Help KB to walk again ?

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Perth, Western Australia, Australia

Supporters

I’m a third year medical student at Notre Dame Fremantle. This means that I spend my time on clinical placement in hospitals. Last September, after trying numerous ways to be seen by a neurosurgeon, I developed cauda equina syndrome because of an fragmented disc, and needed emergency surgery. CES affects the nerves below the spinal cord. These nerves go to the legs, feet, bladder, bowel and sexual organs. I worked hard to get the power back in my legs, while dealing with a neurogenic bladder and bowel.

Unfortunately, in January, I woke up in pain and my legs wouldn’t hold me. Upon investigation they found the disc had reherniated and was putting pressure on the S1 nerve. The neurosurgeon thought this happened because of hypermobility syndrome – this causes lax joints and hyperflexibility. I went back to rehab, but in May on the way home from placement, my car was rear-ended.

The first sign that something was wrong was I could no longer pee- I spent the weekend in hospital because my bladder stopped working. A few days later I had an increase in pain – it got to the point where I couldn’t walk, bend my neck or straighten my leg without electric shocks running from my feet to my back. I was in hospital for 6 days – the doctors decided to do an epidural and other injections into the spine to stop the pain. The procedure was successful and I battled on; back to rehab and placement.

I cancelled all social events except placement; as I was now experiencing anxiety and nightmares about the pain returning. I worked hard at rehab, and within a month, I had almost full power in my leg and I could do heel raises. I finally felt strong.

This was only days before what has become something of a bad dream – on Monday I woke with pain in my leg. I consulted my specialists and we attempted to get it under control. On Thursday, I got home from placement and noticed the pain was very similar to before my first surgery. My leg felt heavy when I tried to walk and within an hour it no longer held me and I couldn’t lift it off the floor.

The emergency MRI showed the disc completely compressing S1 nerve. I underwent difficult emergency surgery for the second time in less than a year. The surgeon has told me that I didn’t do anything wrong – it was just pure back luck that I am one of the 10% who need to have redo surgery. Leading up to this surgery, all my specialists were thrilled with my progress, and find it hard to fathom that this has happened again.

I did not have private hospital insurance prior to the first surgery. I thought I was fit and healthy and wouldn’t need it. I have since purchased it but I am still waiting for the 12 month period to pass for pre-existing injuries to be covered. It costs approximately $90 to $120 per appointment with the spinal physio. I also have appointments with other specialists such as a urologist ($600) and have to pay for medications that are not listed on the PBS.

My extras health insurance covers about $20 of a physio appointment. My surgeon has said I am going to need physio, physio, physio to be able to walk again. From previous experiences my best outcomes will come from seeing the private spinal physio. I am no longer able to work so I am not sure how I will afford to pay for these appointments, as Centrelink barely covers the cost of rent and food for two weeks.

I have never asked for help before. I have done the past 12 months of rehab alone with some minimal financial support from my dad. It has cost me thousands of dollars.

Lots of people have asked me how they can help; and I have realised that financially supporting my rehab is going to mean I have access to the best care. It also means I don’t have to chose between eating food and seeing a physio/doing hydro.

If you would like to donate the amount you would have spent on flowers or a get well gift, that would be amazing. All money will be used to support rehabilitation. My life is pretty simple – I just want to be well enough to finish my med degree and move back to the Pilbara – where my people are.

