Share

cover art for Burning Nights: CRPS and Double Amputations: Chronic Illness Podcast

Invisible Not Broken - Chronic Illness Podcast Network

Burning Nights: CRPS and Double Amputations: Chronic Illness Podcast

Subscribe

Sign up with your email address to receive news and updates.

Email Address Sign Up

We respect your privacy.

Thank you!


What is your disorder? *

Complex Regional Pain Syndrome (CRPS)

At what age did your disorder become a daily issue? *

24

Who were you before your illness became debilitating? *

I was a trained Barrister (lawyer), I was lecturing in Law and became Head of Law at a college. I was happy, content with life, in love with a gorgeous Armed Forces man, just bought our 1st house and we were looking at planning a family

What would you do if you were not dealing with your invisible illness? *

I would have continued my legal career as a Barrister in Family law

What would you like people to know about your daily life? *

I am now confined to a wheelchair and am an above knee amputee due to the CRPS. I live in extreme burning and freezing excessive pain every day and suffer from wild temperature issues, swollen stumps as well as suffering from tremors and spasms on a daily basis. It’s so difficult and simple tasks such as getting dressed can take so long to do. I have to be careful what clothes I wear as they have to be light due to the hypersensitivity of both my remaining stumps. But I have the fantastic support of my husband. I also founded a charity - Burning Nights CRPS Support in the U.K. which I run along with 6 other volunteers.

What would make living and moving in the world easier for you? *

Finding a cure for CRPS to get rid of the stabbing, burning pain and other signs and symptoms. Also Better access to buildings, shops, bars etc for wheelchairs

Do you have any life hacks? *

Using your iPhone to control the heating. Get a doorbell that comes through to your phone to tell the person where to leave the parcel or the doorbell that comes through to the iPhone and you press a button on your phone that opens the door. Learn to adapt clothes for your disability or use safety pins to help keep clothes stay shut! I’ve had to adapt clothes so they don’t get trapped in my wheelchair for example.

What kind of support do you get from family or friends? *

I get amazing support from my husband and sometimes from my family. I couldn’t do without my husband as he is my full-time carer

Would you care to relate the details of what happened when someone didn't believe you were disabled?

I was told that I couldn’t be in this much pain as I looked too well. I was also told that my condition couldn’t make me disabled as it was a psychiatric illness

How has your invisible illness affected your relationships? *

It has been strained occasionally but he is always with me. It’s been tough but I love him.

Is there anything you are afraid to tell even the people closest to you? *

When I’m feeling low and depressed I don’t like telling my husband and Family because I feel I’m burdening them. I always try not to tell them how much pain I’m in. I always say I’m fine.

Does the fact that your disease is invisible change how healthcare professionals treat you? *

Yes

What is your best coping mechanism? *

Distraction techniques - definitely

What are you the most fearful of and hopeful for in the future? *

I would like to hope that the condition would get either a specific medication or cure. However, I’m fearful that it won’t happen. I also hope that my condition does not worsen at any time in the future

What is your favorite swear word?

Shit

Is there anything you want to make sure we talk about during the interview?  

If we possible could we mention the U.K. charity that I founded - Burning Nights CRPS Support and the work we do including raising awareness of CRPS and supporting all those affected by the condition. I would also like to include our web address, mention we’re on social media and we have a U.K. helpline

Any questions you think we should add to this list?

Maybe ask how I got CRPS ie what caused it in the first place and when?

What is the hardest and/or best lesson your condition has taught you?

The hardest lesson is that you soon know and realize who your real friends are when you are diagnosed with a chronic illness especially one that is invisible

What is the best purchase under $100 that helped your life

Grab stick to pick up things from the floor

What is the biggest lesson your illness has taught you?

Live each day as if it was your last

More episodes

View all episodes

  • Vulnerability, Resiliency, and Advocacy with Tim Reitsma

    47:06
    Monica Michelle is joined by consultant and podcast host Tim Reitma.Tim lives with Crohn's Disease.In this episode, Monica and Tim discuss: Tim’s resiliency through managing his Crohn’sThe importance of self-advocacy, especially in the workplace Tim’s podcast why he shares stories of those with invisible illness TIMESTAMPS00:47 - Tim's diagnosis 06:31 - How and why Tim applies self advocacy15:41 - Why Tim started his podcast22:42 - Invisible condition etiquette31:00 - What HR can do better for employees with invisible illness39:31 - Tools Tim uses to care for his Crohn’s outside the homeThe full transcript and all links mentioned can be found on the episode page on invisiblenotbroken.com
  • Tech and Disability: What VR Offers the Disabled Community with Sunny Ammerman

    01:10:27
    Monica Michelle is joined by artist and disability advocate Sunny AmmermanSunny lives with Septo-optic dysplasia, panhypopituitarism, Optic Nerve Hypoplasia, and is missing a membrane in the brain called the "septum pellucidum".In this episode, Monica and Sunny discuss: Sunny’s complex disorders and how she copes with themEverything VR provides from accessible gaming, social platforms and the potential for better online education.Various VR/AR games and their gameplay Sunny’s VR support groupTIMESTAMPS00:45 - What VR/AR offers for chronically ill and disabled folks11:57 - Sunny’s conditions and how she copes with them17:55 - Features that make VR games accessible or inaccessible as well as different games and their play experiences37:13 - The social aspects of virtual gaming51:32 - What opportunities VR has for the future1:04:49 - Sunny’s VR support group The full transcript and all links mentioned can be found on the episode page on invisiblenotbroken.com
  • Reporting on Chronic Illness and Disability with Journalist Julia Metraux

