So on June 26
this happened:
And now I'm thinking that I definitely don't have FND, functional neurological disorder for those of you who haven't seen my last post. Basically FND is caused by stress and your symptoms get worse when you're more stressed. I was extra stressed on the day that I started being able to walk again and I've been able to walk ever since. I definitely overdid it on the day I started being able to walk again, but I don't regret it. My legs were so sore the day after that. I've been walking just a little bit each day and using my wheelchair the rest of the time so my leg muscles can get built up slowly.
As far as what I have that makes my legs stop working sometimes? I don't know for sure but it seems like gluten ataxia could be the culprit. I thought that I just discovered gluten ataxia on June 26 of this year but a look back at my Facebook page showed me that I learned about it last year and then I completely forgot, because brain fog. As far as brain fog is concerned that lifted too when I started being able to walk again. If you've seen those Claritin clear commercials it's kind of like that. The world was just in a fog all of the days that I couldn't walk and then on the worst brain fog days it was more like being underwater. So now I am relearning how to walk and trying to get my stomach nonsense figured out. I have a gastric emptying test on Friday and have been eating mostly only liquid foods for a month because solid foods haven't been digesting.
Sunday, July 9, 2017
I Don't Have FND?
From the brain of
Jessica
when the clock struck
5:58 PM
0
of you tumbled down the rabbit hole
categorized as:
health update
Sunday, May 14, 2017
Processing my New Diagnosis
I have a diagnosis: Functional neurological disorder
"Functional neurological disorder (FND) is a condition in which patients experience neurological symptoms such as weakness, movement disorders, sensory symptoms and blackouts. The brain of a patient with Functional Neurological Disorder is structurally normal, but functions incorrectly." - Wikipedia
Basically what's happening, as the neurologist explained it, is my brain stopped sending messages to my legs for some reason. She said it's like if your computer freezes and you have to reboot it. I will be going through a process of both cognitive behavioral therapy and physical therapy to identify stress triggers and learn how to respond to them and also to learn how to trick my legs into doing what I want them to. It may take a very very long time but it is possible for me to get better. I am definitely willing to put in the work required.
I've had this for at least 6 years so it will take a long time to get better, maybe even years. And it's weird to me because I should be happy that I can get better, and I am, but at the same time I had accepted the fact that I may never get better and I even believed that I would never get better but I was okay with that. And I was used to it. I connected with other people like me who have illnesses that there is no cure for. And we supported each other and helped each other through the tough times. And I still have a chronic illness but I kind of feel guilty because I can get better but so many of my friends can't. It's almost like I don't know who I am anymore again. I have gotten used to being sick all of the time and as weird as it sounds a future where I'm healthy seems a little bit scary. I guess that's my anxiety and my difficulty responding to change. I think that what scares me more is that if I don't get healthy then it's kind of my fault. I'm honestly still processing everything and there are a lot of emotions involved and I don't understand all of them.
I am very grateful for all of the people who support me no matter what happens, for the community of chronically ill people who include me despite the specifics of my illness. One of my first feelings was that I don't know where I fit in anymore but they assured me that I fit in there no matter what happens. My immediate future holds a lot of pain, ups and downs, but also hope. And all of the people who are happy with me during my ups and encourage me during my downs will help me get through this.
"Functional neurological disorder (FND) is a condition in which patients experience neurological symptoms such as weakness, movement disorders, sensory symptoms and blackouts. The brain of a patient with Functional Neurological Disorder is structurally normal, but functions incorrectly." - Wikipedia
Basically what's happening, as the neurologist explained it, is my brain stopped sending messages to my legs for some reason. She said it's like if your computer freezes and you have to reboot it. I will be going through a process of both cognitive behavioral therapy and physical therapy to identify stress triggers and learn how to respond to them and also to learn how to trick my legs into doing what I want them to. It may take a very very long time but it is possible for me to get better. I am definitely willing to put in the work required.
I've had this for at least 6 years so it will take a long time to get better, maybe even years. And it's weird to me because I should be happy that I can get better, and I am, but at the same time I had accepted the fact that I may never get better and I even believed that I would never get better but I was okay with that. And I was used to it. I connected with other people like me who have illnesses that there is no cure for. And we supported each other and helped each other through the tough times. And I still have a chronic illness but I kind of feel guilty because I can get better but so many of my friends can't. It's almost like I don't know who I am anymore again. I have gotten used to being sick all of the time and as weird as it sounds a future where I'm healthy seems a little bit scary. I guess that's my anxiety and my difficulty responding to change. I think that what scares me more is that if I don't get healthy then it's kind of my fault. I'm honestly still processing everything and there are a lot of emotions involved and I don't understand all of them.
