The DISabled to ENabled podcast for people with chronic illnesses

By Jessie Ace

Listen to a podcast, please open Podcast Republic app. Available on Google Play Store and Apple App Store.

Image by Jessie Ace

Category: Mental Health

Open in Apple Podcasts


Open RSS feed


Open Website


Rate for this podcast

Subscribers: 14
Reviews: 0
Episodes: 211

Description

DISabled to ENabled podcast is the podcast for people with chronic illnesses. Join British host Jessie Ace as she interviews inspiring people affected by chronic illness who turned their diagnosis into something unexpected. Listen to people such as celebrities/CEOs/athletes/marathon runners as well as real-life stories as they let you into their lives and how they did something awesome despite their chronic illness diagnosis. Learn their tips, tricks, and advice for living your best life with your chronic illness. We discuss hard topics with a side of positivity and humor as we navigate life.

Episode Date
184. Katie Collett | WAVY-TV | Part 3: on the NBA court!
Jan 01, 2021
182. Katie Collett | WAVY-TV | Part 2: teamwork in TV
Dec 30, 2020
182. Katie Collett | WAVY-TV | Part 1: MS on TV
Dec 28, 2020
181. Damian Washington | NoStressMS | Part 3: ...coffee, anyone?
Dec 25, 2020
180. Damian Washington | NoStressMS | Part 2: vlogging and being on film
Dec 23, 2020
179. Damian Washington | NoStressMS | Part 1: my wife knows her stuff!
Dec 21, 2020
178. Fiona Cray | MS Nurse Specialist | Part 5: Q+A!
Dec 18, 2020
177. Fiona Cray | MS Nurse Specialist | Part 4: Symptoms and Treatments
Dec 17, 2020
176. Fiona Cray | MS Nurse Specialist | Part 3: MS Myths
Dec 16, 2020
175. Fiona Cray | MS Nurse Specialist | Part 2: What is MS?
Dec 15, 2020
174. Fiona Cray | MS Nurse Specialist | Part 1: Who are you?
Dec 14, 2020
173. Marissa Green | The MS Trust | Part 3: not giving a bleep and firewalking!
Dec 11, 2020
172. Marissa Green | The MS Trust | Part 2: Watermelon challenge?
Dec 09, 2020
171. Marissa Green | The MS Trust | Part 1: double diagnosis and why didn't I ever
Dec 07, 2020
170. Daana & Dawn | Myelin and Melanin | Part 3: private to public on the podcast
Dec 04, 2020
169. Daana & Dawn | Myelin and Melanin | Part 2: being the change we needed to see
Dec 02, 2020
168. Daana & Dawn | Myelin and Melanin | Part 1: Lesions and Lemtrada
Nov 30, 2020
167. Nikky | Innabox | Part 3: lots of lemons and taking that leap!
Nov 27, 2020
166. Nikky | Innabox | Part 2: Brain Frog and Kickstarter Campaigns
Nov 25, 2020
165. Nikky | Innabox | Part 1: hormones and belly buttons!
Nov 23, 2020
164. Dr. Conor Kerley | Phytaphix | Part 4: books and kneecaps!
Nov 20, 2020
163. Dr. Conor Kerley | Phytaphix | Part 3: ENabled Warriors Q + A Special!
Nov 18, 2020
162. Dr. Conor Kerley | Phytaphix | Part 2: fruit, veg and vitamin D
Nov 17, 2020
161. Dr. Conor Kerley | Phytaphix | Part 1: diagnosed at 15 and coming off medication
Nov 16, 2020
160. Dr. Lee Phillips | Part 3: being mindful to uncertainty
Nov 13, 2020
159. Dr. Lee Phillips | Part 2: body blueprints!
Nov 11, 2020
158. Dr. Lee Phillips | Part 1: therapy and empathy
Nov 09, 2020
157. Mathew Embry | MS Hope | Part 3: spontaneous flight!
Nov 06, 2020
156. Mathew Embry | MS Hope | Part 2: Living Proof
Nov 04, 2020
155. Mathew Embry | MS Hope | Part 1: part of a bigger plan?
Nov 02, 2020
154. Ryan Prior | CNN | Part 3: pet sitting problems!
Oct 30, 2020
153. Ryan Prior | CNN | Part 2: walking along the Berlin Wall
Oct 28, 2020
152. Ryan Prior | CNN | Part 1: Exercise, exertion and exhaustion
Oct 26, 2020
