the reasons why here. tell a friend

 

The person who has become ill or injured is going through a process of re-defining themselves. They may not be fully aware they are going through this process. It involves figuring out who they are now as a result of the illness/injury and who and what they want to become. That unfolds as they go about living their life with the consequences of the illness or injury, figuring out what they are capable of now, etc. And this is the only way to do it. It’s not a process where you arrive at an end destination, find your new self, put it on and go, ‘Ta da! Here I am world! The NEW ME!’

 

Pic of person trying to buy their new self-identity and sales person telling them it's free out there in the world

Finding your sense of self again isn’t like buying something. You have to live your life to discover your new identity.

 

Also, many of their personal traits, characteristics, likes, dislikes, mannerisms, etc. that existed before the illness/injury are still there. This also needs to be integrated with who they are becoming.

This process of redefining themselves is about integrating the person they were before with the person they are becoming so they can function in their life in the way they want. It is no small psychological effort. We aren’t given a handbook when we get ill or injured on how to go through this process.

As the supporter, you too are going through a similar process. Your life and relationship are also different after the person’s illness/injury.

When you are supporting someone, particularly if you live with them, there are two of you going through this process at the same time (more or less) in addition to dealing with the realities of the person’s illness or injury. That’s a lot.

And if you have children, they too are going through a variation of this. Everyone is evolving and adjusting, trying to figure things out. It’s no wonder there can be an upheaval in family relationships after an illness/injury/disability enters the family.

 

Support for carers 4 – Giving new meaning to the relationship

 

The person who has acquired an illness or injury may no longer be able to participate in activities that were a key feature of your relationship – taking turns on doing everyday activities like running errands, cleaning or mowing the lawn, cuddling together on the couch on a Friday night, sex, spending a leisurely weekend afternoon in a pub drinking, walking up a mountain, etc.

You may be wondering what does the relationship consist of now? What gives it meaning?

The relationship can feel like it is in a very uncertain no-man’s land. Not everyone can exist in such a place and travel though it to come to a new place regarding the relationship. It’s important that you both find ways to talk about it with each other and you both have a variety of support (keep in mind that it’s very hard to be everything to one person). Working together to adapt how you approach activities you used to do together and finding new activities can help ensure your relationship stays on a path you are both satisfied with.

Pic of support for carers 4 things to consider in the caring role

Support for carers – 4 things for carers to consider

 

And more support for carers…

 

Finally, whilst writing this series, I came across this report called ‘Good and bad help: How purpose and confidence transform lives’. It echoes ideas I have been sharing across this series on the dark side of helping.

This report focuses on providing good help at the organisational level: NHS services, social care, or help in the community. Yet the ideas contained within can be applied at the individual level. Have a read! It’s very good.

The report was published by Nesta, a UK charity which is an innovation foundation working on the big challenges of our time in partnership with governments, businesses and charities. I’m including it here on my own initiative, Nesta hasn’t asked me to. But they are aware I am mentioning it.

 

What’s it like for you?

 

Do you recognise these four phenomena? What has your experience been like in dealing with them? Is there any other support for carers you found helpful? Share your thoughts in the comments below.

If you are living with a serious health issue, which may be a serious illness or injury or chronic illness, or are caring for someone who is, and would like support for yourself, have a look at how we can work together and get in touch for a free no obligation consultation.

 

Help with research on acceptance

 

If you or a loved one experienced a serious health issue in the past 2 years and are struggling or wondering if you can accept what has happened, I would love to speak with you. I am researching the concept of ‘acceptance’ within the context of a serious health issue by collecting people’s experiences with it. Click here to find out more. And in exchange, I offer you a free 1 hour coaching session.

 

Pass it forward

 

Although this blog is written in the context of living with a serious health issue, the ideas contained within are applicable to everyone. If you think someone you know would benefit from reading this blog, or you just want to spread the ideas, click on the icons to share.

© Copyright Barbara Babcock 2018

What the dark side of helping people who have a serious health issue is like – Part 2

What the dark side of helping people who have a serious health issue is like – Part 2

We continue our series on the dark side of helping people affected by illness or injury by talking about the reasons they may not want your offers of help (however well-meaning they are).

As I said in the earlier post, helping others is a good thing and recognised as being good for us (Mental Health Foundation, 2018; Psychology Today, 2018; NPR, 2018).

Yet there are times when providing the help doesn’t fulfil the helper’s original intentions to help, nor help the person. This blog series is exploring that situation.

This post will explain the views of people on the receiving end of such help and give some ideas and tips to give you more choices on when to offer and withhold your help. It’s important as relationships you value can end as a result of the dark side of helping. And this is often not your intention when helping someone.

 

Pic of man in wheelchair and woman with sticks saying they are going to share their thoughts on helping

 

My aim is to share my learning from having operated at times from the dark side of helping so you can make mindful choices when to offer your help and when not to. Many of us have been there and done it. The important thing is learning from it.

 

What is the dark side of helping?

