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39:26

My rare disease

by Katy Baker

Welcome to 'My rare disease' podcast. This is a platform where I raise awareness of something that affects 1 in 15 people, rare disease. By chatting to patients, health professionals and advocates, we talk about all aspects of rare disease including relationships, mental health and much more. I cannot wait for you to hear some truly inspiring stories from some absolutely amazing people. From being diagnosed with a rare disease myself at 10 weeks old, it has given me the motivation to give others in the rare disease community an opportunity to share their thoughts and experiences.

Copyright: Katy Baker

Episodes

Having a sister with a rare disease - Lucy Baker

35m · Published 14 Nov 18:11
This episode features a very special guest, my sister! Lucy is 22 years old, she’s a trainee Lawyer and we love spending time together when we can. In this episode, Lucy and I speak openly about what she thinks about my rare disease, Scimitar Syndrome, what it's like having a sister with an illness there is so little information on and some of the memorable experiences that stand out for her. It has been really interesting listening to how a rare disease can affect the whole family, not just the person with the condition and how Scimitar Syndrome has had an impact on her life.

Mental health - Fiona Shepherd

29m · Published 12 Oct 12:47
This episode is all about one of my friends from Uni Fiona and her mental health. Throughout Uni, Fiona went through multiple hospital admissions for her physical health and this led to a stay at an inpatient mental health hospital. In this episode, we are talking about Fiona's experiences in hospital, discussing the stigma that comes with mental health and advice Fiona would give to people struggling. Below are numbers and support you can access if you need to reach out, please talk to someone if you are struggling, your feelings are valid and you are so loved. Samaritans: 116 123 (available 24/7) MINDinfoline: 0300 123 3393 The Mix: www.themix.org.uk (online chat) Crisis text line: text 'shout' to 85258

Cholesteatoma - Daisy Marriott

34m · Published 05 Oct 10:38
In this episode I chat to Daisy who has Cholesteatoma, a condition which mainly affects her hearing but has caused anxiety, low mood and years of being misdiagnosed. In this episode we discuss being a young person with rare disease and having to miss out on what a 'normal' young person can sometimes take for granted, how much rare disease can affect your mental health and the lack of support in this area when being diagnosed with a life-changing condition but also how Daisy's rare disease has given her the motivation to work in the rare disease sector and give other young people a platform to feel empowered and share their inspiring stories.

Occupational Therapy - Chloe Holmes

18m · Published 30 Sep 11:05

In this episode I talk to Chloe who studied Occupational Therapy at the University of Northampton and is now working as a paediatric OT supporting children with a range of additional needs. Occupational Therapists are important in helping people of all ages for different reasons e.g ageing, mental ill-health and physical disabilities and in this episode, we touch on one experience Chloe had with a child with Rett syndrome.

Cavernous malformation (CCM) - Sadie

32m · Published 26 Sep 17:08
This episode features Sadie who is a 3rd year Politics and International Relations student at the University of Westminster. Sadie was diagnosed with Cavernous Malformation at 19 years old resulting in chronic fatigue, migraines and difficulty in dealing with emotion. In this episode we discuss how an illness affects the whole family, the mental health struggles that can come with having an illness, extra hurdles Sadie has come across along the way and the services that the Cavernoma Alliance and Cavernoma Society have to support people living with the condition. 

Lyme disease and mental health - Sophie Ward

29m · Published 09 Sep 11:10
7th Sept is Youth Mental Health Awareness Day and I am so lucky to have one of my friends Sophie chat to me about her rare disease and how much a rare disease can affect your mental health. In this episode, we discuss grief that comes with illness, how your life can be completely changed when you become suddenly unwell and we share our views on statistics I have found on just how many people are affected my ill-mental health.

Idiopathic Hypersomnia - Matt Baker

1h 7m · Published 07 Sep 08:54
To mark Idiopathic Hypersomnia awareness week,  this episode features Matt who suffers with the condition but also has made it his mission to be a patient advocate across the UK. In this episode we talk about how Matt was diagnosed, the debilitating symptoms he experiences, how the word 'idiopathic' can cause so much uncertainty and some of the  medical highs and lows Matt has been through.

Ulcerative Colitis & Arthritis - Ellie Sanders

59m · Published 25 Aug 16:18
This first episode I speak to one of my best friends and old housemates Ellie. Ellie has a couple of chronic illnesses but they haven't stopped her from achieving a first class degree, a full-time job and she has ambitions to become a Children’s Psychologist. In this episode we discuss Ellie's health journey, the different health professionals she's come in to contact with as well as how illness can affect mental health and much more.

My rare disease - Podcast trailer

41s · Published 10 Aug 16:25
Welcome to my podcast! Each month I will be speaking to a patient with rare disease, a health professional or chronic illness advocate with the aim of raising awareness of all aspects of managing an illness from mental health to relationships, friendships to work life balance. I have heard some truly inspiring stories which I can’t wait to share.

My rare disease has 29 episodes in total of non- explicit content. Total playtime is 19:03:41. The language of the podcast is English. This podcast has been added on December 23rd 2022. It might contain more episodes than the ones shown here. It was last updated on April 28th, 2024 09:40.

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