I am very grateful for all of the people who support me no matter what happens, for the community of chronically ill people who include me despite the specifics of my illness. One of my first feelings was that I don't know where I fit in anymore but they assured me that I fit in there no matter what happens. My immediate future holds a lot of pain, ups and downs, but also hope. And all of the people who are happy with me during my ups and encourage me during my downs will help me get through this.
From the brain of
Jessica
when the clock struck
3:04 PM
0
of you tumbled down the rabbit hole
categorized as:
chronic illness,
diagnosis
Monday, March 6, 2017
Easy Ways to Practice Self Care
If you've been on the internet and have a chronic illness or mental health difficulties (or even if you don't) you've probably seen people talk about self care. There are all these lists of things you can do to take care of yourself and help yourself fell better over time. And they're good suggestions and they do work, but here's the big issue: you have to be motivated enough to do the things. When you have a chronic illness and you're having a low energy day or when you have mental health issues and you're lacking motivation it's really hard to actually do those things on the lists. Real life example: yesterday my depression was pretty bad and my anxiety was really bad. In my head I knew that self care would help me but I also lacked the motivation to do any of those things, such as make myself a cup of tea, do a face mask, turn on my favorite music, so I didn't do any of it. The other huge problem is that when you're really depressed you might feel like you don't actually deserve to feel better so you just won't do anything that might help you feel better. For these situations I have come up with a sort of self care cheat sheet. This is a list of the easiest possible things I could think of that can help you feel just a little bit better. It's great for low-energy days or days where you're lacking motivation. I am personally going to try to do at least one of these things every day. Some days you might be able to do every single one since they're things that don't require a lot of energy or motivation, and none of them cost any money! So here it is, my list of small ways to feel a little bit better every day:
Drink water, go outside if even for just a minute (if you can't bring yourself to go outside, look out a window at outside for even just a minute), do something nice for someone else (even if it's just sharing someone's post online with your friends), take deep breaths when it gets difficult, rest when you need to. If you didn't do so well today try again tomorrow. Remember you're not alone.
Read more mental health blog posts like this one at my new blog: https://www.honeybeealley.com/blog
Drink water, go outside if even for just a minute (if you can't bring yourself to go outside, look out a window at outside for even just a minute), do something nice for someone else (even if it's just sharing someone's post online with your friends), take deep breaths when it gets difficult, rest when you need to. If you didn't do so well today try again tomorrow. Remember you're not alone.
Read more mental health blog posts like this one at my new blog: https://www.honeybeealley.com/blog
From the brain of
Jessica
when the clock struck
2:37 PM
0
of you tumbled down the rabbit hole
categorized as:
anxiety,
chronic illness,
depression,
mental health,
self care
Wednesday, February 15, 2017
Life Lately #1
I'll be posting these every so often as a sort of check-in post to share what I've been up to lately. These photos are mostly from my Instagram.
We moved in October and I love our new apartment so much. The natural light makes taking product photos super easy, and I love how there is actually a space for all of our stuff. We have so many cupboards and closets! And the bathtub has made my life about 1000% better every day that I have super sore muscles. I need to get more bath bombs though because I have used up just about all of the ones I had.
| sketches of my crystals |
| new fashion: damask Nightmare Before Christmas long sleeve shirt that is so soft, and wheelchair gloves |
| my "office", love these big windows |
| bookshelf! still waiting to find the perfect bookends |
| one of my woven projects; originally made this for a friend but I tied it too tight at the ends, after taking this photo, and it squished the feather so I kept it instead |
| new products in my Etsy shop: spiral end hair pins and bracelet helpers |
| organized my stones and re-discovered some real beauties from before I knew stone names, including some on my wishlist: ocean jasper and crazy lace agate |
We moved in October and I love our new apartment so much. The natural light makes taking product photos super easy, and I love how there is actually a space for all of our stuff. We have so many cupboards and closets! And the bathtub has made my life about 1000% better every day that I have super sore muscles. I need to get more bath bombs though because I have used up just about all of the ones I had.
From the brain of
Jessica
when the clock struck
9:32 PM
0
of you tumbled down the rabbit hole
categorized as:
life,
new apartment,
photos
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