Hannah Keen

6 years ago

$100

Luke Spagnoletti

6 years ago

$50

Linda Guiraldenq

6 years ago

$50

Anonymous

6 years ago

$100

Ashleigh Boyce

6 years ago

$25

Anonymous

6 years ago

$50

Shannon Wilson

6 years ago

$50

Tess Hooper

6 years ago

$25

Imogen Merlo

6 years ago

$50

Eryn Fullard

6 years ago

$50

Steve Butler

6 years ago

$100

Amy Pollock-Hall

6 years ago

$50

Angus Henderson

6 years ago

$50

Troy Davies

6 years ago

$25

Marc Darbyshire

6 years ago

$100

Alister Hay

6 years ago

$100

Madelaine Landini

6 years ago

$25

Anonymous

6 years ago

$25

Jasmine Rowe

6 years ago

$40

Kim and Kev Harber

6 years ago

$100

Kelly Bell

Hello! Apologies if you didn’t anticipate ongoing updates but it felt right to email you as I approach the one year anniversary since discharge from the spinal unit. That milestone rolls around tomorrow! It’s hard to believe that it has been a year since I tentatively walked out – not very well mind you. So much has happened, it feels like a lifetime but also like yesterday. On August 3, after a 5 month wait, I had what I really hope is the final spinal surgery I’ll need. It has been god damn awful. I thought I knew a thing or two about spinal surgeries – then I had an anterior fusion. And well, just for laughs, we threw in major abdominal surgery as well. I still can’t cough or sneeze without pain – they went through my stomach to access my back and those abdo muscles are right pissed off. BUT, and it’s a big but, this surgery has also been the best thing to happen to me (the god damn worst as well). I have not been in hospital for more than 4 months! This is massive…and I am the furthest I’ve ever got in a rehab program. I can lift small amounts of weight and I don’t have constant burning pain in my legs. I’m still taking pain medication but long term, we would hope to reduce this once I hit 6 months post op in February. I will also have an x-ray to confirm the bone graft in the fusion has grown. While we can’t change the past, 2019 would have looked very different for me if this fusion had been done during the second emergency surgery. In other good news, next Monday, Dec 16, I will receive my results for third year medicine. It has taken 2 years and a lot of bloody heartache, as well as awful mental health and more medication than I ever imagined I would need, but I got there. I sat my exams and have spent the past week in Victoria with my sister. I met my new niece who was born two days before my surgery and I’ve got to spend time with her brothers. This is the first major break I’ll have since the first surgery in 2017. Financially, things are still very tough, but I am so grateful for your contributions in 2018, as there is no way I would have survived 2019 without them – and may limp into 2020. I’m really hoping that with continued rehab I can head into my final year of med without significant pain; and have a year where I don’t need a bloody spinal surgery. Merry Christmas to you all! May 2020 be full of wellness and love xx

Hello!

Apologies if you didn’t anticipate ongoing updates but it felt right to email you as I approach the one year anniversary since discharge from the spinal unit. That milestone rolls around tomorrow! It’s hard to believe that it has been a year since I tentatively walked out – not very well mind you.

So much has happened, it feels like a lifetime but also like yesterday. On August 3, after a 5 month wait, I had what I really hope is the final spinal surgery I’ll need. It has been god damn awful. I thought I knew a thing or two about spinal surgeries – then I had an anterior fusion. And well, just for laughs, we threw in major abdominal surgery as well. I still can’t cough or sneeze without pain – they went through my stomach to access my back and those abdo muscles are right pissed off.

BUT, and it’s a big but, this surgery has also been the best thing to happen to me (the god damn worst as well). I have not been in hospital for more than 4 months! This is massive…and I am the furthest I’ve ever got in a rehab program. I can lift small amounts of weight and I don’t have constant burning pain in my legs. I’m still taking pain medication but long term, we would hope to reduce this once I hit 6 months post op in February. I will also have an x-ray to confirm the bone graft in the fusion has grown. While we can’t change the past, 2019 would have looked very different for me if this fusion had been done during the second emergency surgery.

In other good news, next Monday, Dec 16, I will receive my results for third year medicine. It has taken 2 years and a lot of bloody heartache, as well as awful mental health and more medication than I ever imagined I would need, but I got there. I sat my exams and have spent the past week in Victoria with my sister. I met my new niece who was born two days before my surgery and I’ve got to spend time with her brothers. This is the first major break I’ll have since the first surgery in 2017.

Financially, things are still very tough, but I am so grateful for your contributions in 2018, as there is no way I would have survived 2019 without them – and may limp into 2020.

I’m really hoping that with continued rehab I can head into my final year of med without significant pain; and have a year where I don’t need a bloody spinal surgery.

Merry Christmas to you all! May 2020 be full of wellness and love xx

5 years ago

Kelly Bell

Hello everyone, Just thought I’d stop by and update you all. Thank you again for the generous donations. Without them, I wouldn’t have survived the past few months. Since December 13, I have been discharged, went home to see my family, moved house and have been back at uni. Unfortunately, I have had quite a bit of time off because…would you believe it? I have reherniated the same disc again. I was admitted to Charlie’s on Feb 26 after an increase in pain. The S1 nerve root is again compressed on both the right and the left. The new MRI confirmed that I had herniated the disc in Oct when I was sent back to Charlie’s during my rehab stint. It has doubled in size between then and the MRI on Feb 26. So, for the past 6 weeks or so, I have been waiting for appointments with a new neurosurgeon and an vascular surgeon. The plan is to do an anterior approach interbody fusion. In layman’s terms, that means they are going to go through my stomach/side, move the major blood vessels out of the way, take all of what is left of the disc and replace it with a cage/bone graft. I stupidly made the mistake of googling the surgery and watching a bit of the video. I don’t recommend doing that. It’s a major surgery and it isn’t one I want to have but I don’t have a lot of options now. This disc has continually reherniated with normal increases in activity. I should be able to go back to uni and walk a round on the wards without the disc herniating. It’s frustrating and to be honest, I’m pretty over it. I was given a nerve sleeve injection prior to discharge and that has helped with pain. I’m still seeing physio once a week and attempting to get in the hydro pool as much as possible. I try to remind myself that once this is done, I’ll get on with my life and live for another 50 years. Unlike some of the patients who I have seen on placement. Big love, Kelly x

