Darin, Godspeed to you brother. My wife was diagnosed with als December 2023. Took over a year and half to get diagnosed and it all started with voice loss, respiratory failure in September 2023. She’s currently on 24hr oxygen through a trachea. We are a young couple both turned 42 this year. I have become her primary caregiver. We have a lot of family help and supports. And like you said you find out real quick who your true friends are and what family really means. I will follow you in your journey and will keep you updated on ours. You and your family will also remain in my prayers. I have found some joy in you and your vlog. I will continue to go and find some joy in such a difficult time. I admire your courage.
My mom had ALS and I had to buy her a wheelchair on eBay. The insurance company didn't think a wheelchair (just a basic one that I could push her in...not a fancy electric wheelchair) was worth the expense when you consider that the average lifespan after diagnosis is only about two years (or at least it was at that time).
It would be so hard to go through ALS, and I’m so sorry you are going through it! It’s wonderful that your students were given an opportunity to support you with hugs! What a beautiful thing for you and for them!
Go find some joy! Thank you for sharing! I was diagnosed 4 months ago with ALS. In a wheelchair full time. Sounds like you are an amazing teacher. 🙏 that you will be able to continue teaching
Go find some joy! Another teacher Greg who calls his channel Gregisms always ends his videos with “find your joy”. It has become a mantra for me! I will now add yours as my mantra too! I am learning from you so I can support my Bestie whose husband has been recently diagnosed! I can’t help them because of my own health issues but I can give emotional support! God Bless on this journey! Thanks for being the inspiration that you are!🌈🙏🏻👼🙏🏻😇🙏🏻🌈☀️🌷☀️
You’re not alone my PALS (people with ALS). I’m 40 3 years since symptom on set. I can no longer walk or sit up right for long. My tongue feels a little swollen all the time & my respiratory function levels went from 115% 9 months ago to 80% last checked. I’ve also been diagnosed with a piggyback neuromuscular disorder, called clonic spastic seizures. I’ve such severe fasciculations and spasticity that I’m on a lot of medication just to keep my body under a manageable level. When the ALS hit my body, my neuromuscular system decided to go into a shock trauma, so that is why I have the second disease to deal with. There’s not many of us out there that have this, but unfortunately, it’s speeding up my progression. I try to find the happiness and peacefulness in every day and love my family and friends just so much stronger than I used to. Just remember to take it one day at a time 🩵💙
I’m so sorry to read this. None of the online TH-cam educators shared this. Online teaching could be a work option since it’s working from home. Prayers sent to you and your family. #GoFindSomeJoy
Just came across your videos and I love your spirit. ALS will never take your sparkle and glowing spirit. Keep finding your joy and I wish you peace and restorative rest on your journey. New subbie and I'd love to snag one of those bracelets 😊 sending love and light your way friend ❤❤❤
You are amazing my friend! Even in this trying season your optimism and determination to find joy shines through. I hope you continue to get all the rest you need, but check your schedule to see if you have a hour our two one your old friend. 😉
I was told I have CSM by a neurosurgeon after seeing my MRI imaging. I saw two different neurosurgeons and neither one said anything about having my PC refer me to a neurologist. I finally took it upon myself to get a referral. She wanted to do an EMG with nerve conduction to rule out MND. I decided I just didn't want to be told I have ALS . I'm going to stick with the diagnosis of CSM .I probably should get another testing appointment. I pray you have a slow progression and have many more years with your beautiful family 🙏
Thank you for sharing; love your attitude! I was also diagnosed around 7 months ago--bulbar onset, which means I'm still strong below the neck but my speech is complete trash and I choke all the time. It's criminal that you're being denied coverage for the prescriptions, but to be honest, you're not missing much with those two drugs. At best (and it's a stretch at that), they buy us an extra several weeks before needing a trach. Not worth the $100K+ per year.
My heart goes out to you. My Grandfather passed away from ALS. Enough said. I live in MN. Once of our State Legislators, David Tomossoni, was diagnosed. He had a larger than life persona. MN, in his honor, passed a bill that gave a large sum to research, caregiving, etc., for ALS. I wonder if it's possible for you to receive some counsel through the Mayo Health Clinic. I just wonder. It's tough to hear that your insurance has denied you for the meds. In America, how could this happen? Keep speaking up, keep advocating and getting rest! Thanks for being you!
