Vlog | Black Women Dating While Living Abroad: Will Italian Men Feed You Pasta?

DatingAfter four years of living in Rome, I’ve learned a bit about dating, especially as a Black woman. In this video, I offer up my thoughts on possible dating experiences that Black women may meet while living abroad, the (ir)relevance of beauty standards, and reasons for travelling abroad, including cultural expectations.

Hope you enjoy it! If you do, please “like” (thumbs up) the video. Thanks!

 

Quote Of the Day | Yagazie Emezi

photo from Yagazie Emezi on Tumblr. Click to visit.

photo from Yagazie Emezi on Tumblr. Click to visit.

FMS | FibroArt Project Continues (got fibro? get life.)

gotfibro

 

A work in progress. I am happy with it so far. 🙂

Travel | JCU Students Speak About Study Abroad Experience: Black in Rome!

Alexandria Maloney, JCU graduate and Founder of the Women’s Leadership Initiative. (Image from LinkedIn. Click to visit her profile.

Really wonderful video put together by Alexandria Maloney to address the issues that young Black students may encounter when studying overseas, particularly in Italy.  Please, take time out to watch & share. 🙂

Until Tomorrow,D.

 

FMS | FibroArt Monday

never look away, (series: got fibro? get life.), digital media, Diedre Blake (2015)

never look away, (series: got fibro? get life.), digital media, Diedré M Blake (2015)

This is the first piece from a series that I’m working on called “got fibro? get life.” I’ve been wanting to find a way to explore the shift in attitude towards fibromyalgia and how it impacts my life.

It’s always sometimes challenging to write about your own art, so I’ll leave it here. Of course, your comments are always appreciated.

Happy Monday!

Until Tomorrow,

D.

Vlog & FMS | Funny ‘Ish’ People Say If You Have Fibromyalgia (“You Don’t Look Ill”)

Snapshot 1 (25-Jan-15 17-36)

Over the years, I’ve heard a lot of interesting comments about fibromyalgia, whether directed at me or at others. Just for fun, I decided to put together a little video sketch about these experiences.

If you have fibromyalgia, then I hope you will connect with this video and have little laugh about our shared experiences.

If you don’t have fibromyalgia…then one of these character might be you. 😉

Enjoy!

Travel | Garbatella (Rome)…Even Gandhi Had to Visit!

New Cover Art for  YouTube. Click to Visit Vlog: Rome Off the Beaten Path.

New Cover Art for YouTube. Click to Visit Vlog: Rome Off the Beaten Path.

I have a newfound respect for vloggers…actually, for anyone who films and edits anything.  Yes, indeedy, I do.  Windows Movie Maker and YouTube Video Manager have occupied my soul for the past 72 hours.  Although filming is fun, to be frank, it takes a whole lot of balls to pick up a camera, head outside and record yourself. 😉

Below is a playlist of videos on Garbatella, a neighbourhood that was developed just before the rise of Fascism and was later taken over by the Fascists who relocated people (many communists) they evicted from the historic center.

I welcome you to watch, and hope you will like them.  Feel free to  offer suggestions.  Places you’d like to see, subjects you’d like discussed, etc.

Also…

Thank You So Very Much For Being There Even When I am Not Here!

Vlog | What? Fibromyalgia, Living in Italy (Plus Being Black, Queer & Vegan)

I’ve decided to begin a YouTube channel. 😉  It’s something that I’ve been wanting to do for some time, and now I’ve finally taken this first step.

I hope to share with you the lessons I’ve learned living with fibromyalgia, and also living abroad as a woman of color.  I look forward to your feedback and to answering questions that you may have.

Now, you have a voice to with the face! 😀

FMS | Consistently Embrace the Inconsistency of FMS (The 5 Gs)

Image from fellow blogger Shauntee’s article “Dating Pet Peeves: The Invisible Third Person.” Click image to read.

 

I shouldn’t be writing this post.

No, seriously, I really ought to be writing something else, something relevant to advancing my studies or career or something else that I know is more important.

Even more seriously, typing this actually hurts. My hands, arms, chest, back, stomach, sides, thighs, knees, calves and ankles hurt. You name it, it hurts.  There are parts of me that are hurting that I didn’t know could hurt.  Then I remember:

This is the nature of fibromyalgia. 

 I am used to the pain. Thus, I cannot truly complain about it. This post is not about that.  It is about how to deal with the randomness of the pain or any other FMS symptoms, of being the unsuspecting victim of your own body.

So, What Do I Do?

Image from WOLB Baltimore’s article “Can Listening to Music Improve Your Health?” Click image to read article.

THE 5 Gs

GIVE (IN)| GET (ORGANIZED) | GRATITUDE  | GROW | GATHER

1. Give in / Give up –  Not on getting better, but on denying your experience.  What it basically means is accepting the reality of the situation. For a long while, I was really hard on myself whenever I had a significant flare-up.  I was constantly seeking to figure out when I would feel better, as though there were a timer ticking away and counting down to zero.  Give it up, that’s not the way it goes.

2. Get Organized –  Take a look at your obligations and figure out what can be put on the back-burner, what can be modified, and what needs to be immediately addressed.  The next step is to notify anyone who may be directly impacted by your current state.  Don’t leave others in the lurch just because you are ill.  Be clear with everyone about what you can do and when you can do it, if at all.  

3. Go for Gratitude –   The world didn’t collapse because you are having a flare-up. It’s not that serious.  Be grateful for what you can do, what you have already accomplished, and what you will be able to do.  Wallowing in self-pity will get you nowhere very, very quickly.  So, try not to be about that life.

4. Get Ready to Grow – Every moment, regardless of the value we assign to it, is an opportunity for personal growth.  Use this time to explore yourself. If you are able to do something, read something new.  If you aren’t able to do anything at all, listen to music or close your eyes and allow your imagination to take you on new adventures.  Do your best to remember that you are more than this moment. 

5. Gather Positivity – Whether alone or with loved ones, choose activities that reinforce the positives of your life, rather than focus on the negative.  I find it best to avoid discussing my current state.

Sometimes you may encounter people, I call fixers, who are very invested in solving your illness, and who will bombard you with seemingly never-ending questions–politely refuse to answer or simply avoid them.

Some people have limited patience for your illness, and these are people who you most definitely should do your best to avoid.

Negativity will only serve to bring you down, causing you to feel stressed and may severely impact your recovery time.  Gather around you people who bring with them a bit of sunshine, especially in the winter months. 

 

No Matter What, Keep It Positive While You Find Your Way Back On Your Path.

Until Next Time,

D