The DISabled to ENabled podcast
10. Stem cell treatment, MS camp, best nutrition and exercise advice, diagnosed at 15 with MS!

10. Stem cell treatment, MS camp, best nutrition and exercise advice, diagnosed at 15 with MS!

July 17, 2019

We discuss the ins and outs of the new stem cell treatment for MS and how Jess will be posting everything about her journey with it live on her Instagram (link below). We also discuss what she does for the MS Society in Canada and Jess also shares her best advice for nutrition and exercise that she’s learnt from her 2 degree qualifications in dietetic science and holistic nutrition and with living with MS since she was 15 years old. She’s a runner and boxer whilst fighting through chemo. She’s incredible.

Connect with Jess (and follow her stem cell treatment)
Insta: @Alltherightbites

Take a look at ‘Wrap me cool’ and use code JESS for a 5% discount

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Read Jessie Ace's blogs here: www.JessieAce.com

 

9. Drop foot running and MS, her diagnosis story and the importance of setting goals

9. Drop foot running and MS, her diagnosis story and the importance of setting goals

July 10, 2019

We talk to Leslie Touchton about her MS diagnosis and hows she’s come to terms with it and told it ‘no’. Leslie lives an amazingly active lifestyle and she shares with us her tips for energy management and the importance of goals to live a life that’s full and awesome. We also discuss how she’s managed to continue running despite having heavy foot drop feet!

 

Connect with Leslie:

Here: https://www.facebook.com/leslie.touchton.1

 

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Insta: @jessieaceofficial

www.jessieace.com

 

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8. ENabled inventor, travelling around the world alone with cerebral palsy and her shocking diagnosis story!

8. ENabled inventor, travelling around the world alone with cerebral palsy and her shocking diagnosis story!

July 3, 2019

What happens when you get a creative inventor mixed with an invisible illness? A lot of cool stuff to help ENabled people to live their best lives possible! We also discuss Jessica's travel tips and stories of when she travelled ALONE around the world with an invisible illness! Say what?! Public speaking events and how’s she’s teaching businesses to include disabled people instead of fearing them. 

Connect with Jessica:

Twitter - @D_Disability

Instagram - @D_Disability 

Facebook - Design for Disability

LinkedIn - Design for Disability

And her main website http://designfordisability.co.uk

 

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Comment below with who else you would like to see me interview! 

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And join the tribe! 

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Insta: Enabled_Warriors

www.jessieace.com

7. Things I’ve learnt from talking to people about their MS on MS Connection.org

7. Things I’ve learnt from talking to people about their MS on MS Connection.org

June 26, 2019

Senior Content Development specialist for MSConnection.org blog Christy Kim talks to us about everything she’s learnt from the reading the blogs written by people with MS. We talk about our love of writing and reading, how invisible symptoms are portrayed by the public and how people with MS can be better together. Episode #6

 

Connect with Christy:

Insta - @Clhkayy 

www.MSConnection.org

 

If you love this podcast please subscribe! 

Comment below with who else you would like to see me interview. 

And leave a rating and review

And join the tribe! 

Facebook: ENabled Warriors 

Insta: Enabled_Warriors

Website: www.Jessieace.com

0. What is this podcast all about? Plus who the heck is Jessie Ace?

0. What is this podcast all about? Plus who the heck is Jessie Ace?

June 25, 2019

In this special podcast episode, you'll learn what the DISabled to ENabled podcast is all about and who the heck is Jessie Ace? 

I hope you love this podcast as much as I loved making it. There was nothing like this when I was diagnosed at 22 years old! 

 

Follow the warrior tribe!

If you love this podcast please subscribe! 

Comment below with who else you would like to see me interview. 

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And join the tribe! 

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www.jessieace.com

6. 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!

6. 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!

June 19, 2019

The new CEO of the MS Society Mr Nick Moberly answers your questions asked across social media groups. We discuss his plans for the future of the MS Society - and they might surprise you! He answers topics such as: how we can give people a voice in the community? What help and support needs to be improved, particularly for young people? And how is that £5million budget allocated between the different areas? Also we discuss why you need to campaign to get your voice heard. Episode #6

Follow Nick:

MSSociety.org.uk

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Facebook: ENabled Warriors

Insta: Enabled_Warriors

5. Energy hacks, accessibility goals, kids and MS - can ‘The Simpsons’ help explain MS symptoms? With Kaz Laljee Ep #5

5. Energy hacks, accessibility goals, kids and MS - can ‘The Simpsons’ help explain MS symptoms? With Kaz Laljee Ep #5

June 12, 2019

HR manager at Tesco turned social media legend Kaz Laljee has fully embraced his MS diagnosis setting up not only his social media business (Soc-Med.com) but also his site ‘Positive About MS’ he continues to push the limits of his primary progressive MS. We discuss everything from energy hacks to combat fatigue, how to discuss MS with your kids using ‘The Simpsons’ and why you shouldn’t use toilet rolls for bowling in supermarket aisles!

 

Follow Kaz:

Instagram - @positiveaboutMS

Facebook - @positiveaboutMS

Email - kaz@positiveaboutms.com

Web - www.positiveaboutms.com

 

If you love this podcast please subscribe!

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Click the links below to join the tribe!

Facebook: ENabled Warriors

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4. Meds, how to tell kids you have MS and climbing mountains Ep #4

4. Meds, how to tell kids you have MS and climbing mountains Ep #4

June 5, 2019

Gary Pinder explains how he took his MS diagnosis and made it into something extraordinary. We talk about everything from medications, how Gary told his kids he had MS and how he managed a trip to Everest Base Camp. We also discuss how to stay cool when exercising with an invisible illness. 

Remember if you like this podcast click the subscribe button and keep up to date! 

You can also follow the ENabled Warriors on Facebook, Instagram and Youtube - just search - ENabled Warriors.

Follow Gary here - @MSThrivers

3. What’s an AFO? Bad English accents, toilet humour plus warrior mind hacks Ep #1

3. What’s an AFO? Bad English accents, toilet humour plus warrior mind hacks Ep #1

May 29, 2019

Marisa says NO to her MS. She goes running, works out, does marathons. She’s even set up the movement Fight for Mobility to inspire others living with an invisible illness. We talk bad English accents, humorous MS bathroom issues and her ultimate warrior mindset hacks. Let’s focus on what you are able to today.   

“What are you able to do today? Have those words be ‘I can’”

Follow Marisa:

Instagram - @Risamoe

Youtube - https://www.youtube.com/channel/UCXIFDrb0ihtyl2joYIBPraQ

 

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2. MS in a logo, photography vs. illustration showdown and ‘anti victim’ advertising. Ep #2

2. MS in a logo, photography vs. illustration showdown and ‘anti victim’ advertising. Ep #2

May 29, 2019

The creator of the face for The National MS Society tells all about how the National MS Society’s brand has evolved over the last few years, how the role of photography is especially important because nobody wants to be the face of bladder issues! BUT illustration is also important! And how the NMSS create ‘anti-victim’ advertising.

 

Follow the National MS Society: https://www.nationalmssociety.org/

Follow the NMSS behind the scenes and Marks adventures on Insta - @Mark_Serratoni  

 

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