Hello everyone,

Just thought I’d stop by and update you all. Thank you again for the generous donations. Without them, I wouldn’t have survived the past few months. Since December 13, I have been discharged, went home to see my family, moved house and have been back at uni.

Unfortunately, I have had quite a bit of time off because…would you believe it? I have reherniated the same disc again. I was admitted to Charlie’s on Feb 26 after an increase in pain. The S1 nerve root is again compressed on both the right and the left. The new MRI confirmed that I had herniated the disc in Oct when I was sent back to Charlie’s during my rehab stint. It has doubled in size between then and the MRI on Feb 26.

So, for the past 6 weeks or so, I have been waiting for appointments with a new neurosurgeon and an vascular surgeon. The plan is to do an anterior approach interbody fusion. In layman’s terms, that means they are going to go through my stomach/side, move the major blood vessels out of the way, take all of what is left of the disc and replace it with a cage/bone graft. I stupidly made the mistake of googling the surgery and watching a bit of the video. I don’t recommend doing that.

It’s a major surgery and it isn’t one I want to have but I don’t have a lot of options now. This disc has continually reherniated with normal increases in activity. I should be able to go back to uni and walk a round on the wards without the disc herniating.

It’s frustrating and to be honest, I’m pretty over it. I was given a nerve sleeve injection prior to discharge and that has helped with pain. I’m still seeing physio once a week and attempting to get in the hydro pool as much as possible. I try to remind myself that once this is done, I’ll get on with my life and live for another 50 years. Unlike some of the patients who I have seen on placement.

Big love,

Kelly x

6 years ago

Kelly Bell

Hello! Quick update: I’m currently still on the spinal unit at FSH but likely to be discharged this coming Thursday, 12th or Friday, 13th. Lots has happened since I returned from Charlie’s – I’ve had heaps of specialists come, and plenty of testing. We’ve found out things about my bladder, and I have learnt the hard way that once I leave here for good, I still have a long road ahead of me. I’ve had two weekends at home – the one that just passed, wasn’t the best. Pain is still a factor in the things I do, and I’ve realised I still don’t have much exercise tolerance so about an hour of activity/standing/sitting is about all I can manage at the moment. It’s a bit of a rude shock, but it is what it is. Time will heal. I’m going to be referred back to outpatient rehab at Fremantle Hospital and will continue with physio/hydrotherapy/continence physio – as well as the myraid of other specialist appts that I’ll have at Charlie’s. Unfortunately, my grandfather had a fall, which required emergency surgery while I was on hiatus at Charlie’s. It’s been pretty stressful – so I’m looking forward to getting on that plane back to Victoria next week. I haven’t seen my family for any substantial amount of time since 2016. Seeing them is now my priority and other things, like finding somewhere to live, have had to wait (but if you know someone with a house or room in North Fremantle, I’m looking!!!) Good news: my walking has improved significantly. I still have to concentrate, but it should continue to get better with time. I can manage stairs comfortably and I’m not afraid of falling. The restrictions I had on my movement have also ended so I can bend over and pick something up off the ground (yayay!). But, there will be no power lifting anytime soon, as I’m not allowed to lift anything heavier than 5kg. Soooo, come Friday, I’ll end my 13 week stint in hospital (13 weeks on the 13th hey!) The one thing I would change would be keeping a diary of all the things that happened while here. It’s been rough, but I’m proud of how well I’ve coped, and what my body has done to recover. I’m also incredibly grateful for the team that’s helped me get to this point, and for everyone who has shown support (in whatever way). People keep saying this experience will make me a better doctor, and bloody hell, it sure feels like it at the moment. Merry Christmas everyone. Stay safe, hug your family and friends, and don’t forget to record, and enjoy the little moments. Here’s a pic of me attempting walking in the real world (look up gal!) Big love xxxx

Quick update: I’m currently still on the spinal unit at FSH but likely to be discharged this coming Thursday, 12th or Friday, 13th. Lots has happened since I returned from Charlie’s – I’ve had heaps of specialists come, and plenty of testing. We’ve found out things about my bladder, and I have learnt the hard way that once I leave here for good, I still have a long road ahead of me.