Like ALS, lupus affects everyone differently. Only a couple medications and it never goes away. It not terminal but it can kill you and I’ve had a few close calls in my 23 yrs dealing with this. Keep strong!
Go find some joy! You remind me of Brooke Eby who also documents her ALS journey here In youtube - not waiting inevitable but living each day fully not forgetting laugter and humour. I salute you both❤!
I have Long Covid and feel like I’m in a similar situation. Im a sped teacher. I have chronic muscle pain, fatigue, and frequent crashes. Since it’s so new, they don’t know how to help us. It’s frustrating.
My Mom was diagnosed with Bulgar ALS after being mis diagnosed with a stroke. She lasted 2 years and unfortunately it is the most horrible disease ever.It was blessing when she passed. Would not wish this on my worst enemy. God bless and good luck
i was diagnosed one month ago. it is hurtful when i see " it was a blessing when she passed". how is this helpful? should we all just go off ourselves now? spare others our illness?how is this different than those with terminal cancers ? seriously. please think
Yep, please consider that lots of people with ALS will read this, myself included. This is a video of someone going through the same journey your mum did - would you have wanted her to read this?
My dad had Parkinsons and his insurance refused him the most important meds he needed. However, we prayed and the dr was able to fight for him and change their minds. He was able to get it eventually. It’s horrible that insurance has the ability to do that.
I have been watching you since you taught 4th grade. I also taught 4th at the time. Had a friend that passed from ALS in Baltimore. There is a foundation called Brigance Brigade that helped her, and we walk and raise money for research. Reach out and see if they can help. God bless...
Go find some joy in that wheelchair...it looks nice! My mom had ALS and her insurance wouldn't cover anything either. I had to buy her a very basic wheelchair on ebay 🤦♀️😡. It's been many years but I'm still bitter. I should probably release that negativity and go find some joy 😊.
![[LIVE] : ONE ลุมพินี 85 | คู่เอก "ยอดเหล็กเพชร vs ผึ้งหลวง"](http://i.ytimg.com/vi/Qq_19bnnxEo/mqdefault.jpg)
Darin, Godspeed to you brother. My wife was diagnosed with als December 2023. Took over a year and half to get diagnosed and it all started with voice loss, respiratory failure in September 2023. She’s currently on 24hr oxygen through a trachea. We are a young couple both turned 42 this year. I have become her primary caregiver. We have a lot of family help and supports. And like you said you find out real quick who your true friends are and what family really means. I will follow you in your journey and will keep you updated on ours. You and your family will also remain in my prayers. I have found some joy in you and your vlog. I will continue to go and find some joy in such a difficult time. I admire your courage.
This is heartbreaking, I am so sorry.
@@ngs5554hi Nancy I appreciate your message
have you done a genetic test
I was so taken back with your students crying - speaks volumes of who you are. Teachers like you, are a rarity, thank you - Go find some joy!!
No insurance company should be allowed to deny anyone with ALS anything. Period! I am outraged for you.
My mom had ALS and I had to buy her a wheelchair on eBay. The insurance company didn't think a wheelchair (just a basic one that I could push her in...not a fancy electric wheelchair) was worth the expense when you consider that the average lifespan after diagnosis is only about two years (or at least it was at that time).
I agree 100% !!!
They do this with other illnesses too. It is sickening that patients have to navigate and fight insurance as well as their diseases
It is criminal … and disgusting.
It would be so hard to go through ALS, and I’m so sorry you are going through it!
It’s wonderful that your students were given an opportunity to support you with hugs! What a beautiful thing for you and for them!
Go find some joy! Thank you for sharing! I was diagnosed 4 months ago with ALS. In a wheelchair full time. Sounds like you are an amazing teacher. 🙏 that you will be able to continue teaching
Go find some joy! Another teacher Greg who calls his channel Gregisms always ends his videos with “find your joy”. It has become a mantra for me! I will now add yours as my mantra too! I am learning from you so I can support my Bestie whose husband has been recently diagnosed! I can’t help them because of my own health issues but I can give emotional support! God Bless on this journey! Thanks for being the inspiration that you are!🌈🙏🏻👼🙏🏻😇🙏🏻🌈☀️🌷☀️
You’re not alone my PALS (people with ALS). I’m 40 3 years since symptom on set.
