Tessa Colliver
Tessa’s Path from Grief to Strength and Purpose
Tessa survived her brother's sudden death, MS at 16, and her father's suicide. Thirty years later, she walks daily and works.
Hear this story

Tessa Colliver
Tessa survived her brother's sudden death, MS at 16, and her father's suicide. Thirty years later, she walks daily and works.
Hear this story
Tessa grew up on a farm in rural South Australia, riding bikes and motorbikes, spending summers at the beach with family. When she was ten, her brother Nathan died suddenly from a congenital heart condition. A year later, at sixteen, her fingers stopped working. She couldn't hold a pen during a history project in the cemetery. Weeks or months passed before she saw a neurologist and got her MS diagnosis. While waiting, she spent school days isolated in the typing room. IV steroids helped her hands recover during a family holiday to the Northern Territory, and she watched her handwriting improve day by day in her diary.
In her twenties, living in Melbourne, Tessa started injectable disease-modifying treatment three times a week. She moved back to Adelaide in 2006 to be closer to family, but arrived just in time to watch her father's health unravel. He had Graves disease, which brought depression and anxiety. On 10 July 2006, he took his own life. Tessa was 28. Months later, in early 2007, she had a severe MS relapse that left her barely able to walk or drive. For the first time, she was genuinely frightened about her future.
Tessa got involved with peer support groups for suicide loss, which helped her heal. Nearly ten years ago, she got Boss, a Jack Russell cross. Walking him every day gradually rebuilt her fitness and stamina. Now, thirty years into living with MS, Tessa works as a consultant from home, lives independently, drives, and walks her dog daily. She has found meditation lifechanging, especially the Calm app for slowing her breathing when stress builds. She watches her brother's children grow up and focuses on what she can do rather than what she cannot.
⚠️ Content advisory: this episode discusses suicide & self-harm prevention, which some listeners may find distressing.
If you need support, you're not alone. Help is available: • Lifeline (24/7 crisis support): 13 11 14 · lifeline.org.au
“After 30 years now of living with MS I feel incredibly grateful to still be able to live independently and drive and walk my dog and all those things that you just take for granted. The main thing is focusing on what I can do and just enjoying life for what it is.”
“I think the trick is finding someone who you can talk openly with but also someone who has the skills that you need at the time. Not all counselors are the same so sometimes you have to shop around to find the right one.”
“When I got my dog nearly 10 years ago I never walked anywhere because I'd had so many problems with my legs with the MS. When I got him I knew that I'd need to walk him every day. Every morning after I had my coffee off we'd go for a walk and we started very slowly but gradually build up and probably got up to walking about an hour every day.”
The hero, today
After thirty years with MS, Tessa focuses on what she can do rather than what she cannot, which has allowed her to live independently, drive, and walk her dog. Finding the right therapist matters more than having any therapist, and sometimes you have to try more than one before finding someone who can help you challenge yourself and think differently. Meditation, specifically using an app to slow her breathing when stress would otherwise cause her to hyperventilate, has been lifechanging for Tessa over the past five or more years. Getting a dog forced daily walking that gradually rebuilt Tessa's fitness and stamina, making international travel feel liberating rather than exhausting for the first time. Peer support groups and involvement in suicide prevention work in her community helped Tessa heal from her father's death and gave her a way to use her experience to help others.
Yes. Tessa Colliver is a real person who shared their own story in their own words. Kintsugi Heroes is a not-for-profit that shares first-person stories of overcoming adversity, told with the person's consent.
Kintsugi Heroes, a registered Australian not-for-profit. Every story is shared with the hero's own consent and reviewed under Kintsugi Heroes' trauma-informed content standard before it goes public.
After thirty years with MS, Tessa focuses on what she can do rather than what she cannot, which has allowed her to live independently, drive, and walk her dog.
Finding the right therapist matters more than having any therapist, and sometimes you have to try more than one before finding someone who can help you challenge yourself and think differently.
Meditation, specifically using an app to slow her breathing when stress would otherwise cause her to hyperventilate, has been lifechanging for Tessa over the past five or more years.
