Showing posts with label EDS. Show all posts
Showing posts with label EDS. Show all posts

Saturday, December 5, 2020

Holiday Gift Guide - Ehlers Danlos/Rare Disease Zebra Edition

This post contains referral links which means that if you purchase from one of my links, I will receive a small percentage of the sale.  Don't worry, this won't cost you any extra!

If you're looking for the perfect gift for the Ehlers Danlos Syndrome or rare disease zebra in your life (or maybe for yourself), look no further! I've put together a list of gift ideas with something for every budget. Enjoy!




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Holiday Gift Guide - Ehlers Danlos/Rare Disease Zebra Edition : https://bit.ly/2JtX7IL
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Did you find anything you liked, either for a gift or for yourself? Drop a comment and let me know what your favorite item from the list is!











Thursday, August 13, 2020

What Not to Say to a Parent with a Chronic Illness (and What to Say Instead)

This post contains referral links which means that if you purchase from one of my links, I will receive a small percentage of the sale.  Don't worry, this won't cost you any extra!

Being a parent is hard, especially in today's world where an innocent picture of your kid eating a graham cracker on Instagram can be bombarded with criticism or "helpful" suggestions. 

"Isn't your kid too young to be eating graham crackers by himself? He doesn't look any older than six."

"Why are you taking pictures instead of watching your kid so he doesn't choke to death?!? You're a horrible parent."

"Is that a toy on the ground behind him? Don't you know that a messy house stunts your child's growth?"

I may be exaggerating a little, but you get the picture. It doesn't just happen on social media either. Sometimes people mean well, but their comments can be insensitive to say the least.

Now, take all of those up-in-your-business, critical, hurtful comments and multiple them by at least 10 and you have an idea of what it's like to be a parent who lives with a chronic illness. I've encountered so many people who think they can "fix" me or tell me how I've messed up my kids and my health. From the lab technician who asked why in the world I would ever have children knowing that I could pass Ehlers Danlos Syndrome on to them, to the “friend” who informed me that I caused my whole family to have EDS by vaccinating my children (um, that’s not how a genetic disorder works…), to the other "friend" who told me that I only had my health conditions because I "wanted" them, I've heard some doozies that have ranged from mildly insensitive to downright hurtful and I can tell you...the mom guilt is real.

What Not to Say to a Parent with a Chronic Illness (and What to Say Instead)


People think they’re helping but sometimes all they’re doing is hurting. With that in mind, I put together a helpful list of things never to say to a parent with a chronic illness. Some of them are a little tongue in cheek because I think we could all use a chuckle now and then. Also, every single thing on the list has either been said to me or another chronically ill mom I know. I wish I were kidding about that, but I’m not. 

"You don’t look sick!" 
This is usually meant as a compliment, but it sure doesn’t feel like it. Many of us have spent our whole lives trying to prove to our friends, families, and even doctors that we’re not just faking it and that there truly is something wrong. Telling us that we don’t look sick makes us feel like you think we’re just faking the whole thing. And believe me, we wish we were! 
Instead, try saying: ​You’re looking good today, but how are you feeling? 
"I know how you feel."
Um, no. Unless you also have a debilitating chronic illness, you really don’t. 
Instead, try saying: I don’t know how you feel, but I’d like to understand better.

"Well, I’m tired too." 
Yeah, I thought I knew what tired felt like too before my chronic fatigue increased in intensity. Believe me, nothing can compare to this level of “tired.” It’s so intense that at times, I can’t even lift my fingers to type on my computer. 
Instead, try saying: ​I can’t imagine how you feel, but help me try to understand.

I’ve found the people who ask these kinds of questions are often trying to get me to buy a product that they sell. Sometimes, they’re genuinely trying to help though, and while I appreciate the thought, it’s not helpful. I spend a lot of my time researching new treatments and possibilities as well as discussing things with my doctors. If there’s something out there that I haven’t ​tried, it’s for a reason. 
Instead, try saying: ​I can tell that you’re working hard to research the best options for your illness.