I can no longer walk or sit up right for long. My tongue feels a little swollen all the time & my respiratory function levels went from 115% 9 months ago to 80% last checked.
I’ve also been diagnosed with a piggyback neuromuscular disorder, called clonic spastic seizures. I’ve such severe fasciculations and spasticity that I’m on a lot of medication just to keep my body under a manageable level.
When the ALS hit my body, my neuromuscular system decided to go into a shock trauma, so that is why I have the second disease to deal with. There’s not many of us out there that have this, but unfortunately, it’s speeding up my progression.
I try to find the happiness and peacefulness in every day and love my family and friends just so much stronger than I used to. Just remember to take it one day at a time 🩵💙
You are incredibly strong. ❤
Prayers
I’m so sorry to read this. None of the online TH-cam educators shared this.
Online teaching could be a work option since it’s working from home.
Prayers sent to you and your family. #GoFindSomeJoy
Just came across your videos and I love your spirit. ALS will never take your sparkle and glowing spirit. Keep finding your joy and I wish you peace and restorative rest on your journey. New subbie and I'd love to snag one of those bracelets 😊 sending love and light your way friend ❤❤❤
Praying for you! 🙏🏾🙏🏾🙏🏾🙏🏾 Pray to GOD for healing! Miracles happen everyday.❤
Go find some joy! Thank you for sharing your journey with us and bringing us so much joy! 🙏💫💖
You are amazing my friend! Even in this trying season your optimism and determination to find joy shines through. I hope you continue to get all the rest you need, but check your schedule to see if you have a hour our two one your old friend. 😉
Go find some joy! You inspire me! Been listening to you several years. So glad I found this!💗
I was told I have CSM by a neurosurgeon after seeing my MRI imaging. I saw two different neurosurgeons and neither one said anything about having my PC refer me to a neurologist. I finally took it upon myself to get a referral. She wanted to do an EMG with nerve conduction to rule out MND. I decided I just didn't want to be told I have ALS . I'm going to stick with the diagnosis of CSM .I probably should get another testing appointment. I pray you have a slow progression and have many more years with your beautiful family 🙏
Go find some joy! You are truly an inspiration to all!
Go find some joy. I always loved your big heart and positive teacher community you’ve created here. ❤❤❤
Go find some joy!! You are an inspiration. God bless you
Go find some JOY!❤
Go find some joy ❤😊 I’m sending you so much love always xxx
Go find some joy!!!🙏🏻🙏🏻🙏🏻
Your daughter is lovely. You and Mrs. N had a great time I’m sure. Just subscribed. Life really sucks sometimes - i will be praying for you. ❤️🇨🇦🙏
Keeping you in my thoughts while you keep adjusting to this life and stay stable as long as a possible
Go find some joy! Thank you for inspiring me and so many. 🌺❤️ Sending love, peace, courage.
Go find some joy!!! ❤
Go find some joy! You're truly an inspiration.
Thanks for putting the word out about this disease. You are brave, respect 👊🏼
Go find some joy. Bless you ❤
Go find some joy Mr. N. As a fellow teacher, you are an inspiration to me.
Got your bracelets yesterday Darin! I’m gonna go find some joy too!! Keeping you and your family in my thoughts!! ❤
Go find some joy!!
Go find some joy!
Go find some joy! ❤
I am going to find some joy. ❤
Find Joy 💜❤️🇨🇦🙏
Prayers for Us 🙏 all
GO FIND SOME JOY!!!!
Thank you for sharing; love your attitude! I was also diagnosed around 7 months ago--bulbar onset, which means I'm still strong below the neck but my speech is complete trash and I choke all the time.
It's criminal that you're being denied coverage for the prescriptions, but to be honest, you're not missing much with those two drugs. At best (and it's a stretch at that), they buy us an extra several weeks before needing a trach. Not worth the $100K+ per year.
Go find some JOY!!
Go find some joy❤
~Go Find Some Joy!~
Go find some joy! Thank you for sending the bracelets! ❤
My heart goes out to you. My Grandfather passed away from ALS. Enough said. I live in MN. Once of our State Legislators, David Tomossoni, was diagnosed. He had a larger than life persona. MN, in his honor, passed a bill that gave a large sum to research, caregiving, etc., for ALS. I wonder if it's possible for you to receive some counsel through the Mayo Health Clinic. I just wonder. It's tough to hear that your insurance has denied you for the meds. In America, how could this happen? Keep speaking up, keep advocating and getting rest! Thanks for being you!