Getting a dog forced daily walking that gradually rebuilt Tessa's fitness and stamina, making international travel feel liberating rather than exhausting for the first time.
[Music] welcome back to kugi Heroes helping people tell the stories they need to share so you can find the stories that you need to hear we're delighted to welcome Tessa civer a valued member of our team who joined us as a grand writer in 2024 Tessa's story is truly remarkable having faced significant personal challenges in including profound losses and living with multiple sclerosis since her teens she's gained valuable insights into the meaning of resilience by sharing her journey Tessa hopes to inspire others facing adversity to find strength and keep moving forward we're honored to have Tessa with us today not just as part of our team but as a true kugi hero [Music] hello Tessa thanks for joining us on kugi Heroes podcast thank you Natalie it's a pleasure to be here well Tessa we met last year when you joined the kugi heroes team and it's been really interesting and a great pleasure to get to know you and The more I've got to know you the more I real have learned that you have come through quite a number of challenges and you have not only survived and coped but you have you've recovered and you have a lot to to offer our audience with with your with your resilience story so let's start from the beginning of your early childhood and we look forward to hearing your journey thanks Natalie um so in know I had a great childhood in a lot of ways grew up on the Family Farm in rural South Australia my dad was a farmer my mom was State home mom um at least till I was in high school when she did go back to work I had two younger brothers Nathan who was two years younger than me and Sam who is uh seven and a half years younger than me and um living on a farm I think gave us a lot of freedom in a lot of ways we used to love riding our push bikes around the place as when we got older motorbikes were um a lot of fun as well learning to drive the you in the padic um all those sort of things that are unique to growing up as a farm kid and um yeah got like a lot of great memories um we used to go for a summer holiday just at a local Beach just 30 minutes away but two other local families went down as well so big gr at the Caravan Park you with your friends jelly jumping days on the beach all um all good stuff um my mom was originally from adade so we did um like I remember from when I was quite young always spending time back in adad with her side of the family and um my auntie and uncles um but there was always a bit of an undercurrent even even as a child that my brother Nathan was born with a congenital heart condition and um he had major Ser surgery um just when I was beginning year four at school and um which I remember very clearly because I had a kidney infection and actually vomited all over my desk on the first day of school um but Mom and Dad were in Nathan with Nathan in Melbourne while he had this big operation and um and I think that was sort of the first time I realized how serious his condition actually was um and then in um 1993 we just started the school year I had just started year 10 Nathan year8 and um Nathan died really suddenly and that was just um totally unexpected and obviously just well devastating for our family unit Nathan was um um very had such a big personality and I don't know if that was just just who he was or part of his journey but it's really um I really love that he's he's been gone 32 years now but he's still very well remembered certainly um amongst people we were close to at that time and um obviously that had um shock waves through our family and the community and just um yeah um totally unexpected and also he died suddenly which was not something my parents had been prepared for and in fact they had been told by his specialists that um that would never happen and that um you know he would deteriorate slowly and they'd be time to get help and all of that sort of thing which which unfortunately was not what happened at all um but I guess as a family we um we banded together had a lot of um you know a lot of beautiful friends offering support and um I think my my mom's sister came over for a while and you know gradually life got back to a bit of a new normal um but then the the following year in 94 uh probably around July um we were doing a history project at school and we were outside in the in the local Cemetery which was a bit creepy and it was really cold and um I remember being frustrated because I I couldn't hold a pen to write notes for the assignment we were working on and um I just assumed it was CU it was so cold and when I got back into the classroom my fingers would th out and I would be able to hold a pen again um but unfortunately got back to the classroom I still couldn't hold a pen and also developed a funny almost buzzing sensation in my hands um so I went off to the first air room and no one really knew what to do with me so um one of my parents came to pick me up from school and um and I remember even then we went and saw a a local GP who was a farmer's wife who lived um very close to our farm and I think right away mple sclerosis was something that she mentioned even right back then um but I did then have to wait quite quite a while um thinking weeks if not months to get an appointment with a neurologist um and in the meantime I was just spending all of my