I’ve had two weekends at home – the one that just passed, wasn’t the best. Pain is still a factor in the things I do, and I’ve realised I still don’t have much exercise tolerance so about an hour of activity/standing/sitting is about all I can manage at the moment. It’s a bit of a rude shock, but it is what it is. Time will heal.

I’m going to be referred back to outpatient rehab at Fremantle Hospital and will continue with physio/hydrotherapy/continence physio – as well as the myraid of other specialist appts that I’ll have at Charlie’s.

Unfortunately, my grandfather had a fall, which required emergency surgery while I was on hiatus at Charlie’s. It’s been pretty stressful – so I’m looking forward to getting on that plane back to Victoria next week. I haven’t seen my family for any substantial amount of time since 2016. Seeing them is now my priority and other things, like finding somewhere to live, have had to wait (but if you know someone with a house or room in North Fremantle, I’m looking!!!)

Good news: my walking has improved significantly. I still have to concentrate, but it should continue to get better with time. I can manage stairs comfortably and I’m not afraid of falling. The restrictions I had on my movement have also ended so I can bend over and pick something up off the ground (yayay!). But, there will be no power lifting anytime soon, as I’m not allowed to lift anything heavier than 5kg.

Soooo, come Friday, I’ll end my 13 week stint in hospital (13 weeks on the 13th hey!) The one thing I would change would be keeping a diary of all the things that happened while here. It’s been rough, but I’m proud of how well I’ve coped, and what my body has done to recover.

I’m also incredibly grateful for the team that’s helped me get to this point, and for everyone who has shown support (in whatever way). People keep saying this experience will make me a better doctor, and bloody hell, it sure feels like it at the moment.

Merry Christmas everyone. Stay safe, hug your family and friends, and don’t forget to record, and enjoy the little moments.

Here’s a pic of me attempting walking in the real world (look up gal!)

6 years ago

Kelly Bell

Hi friends, So random, but I actually started writing this message about a week and a half ago. At the time, I was really struggling with self catheterisation (inserting a sterile plastic tube into your bladder to release urine), and wouldn’t have imagined having to head back to the surgeons. That night, I had a sudden onset of quite severe coccyx pain – an MRI showed I have reherniated the disc that was operated on. Honestly at this point, it is probably my best skill in life. Third time lucky hey? Presently, I am in Sir Charles Gairdner Hospital (I was transferred from the rehab unit), listening as a patient across the hall cries about the amount of pain she is in (they’re trying to move her so she doesn’t get a pressure injury). I can definitely say that I have experienced similar at multiple points in this journey. After a stressful few days waiting, my surgeon decided that she didn’t need to operate again. I had some testing done on my leg to see what was happening with the nerves, and while I likely have nerve damage (I did in Jan when they last tested), there is no direct compression of the nerve roots at the moment that needs surgical intervention. I’ve lost a bit of movement and strength and walk in some muted fashion – the specialists say there is global dysfunction of the muscles (likely caused by a combination of ongoing compression over the past 2 years, multiple surgeries and pain). This should improve with physio and time. So I’m currently just hanging out on vacation at Charlie’s waiting fo transfer back to rehab (please happen tomorrow!). Rather frustratingly, tomorrow (Nov 5) was going to be my discharge date. But it looks like it will be another two weeks or so. I’m currently sitting at 7 and a half weeks in hospital. The biggest issue for me, at the moment, is my bladder. I am catheterising again but as a result of a combination of things, have been unwell with a bladder infection for two weeks. It doesn’t sound like much but because I have no feeling, it can make me feel really rubbish because I don’t get the usual onset symptoms. I have worked out that if I have pain when I push on my bladder, then it usually means I have an infection. If there is no pain, I won’t realise I am an infection, until there is blood in my urine; which is never fun. I’m praying for a transfer to rehab tomorrow so that we can get on with the testing I need on my bladder function – once that is done and we have a solid plan in place. then I can feel confident going home. My continence (bladder and bowel function) is my number 1 priority. Just to throw a spanner in the works, my landlady (who I live with) has decided to renovate our house next year – so I also need to find another house to live in for the rest of my degree. Some of the money may be used to purchase the things I need to move into a new place – I currently live in a furnished place so I don’t have a bed or any of the basics (I think I own like two towels haha). Meanwhile, my cohort at uni sat their second exam today. It’s been an interesting week – I feel for them and also just feel like I’m going to wake up, and be sitting my exams with them as well. It doesn’t feel real that I will be in 3rd year again next year. It’s funny how the brain does that. Below is my pisstake of an outfit for Derby Day haha 🙂 KB x

