In March of 2010, my daughter was involved in a serious car accident that left her battling the chronic neurological pain disorder Complex Regional Pain Syndrome (CRPS/RSD) and changed our lives forever. Follow us along on our journey. Our suitcases have no room for negativity.

4th September 2012

Link reblogged from Project3x5 with 137 notes

Project3x5: HOORAY! It's September! It's Pain Awareness Month! →

project3x5:

Did you know that September is National Pain Awareness Month?!?

Even better… do you know that there are a ton of exciting events going on all over the USA (and the web, so no excuses!) to raise awareness & education for the cause and to allow us to meet each other for support?!

Yup!…

Tagged: AwarenessCRPSRSDComplex Regional Pain SyndromeReflex Sympathetic DystrophyInvisible IllnessChronic PainFaithHopepain awareness month

28th August 2012

Post reblogged from Believe In Recovery with 23 notes

chosen-positivity:

Having a rough day? Even if you’re having a wonderful day, here’s a tiny reminder that you are so strong and can do any positive thing you put your mind to. Never stop believing in yourself.

Tagged: RSDReflex Sympathetic Dystrophy. CRPSComplex Regional Pain SyndromeFaithHopePaininvisible illness

Source: chosen-positivity

23rd August 2012

Photo reblogged from Project3x5 with 11 notes

project3x5:


Because every week should start off with something beautiful, something blue, and something to inspire and be coveted by you… xx
*Boys, please hang around for this one! I promise, it’s more than just a girly shoe post! 
It is my absolute honor to lead y’all to a super fun fashion-image blog I recently discovered. Named MTV fashion and showcasing pieces of absolutely impeccable, yet still trendy, taste; I was thrilled to find it while browsing for something to distract me from my way-over-reactive nerves yesterday. 
Now, if you thought that the above-mentioned shoes were something special, you’re in for even more of a treat…
Imagine my surprise when, while navigating amongst a sea of chic, I discovered a teeny, tiny blurb explaining the blog to be run by a fellow CRPS/RSD warrior named, Alicia. Having been born in Paris, but now hailing from New Zealand, Alicia uses the whimsy of fashion as an escape from the fact that, ironically, the disease has taken away her ability to walk at the far too early age of only 15 years old. 
She’s beautiful, smart, confident, and has gorgeous taste. Life is cruel, but we are kind. As Spoonies, let’s rally around this lovely lady (whose other blog - a diary of her life with CRPS/RSD may be found here) and show her all the love that we can. x
Loads of love to you all & be well! 
Danielle xx
Ps: Although this was not the case with Alicia, should there be another CRPS/RSD warrior/blogger that you think needs featuring, write to me and let me know why! I love hearing about experimental treatments, books, etc. also!
I’m available at: theproject3x5@gmail.com or on twitter at: theproject3x5. Don’t forget that I always love hearing from you :) xx

project3x5:

Because every week should start off with something beautiful, something blue, and something to inspire and be coveted by you… xx

*Boys, please hang around for this one! I promise, it’s more than just a girly shoe post! 

It is my absolute honor to lead y’all to a super fun fashion-image blog I recently discovered. Named MTV fashion and showcasing pieces of absolutely impeccable, yet still trendy, taste; I was thrilled to find it while browsing for something to distract me from my way-over-reactive nerves yesterday. 

Now, if you thought that the above-mentioned shoes were something special, you’re in for even more of a treat…

Imagine my surprise when, while navigating amongst a sea of chic, I discovered a teeny, tiny blurb explaining the blog to be run by a fellow CRPS/RSD warrior named, Alicia. Having been born in Paris, but now hailing from New Zealand, Alicia uses the whimsy of fashion as an escape from the fact that, ironically, the disease has taken away her ability to walk at the far too early age of only 15 years old. 

She’s beautiful, smart, confident, and has gorgeous taste. Life is cruel, but we are kind. As Spoonies, let’s rally around this lovely lady (whose other blog - a diary of her life with CRPS/RSD may be found here) and show her all the love that we can. x

Loads of love to you all & be well! 

Danielle xx

Ps: Although this was not the case with Alicia, should there be another CRPS/RSD warrior/blogger that you think needs featuring, write to me and let me know why! I love hearing about experimental treatments, books, etc. also!