151. Caroline Craven | Girl With MS | Part 3: hilarious Halloween costumes!
Oct 23, 2020
150. Caroline Craven | Girl With MS | Part 2: blogging and building community
Oct 21, 2020
149. Caroline Craven | Girl With MS | Part 1: going rogue in Guatemala
Oct 19, 2020
148. Hannah Ensor | Stickman Communications | Part 3: a scary hospital stay!
Oct 16, 2020
147. Hannah Ensor | Stickman Communications | Part 2: stickmen and medical retirement
Oct 14, 2020
146. Hannah Ensor | Stickman Communications | Part 1: how it all changed
Oct 12, 2020
145. Eva Minkoff | Wellacopia | Part 3: rein-free riding!
Oct 09, 2020
144. Eva Minkoff | Wellacopia | Part 2: natural treatment and Wellacopia
Oct 07, 2020
143. Eva Minkoff | Wellacopia | Part 1: fibro and hypermobility syndrome
Oct 05, 2020
142. Michael Wentink | Part 3: I froze myself!
Oct 02, 2020
141. Michael Wentink | Part 2: writing about it
Sep 30, 2020
140. Michael Wentink | Part 1: Fortune 500 to Father at home
Sep 28, 2020
139. Natalie Suppes | For The Health | Part 3: fears of air and sea!
Sep 25, 2020
138. Natalie Suppes | For The Health | Part 2: Coaching and Nutrition
Sep 23, 2020
137. Natalie Suppes | For The Health | Part 1: Crohn's and Pregnancy
Sep 21, 2020
136. Claire | Through The Fibro Fog | Part 3: sky garden and sleep studies!
Sep 18, 2020
135. Claire | Through The Fibro Fog | Part 2: Instagram and Histamine
Sep 16, 2020
134. Claire | Through The Fibro Fog | Part 1: my merging conditions
Sep 14, 2020
133. Amanda Webster | Part 3: Halloween at Hogwarts!
Sep 11, 2020
132. Amanda Webster | Part 2: defying the odds to find happiness
Sep 09, 2020
*COVID 19 Special | Michael Wentink: a drive-by situation*
Sep 08, 2020
131. Amanda Webster | Part 1: childhood, loss and life on that ledge
Sep 07, 2020
130. Daralyse Lyons | Part 3: a 12 hour trip to Chicago!
Sep 04, 2020
129. Daralyse Lyons | Part 2: mindset and the healing journey
Sep 02, 2020
*COVID 19 Special | Eva Minkoff: March in NYC *
Sep 01, 2020
128. Daralyse Lyons | Part 1: bulimia, mental health and control over food
Aug 31, 2020
127. Amy Thompson | But you don't look ill | Part 3: free-falling!
Aug 28, 2020
126. Amy Thompson | But you don't look ill / MS Together | Part 2: invisibility awareness
Aug 26, 2020
*COVID 19 Special | Natalie Suppes: Pregnant Pandemic*
Aug 25, 2020
125. Amy Thompson | But you don't look ill | Part 1: symptoms in Paris
Aug 24, 2020
124. Courtney Ng | Part 3: frogs and skydiving!
Aug 21, 2020
123. Courtney Ng | Part 2: Hope for Ataxia and different perspectives
Aug 19, 2020
*Special Blooper Episode - 3!*
Aug 18, 2020
122. Courtney Ng | Part 1: my ARCA 1 diagnosis
Aug 17, 2020
121. Edward Payson | Part 3: special effects and sneaking out!
Aug 14, 2020
120. Edward Payson | Part 2: making the documentary
Aug 12, 2020
*COVID 19 Special |Amanda Webster: missing the gyms*
Aug 11, 2020
119. Edward Payson Filmmaker | Part 1: meeting Jon
Aug 10, 2020
118. Carley Gordon Peony HC | Part 3: podcasts, peeling and PeonyHC
Aug 07, 2020
117. Carley Gordon Peony HC | Part 2: easing the burden and being organised
Aug 05, 2020
*COVID 19 Special | Daralyse Lyons: zoom connections *
Aug 04, 2020
116. Carley Gordon Peony HC | Part 1: weight, waiting and being watched
Aug 03, 2020
115. Lori DePorter | Part 3: fans, Hawaii and helicopters
Jul 31, 2020
114. Lori DePorter | Part 2: boxing, tango and ironic writing
Jul 29, 2020
*COVID 19 Special | Amy Thompson: quizzes, murder mysteries and bottomless brunch!
Jul 28, 2020
113. Lori DePorter | Part 1: diagnosed with Parkinson's and being a Mom
Jul 27, 2020