 

A quick recap – The dark side of helping is when someone helps another, and the person helping hasn’t asked if it’s needed. It’s a proactive form of help, which our society feels is a good thing. But the helper as assumed the person being helped needs or wants it. The person being helped hasn’t asked for it, so we don’t know if it is wanted or needed.

 

Pic of man insisting on helping a person who uses is sticks and is carrying a bag, the dark side of helping

 

The impact of the dark side of helping

 

People who get around using a wheelchair, stick or walking frame have often told me it doesn’t feel good to be on the receiving end of this kind of help. They gave four reasons why. These reasons can also apply to people living with invisible illnesses. So have a read to learn what to do to make sure you don’t end up inadvertently wandering in the dark side of helping.

You want to help someone who has a #serioushealthissue #seriousinjury #chronicillness But they don’t want your help. Read the four reasons why here tell a friend

 

Reason 1: It’s an invasion of personal space

 

It some cases it can be when it involves you physically doing something for someone.

 

Reason 2: It can feel demeaning

 

People I’ve spoken said it can come across as if the person helping assumes the person is no longer capable of doing what they are setting out to do because of the illness or injury. To live with people treating you as if you do not have the capability can erode your sense of self-efficacy (your belief in your ability to accomplish a task or succeed in a particular situation), self-esteem and self-worth over time.

As the person helping, you may say that the person is no longer capable of doing that activity. This can go several ways.

Ask yourself how you feel watching the person doing the activity. Are you thinking they can’t do it? Are you worried they will hurt themselves or drop something? Is it taking longer? And you’re busy and don’t have the time to wait for them to finish. Does it feel more laborious to you? Do you think you can do it more quickly or better? These are common reactions and they can often highlight your assumptions, standards, expectations, wants or needs.

If you find yourself feeling this way, that’s ok. Just notice it and you don’t have to act on it. The downside of acting on these feelings is you inadvertently transfer them to the person you are trying to help even if you don’t say anything about how you are feeling. For example, if you help someone because you can’t stand how much effort it is taking them to do what is expected to be a simple task… you get the feeling.

It’s not nice being on the receiving end of that kind of help. It’s difficult to understand. The person may wonder if they have done something wrong. Or be upset because they were trying to exercise their independence. It can also be confusing and uncomfortable when you don’t know the person trying to help you.

If you don’t know the person at all or only a little, ask before you help.

If you know the person and there is a time element to the situation where you both have to be somewhere, or it’s an issue of keeping the person safe (a safeguarding issue), I recommend finding a way to talk about when your help might actually be recommended or necessary. This can be a talk of a more delicate nature and warrants a separate article for another day.

 

Pic of woman having taken over of making tea for a man in a wheelchair

Wanting to try doing things for yourself when living in a changed body.

 

Reason 3: It disempowers the person you are helping

 

The person you are supporting may no longer be capable of doing the activity how they used to do it pre-illness/injury. But they may be able to find a new way of doing it. This a key process for people living in a changed body to go through. It fosters adaptability and flexibility which are key qualities they need to deal with the ongoing impact of their illness/injury, to look after themselves, and regain a quality of life.

When you rush in to help someone without asking, it’s focusing on what the person cannot do and that isn’t empowering. When you support someone to figure things out, you are focusing on the possibilities that exist for them and what they can do. They may not always be sure what they can do, so you can give some suggestions (if they are open to them and you may need to ask them that too). You can also give them your moral support and belief in them, both which can be incredibly empowering for the person.

This kind of help on your part fosters a reciprocal partnership. It strengthens the person’s resolve that they can figure out a new way to do things, what they can do on their own and what they cannot. They may make a mess, drop things, and take a long time. They will express frustration. But they learn, and it can be empowering to find a new way of doing things. It feeds their sense of self-worth. So voluntary help can actually prevent people from going through this helpful process.

When you support someone with a #serioushealthissue to figure things out for themselves, you are focusing on the possibilities that exist for them and what they can do #empowerment #inclusivity #disability tell a friend

 

Reason 4: It takes away control

 

The person may actually no longer have the capability to do what they want. But for some people they have to go through the process of figuring this out for themselves. It will contain more meaning for them than someone telling them they are no longer capable. Even though it is hard for them to digest this realisation and for you to witness.

They retain a sense of control in making the decision knowing what they are capable of and not. When someone tells you verbally or through their actions that you are not capable, it highlights a difference between you and the person/people telling you. Your sense of belonging can feel threatened. It feels like you can’t decide for yourself anymore. You can feel ‘less than’. This can erode your sense of self-efficacy and self-esteem as mentioned above.

Over the long-term, it can foster resentment for both people in the relationship:

Supporter: I resent you because you can no longer do what you used to do and now I have to do it.

Person being helped: I resent you having to do things for me.

This resentment can result in malfunctioning co-dependent relationships.

This realisation process of learning what one is capable or not capable of is tough because it involves the person acknowledging the loss of capability due to their illness or injury. And they may not be ready to do that just yet, particularly if they (and you) really valued the lost capability. It can take time.