I’m available at: theproject3x5@gmail.com or on twitter at: theproject3x5. Don’t forget that I always love hearing from you :) xx

Tagged: RSDCRPSPainchronic Paincomplex Regional Pain SyndromeReflex Sympathetic DystrophyHopeInspirationfaith

4th July 2012

Photo reblogged from Project3x5 with 20 notes

project3x5:

It’s one of those bad, bad pain days today.
Ouch! Ouch! Ouch! 
Thinking about it though, it’s so wonderful how tomorrow is another day, isn’t it?
It may always hurt, but (fingers crossed), at least tomorrow it may hurt just that little bit less. Enough to get us through and allow us to deal with things just that much easier. :) xx
(Source: pleaseholdmecloser)

project3x5:

It’s one of those bad, bad pain days today.

Ouch! Ouch! Ouch! 

Thinking about it though, it’s so wonderful how tomorrow is another day, isn’t it?

It may always hurt, but (fingers crossed), at least tomorrow it may hurt just that little bit less. Enough to get us through and allow us to deal with things just that much easier. :) xx

(Source: pleaseholdmecloser)

Tagged: RsdCRPScomplex regional pain syndromeReflex Sympathetic DystrophyPaininvisible illnesshopefaithCureHelpChronic PainHopeSmileHappiness

14th June 2012

Photo reblogged from The Facets Magazine with 4 notes

facetsmag:

In our June/July issue, Kara Vanderbijl interviews Tumblr’s own Danielle Cosgrove (above) of Project 3x5 about her experience living with Complex Regional Pain Syndrome.
Read the inspiring article now.

facetsmag:

In our June/July issue, Kara Vanderbijl interviews Tumblr’s own Danielle Cosgrove (above) of Project 3x5 about her experience living with Complex Regional Pain Syndrome.

Read the inspiring article now.

Tagged: RsdCRPSChronic illnessPainComplex Regional pain Syndrome

14th June 2012

Photo reblogged from Project3x5 with 6 notes

project3x5:

Happy Feet in Chicago!
I feel as though Chicago is slowly & currently taking the place of home, what with the amount of time spent here for medical treatments and what not.
However, you know what? Looking back on what Chicago has managed to do to my health - that’s kind of somewhat alright with me.
I mean…
Do we see that I’m wearing normal sandals? Or rather, sandals with a little heel, no doubt!
Gone is the era of the public wearing of my sad looking black bedroom slipper things with every single outfit, no matter how bright, how sequined, nor how ladened with tropical flowers (oh yeaaaa, I’m that girl).
Sadly, it didn’t seem to matter to the world that they were oh-so-expensive & UGG’s, everyone just seemed to find them oh-so-overpriced & UGG-LY - which was devastating seeing as longtime readers know my adoration, adulation, & admiration of beautiful footwear. 
And what about the color of my feet in this picture? Yes ok, I’ll give you the fact that there’s a slight difference in color (if you don’t know what I’m talking about click here or here for a greater understanding of CRPS/RSD symptoms), but hardly so when compared to this! Or how about this.
I love you Chicago!
Until my next craving of sun, sand, & sea at least. ;) xx
RELATED POSTS:
- Happy Feet Floating

project3x5:

Happy Feet in Chicago!

I feel as though Chicago is slowly & currently taking the place of home, what with the amount of time spent here for medical treatments and what not.

However, you know what? Looking back on what Chicago has managed to do to my health - that’s kind of somewhat alright with me.

I mean…

Do we see that I’m wearing normal sandals? Or rather, sandals with a little heel, no doubt!

Gone is the era of the public wearing of my sad looking black bedroom slipper things with every single outfit, no matter how bright, how sequined, nor how ladened with tropical flowers (oh yeaaaa, I’m that girl).

Sadly, it didn’t seem to matter to the world that they were oh-so-expensive & UGG’s, everyone just seemed to find them oh-so-overpriced & UGG-LY - which was devastating seeing as longtime readers know my adoration, adulation, & admiration of beautiful footwear. 

And what about the color of my feet in this picture? Yes ok, I’ll give you the fact that there’s a slight difference in color (if you don’t know what I’m talking about click here or here for a greater understanding of CRPS/RSD symptoms), but hardly so when compared to this! Or how about this.

I love you Chicago!