"You need to get out and do more activities with your kids."
Mom guilt on its own is bad enough (am I doing too little for my kids? Am I a good enough mom?), but when you throw in a chronic illness, it intensifies significantly. Why would you want to add to that? Do you really think that I wouldn’t ​love​ to be able to do more with my kids? Having to tell my kids no because of my chronic illness absolutely tears me up inside. 
Instead, try saying:​ You’re doing a good job as a mom. Can I take the kids with me on our next trip to the park? 

"You did it last week, why can’t you do it today?" 
Honey, I did something ​an hour ago​ that I can’t do right now. Every day with a chronic illness is different and sometimes, it narrows down to being different every hour. My body is very unpredictable, and I hate that more than anyone else. 
Instead, try saying: ​Are you up to getting coffee with me today? If not, I understand and in that case, can I bring you a coffee? 



"At least it’s not cancer!" 
Oh. my. word. Comparing illnesses doesn’t help anyone. Ever. We all have trials to work through and each one is huge to the person dealing with it. For example, when I was still relatively healthy and had one relatively healthy baby, I thought that was incredibly hard (Example: my baby has an ear infection...this is the worst thing ever!). Now I’m basically disabled and have four kids with varying special needs who will experience more pain and medical issues as they get older. ​This is hard.​ But that doesn’t negate how hard it was with just one child. Your perspective changes as your situation does. 
Instead, try saying:​ I know it’s hard right now, but I’m here for you.

"You look and sound happy on social media so how bad can it be?" 
Just because I’m in almost constant pain doesn’t mean that I’m never happy. If I waited until I felt good before I was happy, I would be miserable all the time and that’s not a good way to deal with this. Also, I only share things that I want to share on social media which means that you’re probably just seeing my best moments. Would you really want to be friends with me if I did nothing but complain and exude negativity? 
Instead, try saying: ​I’m glad to see that you were able to enjoy your day yesterday!

"You only have your illness because you think you do." 
Are you insinuating that I’m faking it and it’s all in my head or are you telling me to be more positive so my chronic illness will just go away? Either way, ​don’t say this​. Seriously. I know people think I’m faking it. I’m going to let you in on a little secret. I ​am​ faking it. However, I’m actually faking being as well as I am. I work hard and push through a lot of pain so I can lead as normal a life as possible. I’ve had so many people tell me that I’m faking it that I even doubt myself sometimes. Do you have any idea how crushing that is? Thinking positively can definitely have a good effect on mental and physical well-being, but no matter how positively I think, it won’t heal my Ehlers Danlos Syndrome. I will still have pain, and I will still have defective genes. 
Instead, try saying: ​I believe you. Tell me more about your chronic illness. 


"I could never do what you do." 
I didn’t think I could ever do this either. I used to read stories about people in situations similar to my current one and thank God that I didn’t have to deal with that because I ​knew ​I didn’t have it in me. However, that shows a lack of faith in God, and it turns out that you do what you have to do to survive when you literally don’t have any other choice, and you do it with God’s help. Also, please stop painting me to be this amazing brave person who can power through something that most people couldn’t. Sometimes, I’m barely hanging on and hearing something like this can make me feel like even more of a failure. If you only knew what goes on inside my head and behind the scenes, you would know that I struggle just like everyone else. 
Instead, try saying: ​How can I pray for you today?

"If you pray and believe, God will heal you." 
Please don’t turn God into a vending machine. That’s not how He works. I can pray and believe all I want, but if God says no or wait, I am not going to be able to change His answer. Instead, I need to focus on what He is trying to teach me through my chronic illness. Do you remember Paul in the Bible? Remember how he had a “thorn in the flesh” (II Corinthians 12:7) and prayed for God to remove it from him? God didn’t. Instead, He allowed Paul to continue to go through his trial, knowing that it would strengthen his relationship with Christ. 
Instead, try saying: ​How can I pray for you today? 