And during this time, the greatest thing you can be doing for yourself is to make sure you have support and time out (as far as that is possible, I know it’s tough at times to have time out). This will enable you to top up your inner resources of patience, strength and whatever else you need to keep going.

 

Pic of a woman talking to another woman to get some support

Getting support for yourself when you are supporting another is important.

 

Next time

 

Come back in two weeks where I will share the strategies you can use to manage tough situations, help effectively and to support yourself.

 

What’s it like for you?

 

What has your experience of supporting someone or receiving help taught you about the dark side of helping? What advice would you share with others to make sure they didn’t operate from that place? Share your thoughts in the comments below.

If you are living with a serious health issue, which may be a serious illness or injury or chronic illness, or are supporting someone who is, and would like to return to a sense of wellness, have a look at how we can work together and get in touch for a free no obligation consultation.

 

Help with research on acceptance

 

If you or a loved one experienced a serious health issue in the past 2 years and are struggling or wondering if you can accept what has happened, I would love to speak with you. I am researching the concept of ‘acceptance’ within the context of a serious health issue by collecting people’s experiences with it. Click here to find out more. And in exchange, I offer you a free 1 hour coaching session.

 

Pass it forward

 

Although I wrote this blog in the context of living with a serious health issue, the ideas contained within are applicable to everyone. If you think someone you know would benefit from reading this blog, or you just want to spread the ideas, click on the icons to share.

© Copyright Barbara Babcock 2018

 

What health coaching is like for people with serious health issues

What health coaching is like for people with serious health issues

A former client, Wendy H., has graciously shared her health coaching journey to give you a taster of what it is like and how it can support someone to live well with the impact of the health issue they have. Wendy starts her story before we started working together, sharing with you the serious health issue she lives with and everything she tried to help herself before trying health coaching. She then shares what health coaching was like for her. 

I made very little changes to what Wendy wrote. I added in a word here and there and the titles, and moved some sentences. I also drew the pictures. At the end of this article I provide a link to the questions referred to by Wendy. They will help you think about your own situation and what you want to be different. There is also the opportunity to try coaching for yourself for free.

 

Return to wellness: My health coaching experience

 

When my life changed forever

 

It was 7 years ago – in another life – since I was diagnosed with Transverse Myelitis (TM), resulting in a weakened left leg with inevitable muscle wasting, dropped foot and a multitude of other symptoms associated with the condition such as bladder and bowel issues and fatigue.

I had always been sporty and active so over the past few years my rehabilitative journey took on a multitude of self-help strategies, importantly, finding out as much as I could about the condition.  I read books on neuroplasticity, brain training and mindfulness. I joined exercise programmes, the gym, saw a sports physiotherapist, neuro physiotherapist, trained how to do Nordic walking, which led to me taking up hippotherapy (horse therapy, or simply put, horse riding).

I have been measured for orthotic insoles and used a Functional Electrical Stimulation device (FES). I even went to acupuncture for weeks. I was on the verge of sinking into depression so was referred to a clinical psychologist, resulting in a short course of anti-depressants.

 

The irony….

 

Even after all this determination and sheer will power to get back to my previous life, it wasn’t really working.  I did a reasonable job at maintaining my physical strength. However, it seemed I was fighting a losing battle and began to feel ‘exercised out’.  I would put pressure on myself to exercise and scold myself if I didn’t.

I’d watch people running and walking in the street or on TV.  I found myself analysing their gait. How do they do this simple activity…. automatically?

I obsessed about how TM had affected me, was consumed with frustration, anger, loss, depression.

Finally, a few months ago I realized I had become STUCK.

After all this effort.

I was STUCK.

Everything became a mammoth task or a hassle. I’d stopped exercising. I became anxious and tearful.  I lost motivation, interest and confidence in almost everything. I couldn’t move on or come to terms with or adjust to how my world was now.

I still fretted about my past life. I was still angry and frustrated. This mountain was in front of me and I didn’t have the energy to climb it again.

Then it occurred to me – I had been focussing mostly on my physical state and been neglecting my mental health state. I really hadn’t learned how to adjust, accept or come to terms with this long-term medical condition Transverse Myelitis.

Picture of a person with a serious health issue stuck between their old life and the mountain (i.e. figuring out their new life)

Wishing for your old life but starting a new one feels like a large mountain to climb

 

You've done everything you can to live well w/ your #serioushealthissue #seriousinjury #chronicillness but you’re still stuck. Imagine this. A magic wand is waved as you sleep. In the morning, you still have the health issue, but… tell a friend

 

The turning point

 

At this time, an article in a newsletter from the Transverse Myelitis Society reminded members about a bursary to provide health coaching, guided by Barbara Babcock. I did have some apprehension and wondered whether this would be another fruitless journey.

However, having plucked up the courage to contact Barbara, she reassured me about the process and that we would have telephone contact at times to suit us both.  She also provided lots of preparatory articles and questions to think about prior to our first communication, so I felt somewhat relieved and prepared.