school day in the um typing room because I couldn't couldn't hold a pen and couldn't write so um yeah I had to been the typing room to get my work done but you know quite a isolating experience when you're you know 16 years old and um everything was a bit uh strange and not really knowing what was happening um but I had uh a dose of high high dose IV steroids as a inpatient at the Royal adate hospital and gradually my hands went back to normal and um yeah I remember that we went on a family holiday to the Northern Territory and a rock and um back to south Australia on the Gan which was a very memorable memorable family holiday but also I remember keeping a diary and as a as the trip progressed my handwriting got better and better um and I know that my mom spent a lot of time researching Ms and you know what to expect what could happen and I um I just remember I wasn't at all interested but rather I was just glad that the the symptoms went away and um just kept on living my life as a um 16year old got my driver's license and um because I lived on a farm actually got my L's for a motorbike so that I could drive on my own right away and um yeah how how did your your friends react to to your Ms when you're being 16 it's a time in life when people tend to want to conform and not be different they want to be part of the pack so how how how was it socially for you at 16 just being discovering you have MS it to be honest it's hard to remember that far back because it is a long time ago now um but I don't I I um I don't remember anyone being um you know funny about it I think some of might have asked me if it was contagious which obviously it's not um but yeah I I don't remember being treated any differently because of what was happening and um and I just um what I do remember is just it what it was a bit isolating spending so much of my time that year in the typing room and um you know sort of aart away from the class environment but um but I think to at that age there there're certainly a resilience I I feel like I took it on board more than I would have had I first had symptoms in my 30s or 40s now even um when when your life's more settled and and obviously at 60 and I was still living at home and dependent on my parents so it it certainly wasn't the um the disaster I I would have thought if um if I was older and in a different situation so um yeah so the simp symptoms improved and I went off to UNI and um started working and um I guess uh I I did have a few more flare ups of the Ms and had to have the high do steroids again but um but I never spent I don't remember ever spending a lot of time worrying about it because every time I had the IV treatment the symptoms got better um so so I guess back then it it all very manageable and then when I was in my 20s I I spent some time living in Melbourne and um my auntie actually connected me with a lady who she had worked with who had Ms and while that was quite confronting in some ways because she was in a wheelchair um and not working and like quite isolated by then um the upside was that she um directed me to her neurologist and actually started treatment um and um there to inject myself three times a week which was quite horrifying at the time um although of course compared to a diabetic and all the needles they have three times a week would probably sound great to a diabetic um but at the time it was that was all a bit scary with the injecting myself and getting onto th that treatment but I actually ended up being on that drug for 17 years and um I think it really did help slow the disease down which is what it's meant to do um yeah and yeah um and I also spent some time living in Perth and um which beautiful beautiful city but um i' soon realized that as long as I lived in Perth I would never get to travel because I would spend all my money coming home to south Australia um but once I did get back to south Australia I have happily done some um some pretty awesome traveling over the last few years um so in 2006 I moved from Perth back to Adelaide and I was um doing some admin temping work and staying with my staying at my brother's house he was actually away in the Air Force when I got back but um with his now wife and um yeah got back into work and everything and um I'd mve back because I wanted to be closer to family um but unfortunately moving back was just in time to watch my Dad's life unravel and um he'd been having issues with his iite and um he was actually diagnosed with Graves disease but but also we didn't really understand at first that there is um because it affects the thyroid there's very much a mental health aspect to it as well and depression and anxiety and all those sort of things um are very common but this um this certainly wasn't really known to us at the time and um my dad took his own life on the 10th of July 2006 and I think that is still the most shocking devastating yeah day that I've ever experienced and just um I don't know just the disbelief but Devastation grief yeah just um something unimaginable um and I guess I guess for me too when when my dad died I had no idea that male suicide especially is um is actually pretty common in Australia and that unfortunately I think it's six or seven men every day um take their own lives but I um I had no knowledge of that um at that point and it was just um yeah just just such a shocking um shocking event and um also because my dad was an only child um for me and