Tag: ehlers-danlos syndrome
Posted on November 24, 2021
by Chronically Jenni
115 Comments
The Holidays are coming and the Black Friday deals have already begun and for me that means it’s time to get my Christmas Shopping sorted! So whether you’re a spoonie writing your wishlist or looking for a great gift for a chronically ill loved… Continue Reading “Chronic Illness Holiday Gift Guide”
Category: Illness, UncategorizedTags: black friday, christmas, christmas gift guide, christmas gifts, chronic fatigue, chronic illness, chronic illness holiday gift guide, chronic pain, disability, disabled, eds, ehlers-danlos syndrome, gift guide, happy holidays, holiday gift, holiday gift guide, pots, spoonie holiday gift guide
Posted on June 29, 2020
by Chronically Jenni
48 Comments
My personal life is something I’ve always kept fairly private but in the world of social media sometimes this can skew the view of what it is like to be in a relationship whilst being diagnosed with a chronic illness. For the readers who… Continue Reading “Relationships & Chronic Illness”
Category: UncategorizedTags: chronic fatigue, chronic illnes, chronic pain, chronically ill, coronavirus, dating, dating and chronic illness, dating during coronavirus, dear future husband, eds, ehlers-danlos syndrome, love, pots, relationships, relationships and chronic illness, shout out to my ex
Posted on September 29, 2019
by Chronically Jenni
7 Comments
September is coming to a close. This month has brought the feeling of new beginnings as little ones head back to school and an autumnal chill fills the air. I know for sure that I’ve already curled up in a blanket and lit a… Continue Reading “Pain Awareness Month: A Letter to Pain”
Category: Illness, UncategorizedTags: chronic illness, chronic pain, csf leak, eds, ehlers-danlos, ehlers-danlos syndrome, letter, letter to pain, pain, pain awareness month, pots, september
Posted on September 28, 2019
by Chronically Jenni
6 Comments
It’s strange to think, as I sit here in bed in my most comfortable tracksuit with a bloated tummy and sore head, that this time last week I was sat down for a 3-course dinner in a beautiful cathedral, which looked like it had… Continue Reading “Friday Thoughts: The National Diversity Awards”
Category: Illness, UncategorizedTags: awards, chronic illness, disability, diversity, eds, ehlers-danlos, ehlers-danlos syndrome, hsd, hypermobility, Illness, liverpool, national diversity awards, paul sesay, pots, role model, sally phillips, spoonie, vlogger, zebra
Posted on September 20, 2019
by Chronically Jenni
89 Comments
Over the past few years, I have found so many amazing products and hacks to help me with different aspects of my connective tissue disorder (Ehlers Danlos Syndrome). Some of these things are quite specific to EDS but others would be helpful for a… Continue Reading “My EDS Survival Kit (Part 1)”
Category: Illness, UncategorizedTags: chronic fatigue, chronic illness, chronic pain, eds, eds hacks, eds products, eds survival kit, ehlers-danlos, ehlers-danlos syndrome, living with ehlers danlos syndrome
Posted on August 24, 2019
by Chronically Jenni
17 Comments
If I’d have had to write my final university project two years ago, when I was part of the class of 2017, I couldn’t tell you what I’d have written about, since going back to university I always knew that I wanted my project… Continue Reading “All That You Can’t See: Living with Ehlers Danlos Syndrome”
Category: Illness, UncategorizedTags: all that you can't see, awareness, chronic fatigue, chronic illness, chronic pain, chronically ill, docudrama, documentary, eds awareness, ehlers-danlos, ehlers-danlos syndrome, living with eds, living with ehlers danlos syndrome, project, radio, university, zebra
Posted on August 23, 2019
by Chronically Jenni
32 Comments
Recently I’ve had a lot of questions from friends, colleagues and spoonie’s alike about my mobility aids. From how I started using them and accepting them as part of my life to why I do, or don’t, need them from one day to the… Continue Reading “Friday Thoughts: Different Aids for Different Days”
Category: Illness, UncategorizedTags: babe with a mobility aid, chronic illness, chronically ill, different aids for different days, disability, disabled, eds, ehlers-danlos, ehlers-danlos syndrome, hsd, mobility aid, mobility aids, pots, spoonie, walker, walking stick, wheelchair, zebra
Posted on August 21, 2019
by Chronically Jenni
33 Comments
Very Busy Week Last Week! Went back to the gym, had 2 hospital appointments (Neurology at Queens & my year follow up from rehab at RNOH) and went on a date day to Thorpe Park and discovered their Ride Access Pass. I also went shopping… Continue Reading “Chronic Illness Weekly: Back to the Gym, Hospital Appointments & Thorpe Park”
Category: Illness, UncategorizedTags: accessibility, Accessible, appointments, chronic fatigue, chronic illness, chronic pain, eds, ehlers-danlos, ehlers-danlos syndrome, gym, haul, hospital, hospital appointments, pots, Ride Access Pass, RNOH, shopping, Thorpe Park
Posted on December 22, 2017
by Chronically Jenni
7 Comments
Happy December Everyone Sorry I’ve been super quiet on here but a lot has been going on! If you’ve missed it you can see what I’ve been getting up to every day throughout December over on my Youtube channel where this year I’ve got… Continue Reading “Spoonie Vlogmas!”
Category: Illness, UncategorizedTags: christmas, December, eds, ehlers-danlos, ehlers-danlos syndrome, heds, hsd, living with pots, postural orthostatic tachycardia syndrome, pots, spoonie, Vlogmas, zebra
Posted on November 6, 2017
by Chronically Jenni
39 Comments
Dysautonomia Awareness Month may be over but Dysautonomia is something people have to live with every day of the year. I made a video last month with 4 other lovely ladies who were all brave enough to share their story about Living with POTS.… Continue Reading “Dysautonomia Awareness Month & Recent Vlogs”
Category: Illness, UncategorizedTags: adventures, adventures with EDS, awareness month, chronic, chronic illness, chronic pain, dysautonomia, eds, ehlers-danlos, ehlers-danlos syndrome, Illness, living with pots, postural orthostatic tachycardia syndrome, pots, video, vlog, vlogger