Showing posts with label ehlers danlos syndrome. Show all posts
Showing posts with label ehlers danlos syndrome. Show all posts

Monday, August 30, 2021

A New Diagnosis for Davy


Thursday, April 29, 2021

Davy had an appointment with his geneticist that day to find out the results of his Whole Exome Sequencing or WES. It had been a few years since we'd done any genetic testing for Davy, and I was fully expecting the results to be the same as the other tests we'd done with nothing significant found. 

Several years earlier, our geneticist had told me that despite diagnosing Davy with hypermobile Ehlers Danlos Syndrome, she felt that he had another genetic syndrome as well and wanted to keep looking. EDS explained a lot of his issues, but there were still some things that didn't quite fit in that box. Multiple genetic tests had always come back negative so we had taken to writing things off as "that's just Davy!"


Once we were back in the exam room, I tried to keep a very impatient Davy calm and occupied while Hubby and I waited for the geneticist. 

When she entered the room, she had a stack of papers in her hand and a triumphant smile on her face. 

"We have answers!" 


I just about fell off my chair. I had been expecting her to tell us the test was negative, just like we'd been told so many times before over the last seven years

She started asking us questions that she already knew the answers to, having followed Davy since he was a year old: 
Did he have feeding issues? He had to have a feeding tube as an infant to keep him from starving to death.
Was his hair thick and curly? For sure. If we didn't keep it short, it was uncontrollable.
Did he have speech issues? He had a diagnosis of apraxia and struggled to speak and be understood. 
Did he have hypotonia? Yes, definitely.

As the questions continued, I was stunned at how well they fit Davy. It turned out that he had tested positive for a mutation on the CDK13 gene or CDK13 related disorder. It was newly discovered in 2017 and medical literature noted that only 44 individuals worldwide had been found to have it. Our geneticist had never even heard of it before Davy was diagnosed. 


When the geneticist was done talking to us, the genetic counselor sat down to help us navigate our new reality. He recommended joining a CDK13 support group on Facebook that he had stumbled on in his search for some information to share with us. Davy had two more appointments that day and before we had left the clinic, I had already found the group and requested to join. When the administrator contacted me to verify Davy's diagnosis before admitting me into the group, she mentioned that she had been able to easily pick Davy out of my profile picture, which had all four of my kids in it, based on his facial features which are unique to people with CDK13.

Once I joined the group, I found that CDK13, while very rare, isn't quite as rare as what our geneticist thought. We were the 170th family in the world to join the group because of their child's diagnosis and the group continues to grow. After seven years of not having answers to Davy's unique issues, being able to talk to other families and getting to "meet" their awesome CDK13 kiddos (many of whom look like siblings to Davy!) has been so amazing. 
We don't know exactly what Davy's future holds, but we do know that he doesn't have any of the potentially life-threatening issues that people with CDK13 sometimes have such as a heart defect or seizures. He does have quite a few of the other symptoms of it such as unique facial features, thick curly hair, speech issues, developmental delays, hypotonia, feeding issues, autism, gastrointestinal issues, reflux, and more. Some kids with CDK13 tend to be very cuddly and loving and Davy definitely has that trait which is one of the things I love about him. I wouldn't change him for the world. No matter what struggles he faces in life, he is exactly how God designed him and we will support him to always do his best. Davy is an amazing blessing and he is who he is because of his CDK13, not in spite of it. 

This shirt is available at the Sunshine and Spoons Shop

September 2nd is CDK13 Awareness Day. I'd love for you to help spread awareness so hopefully other families can find the answers and support they need. 

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September 2nd is CDK-13 Awareness Day! If you've never heard of it, learn more here: https://bit.ly/3zH4j8U
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I would appreciate it so much if you would share this post! You can also add a frame to your Facebook profile picture by searching for "CDK13" in the frames.






Tuesday, June 1, 2021

Essential Tools for Moms with Brain Fog

 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 have a chronic illness, you probably experience brain fog at least some of the time. 

Confession: I wrote that first sentence and then stared at it blankly for 20 minutes. Brain fog, anyone?

Anyway...like I was saying, brain fog is real and it can make life pretty difficult sometimes. Add in a few kids (hello mom brain!) and it gets really interesting. The struggle is real.

Essential Tools for Moms with Brain Fog

I use a lot of tools to help me manage my brain fog. My smartphone is the biggest one and what I refer to as my "external brain." I also work hard to stay organized with my home and schedule, stick to routines so I don't miss anything, and break down big tasks into smaller, more manageable ones.  

I'm going to share some tips, tricks, and tools for brain fog with you in the hopes that they'll help you as well. 


I used to carry a paper planner with me at all times to keep track of my calendar, but I needed to lighten up my purse to cut down on shoulder strain so I reluctantly made the switch to using a Google calendar. It turns out that I love it! I especially love that I can sync it with my husband and share it with my sister.
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This one's a little less high-tech, but still very useful. I use them to leave reminders for myself around the house, notes for my kids, and I even write Bible verses on them so I can see them throughout my day. You can even get sticky notes pre-printed with Bible verses here
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Phone alarm clock
Thanks to distance learning with four kids who all have virtual classes, I currently have 17 alarms set to go off of my phone throughout the school day. Thankfully, that's not the norm for me, but I do use my phone alarm on a regular basis to help me remember things such as appointments, picking kids up from activities, and just about anything else.
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If you're like me, you're constantly looking for your phone, your keys, your purse, your mind, etc. Tile can't help you when you're losing your mind, but it's great for the other stuff! 
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I don't write by hand as much anymore because it hurts my fingers and hands, but I'm still pretty obsessed with notebooks and always have at least one going at all times. I use it for my devotions, to write lists and reminders down, to plan things, etc. When I discovered smart notebooks, it blew my mind! Write in the notebook with a Pilot FriXion erasable pen, scan it and upload to your favorite cloud service, erase, and start again. I love that what I write can become digital so I can save and easily find it again. Plus, it's endlessly reusable!
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Flaredown App
This app helps you track your symptoms and is available for Androids and iPhones. This can make a huge difference in managing your health and being able to show your doctors exactly what's going on with you. 
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Medisafe App
Do you ever forget to take your medicine or is that just me? If that's something you struggle with too, this app can help remind you to take your medication and can even be synced with others so someone else can check in on you or so you can make sure your child or other loved one is taking their medicine. Oh, and did I mention that it's free??
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I've used this app for about 10 years now and LOVE it. It helps me keep my house from reaching disaster levels by giving me a list of simple chores to do each day. They can be customized and even assigned to others in your house. 
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I haven't personally used this app, but I've heard rave reviews about it from lots of other moms so I thought I better include it in the list. Cozi is a family organizer that keeps your whole family on track and in communication with each other. 
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If you prefer to go old school, this book covers a lot of ground and can make tracking your symptoms and other aspects of your care easy to do and share.
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Need some tips for how to clean your house while minimizing your pain and fatigue? This book covers it all and is a must-read.
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This last one isn't really a tool, but it's a blog post about getting organized from Chronic Illness Warrior Life that I found to be very helpful. Check it out! 

What tools do you use to cope with brain fog?







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.