"I wish I could stay home with my kids and not have to work." 
When I was 17, I had to quit my first job thanks to my health. I cried for days because I was so crushed that I had to give up a job I loved and because quitting made the reality of my health hit me like a load of bricks. Right now, I’m a substitute at the local library and have to turn down a lot of hours because, after about an hour or two on a job that isn’t even that physically taxing, I’m stumbling around like I’m drunk because my legs aren’t working right anymore and practically gasping in pain. I love, love, love working at the library and had originally hoped to be able to go up to full-time when my kids get older, but now, I’m facing the realization that I will not be able to do that. Not being able to work makes me feel worthless at times. 
Instead, try saying: ​Tell me about your hobbies.

"It must be nice to be able to park in the handicapped spots." 
You can have my handicapped placard if you take my disability to go along with it. I’m actually too scared most of the time to use my placard when I need it because people can be mean, judgmental, and forget that not all disabilities are visible. 
Instead, try saying: ​Can I help you carry your bag to your car? 

"You go to the doctor too much." 
Yeah, I agree. I actually hate going to the doctor, but unfortunately, it’s necessary for my health. If I stop going, bad things will happen.
Instead, try saying:​ Would you like me to come along with you to the doctor sometime so we can have coffee afterward?

"God will never give you more than you can handle."  
You will go through more than you can handle, but God can handle it if you let Him. I can’t​ handle this, and you saying something like that to me makes me feel like I must be a terrible Christian. 
Instead, try saying:​ How can I pray for you?

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What not to say to a parent with a chronic illness (and what to say instead) : https://bit.ly/2PPor3x
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The absolute best thing you can say to someone with a chronic illness is “I believe you.” Seriously. What do ​you ​do when someone just isn’t getting the hint about their insensitive words? Well, you actually have several options to choose from and you can use one or all of them, sometimes on the same person. Oftentimes, I go with a combination of the following.

Ignore them. 
When someone says something hurtful to me about my chronic illness, sometimes, I will just smile and then change the subject. Unfortunately, some people just don’t get the hint so you may have to move on to another strategy if this one doesn’t work.

Realize when it’s not worth your energy to argue. 
We all know a few people like this. They just won’t let it go and there’s pretty much no chance of them ever changing their mind on anything. When you run across someone like that, acknowledge to yourself that arguing with them is not going to help and it will more than likely end up using some of your precious energy. Answer their comment or question with something along the lines of, “I know that we don’t agree on this, so I think it would be best if we talked about something else.” Then change the subject and if they bring it up again, use one of the other strategies to deal with them.

Set clear boundaries. 
It’s okay to tell someone that you do not want to talk about your chronic illness with them and that it’s off-limits. Once you’ve let them know that, stick to it because just like a toddler, if you give in once, they’ll think it’s okay to do it forever. Alternatively, you could also send them a link to a website that you know had reputable information about your specific chronic illness and tell them that you would love to discuss their suggestions and thoughts about your condition after ​ they’ve read about it. 

Know when it’s time to cut ties.
If someone is intentionally hurtful or just won’t let up with the insensitive comments and questions, it may be time to cut ties or at least limit interactions. You can unfollow them on social media (sometimes you can do this without deleting them from your friends list/followers so they won’t even know), cut down on social interactions, “miss” their phone calls (caller ID really does come in handy sometimes!), etc.

Look for the intention behind the words. 
This one is hard, but sometimes it’s the best way to avoid hard feelings on either side. Maybe your friend makes insensitive comments about your chronic illness but does it with good intentions. Maybe they truly care and want to help. If that’s the case, gently explain to them that while you appreciate the sentiment, saying and asking things like that is actually hurtful and doesn’t help. Be open and honest with them about ways that they can help encourage you. 

What tips do you have for dealing with insensitive or rude comments?









Monday, March 2, 2020

The Most Important Thing You Can Give Your Chronically Ill Loved One


Maybe they were born with their chronic illness or maybe it developed later in life.  Either way, there's one thing that people with a chronic or invisible illness need more than anything else.

They need you to believe them.

The Most Important Thing You Can Give Your Chronically Ill Loved One

One of the worst parts of having a chronic illness or invisible disability is having people think we're faking it.  That we're doing it to get sympathy or so we can get out of doing things.  That we're hypochondriacs, lazy, wimpy, etc.  