112. Dr. Lynette Louise | Part 3: home is my favourite place
Jul 24, 2020
111. Dr. Lynette Louise | Part 2: travel therapy, neurofeedback and Fix it in 5
Jul 22, 2020
*COVID 19 Special | Courtney Ng: keeping connected *
Jul 21, 2020
110. Dr. Lynette Louise | Part 1: dealing with autism as a parent and doctor
Jul 20, 2020
109. Natalie Van Scheltinga | Part 3: moving country and unplanned trips
Jul 17, 2020
108. Natalie Van Scheltinga | Part 2: The Unchargeables Movement
Jul 15, 2020
*COVID 19 Special | Edward Payson: social media and shopping licenses*
Jul 14, 2020
107. Natalie Van Scheltinga | Part 1: laughing through my diagnosis!
Jul 13, 2020
106. Jess Faulds | Part 5: support through chemotherapy
Jul 10, 2020
105. Jess Faulds | Part 4: all the right bites!
Jul 09, 2020
104. Jess Faulds | Part 3: menopause in my twenties
Jul 08, 2020
103. Jess Faulds | Part 2: Freezing my eggs at 28 years old
Jul 07, 2020
102. Jess Faulds | Part 1: HSCT - what is it and what happens?
Jul 06, 2020
101. Lisa Sniderman | Part 3: gigs, digs and sandals
Jul 03, 2020
100. Lisa Sniderman | Part 2: my mission of creativity and healing
Jul 01, 2020
*COVID 19 Special | Carley Gordon: suburb walks and exercising*
Jun 30, 2020
99. Lisa Sniderman | Part 1:dermatomyositis and being grateful
Jun 29, 2020
98. Daniele Hargenrader | Part 3: hot coals and the Scottish play
Jun 26, 2020
97. Daniele Hargenrader | Part 2: dominating diabetes and mindset
Jun 24, 2020
*COVID 19 Special | Lori DePorter: keeping our Corona Capsule!*
Jun 23, 2020
96. Daniele Hargenrader | Part 1: diabetes diagnosis and loss
Jun 22, 2020
95. Brad Dell | Part 3: green eggs and roman ruins!
Jun 19, 2020
94. Brad Dell | Part 2: writing to help others
Jun 17, 2020
*COVID 19 Special | Dr. Lynette Louise: homeschooling*
Jun 16, 2020
93. Brad Dell | Part 1: cystic fibrosis, lung transplant and deafness
Jun 15, 2020
92. Jameisha Prescod | Part 3: frat parties and rollercoasters!
Jun 12, 2020
*Special Blooper Episode - 2!*
Jun 11, 2020
91. Jameisha Prescod | Part 2: working at the BBC and PIP struggles
Jun 10, 2020
*COVID 19 Special | Natalie Van Scheltinga: strict lockdown and colouring in*
Jun 09, 2020
90. Jameisha Prescod | Part 1: Starting Uni with Lupus
Jun 08, 2020
89. Ardra Shephard | Part 3: eating crickets and donkey!
Jun 05, 2020
*Special Blooper Episode!*
Jun 04, 2020
88. Ardra Shephard | Part 2: devastating illness expert
Jun 03, 2020
*COVID 19 Special | Jess Faulds: immunocompromised in Canada *
Jun 02, 2020
87. Ardra Shephard | Part 1: MS in my invincible 20s
Jun 01, 2020
DISabled to ENabled Podcast's First Birthday!!!
May 30, 2020
86. Natalie Wilson | Part 3: policemen and wet knickers!
May 29, 2020
85. Natalie Wilson | Part 2: I cycled 5000 miles!
May 27, 2020
*COVID 19 Special | Lisa Sniderman: going to hospital and getting shopping*
May 26, 2020
84. Natalie Wilson | Part 1: being diagnosed with EDS
May 25, 2020
83. Matt Lafleur | Part 3: skydiving and escape rooms!
May 22, 2020
82: Matt Lafleur | Part 2: writing, happy hours and life at 34
May 20, 2020
*COVID 19 Special | Daniele Hargenradar: task tracking and keeping busy *
May 19, 2020
81. Matt Lafleur | Part 1: Friedrichs Ataxia
May 18, 2020
80. Lauren Freedman | Part 3: flamingos and mooning!
May 15, 2020
79. Lauren Freedman | Part 2: uninvisible pod and medical gaslighting
May 13, 2020
*COVID 19 Special | Natalie Wilson: virtual support and hobbies*
May 12, 2020
78. Lauren Freedman | Part 1: hashimoto's and sleep apnea
May 11, 2020
77. Paul Ace | Part 3: miracle morning and playing music
May 08, 2020