 

Health coaching journey – One of enlightenment, empowerment and self-awareness

 

Over the weeks that followed, my health coaching journey became one of enlightenment, empowerment and self-awareness.  I was amazed with how comfortable it was talking to Barbara on the phone and I soon realized that she didn’t put pressure on me to fulfil her agenda.

This was totally me guiding the script and pouring out my anxieties, stresses, frustration and anger. And importantly, we tackled the obstacles in my way, with a much more energetic and positive attitude.

I learned how to recognise my feelings within my body, not just the negatives, but the positives too.  It was frightening that I rarely felt these ‘positives’ because I had focussed on the negatives for so long.  It took practice, but I now consciously recognise when something feels ‘good’ and that this is the ‘anchor’ I needed.

I became more attuned to acknowledging anger and anxiety and importantly, how to manage, process and take control.  With Barbara’s guidance and simple strategies, I learned how to ‘feel’ where in my body the emotion was and what thoughts arose.

By simply giving the emotion a name and spending time with it, enabled me to process these thoughts and feelings.  This may sound daunting, but the nature of talking about your underlying feelings, in this safe environment, or writing them down was incredibly powerful.

Picture of a person writing about their feelings which is a powerful thing to do

The power of writing about your feelings.

 

The nature of talking about your underlying feelings in this safe environment of #health #coaching, or writing them down, was incredibly powerful. #serioushealthissue #chronicillness #spinalcordinjury #TransverseMyelitis tell a friend

 

 

Health coaching empowered me to focus on what I can do

 

My health coaching journey has now ended, but my journey to wellness and normality continues.  This is my new philosophy.

If you feel you have a mountain to climb or feel ‘stuck’ and have determination and the willpower to want to take your first steps, I would strongly recommend health coaching.

Be prepared to be open and honest and be aware that emotions may become overwhelming and distressful. And be prepared to work at it.

Barbara will pose unexpected questions and prompt when you are off your guard. If you expect Barbara to tell you what to do and how to do it, you will realise that this is not how it works and you will not reap the benefits.

I am learning to focus on what I can do now, and although I still have a mountain to climb, I can tackle it in smaller chunks.  I am more positive and less fatalistic. I am able to recognise anger. I am now able to move on. I am managing fatigue. I have resumed physical activities and registered for a one-mile open water swim.  I no longer feel ‘stuck’.

Wendy H, York

 

Picture of a person having found her path to wellness and a new normality because of health coaching

Finding your own path towards wellness and your new normality

 

What’s it like for you?

 

In what ways did Wendy’s story mirror your own or someone you know? How do you think health coaching could help you? Share your thoughts in the comments below.

If you are living with a serious health issue, which may be a serious illness or injury or chronic illness, or are caring for someone who is, and would like support to return to a sense of wellness, have a look at how we can work together and get in touch for a free no obligation consultation.

You can also download the questions I sent to Wendy for her to think about ahead of our first session via this blog post.

 

Help with research on acceptance

 

If you or a loved one experienced a serious health issue in the past 2 years and are struggling or wondering if you can accept what has happened, I would love to speak with you. I am researching the concept of ‘acceptance’ within the context of a serious health issue by collecting people’s experiences with it. Click here to find out more. And in exchange, I offer you a free 1 hour coaching session.

 

Pass it forward

 

Although this blog is written in the context of living with a serious health issue, the ideas contained within are applicable to everyone. If you think someone you know would benefit from reading this blog, or you just want to spread the ideas, click on the icons to share.

© Copyright Barbara Babcock 2018

 

My story of coping with a serious rare illness Transverse Myelitis #RareDiseaseDay

My story of coping with a serious rare illness Transverse Myelitis #RareDiseaseDay

For Rare Disease Day, I am sharing my story of coping with a serious rare illness called Transverse Myelitis, which I got in October 2008. I realised I never shared my personal story with serious illness in any detail and given Transverse Myelitis is rare, it feels appropriate to share it today. I originally wrote this article in 2016 for the Transverse Myelitis Association in the USA and it first appeared here. I have made some changes to the original article.

 

About Transverse Myelitis

 

Transverse Myelitis, which I’ll refer to as TM, is a rare neurological inflammatory condition resulting in inflammation in the spinal cord. The inflammation can be at any point along your spinal cord and you will be affected in your body from that point downwards. For example, if you have inflammatory lesions in the cervical region, your arms, torso and legs will be affected. If the lesions are in the thoracic region, your torso and legs will be affected but not your arms.

It is an auto-immune disorder which means that your immune system attacks your body instead of the virus, infection or whatever it was supposed to be dealing with. So it is not an illness you ‘catch’ from anything or anyone; it’s not contagious or genetic.

Transverse Myelitis is in the same disease family as Multiple Sclerosis, just much more rare. Approximately 300 people per year are diagnosed with TM in the UK.