Hi friends,

So random, but I actually started writing this message about a week and a half ago. At the time, I was really struggling with self catheterisation (inserting a sterile plastic tube into your bladder to release urine), and wouldn’t have imagined having to head back to the surgeons. That night, I had a sudden onset of quite severe coccyx pain – an MRI showed I have reherniated the disc that was operated on. Honestly at this point, it is probably my best skill in life. Third time lucky hey?

Presently, I am in Sir Charles Gairdner Hospital (I was transferred from the rehab unit), listening as a patient across the hall cries about the amount of pain she is in (they’re trying to move her so she doesn’t get a pressure injury). I can definitely say that I have experienced similar at multiple points in this journey.

After a stressful few days waiting, my surgeon decided that she didn’t need to operate again. I had some testing done on my leg to see what was happening with the nerves, and while I likely have nerve damage (I did in Jan when they last tested), there is no direct compression of the nerve roots at the moment that needs surgical intervention. I’ve lost a bit of movement and strength and walk in some muted fashion – the specialists say there is global dysfunction of the muscles (likely caused by a combination of ongoing compression over the past 2 years, multiple surgeries and pain). This should improve with physio and time. So I’m currently just hanging out on vacation at Charlie’s waiting fo transfer back to rehab (please happen tomorrow!).

Rather frustratingly, tomorrow (Nov 5) was going to be my discharge date. But it looks like it will be another two weeks or so. I’m currently sitting at 7 and a half weeks in hospital.

The biggest issue for me, at the moment, is my bladder. I am catheterising again but as a result of a combination of things, have been unwell with a bladder infection for two weeks. It doesn’t sound like much but because I have no feeling, it can make me feel really rubbish because I don’t get the usual onset symptoms. I have worked out that if I have pain when I push on my bladder, then it usually means I have an infection. If there is no pain, I won’t realise I am an infection, until there is blood in my urine; which is never fun.

I’m praying for a transfer to rehab tomorrow so that we can get on with the testing I need on my bladder function – once that is done and we have a solid plan in place. then I can feel confident going home. My continence (bladder and bowel function) is my number 1 priority.

Just to throw a spanner in the works, my landlady (who I live with) has decided to renovate our house next year – so I also need to find another house to live in for the rest of my degree. Some of the money may be used to purchase the things I need to move into a new place – I currently live in a furnished place so I don’t have a bed or any of the basics (I think I own like two towels haha).

Meanwhile, my cohort at uni sat their second exam today. It’s been an interesting week – I feel for them and also just feel like I’m going to wake up, and be sitting my exams with them as well. It doesn’t feel real that I will be in 3rd year again next year. It’s funny how the brain does that.