We desperately want to be "normal" and to be able to do everything that you do, but our bodies simply won't cooperate.

I spent most of my life thinking that all of my pain, my weird symptoms, my inability to keep up with my siblings was in my head.  Doctor after doctor ran tests, shook their heads, and told me, once again, that they couldn't find anything wrong with me so I must be fine.

And then, when I was 30 years old, I finally had a doctor look me in the eye and gently say, "It's not in your head.  You have Ehlers Danlos Syndrome, and it explains everything."

She made me cry, but they were happy tears because my whole life had finally been validated.  I could finally stop lying to everyone and hiding how awful I really felt and how hard I struggled to get through each day.  I could finally slow down and take care of myself.

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Do you know what the most important thing you can give your chronically
ill loved one is? Find out here: https://bit.ly/2x1ffmt
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I thought having a name for my health issues would finally make everyone believe me when I said there was something wrong.

Nope.
It hurts worse now than it did before I was diagnosed because even though I have medical documents and specialists to back me up, some people still don't believe me.  It doesn't help that Ehlers Danlos Syndrome is something that many people haven't heard of or know much about.  Sometimes I wonder if it would make a difference if I had a "real" disease, you know, one that people know about. But deep down, I know it wouldn't. People will either believe me or they won't. I'm not going to waste my low supply of energy trying to prove myself to people who have already made up their minds.

So sit down with your loved one today, look them in the eye, and give them the best gift you can.

Tell them you believe them.












Monday, October 22, 2018

The Ultimate List of Ehlers Danlos Resources


In case you haven't noticed, I'm kind of passionate about raising awareness and understanding for the Ehlers Danlos Syndromes (which I've been told is now the right way to say it.)  I have this passion for five reasons.

Reasons 1-4: My kids.  Katie (10), Nano (8), Anna (6), and Davy (4) all have Hypermobile Ehlers Danlos Syndrome or hEDS which they inherited from me.  I want them to grow up in a world that I didn't grow up in...one that acknowledges and understands their condition and where doctors know what it is and how to treat it.

Reason 5: Everyone else with EDS.  Most people with EDS spent the majority of their lives being told it's all in their heads when that couldn't be further from the truth.  We're already at high risk for depression and suicide due to living in chronic debilitating pain and all of the other EDS symptoms.  Not being believed or understood makes everything so much worse.

The Ultimate List of Ehlers Danlos Resources

So, with that in mind, I put together a list of EDS resources, printables, freebies, awareness products, etc.

Tuesday, October 16, 2018

10 Facts About Handicapped Parking


I'm 33 years old, and I have a handicapped placard in the glove box of my car.  I got it about a year or so ago, but I've only used it a few times.  There are three reasons for that.  The first is that I only use it on my really bad days when I literally can't handle walking very far.  The second is that often all of the handicapped spots are full, sometimes with vehicles that are parked there illegally.  The third is that I'm scared of backlash because I look healthy and normal unless I'm using one of my mobility devices, and people can be cruel about invisible disabilities.  Stories like this, this, or this seem to pop up at least several times a month, and I know that I just don't have it in me to deal with something like that on my bad days.

So, in light of all the misconceptions surrounding handicapped parking, here are 10 facts about it that might shed some light on their proper use.

10 Facts About Handicapped Parking

1. You can have my placard if you take my disability to go with it.

Monday, September 3, 2018

10+ Books About Ehlers Danlos Syndrome

This post contains referral links which means that if you purchase from one of my links, I will receive a small percentage of the sale.  Don't worry, this won't cost you any extra!

When it comes to information on the Ehlers Danlos syndromes or EDS, the selections are pretty slim.  As the disorder is still classified as rare (although it's NOT rare, it's just rarely diagnosed), there just aren't a lot of books about it out there.  However, as awareness is increasing, the number of books has been slowly increasing as well.  I put together a list of the best books to learn more about living with and loving someone with one of the Ehlers Danlos syndromes.


Thursday, May 10, 2018

Too Much EDS Awareness?