Go find some joy🌞! I am a teacher too ! Enjoy the summer to rest !
Like ALS, lupus affects everyone differently. Only a couple medications and it never goes away. It not terminal but it can kill you and I’ve had a few close calls in my 23 yrs dealing with this. Keep strong!
Go find some joy! Lifting you up in prayer! 🙏✨
Go find some joy! 🙏🏼 🤗 😊
Go Find Some Joy❤
*There is joy to be found everywhere if we look and know He is with us.
Go find some joy!! ❤
Go find some joy🥰
Go find some joy!! 🎉
the medications don't do much to extend your life and sometimes make people worse
Go find some joy!!!!
🌟Go find some joy!🌟.....🙏🙏🙏
Go find some joy! You remind me of Brooke Eby who also documents her ALS journey here In youtube - not waiting inevitable but living each day fully not forgetting laugter and humour. I salute you both❤!
Oh thank you!
Praying for you. #GoFindSomeJoy 9:59
Go Find Some Joy! Love this so much
GO FIND SOME JOY!
I have Long Covid and feel like I’m in a similar situation. Im a sped teacher. I have chronic muscle pain, fatigue, and frequent crashes. Since it’s so new, they don’t know how to help us. It’s frustrating.
My Mom was diagnosed with Bulgar ALS after being mis diagnosed with a stroke. She lasted 2 years and unfortunately it is the most horrible disease ever.It was blessing when she passed. Would not wish this on my worst enemy. God bless and good luck
i was diagnosed one month ago. it is hurtful when i see " it was a blessing when she passed". how is this helpful? should we all just go off ourselves now? spare others our illness?how is this different than those with terminal cancers ? seriously. please think
Not helpful, at all.
Yep, please consider that lots of people with ALS will read this, myself included. This is a video of someone going through the same journey your mum did - would you have wanted her to read this?
How are you now @@leaveittolefty
@@Tayyab-hr1gp i am doing ok. i have appt with dr tomorrow see how it’s going
The insurance thing infuriates me! I am so sorry you are going through this 😢
You should not be denied the medicine you need. Can the school system fight for you to get the medicine you need? Unbelievable.
Go Find Some Joy!!!
Go find some joy. 😊
Go Find Some Joy 🙏🏻❤️
Definitely reach out to Team Gleason for assistance!
My dad had Parkinsons and his insurance refused him the most important meds he needed. However, we prayed and the dr was able to fight for him and change their minds. He was able to get it eventually. It’s horrible that insurance has the ability to do that.
How can i get. Bracelet ? Would love to have one
Go find some joy
Go Find Some JOY!!!!
Go Find Some Joy!
🙏🏻🙏🏻
Go Find Some Joy❤
You need to counter the insurance denial for Radicava ORS. It’s part of the red tape
Go find some joy :)
❤
Would starting a Gofundme help with meds and wheelchairs etc?
Go find some joy.
When you suffer in ALS?
The only medicine They gave my mom is Neudexta . There’s no real treatment. 😢
Go find some joyx
Go find some joy -
I have been watching you since you taught 4th grade. I also taught 4th at the time. Had a friend that passed from ALS in Baltimore. There is a foundation called Brigance Brigade that helped her, and we walk and raise money for research. Reach out and see if they can help. God bless...
Go find some joy in that wheelchair...it looks nice! My mom had ALS and her insurance wouldn't cover anything either. I had to buy her a very basic wheelchair on ebay 🤦♀️😡. It's been many years but I'm still bitter. I should probably release that negativity and go find some joy 😊.
Please name your insurance company. They need to have a light shone on them.
Voice bank asap
Get rid of all carbs
(Please Research this)
CARNIVORE DIET
Bulbar Als
Try the carnivore diet.
And don't take anymore vaccine.
Sue someone please. It is from the crapcines
Damn brother 😞😞😞
Go find some joy 🥹 ❤
Go Find Some Joy (GFSJ)!!❤
Go find some joy! 💚💙🧡
Go find some joy!
Go find some joy!!
Go find some joy! ❤
Go find some joy❤
GO FIND SOME JOY!!!!
Go Find Some Joy!
Go find some joy
Go find some joy!!! ❤