Below is my pisstake of an outfit for Derby Day haha 🙂

KB x

6 years ago

Shannon Wilson

Sorry it’s not more. Send more next week x

6 years ago

Kelly Bell

@Shannon Wilson don’t be silly. Just sent Tommy videos xx

6 years ago

Shannon Wilson

Sorry it’s not more. Send more next week x

6 years ago

Tess Hooper

Big love Kel xxx

6 years ago

Kelly Bell

@Tess Hooper I’m looking forward to your return from the North Pole 😉 xx

6 years ago

Kelly Bell

Hello from Ward 1A, bed 109 at Fiona Stanley Hospital, Who would have thought that this time a month ago, I would wake up with a pain in my knee that would end up with another bout of emergency surgery. I will have been at the rehab centre 3 weeks this Friday. I am progressing well physically, and “walked” in shoes for the first time yesterday. My toes still drag on the ground, but nowhere near as bad as it was. I can now get up and take myself to the toilet and walk short distances around the ward. On Monday next week, I will be able to start in the hydrotherapy pool, which is pretty exciting. I never thought that I would be excited to be in any hydro pool ever, but here we are. I’m hoping the water makes me feel a bit more balanced and less inclined to fall. We are still having plenty of issues with my bladder and bowel function, and are in the process of changing the way these are managed. It is important that we have the best plans in place as possible, to ensure that I don’t end up losing my bladder all together. Unfortunately, I also had to make the decision to defer this year of study (I was only 8 weeks from finishing, after completing more than 30 weeks). It means that I will need to repeat 3rd year medicine again in 2019. It was a pretty devastating decision to make, but I also need this body to last me another 50 to 60 years, so I have to give it the time to heal…and I figure I’m just going to be reallly good at 3rd year haha. I’d like to take this opportunity to thank you for the financial support you have provided me with. It is very difficult for me to accept help, but I would not be able to do this again, without it. I am already planning ways that I can give back to the spinal unit once I have been discharged. I would like to somehow contribute to the experience and outcomes of other patients who find themselves here. Big love, KB

Who would have thought that this time a month ago, I would wake up with a pain in my knee that would end up with another bout of emergency surgery.

I will have been at the rehab centre 3 weeks this Friday. I am progressing well physically, and “walked” in shoes for the first time yesterday. My toes still drag on the ground, but nowhere near as bad as it was. I can now get up and take myself to the toilet and walk short distances around the ward.

On Monday next week, I will be able to start in the hydrotherapy pool, which is pretty exciting. I never thought that I would be excited to be in any hydro pool ever, but here we are. I’m hoping the water makes me feel a bit more balanced and less inclined to fall.

We are still having plenty of issues with my bladder and bowel function, and are in the process of changing the way these are managed. It is important that we have the best plans in place as possible, to ensure that I don’t end up losing my bladder all together.

Unfortunately, I also had to make the decision to defer this year of study (I was only 8 weeks from finishing, after completing more than 30 weeks). It means that I will need to repeat 3rd year medicine again in 2019. It was a pretty devastating decision to make, but I also need this body to last me another 50 to 60 years, so I have to give it the time to heal…and I figure I’m just going to be reallly good at 3rd year haha.

I’d like to take this opportunity to thank you for the financial support you have provided me with. It is very difficult for me to accept help, but I would not be able to do this again, without it. I am already planning ways that I can give back to the spinal unit once I have been discharged. I would like to somehow contribute to the experience and outcomes of other patients who find themselves here.

6 years ago

Steve Bell

You are an amazing young woman Kelly and I’ve seen your strength for myself. I’m staggered that you have managed to keep up with your med degree on top of everything else! Although we’ve chatted a bit at Uni, I’m really pleased to be able to do something tangible. Wishing you all the best! Sharon.

6 years ago

Kelly Bell

@Steve Bell I’m really looking forward to getting back to uni xx

6 years ago

Warren McDonogh

Sending you lots of positive vibes for a speedy recovery. Keep your chin up and make sure you listen to the Occupational health peeps.

6 years ago

Kelly Bell

@Warren McDonogh they hound me. Doing all they say x

6 years ago

Lucindy Sartor

Good luck and hope it works out for you. Take care !

6 years ago

Kelly Bell

@Lucindy Sartor thanks so much x

6 years ago

Lucindy Sartor

Good luck and hope it works out for you. Take care !

6 years ago

Jason Squires

Rip in KB, ya be back in the Pilbs before ya know it mate

6 years ago

Kelly Bell

@Jason Squires the pair of us hey! At least you get fancy plaster!

6 years ago

Rose Felle

Wishing you a safe and speedy recovery KB. Thinking of you. Lots of love xx

6 years ago

Heather & Graeme Baldock

Hoping and praying for your full recovery Kelly xxxxx

6 years ago

Shae Spry

Never feel bad for asking for help – we are all thankful for the opportunity (and this is what community is for!) I only wish I could give you more 🙂 I’m so pissed off that you’ve had to self fund your rehab… you shouldn’t have to have private health to get the services you need. Sending love x

6 years ago

Denise Bevins

Best of luck with your recovery Kelly!!! ❤️❤️

6 years ago

Kelly Bell

@Denise Bevins I hope you are well xxx

6 years ago

Regine Andersen

Lots of love and best wishes for a total recovery

6 years ago

Sam Bell

One Step at a time Lovely Lady back to Full health and Happiness X

6 years ago

Katie Allen

Wishing you a speedy recovery Kell… feel better soon xx

6 years ago

Voula Keating

Let me know if you need anything. Wishing you a speedy recovery xo

6 years ago

Lisa and Andrew Lock

You got this KB – and we got you xxx

6 years ago

Lisa Lock

Kelly Bell