May is Ehlers Danlos Syndrome awareness month and in the two years since I was diagnosed, I've thrown myself into it fully each May.  With a shockingly small number of doctors who are EDS knowledgeable and most of the general public having never heard of it, raising awareness is a very important step towards furthering research for EDS.  


For many years, doctors have been very hesitant to diagnose Ehlers Danlos Syndrome because it is considered to be a rare disease, too rare in fact to diagnose or see a case of during their medical career.  However, the truth is that it's not rare, it's rarely diagnosed.  It's also a hereditary genetic condition which means that a parent who has it has a 50% chance of passing it on to each one of their children.  In the case of my family, I passed it on to all four of my children.  EDS is definitely not rare in my family or in many other families either.

https://www.facebook.com/sunshineandspoons/photos/a.294103583951875.87052.181409978554570/2035565373139012/?type=3&theater


In the two short years since my kids and I were first diagnosed with Ehlers Danlos Syndrome, I've noticed a huge increase in the awareness of EDS.  The EDS groups on Facebook are growing in leaps and bounds as more people hear about it and realize that this may be the answer to their many unexplained medical issues.  More doctors actu
ally know what it is even if they don't necessarily know how to treat it, and it's becoming more common for people to respond with, "I know someone else with that too!" when I tell them that I have it.  The Ehlers Danlos Society recently received an anonymous $1 million dollar donation to be used on research of the hypermobile type of EDS which is the most common type. The American Journal of Medical Genetics released new criteria for diagnosed hEDS in March 2017.  This is all huge, and we're making amazing strides.  It's exactly what I and others with EDS have been fighting for.

Tuesday, January 16, 2018

25+ Products That Make Life with Chronic Illness Easier

This post contains referral/affiliate links which means that if you purchase from one of my links, I will receive a small percentage of the sale.  Don't worry, this won't cost you any extra!

Having a chronic illness definitely makes life harder.  I'm assuming that, like me, you don't have the resources to hire a full-time nanny, chef, housekeeper, personal assistant, etc. either.  So, until I win the lottery (which will probably be tricky to do as I don't even play the lottery), I will have to go on finding products that work for me to make my life with a chronic illness easier.  

25+ Products That Make Life with Chronic Illness Easier

Here's what I've come up with so far.  Some are things I already use, some are on my wishlist (my birthday's in May if anyone wants to just go ahead and buy me everything on my wishlist! Hey, doesn't hurt to try, right?!?) and some are highly recommended by other spoonies.  Feel free to add your own suggestions in the comment section!

Monday, November 20, 2017

Christmas Traditions: Ornaments for Every Occasion From Etsy

This post contains referral links which means that if you purchase from one of my links, I will receive a small percentage of the sale.  Don't worry, this won't cost you any extra!

Every year on Christmas morning, my kids know that they will find a new ornament in their stockings.  Each of their ornaments mark a milestone they experienced in the past year or note something that they're currently interested in.  This year, Katie will be receiving a basketball ornament as she just started playing basketball, Nano will get a tractor ornament because he's really getting into farming with Hubby, and Anna and Davy will each get a first year of preschool ornament as they both started school this year (Anna is in 4/5 preschool and Davy is in 3/4.)

I have a lot of fun carefully picking out a special ornament every year for each of my children.  Someday, when they move out to their own place, they will already have a collection of ornaments for their Christmas tree.  I hope this is a tradition that they will someday pass on to their own children. 

Christmas Traditions: Ornaments for Every Occasion From Etsy

One of my favorite places to get ornaments is Etsy.  I love how unique every ornament is and how easy it is to find personalized ones.  A great bonus to shopping on Etsy is being able to help support fellow small business owners like me. 

Here are some of my favorite ornaments that I found on Etsy this year...

Monday, November 13, 2017

30+ Books for Kids with Special Needs Siblings: The Ultimate List

This post contains referral links which means that if you purchase from one of my links, I will receive a small percentage of the sale.  Don't worry, this won't cost you any extra!