    39:16
    Monica Michelle is joined by Journalist Julia Metraux.Julia lives with vasculitis, mild to moderate hearing loss, and has experienced long COVID.In this episode, Monica and Julia discuss: Julia's diagnosis with vasculitis and how it influences her journalistic lensHow community impacts the mental health of those with chronic illnessHow Julia and Monica find positives and negatives in the internet spaces for chronically ill and disabled folksThe politics of how government, businesses, and celebrities influence the chronic illness community TIMESTAMPS00:32 - Julia's diagnostic journey07:02 - Julia’s work reporting on the online community of chronic illness 16:32 - The effect of Internet communities on chronically ill and disabled folks26:46 - How Julia’s illness impacts her work, both in what she writes about and how she manages her lifestyleThe full transcript and all links mentioned can be found on the episode page on invisiblenotbroken.com
  • Author of “Pain: The Ultimate Mentor,” Physiotherapist Kevin Hunt

    31:29
    Monica Michelle is joined by author & physiotherapist Kevin Hunt.Kevin lives with chronic pain.In this episode, Monica and Kevin discuss: Kevin’s philosophy of pain management as a physiotherapist who experiences chronic pain. The Hexagon Model, a life-management tool for focusing on what’s important to you.Kevin’s idea behind his new book.Using pain as a guide.TIMESTAMPS00:34 - Kevin’s work as a physiotherapist specializing in the experience of pain 06:44 - The Hexagon Model for managing your life’s needs14:00 - Putting aside the idea of a “quick fix”19:45 - Kevin’s personal experience with pain and how he uses it with patients28:44 - Kevin’s book, “Pain: The Ultimate Mentor”The full transcript and all links mentioned can be found on the episode page on invisiblenotbroken.com
  • Author of “Through the Pain: The Silent Suffering & Triumph of a Personal Trainer”: John K. Frazier

    28:35
    Monica Michelle is joined by author & personal trainer John K. Frazier.John lives with ankylosing spondylitis.In this episode, Monica and John discuss: John’s work as a physical trainer and authorChronic pain comparisonsPersonal triumphTIMESTAMPS00:50 - John’s business & diagnosis07:19 - Chronic pain olympics09:31 - Talking about & hiding a diagnosis15:09 - Personal triumph18:24 - Staying in the present23:29 - The superman complexThe full transcript and all links mentioned can be found on the episode page on invisiblenotbroken.com
  • The Creative Process, Self Worth, and Dating with Disability: Laura Mustard

    31:08
    Monica Michelle is joined by musician Laura Mustard.Laura lives with VATER syndrome.In this episode, Monica and Laura discuss: Laura’s inspiration for her upcoming musical EP.How Laura’s illness impacted her recent relationship & self-image.Laura’s creative process, new music, and social media pressure.TIMESTAMPS00:30 - Laura’s new EP / Monica’s recent COVID experience05:32 - Relationships with chronic illness11:20 - Image and self acceptance with disability15:32 - Laura’s creative process and current projects20:05 - Pursuing creativity despite social media attentionThe full transcript and all links mentioned can be found on the episode page on invisiblenotbroken.com
  • Author of “The Girlfriend’s Guide to Lupus”: Amanda Chay

    30:43
    Monica Michelle is joined by author Amanda Chay.Amanda lives with Sjögren’s and Lupus.In this episode, Monica and Amanda discuss: Amanda’s book & diagnosisOutlooking on work & writingNavigating chronic illness with kids & familyTIMESTAMPS00:26 - Intro + The Girlfriend’s Guide to Lupus02:17 - Amanda’s diagnosis10:09 - Amanda’s outlook on writing17:11 - Navigating chronic illness with kids & family23:29 - Labels and roles26:24 - Flare reads & closing remarksThe full transcript and all links mentioned can be found on the episode page on invisiblenotbroken.com
  • Author of “Compass Points the Way”: Alexis Kline

    23:14
    Monica Michelle is joined by author Alexis Kline.Alexis lives with Dysautonomia.In this episode, Monica and Alexis discuss: Being a sick teenagerHaving an isolated diagnosisProductivity workflowsTIMESTAMPS00:28 - Alexis’s diagnosis & dog07:18 - Sick teenager road map10:00 - Alexis’s book & workflow16:25 - Having an isolated diagnosis20:50 - Wildlife photography, purchases The full transcript and all links mentioned can be found on the episode page on invisiblenotbroken.com
  • Author of “From the Sidelines to the Finish Line”: Emily Falcon

    36:47
    Monica Michelle is joined by author Emily Falcon.Emily lives with ALCAPA.In this episode, Monica and Emily discuss: Growing up sickPost-surgery supportHaving a public bodySelf-motivation and adventuringTIMESTAMPS00:28 - Being a sick kid & Emily’s book title07:28 - Mortality10:16 - Portrayal of disability in media12:21 - Post-surgery support19:23 - Having a public body23:43 - Self-motivation29:46 - Emily’s tips for adventuresThe full transcript and all links mentioned can be found on the episode page on invisiblenotbroken.com