76. Paul Ace | Part 2: needles and being logical
May 06, 2020
*COVID 19 Special | Brad Dell : ritual self care*
May 05, 2020
75. Paul Ace | Part 1: my partner's diagnosis
May 04, 2020
74. Hanna Boethius | Part 3: dreaming about sugar!
May 01, 2020
73. Hanna Boethius | Part 2: learning from my mistakes
Apr 29, 2020
*COVID 19 Special | Paul Ace: Online business bubbles*
Apr 28, 2020
72. Hanna Boethius | Part 1: living with diabetes and hashimoto's
Apr 27, 2020
71. Sneha Dave | Part 3: climbing forbidden walls!
Apr 24, 2020
70. Sneha Dave | Part 2: my health advocacy achievements
Apr 22, 2020
*COVID 19 Special | Jameisha Prescod | hydroxychloroquine issues for Lupus
Apr 21, 2020
69. Sneha Dave | Part 1: ulcerative colitis diagnosis
Apr 20, 2020
68. Amin Zayani MedAngel | Part 3: obsessed with fridges and work
Apr 17, 2020
67. Amin Zayani Medangel | Part 2: my insulin froze!
Apr 15, 2020
*COVID19 Special* What we drinkin'? Ardra Shepard | Tripping On Air
Apr 14, 2020
66. Amin Zayani MedAngel | Part 1: my diabetes diagnosis
Apr 13, 2020
65. David Lyons MS Fitness Gym co-founder | Part 3 I drank raw eggs!
Apr 10, 2020
*COVID 19 Special | Matt Lafleur: being serious and seeing positives*
Apr 07, 2020
63. David Lyons MS Fitness Gym co-founder | Part 1: my MS diagnosis
Apr 06, 2020
62. Sally Hatton | Part 3: Advice and super quick secrets | Patient advocate XLH
Apr 03, 2020
61. Sally Hatton | Part 2: How I became a patient advocate for XLH
Apr 01, 2020
*COVID 19 Special | Lauren Freedman: How has the virus changed things where you are?*
Mar 31, 2020
60. Sally Hatton | Part 1: My Diagnosis | XLH patient advocate
Mar 30, 2020
59. David Francisco | Part 3: man's search for meaning and crab brain soup
Mar 27, 2020
58. David Francisco | Part 2: I forgave the person who paralysed me, now I teach kids about it in schools
Mar 25, 2020
*COVID 19 Special | Hanna Boethius: How Switzerland and the UK are coping differently*
Mar 24, 2020
57. David Francisco American Idol Star | Part 1 My accident left me paralyzed
Mar 23, 2020
56. Celestine Fraser | Secrets of a film maker | Part 3
Mar 20, 2020
55. Celestine Fraser | Part 2 ill, actually a documentary about disability
Mar 18, 2020
*COVID 19 Special | Sneha Dave: How COVID-19 is affecting people with chronic illness*
Mar 17, 2020
54. Celestine Fraser | Glowworm Films Founder | EDS + P.o.T.S diagnosis
Mar 16, 2020
53. Nitika Chopra | Part 3: My advice and the not-so-super-quick secrets | TV presenter & founder of Chronicon
Mar 13, 2020
52. Nitika Chopra | Part 2: How I planned events/became a tv presenter and ran a magazine
Mar 11, 2020
51. Nitika Chopra | Part 1: My diagnosis | TV presenter & Founder of Chronicon
Mar 09, 2020
50. Megan Finch | Part 3: not-so-super-quick secrets
Mar 06, 2020
49. Megan Finch | Part 2: Planning my wedding around my chronic illness
Mar 04, 2020
48. Megan Finch | Part 1: My diagnosis story |
Mar 02, 2020
47. Chris Holland | Part 3 | Super quick secrets
Feb 28, 2020
46. Chris Holland | Part 2: After diagnosis TV fame | 3x winner of Food Network's Chopped
Feb 26, 2020
45. Chris Holland | Part 1: My Diagnosis Story | 3x Winner of Food Network's 'Chopped'
Feb 24, 2020
44. George Pepper | Before I knew it is was on my plate.
Feb 21, 2020
43. George Pepper | How I started Shift.ms
Feb 19, 2020
42. George Pepper | My Diagnosis
Feb 17, 2020
41. Shelby and Luna | the benefits of having a service dog
Feb 12, 2020
40. Geoff Allix | Overcoming MS Podcast host
Feb 05, 2020
39. Joanna Livermore: MS taught me a vital life lesson
Jan 29, 2020
38. BE Alink: Founder of the Alinker bike