When my youngest son Davy was born, my three older kids were 6, 4 and 17 months old.  The next year or so was very hard on my whole family as Davy spent countless hours at doctors' appointment, was hospitalized five times and, and required one-on-one care during most of his waking hours.  The guilt of not being able to care for all my kids' needs was crushing and made even worse when people would "helpfully" point out that I had three older kids who needed me too.  I knew that having a medically complex, special needs sibling was hard on my kids and I didn't want them to resent him or feel left out.

When Davy was around six months old, I found a book about kids with G Tubes on Amazon and got it to read to the older kids.  It helped them see that their brother's button wasn't scary and other kids had them too.  That got me thinking of how helpful books could be for kids who have siblings with special needs.

30+ Books for Kids with Special Needs Siblings: The Ultimate List

Keep reading for a list of over 30 books for kids with special needs siblings.

Tuesday, November 7, 2017

10 Things Guaranteed to Cure Whatever Ails You

This post contains referral links which means that if you purchase from one of my links, I will receive a small percentage of the sale.  Don't worry, this won't cost you any extra!

As someone with Ehlers Danlos Syndrome, Postural Orthostatic Tachycardia Syndrome, asthma, acid reflux disease, eczema, etc, I've heard it all.  On top of that, all four of my kids have Ehlers Danlos Syndrome as well, and three of them also have asthma and eczema.  My youngest son, Davy, had to have a feeding tube until he was 18 months old due to the severity of his issues.

10 Things Guaranteed to Cure Whatever Ails You

With all that, there's no shortage of unsolicited advice and cures.

"You only have your disease because you've 'claimed' it."

"You'd feel better if you would exercise more and eat better."

"Your *insert condition here* could be cured if you tried this supplement."

"Your EDS was caused by vaccinations."

Thanks to all the helpful advice I've received, I was able to put together a list of things that will cure any problem you have.  You're welcome.

Thursday, October 26, 2017

50+ Books for Special Needs Kids: The Ultimate List

This post contains referral links which means that if you purchase from one of my links, I will receive a small percentage of the sale.  Don't worry, this won't cost you any extra!

If your child has special needs of any kind, reading them a book about another child with similar issues can make them feel less alone.  

When I got my kids a copy of "Special Like Me" which is a book about a boy with Ehlers Danlos Syndrome just like they have, they were pretty excited.  I even took it to the school and read it to each of my two oldest kids' classes.

For children with special needs of any kind, reading them a book about another child with similar issues can make them feel less alone.  

50+ Books for Special Needs Kids: The Ultimate List

Books that focus on special needs of any kind are not just a great idea for the kids who have them, but for their peers, family, and anyone else who could benefit from learning more about the condition (hint: that would be everyone).

With that in mind, I spent several days researching and compiling this list of children's books about various special needs and disabilities.  I hope you find a book that works for your family!   

Monday, October 2, 2017

What are Dysautonomia and POTS?

Did you know that October is Dysautonomia Awareness Month?

Let me back that up a little....do you know what dysautonomia is?

If you said no, you're not alone.  Most people have never even heard of it.  I didn't know what it was either until I was diagnosed with it.

What are Dysautonomia and POTS?

Thursday, September 7, 2017

How to Make No Sew DIY Rice Heating Pads

This post contains referral links which means that if you purchase from one of my links, I will receive a small percentage of the sale.  Don't worry, this won't cost you any extra!

There are five people in my family who have Ehlers Danlos Syndrome, which means that pain is a normal occurrence around.  I prefer to try alternative methods of pain relief such as using essential oils (Panaway is a great one for muscle pain!), massage, ice, and heat before turning to tylenol.

A few weeks ago, I had all four of my wisdom teeth removed and was in excruciating pain for 10 days straight.  After applying ice to both sides of my face for the first 48 hours, the oral surgeon recommended switching to heat.  He said I could heat up the ice packs he'd sent home with me, but they just didn't seem to hold the heat very well so I decided to grab one of our trusty rice socks that I'd made with one of Hubby's (clean!) tube socks instead.  The problem was that it was too big and bulky to work well for my face.  In a rare moment of clarity, I grabbed a leg warmer from the kids' mis-matched sock basket and turned it into a perfectly sized rice heating pad.  