The onset of TM can be sudden over a few hours, or more gradual over days, weeks or even months. Red flag symptoms can include back pain (not just lower back pain), paralysis or muscle weakness in arms and/or legs (and hence mobility issues), bladder and bowel issues, sexual dysfunction, sensory disturbance (like a numbing sensation), and pain which can feel like a shooting, stabbing, crawling, freezing, hot or banding like pain.

TM is typically a one-off episode which can leave a person with ongoing residual symptoms such as paralysis, weakness, mobility issues, bladder and bowel issues, sensory disturbance, neuropathic pain, fatigue, and depression. The recovery process is a very uncertain one and doctors cannot predict how much functionality a person will regain and how long it will take. Recovery will start a few weeks to months after onset and can continue for more than two years.

Every person is affected differently by TM. Some people can be left with a lifelong disability, others can make a good recovery. For some people, TM is the first presentation of Multiple Sclerosis or Neuromyelitis Optica. For a small percentage of people, TM can be recurrent.

Awareness ribbon for Transverse Myelitis

 

My story of Transverse Myelitis – The onset

 

Today is 13 October 2016 (when I originally wrote this article), 8 years to the day I was advised by my GP to go to A&E (Accident and Emergency) as soon as possible. I was feeling strong pins and needles, and shooting, stabbing pain all throughout the saddle area. Sitting for any length of time was painful. So was standing. I felt like I poo-ed my pants and was constantly checking whether I had. I hadn’t. Walking was painful. I was due to deliver a presentation that evening, but cancelled it as going to A&E took priority.

In A&E, a host of tests were done. Despite being in pain, I was pretty relaxed, chatting with my other half and making my way through a bag of Haribo sweets I asked him to bring me. (Learning: Do not eat sweets whilst in A&E. It wreaks havoc on your blood sugars, and the nurses ask you all sorts of questions about whether you are diabetic and may not be convinced if you tell them no.) They wanted to admit me. I was meant to fly to the USA in three days for my sister’s wedding, so I wanted to return home. They strongly advised me to follow their advice. I did.

Tests commenced. Long sessions in the MRI scanner. A lumbar puncture that required a longer needle than what the doctors were initially using, and 3-4 tries before they got a clean sample of my cerebrospinal fluid. I had to remind the very excited medical students that there was a patient at the end of the needle who was scared, in discomfort and needed to be looked after.

With each passing day, the pins and needles and stabbing and shooting pain progressed down my body. Banding pain joined the noisy party inside of me. I felt like I couldn’t breathe and I could feel the panic rising. I finally figured out I could breathe and that what I was experiencing was some kind of pain.

Walking felt like pushing through the heaviest of treacle and my legs felt twice the size they actually were. I couldn’t walk more than 10 steps so acquiesced to using a wheelchair. I never made it to my sister’s wedding.

The pain, odd sensations and banding crept above my waist. More tests were ordered. Water hitting my skin and wearing clothes became very painful. I couldn’t sense temperature either. I still showered telling myself I was going to maintain a routine and be clean despite everything. Time feels plentiful in hospital so I laid there doing visualisations of a healing white light going up and down my spine and forced myself to walk as far as I could however badly I was walking.

A surprise for me and a highlight for the neurologist leading my case was accidentally discovering that I have another rare neurological condition in her area of expertise of movement disorders – geniospasm. It is a rare hereditary movement disorder where the chin shakes at random times and often for no reason. So I was discharged from hospital with two rare neurological conditions. I’ve had geniospasm all my life and never knew it was a recognised disorder and rare.

In relation to Transverse Myelitis, they didn’t tell me I had that. They only told me that I had ‘inflammation of the spinal cord’ with two lesions at C4 and C5, was seriously ill, should not work for several months and rest. I was worried as my job had been made redundant earlier in the summer and I had been actively looking for work.

 

After hospital – Learning to live with Transverse Myelitis

 

I returned home from hospital after 2 weeks. I had to rest a lot because of the fatigue and pain. A two block walk to the store and back would tire me out so much I slept for the rest of the day. As we were technically on holiday, my other half was able to be at home with me for a few days to make sure I could look after myself. The day he returned to work, he learned that his job was being made redundant.

Picture of a person with fatigue sleeping on a sofa

When fatigue is present, resting is important

 

I learned of my diagnosis in a letter the neurologist sent to my GP, a copy of which was sent to me. In it was written ‘cervical myelitis’. So I naturally turned to Google and what I read scared me. I experienced so much anxiety and fear for my health, my future and my life. The quality of my sleep wasn’t great due to the anxiety, pain and geniospasm (for some reason the TM re-triggered the geniospasm and my badly shaking chin would wake me up at night).

I couldn’t do much at all and was bored senseless. So I started genealogical research. Although it was painful and slow to type, it was a good temporary distraction from my health issues. And I usually had an interesting piece of info to share with my husband about my family at the end of the day.

In time, I found the Transverse Myelitis Association in the USA and the Transverse Myelitis Society in the UK where I live. The information was limited at that time but a talk by a neurologist at the TM Society’s London support group answered some of my questions. I also had regular follow-up visits with the neurologist which helped too. I was one of the lucky ones to see a neurologist regularly post-diagnosis and I think the geniospasm had a role to play in that.