Jan 22, 2020
37. Cheryl Hile: 53 marathons and 287 participants round the world
Jan 15, 2020
36. Effie Koliopoulos | Juvenile idiopathic arthritis | My Story
Jan 08, 2020
35. Gynaecologist Dr Jonathan White: What you need to know about MS
Jan 01, 2020
34. Irene Eagle: A parent’s perspective on their child’s diagnosis.
Dec 25, 2019
33. Susan Carey - My 21st birthday was at one of my infusions!
Dec 18, 2019
32. Harper Spero: I have mould constantly growing in my lungs. Made visible podcast host
Dec 11, 2019
31. MBE Kadeena Cox: Smash the rules, achieve your dreams.
Dec 04, 2019
30. Beccy Huxtable: I was grateful to be diagnosed with MS live on air! Radio producer
Nov 27, 2019
29. Shelley Ramsey DeJongh | I started my life again... addiction free with Multiple Sclerosis
Nov 20, 2019
28. Heather and Dizzy 'With Multiple Sclerosis you have to cancel plans and I hate that'
Nov 13, 2019
27. Gina Johnson. Doctor: do you want to have a career or do you want to be alive?
Nov 06, 2019
26. Ciena Rae: My fingernails just started falling off one-by-one
Oct 30, 2019
25. Chanel White: 'There are two times I wish I just died'
Oct 23, 2019
24. Jenny Clarkson | I did my exams whilst being diagnosed with MS
Oct 16, 2019
23. Sandy Bista | I feel blessed to have Fibromyalgia
Oct 09, 2019
22. Dara Shashoua | I wore an eye patch to my shop and just pretended to be a pirate
Oct 02, 2019
21. Conor Devine: Anxious man to Ironman
Sep 25, 2019
20. Scott Mills - Radio 1 DJ 'My mum couldn't run for a bus'
Sep 22, 2019
19. Alicia Aiello | I pooped in my car
Sep 18, 2019
18. People's Strictly Come Dancing Star Trishna Bharadia: ‘I was left in what felt like a black hole with no information’
Sep 11, 2019
17. I was in a constant state of adrenaline, my pulse was 181 per minute! - Faith Abbott/Ashenden
Sep 04, 2019
16. Sheryl Chan | You can die in Singapore but you can’t get sick - it’s too expensive! A Chronic Voice Blogger
Aug 28, 2019
15. Dr Gretchen 'the one secret doctors won’t tell people with chronic illness'
Aug 21, 2019
14. I fight my rare autoimmune disease to plan celebrity events and be a pageant queen
Aug 07, 2019
13. Exercise trainer for people with chronic illnesses, what exercise and food does to your body and how it can help you be awesome.
Jul 31, 2019
12. Zumba with Colitis, PTSD, Anxiety and MS working in mental health and still taking on the world!
Jul 24, 2019
11. Stem cell treatment, MS camp, best nutrition and exercise advice, diagnosed at 15 with MS!
Jul 17, 2019
10. Drop foot running and MS, her diagnosis story and the importance of setting goals
Jul 10, 2019
9. ENabled inventor, travelling around the world alone with cerebral palsy and her shocking diagnosis story!
Jul 03, 2019
8. Things I’ve learnt from talking to people about their MS on MS Connection.org
Jun 26, 2019
1. What is this podcast all about? Plus who the heck is Jessie Ace?
Jun 25, 2019
7. CEO talks future plans for the MS Society, a need for MS nurses, how we can give people a voice and why in a family of Doctors he’d prefer to be the boss!
Jun 19, 2019
6. Energy hacks, accessibility goals, kids and MS - can 'The Simpsons' help explain MS symptoms? With Kaz Laljee
Jun 12, 2019
5. Meds, how to tell kids you have MS and climbing mountains
Jun 05, 2019
2. What’s an AFO? Bad English accents, toilet humour plus warrior mind hacks
May 29, 2019
3. MS in a logo, photography vs. illustration showdown and ‘anti victim’ advertising
May 29, 2019
4. Weight loss, marathons, how to manage energy and peeing at the side of the road
May 29, 2019