How to Make No Sew DIY Rice Heating Pads

Want to make your own rice heating pads that are the perfect size for kids AND adults?

Tuesday, August 15, 2017

What Chronically Ill People Want You To Know

Just about everyone who has a chronic illness fights not just their illness, but the preconceptions and judgments of their friends, family, and even complete strangers.  Stories like this or this happen way too often.

I asked people on my Facebook page and in several chronic illness Facebook pages what they wish people knew about their chronic illnesses.  The answers were pretty eye-opening.  

If you love someone with a chronic illness of any kind, read thisFor them. You'll come away with a greater understanding of what they are going through everyday.    

What Chronically Ill People Want You To Know

For me personally, I wish people knew that I feel like I have the flu just about everyday.  Imagine that...waking up in the morning aching intensely all over, so exhausted that you can barely put one foot in front of the other and that it gets worse throughout the day.  Now imagine waking up like that every single day and knowing that it will never get better.

Monday, July 17, 2017

Why God Hasn't Healed Me

This post contains referral links which means that if you purchase from one of my links, I will receive a small percentage of the sale.  

When I was 17, I went to an outdoor Christian music festival for 2 days with some friends.  That's when I found out that I have a heat and sun intolerance and also when it got kicked into overdrive.  I spent most of my time sleeping in the tent, and it took me several months to recover.

Why God Hasn't Healed Me

Since then, things have gotten worse.  Each one of my pregnancies intensified my heat and sun intolerance, and now it's so severe that I often joke that I'm a vampire because I stay out of the sun as much as I possibly can.  Just a few seconds in the sun or heat, and I start feeling dizzy, nauseous, weak, and like my head is going to explode.  I panic when I get into a hot car until the air conditioner is running at full blast, I will go out of my way to walk in a shaded area versus a sunny one, and I stay indoors whenever possible.

Tuesday, June 20, 2017

Ehlers Danlos Syndrome Awareness Bundle Giveaway!

This post contains referral links which means that if you purchase from one of my links, I will receive a small percentage of the sale.  

If you have Ehlers Danlos Syndrome, you know how important it is to raise awareness for the disorder. Most people you encounter have never even heard of it and many doctors don't know much about EDS or have incorrect information on it.

If you're looking for ways to help raise awareness, I have an entire post devoted to that here.

You want to hear something really awesome though?

I'm co-hosting a giveaway for an Ehlers Danlos Syndrome awareness bundle with five other awesome bloggers!!  My co-hosts are Sarah from My Stripy Life, Brittany from A Southern Celiac, Sara from A Zebra Writes, Jenni from 1visibl3Girl, and Mary from The Headache Heroine.


Enter to win an EDS awareness bundle giveaway worth over $75!

Wednesday, May 10, 2017

What It's Like To Be a Kid With Ehlers Danlos Syndrome

This post may be a little hard for you to read. I know I had tears in my eyes more than once while typing this up.

If you've been hanging around Sunshine and Spoons for very long, you know that at least 3 of my 4 kids have hypermobile Ehlers Danlos syndrome, which they inherited from me. Davy (3) and Nano (7) don't really understand it yet, but Katie (9) does. She goes back and forth between being proud of being a zebra to asking why God would make her have EDS and all of the pain that goes along with it.


Kids are supposed to be able to run and play. They shouldn't have to deal with chronic pain and fatigue. They shouldn't have to spend their childhoods at doctors' offices, wearing braces and explaining random bruises.

But, that's not how things always work. I interviewed 25 kids who have EDS to see what it's really like to be a child or young person with the disorder. 



What it's like to be a kids with Ehlers Danlos Syndrome

Averie, 10 years old (hEDS) - "The hardest part is telling other kids that I can't do certain things, like play on the monkey bars, or do everything that my classmates are doing in gym class. EDS hurts a lot.  It's frustrating that you can't do as much as your friends, and POTS is really frustrating because I just have to explain myself more when I'm getting up more slowly than others, and have to draw attention to myself."