Until my next craving of sun, sand, & sea at least. ;) xx

RELATED POSTS:

- Happy Feet Floating

Tagged: CRPSRSDPainillnessComplex Regional Pain SyndromeReflex Sympathetic DystrophyHopesupportfaithhealing

3rd June 2012

Photo reblogged from Project3x5 with 10 notes

project3x5:

I’m slowly rapidly becoming a part of of the Chicago Skyline. xx

project3x5:

I’m slowly rapidly becoming a part of of the Chicago Skyline. xx

Tagged: PhotographyRSDComplex Regional Pain SyndromePainIllnessChicagoChronic illnessInvisible IllnessFaithCureScenerytrending.

31st May 2012

Video reblogged from Project3x5 with 14 notes

project3x5:

I’m having surgery again today, hear why in this Vlog!

Also… y’all deserve a proper explanation as to where I’ve been over the past (yikes…!) 8 weeks.

Lots of love. Be well.

Danielle xxxx

Tagged: CRPSRSDpainillnessChronic IllnessDiseasePainComplex Regional Pain SyndromeReflex Sympathetic DystrophySupportFashion

20th May 2012

Photo reblogged from Project3x5 with 7 notes

project3x5:

“Whatever Happens, Happens…”
Lauren (you met her yesterday) and I just before entering the hospital yesterday to find out my not such great news. So close we almost look like the same person, huh?
I was in an extreme amount of pain the moment that the above photo was taken, but you know what - here’s how I choose to look at it (Hint: it really helps!): My Complex Regional Pain Syndrome/Reflex Sympathetic Dystrophy (CRPS/RSD) may be hurtful, but my friendships bring me joy, hope, love, faith, and strength. A wicked combination that nothing - no disease, chronic illness, sickness, pain, etc. - nothing, is stronger than. 
Living in and out of hospitals, being cut into every other month (with no cure to be found) - there is at times so little that brings us laughter, so little that brings us hope, and, even in the best of us, there may be at times a fading or flickering faith that things might not get any better. Chronic illnesses, ugh. I had no idea before I got one, but boy do they take it out of you. 
If there’s one thing I’ve learned though it would be this - chronic illnesses put stuff back in to you as well. And it’s damn good stuff too! 
Living in and out of hospitals, being cut into every other month (with ‘seemingly’ no cure to be found) there’s so little time for drama that your friendships just become true. There’s so little extra strength for pettiness that your experiences just become pure. When dealing with hope, let’s hope it has nothing to do with worrying that some minor inconsequential action of yours has lead to the petty argument between your flatmates. 
And as for love & joy… well I think there’s always enough of those to go around - chronically ill or not. :)
Be well,
Danielle. xx

project3x5:

“Whatever Happens, Happens…”

Lauren (you met her yesterday) and I just before entering the hospital yesterday to find out my not such great news. So close we almost look like the same person, huh?

I was in an extreme amount of pain the moment that the above photo was taken, but you know what - here’s how I choose to look at it (Hint: it really helps!): My Complex Regional Pain Syndrome/Reflex Sympathetic Dystrophy (CRPS/RSD) may be hurtful, but my friendships bring me joy, hope, love, faith, and strength. A wicked combination that nothing - no disease, chronic illness, sickness, pain, etc. - nothing, is stronger than. 

Living in and out of hospitals, being cut into every other month (with no cure to be found) - there is at times so little that brings us laughter, so little that brings us hope, and, even in the best of us, there may be at times a fading or flickering faith that things might not get any better. Chronic illnesses, ugh. I had no idea before I got one, but boy do they take it out of you. 

If there’s one thing I’ve learned though it would be this - chronic illnesses put stuff back in to you as well. And it’s damn good stuff too! 

Living in and out of hospitals, being cut into every other month (with ‘seemingly’ no cure to be found) there’s so little time for drama that your friendships just become true. There’s so little extra strength for pettiness that your experiences just become pure. When dealing with hope, let’s hope it has nothing to do with worrying that some minor inconsequential action of yours has lead to the petty argument between your flatmates. 

And as for love & joy… well I think there’s always enough of those to go around - chronically ill or not. :)

Be well,

Danielle. xx

Tagged: Complex Regional Pain SyndromeRSDCRPSReflex Sympathetic DystrophyPainIllnessStrengthFaithLoveInvisible Illness

13th May 2012

Photo reblogged from Project3x5 with 17 notes

project3x5:

Goodnight! I hope you all had relatively pain-free days. xx

project3x5:

Goodnight! I hope you all had relatively pain-free days. xx

Tagged: RSDCRPSCOMPLEX REGIONAL PAIN SYNDROMEPainFaithLOVEIllnessHopeCure