my brother to sort of have to be looking after our grandparents in a way if you like and also um I remember I had the job of being the one to make phone calls um to let people know what had happened and just um just just really hard stuff because nothing I think prepares you for that and um I think you just just do it because just do what needs to be done and um yeah Tessa how how old were you at how old were you at the time I was 28 when dad died but it was very um I think I'd always been close to my dad because um well I think firstly we had similar sense of humor but also we had a bit of a different dynamic because Nathan was born with the heart condition and there were times when Mom would be with him in hospital and I would be at home with Dad so yeah did sort of have a closeness I think that not not all daughters would necessarily have with their fathers and um yeah so and I think also on top of that was um certainly nearly 20 years ago well 18 years ago very much the stigma associated with suicide and you know it's cowards way out and um just just that sort of unhelpful commentary and um you know people not not wanting to um talk about um Dad even years later I can only assume because of how he died so that's um I think that was something that took a long long time to come to terms with and I think for me one of the best things I did was to get involved with um peer support groups so I did um PE support training with living beyond suicide I got involved with a group in ad bere through suicide and through that got to meet a lot of other people who' been affected um losing their own loved ones but I think through through that for me that that was very healing um and also when I moved back to York peninsula in 2013 being part of um actually setting up a suicide prevention Network for York peninsula um and sort of using using my experience to try and avoid other people going through um that sort of tragedy but um unfortunately just uh just I guess when I thought I was maybe starting to get a grip on dad's death um the MS stuck again very forcefully and I remember it was early 2007 that I had a really severe relapse and you know so I'm 28 years old can hardly walk couldn't drive um again very isolating and um and just a lot to deal with on top of uh top of losing dad only six months before um but again I had the drugs and they did their work their magic again um but then again and this this had never happened before having another relapse within the first 6 months of 2007 and just really for the first time being really frightened I'm going to be a wheelchair before I'm 30 and you know what's what's my life going to look like and and all these fears and um yeah which I probably wasn't good at very good at expressing at the time but um now now all these years later in hindsight I can see you know 2006 2007 was in a very very place and um I had to do a lot of work to to get back out of that and um move move beyond the graef and um sort of comes to terms with um the fact that well Ms is a scary thing to live with because you just you don't know what's coming Tessa you've had to face a serious disease MS and the loss of your brother and later your father father how did you cope what what what strategies or resilience tools did you engage to cope with these very difficult challenges well I think um I think um when my brother died there was like that was just no no Strategies employed at all just more getting on with life and um moving forward and um and really it wasn't until I think after dad's death that I first really um saw a counselor and um or a therapist or you know I've seen a few now over the years and um definitely um I think the trick is finding someone who you can talk openly with but also um someone who you know has has the skills that you need at the time if that makes sense I think um not not all counselors It's well it's like anything um like not all um therapists are the same so sometimes you have to shop around to find the right one I think that's what I'm trying to say and um but when you do find the right one I think that's just hugely beneficial to have someone to challenge you a little bit and maybe get yourself out of your own head and um and think about other strategies that you can use um whether for me personally meditation um I have the Cal app on my iPhone and I absolutely swear by it I would use it every day um and I've probably used that for I don't know five or more years now and I think for me that's been lifechanging because I know for me um before I was using that if I got stressed out I would basically start hyperventilating so learning just to slow down the breath and um breathing and um being present um can make a huge difference I um yeah I think over time there's there's been a lot of little things along the way that have helped with the journey um but yeah I think for me uh therapy of whatever shape or form and um peer support So meting other people going with go through similar challenges and um and meditation for me are probably the three big ones and you have a dog too don't you I do dog play a well a role in your well-being H he does when I when I got my dog nearly 10 years ago I never walked anywhere because I'd had so many problems with my legs with the Ms and um and when I got him I knew that I'd need to walk him every day because it was a three-year-old Jack Russell cross so lots of energy and um so every every morning after I had my