 

Logo for the Transverse Myelitis Society

 

The months passed and bit by bit, I improved. The fatigue started to dissipate. I swam and did yoga. I started a new job and was thankful it was part-time because I was still experiencing fatigue and pain. I started studying for my first coaching qualification and that helped me immensely to come to terms with what happened.

A completely separate issue from the Transverse Myelitis was learning at this time that we would not be able to have children. Between the death of my father in 2007, caring for my mother after she had emergency heart surgery in Spring 2008, my job being made redundant soon after that, getting seriously ill in Autumn 2008, then my husband’s job being made redundant, that news felt like another blow and a particularly cruel one. People with serious health issues and particularly chronic ones often mention about not having a choice to go on, you just do. I get that.

When a #seriousillness or #seriousinjury disrupts your life, people often ask how do you go on. The option of doing nothing doesn’t feel like a great choice to make. So you just get on with your life the best you can. tell a friend

 

Nine months later, I still had sensory disturbance, neuropathic pain, some fatigue, and didn’t have full sensory awareness in my hands. The neurologist said that might be it for the rest of my life. It felt like something finished when I heard that prognosis. A finality. On the outside, I looked and functioned normally. All things considered, my recovery was a good one.

 

Making meaning of my illness experience

 

I got involved with the Transverse Myelitis Society and offered my skillset of NLP (Neuro Linguistic Programming), coaching and adult learning to use for the benefit of members through delivering presentations and writing articles. I had been using my skillset on myself and found it immensely helpful.

In 2010, I was asked to join the TM Society’s management committee. In 2011, I started a masters in coaching psychology and focused my research on the impact of coaching on the wellbeing of people living with TM and their primary caregivers. I included the carer, often a family member, as I saw how they are also affected. I was curious whether coaching could help people find a way to live well (enough) with the impact of the condition. I learned it can. You can read a summary of that research project here.

In April 2013, I became Chair of the UK TM Society for a three-year term which finished in April 2016. It was an opportunity to use my skillset in a greater way for the benefit of our members. This aligned with my values of being in service to others for a good cause and developing myself. I enjoyed introducing new services, events and information for our members: a Coaching Bursary Scheme, an Equipment Grant Scheme, the Family Weekend in the UK, and information such as the TM Condition Insight Report and TM Frequently Asked Questions document. I enjoyed having the opportunity through charities such as the Neurological Alliance, National Voices and Spinal Injuries Association to raise awareness and represent the needs of TM Society members across the charity sector and amongst government officials and the NHS.

 

Life beyond Transverse Myelitis

 

Even though I have stepped back from the Chair role and the TM Society’s management committee, I am still involved as a volunteer. Separately, I am helping a neurologist design a research project on TM and we hope it will get the necessary funding. I have studied Acceptance Commitment Therapy because I wanted to learn different approaches to helping people through the process of acceptance of difficult situations. I’ve also been studying Systemic Constellations to help people resolve issues relating to family dynamics and illness. This all feels like good work to be doing. It is also work I very much enjoy and wonder if ‘work’ is the right word. I am grateful for the opportunity.

So I think back to 9 years ago and to the day I felt like something finished when I was told my prognosis. I notice how my body is now. The constant pins and needles in my hands and hence reduced sensory awareness. How anything I touch feels like sandpaper, and the cramping in my fingers during the winter months. The random sensory disturbance which happens throughout my body. Some bladder and bowel issues which are manageable. The buzzing I feel in my spinal cord whenever I bend my head forward. These symptoms are all invisible and are manageable. I use the symptoms as a reminder to look after myself and live my life well.

 

What we think is broken can actually nurture beauty

 

When living with a #serioushealthissue #chronicillness our bodies may have been wounded and at times they may feel broken. But beauty can spring forth from the brokenness #KintsugiBowls #postraumaticgrowth tell a friend

 

When I reflect on my involvement with the TM Society, the healthcare profession and charity sector in the UK, and my coaching work, I think of Kintsugi bowls. They are Japanese bowls that broke and are mended with gold seams. It’s about honouring the wound and beauty from the brokenness. It is a symbol of rebirth, that nothing is ever truly broken beyond repair.

So our bodies may have been wounded. At times we may feel that they are broken. But beauty can spring forth from the brokenness. And that is my hope for all of us affected by a serious health issue, including our children and families: may we nurture and grow the beauty that we still hold within us.

Picture of a Japanese kintsugi bowl and how life with a serious health issue can be like that

 

What’s it like for you?

 

What has your experience with a serious illness or injury been like? What have you done differently in your life as a result? What would you like to do differently? Share your story in the comments below.

If you are living with a chronic illness or the after effects of a serious illness or injury, or are caring for someone who is, and you would like support to rebuild and renew your life, have a look at how we can work together and get in touch for a free no obligation consultation.

 

Help with research on acceptance

 

If you or a loved one experienced a serious health issue in the past 2 years and are struggling or wondering if you can accept what has happened, I would love to speak with you. I am researching the concept of ‘acceptance’ within the context of a serious health issue by collecting people’s experiences with it. Click here to find out more. In exchange, I offer you a free 1 hour coaching session.

 

Pass it forward

 

Although I wrote this blog in the context of living with a serious health issue, the ideas contained within are often applicable to everyone. If you think someone you know would benefit from reading this blog, or you just want to spread the ideas, click on the icons to share.

© Copyright Barbara Babcock 2018

 

10 tips to manage scanxiety (scan anxiety) during medical procedures

10 tips to manage scanxiety (scan anxiety) during medical procedures

You may need to manage scanxiety – scan anxiety – when living with illness every few months, once a year or on the occasion when something isn’t right and you need to get it checked out. This type of anxiety can also apply to other medical investigative tests.

It’s not fun, I experienced it the other week. And I’ve experienced it many times in the past when I’ve had MRIs, other unpleasant investigative tests, and as a carer. I learned it can be an up and down process – you may get some good news, then some not-so-good news, then some reassurance, and then you wait days/weeks/months for the final verdict.

Feeling a degree of anxiety is normal because as you go through the process of scans, procedures, etc, you don’t know what the medical professionals will find and what it may mean. If you feel the anxiety is getting in the way – how often you think about it, your sleep, or getting through the procedure/scan/treatment itself for example – then here are 10 ideas on how to manage it.

I largely refer to managing the anxiety during the scan or procedure but some of the ideas are also applicable before and after it. When I talk about anxiety in this context, I am not referring to a clinical diagnosis of anxiety. If you have a diagnosis of anxiety, you may find the ideas mentioned here useful.

 

My experience of scanxiety

 

In my case, the scan came about because something wasn’t quite right for a few months – breast pain. Given it was recurring and it felt like something was in the way inside my breast but I couldn’t feel a lump, I saw the GP. The GP referred me for a scan and 11 days later I was sitting in my local hospital.

I saw the consultant. She did a manual exam and couldn’t find any lumps. I felt relief. She sent me for a scan.

I got changed and waited for the scan.

I had the mammogram. It was uncomfortable but went ok.

I sat in the scan seating area. They asked me to come back to redo some of the mammogram scans.

I could feel the anxiety rise a notch.

Afterwards, they came back and said the consultant wanted an ultrasound.

I felt the anxiety increasing.

Whilst doing the ultrasound, the consultant said they found something.

But it was in the other breast that had been ok.

When I get news like that, I have a ‘deer in the headlights’ moment. I can feel the anxiety spike high, and my eyes open wide. I feel very scared in those moments.

Picture of a person with anxiety after receiving a diagnosis and needing a medical procedure

When you get a diagnosis or an unpleasant medical update and feel anxiety

The consultant said it was a lump but one that was well-defined – a fibroadenoma.

I said to her, “I should be asking questions but I can’t. My mind had gone blank.” The anxiety was in control.

She said it was most likely not cancerous, but they wanted to check it out further by doing a biopsy, they could do that at another time but could also do it now. I don’t remember actually saying yes, I may have, but what I was saying and tone of voice indicated yes. She proceeded to prepare for the biopsy.

I was full of nervous chatter during it describing what had happened when I had a lumbar puncture when they had to get a bigger needle so this shouldn’t be so bad. That was a way of me calming myself by telling myself and them I had been through worse.

I was noticing how tense my muscles were and I would remind myself to relax and breathe. At the end the consultant said I had been very brave. I didn’t feel brave. I berated myself silently saying to myself the doctor shouldn’t have to say that to me. Notice that should, because we are coming back to it. I reminded myself to take from the consultant’s words what she was giving – comfort. I then joked with the nurse asking if I could get a gold star.

The scans and procedures finished and it was back to the main waiting area to wait to see the consultant. I suddenly felt emotional. It was a familiar feeling. After a round of being poked and prodded by medical professionals I can feel emotional. Also, I’ve been having tests for other things recently and have a treatment coming up so it just felt like something else to deal with. I just wanted to curl up and be looked after by someone else.

I saw the consultant, who said the lump is usually not an issue and if all is ok, they would leave it where it is. But they would let me know the results of the biopsy in the next week. I referred to the anxiety I was feeling and the doctor said they wanted to be thorough.

And that was it I thought and even said, ‘It’s a balance to maintain between the medical professionals being thorough and the anxiety the patient may be feeling.’ That sounds clumsy but that was the key learning for me.

There’s a balance to maintain between the medical professionals being thorough and the #anxiety you may be feeling during the #medicalprocedure or #scan tell a friend

 

The doctors want to do their best so they will be thorough.

 

Although modern medicine can do so many great and amazing things, it is not always a precise science. So expect the unexpected to happen and if it doesn’t, that’s great.

 

The patient manages their scanxiety as best they can so the doctors can do their scans, tests, etc.

 

Learning and practicing techniques to manage our anxiety is in our control. Given we can control our breath, mind and muscles, those are great starting points to manage any anxiety we may experience.