coffee off we' go for a walk and we started started very slowly but gradually build up and probably got up to walking about an hour every day and um and for me that that was life changing because and I specifically remember um the first big overseas trip I did to the US I didn't have my dog and I remember that being quite uncomfortable at times because I'd be so puffed out and you know if I had to do any walking whereas when I went on another trip about a year later I just remember that being so liberating because I was so used to walking with my dog that I actually felt comfortable getting around cities I was in by for and it was um yeah it it was quite amazing what a difference that made to the experience but also just obviously everyday life I um I still walking religiously and I definitely find Walking time is always good thinking time I don't listen to podcasts or anything while I walk him I just or music I just um just walk and um have my own thoughts and and talk to him sometimes to encourage him to hurry up quite often um but yeah and he's um he's funny because he's actually I joke that he's actually part cat because he's not um he doesn't need to be near me all the time but um at night he definitely likes to snuggle and be next to me on the couch and and yes be in my bed I know some people just cringe at the thought of a dog in a bed but he's my little Snuggle Buddy and um yeah so he's my name is boss and I quite often joke Boss by name Boss by nature and um yeah for me he is Jack R's Al like that aren't they yes yes so a lot of attitude in a very small body but um yeah he he's definitely been life-changing for me so and sort of a form of animal therapy at times as well I'm sure so Tessa can you describe your life what what your life looks like today sure um so still have challenges I um I break my wrist in December so that would that was been and is very challenging that I wasn't able to drive for about eight weeks and just getting back into that now just only being able to type again with two hands um but overall I think um I feel very lucky because I I work as a consultant so I work from home I work with different organizations and um I love um that about my work that I can work and learn about different organizations like cons Heroes um and I I guess for me the big thing is though after 30 years now of living with Ms I feel incredibly grateful to still be able to live independently and drive and walk walk my dog and all those things that you just take for granted um well until you know something happens and you suddenly can't do something but I think um you know there's there's certainly there certainly things I can't do due to Ms and um do have a certain level of disability but I think I think for me the main thing is focusing what I C focusing on what I can do and just enjoying you know enjoying life for what it is um with my dog got a great small group of friends um I love um watching my brother's kids grow up now so um got a niece and two nephews and my um 13-year-old nephew is now actually taller than me which is um a bit SC scary and you know seeing them grow up right before my eyes but um yeah I think um given given the challenges I've faced over the last 30 years who and 32 years since um Nathan passed I um yeah I feel like um come through come a long way and um yeah hopefully have a bit to offer others um who might be fighting their own battles and some suggestions on on what steps to take to um help keep moving forward yeah Tess so what what advice would you give to people who in the audience who may be struggling now perhaps they're facing an unwant serious disease like Ms or perhaps they they're grieving what advice would what final advice would you offer to the audience um I I well I guess a big one for me is take things one day at a time like try not to be thinking too far ahead and U really lean into the people who are there um who are there for you I think you know we all have just those wonderful friends who who are prepared to you know come and visit or take you somewhere or you know just have a chat when you need it and um yeah but like I said before SE seek support seek therapy um I personally have found meditation to be um lifechanging and um peer support I think is really good one as well Tessa thank you very much for joining us on kuki Heroes you're um it's amazing what you have have endured and and survived and your your um your life is is wonderful now and you're contributing to the world and in in so many ways so thanks very much for sharing your story with us thanks Natalie it's been a [Music] pleasure thank you for listening to this episode of kugi Heroes thank you to Colin Lily for permission to use broken as our theme music for this series if you enjoyed this conversation share the podcast with a friend and let us know by leaving a rating and review on Apple podcasts Spotify or wherever you get your podcasts if you'd like to support kugi Heroes and the stories we share head to kugi heroes.com and follow the instructions to make a tax deductible donation thank you for listening and we'll see you next time time [Music]
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This conversation includes growing up on the farm, nathan's surgery and sudden death, fingers that wouldn't hold a pen, typing room and waiting for answers, the northern territory holiday and hands coming back and finding the right neurologist and starting injections.