 

Picture of a scale with a doctor and patient sitting on it and maintaining a balance

The doctor and patient maintaining the balance between being thorough and managing anxiety

 

So here is what I found to keep scanxiety from taking over

 

  1. Read the information they send you in advance so you know what will happen on the day. If you have questions before the appointment, call the hospital.

 

  1. Bring something to do during the times you have to wait like a book or magazine to read, paper to draw or write on, your iPad or phone to watch tv or listen to music, your knitting, whatever. This is a healthy distraction which helps to keep the anxiety at bay.

 

  1. If you will be there for a while, bring food and drink provided you can eat/drink during the procedure you’re having. Sometimes it’s hard to get away as when you are waiting, you don’t always know when you will be called in to see the consultant or have a scan/procedure. So best not to sit there hungry or thirsty.

 

  1. Be prepared with these generic questions in case they want to do another procedure or suggest a new treatment. They will help you to collect the information you need to make an informed decision. You may not have to use them but being prepared can be a comfort.

 

  • What is this procedure/treatment/drug meant to achieve?
  • What are my options? (are there other options for example)
  • What are the specific benefits and potential harm to me? (pros and cons)
  • What happens if I do nothing?
  • What should I watch out for? (after treatment, the procedure or starting new medication, i.e. side effects, having a relapse, etc.)
  • Are there any questions I haven’t asked that other patients typically ask?
  • Who can I contact if I have a follow-up question?

 

(Questions 2, 3, 4 were obtained from this excellent article.)

 

Picture of questions to ask so you can make informed decisions about your medical care

Key questions to ask so you can get the info you need to make informed decisions about your medical care

 

  1. Find a release for your anxiety during the procedure that doesn’t get in the way of completing it – Chattering and joking, when it’s possible, are mine. If that, breathing, counting, or something else helps you to be brave, go for it. I have in the past told medical professionals that I would probably chat or use humour to calm my nerves and get through the procedure. They were never surprised. They’ve seen it all before.

 

  1. Keep yourself in the present moment – Focusing on your breath and breathing is a healthy distraction from wondering how the test is going, what are they finding, etc. However, if breathing has an impact on the procedure (there are procedures where you may have to hold your breath or breathe a certain way), then focus on what is in front of you – what you see, what you are holding on to, etc. Or ask if you can wear headphones during the procedure as you may be able to listen to a podcast or your favourite music.

 

  1. Have a mental happy place you can take yourself to – favourite holiday spot, a place you’ve always wanted to travel to, imaginary dream home, you score the winning goal in the World Cup final (whenever England get there), you achieve something great you’ve always wanted to, etc. This is a day dream that makes you feel happy.

 

  1. Have pen and paper with you to write down how you are feeling or use your phone to type it out while you are waiting. That is how this blog post was born.

 

  1. If thoughts are being pesky like annoying internet pop-up windows, imagine crumpling them up and throwing them in the medical waste bin. Or being taken away by a healthcare professional leaving the room. Or imagine putting the thought on a cloud and watching a strong wind blow it away. And if you find your self-talk containing a lot of ‘I should have…’, stop and remind yourself to be gentle with yourself.

 

  1. If you can, take someone with you to the procedure/treatment. Having someone else to talk to whilst you are waiting for procedures and scans can be a good distraction, enjoyable, and calming. If that is not possible, call or visit a good friend or family member afterwards to talk about it. I dropped in on a friend of mine on the way home (unannounced) and she fed me tasty vegetarian lentils and chocolate cake. Her company and food were very restorative!

 

Here are 10 ways to keep #scanxiety – scan anxiety – at bay during a #medicalprocedure or #scan tell a friend

 

Picture of 10 ways to manage scanxiety (scan anxiety)

10 ways to manage scanxiety (scan anxiety)

 

These 10 tips are a starting point. Keep seeking to learn new techniques and approaches so you have a toolbox of them. That way, if you can’t use one during a procedure or scan, you can use another one.

 

What’s it like for you?

 

What have you found to help you keep scanxiety at bay during procedures, scans and doctor appointment? Share your thoughts in the comments below as we may all learn something new to add to our toolbox.

If you are living with a chronic illness or the after effects of a serious illness, or are caring for someone who is and would like support to manage anxiety and have good relationships with healthcare professionals, have a look at how we can work together and get in touch for a free no obligation consultation.

 

Help with research on acceptance

 

If you or a loved one experienced a serious health issue in the past 2 years and are struggling or wondering if you can accept what has happened, I would love to speak with you. I am researching the concept of ‘acceptance’ within the context of a serious health issue by collecting people’s experiences with it. Click here to find out more. And in exchange, I offer you a free 1 hour coaching session.

 

Pass it forward

 

Although this blog is written in the context of living with a serious health issue, the ideas contained within are applicable to everyone. If you think someone you know would benefit from reading this blog, or you just want to spread the ideas, click on the icons to share.

© Copyright Barbara Babcock 2018

 

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