Amyotrophic Lateral Sclerosis (ALS) with Brooke Eby
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- 게시일 2023. 07. 17.
- At the age of 29, Brooke received a devastating diagnosis. After four years of confusing symptoms in her leg, Brooke Eby was diagnosed with ALS in March 2022. She hopes to spread awareness of amyotrophic lateral sclerosis (ALS) to as many people as possible and laugh along the way. Brooke has appeared as a guest on the Today Show, interviewed by Savannah Guthrie. You can also read the essay she wrote for the Today Show.
Brooke, thank you so much for sharing your story with us. Listeners, you can follow along with her journey across all social media platforms at @LimpBroozkit (TikTok, Instagram, etc.).
Stay tuned for the next new episode of It Happened To Me! In the meantime, you can listen to our previous episodes on Apple Podcasts, Spotify, streaming on the website, or any other podcast player by searching, “It Happened To Me”.
It Happened To Me is created and hosted by Cathy Gildenhorn and Beth Glassman. DNA Today’s Kira Dineen is our executive producer and marketing lead. Amanda Andreoli is our associate producer. Ashlyn Enokian is our graphic designer.
See what else we are up to on Twitter, Instagram, Facebook, KRplus and our website, ItHappenedToMePod.com. Questions/inquiries can be sent to ItHappenedToMePod@gmail.com.
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I have genetic ALS. I relate to so much of your journey! I am 72 and i thank God for letting me live this long!
Amen Brooke this disease and als diagnosis is very hard hard to deal with I considered suicide and cried two. Follow u and yours progress😢
Brooke is a beautiful soul and she looks beautiful too. She will make a difference for this nasty disease. I will definitely be contributing to the fundraising for ALS. I will be praying for this cause. This is a great channel and I will check out your other videos. ❤️🇨🇦🙏
Brooke, you are an inspiration and so brave in the way you are dealing with this. Hopefully you remain slow progressing until they can find a cure. There is a wonderful man over here Charlie Bird that has raised over 3 million euro in one year for MND research. It just needs funding, as I'm sure their is a cure out there. That group for young woman is brilliant, and you can share your positivity with them as well as the rest of the world. You have found your purpose x
What an amazing young woman. I believe you will help many. Sending prayers to you.
You need to have a methylmalonic acid blood test. You might just have a low B12 at the tissue level, which causes symptoms that are often misdiagnosed as ALS. A normal B12 serum test is no good, you need to have the methylmalonic acid test. When this acid is elevated, it means your tissue B12 is low. This acid will eat the myelin sheaths off your nerves. It also blocks enzymes in the urea cycle that convert ammonia to urea, which causes an elevated ammonia level.
I just got the diagnose, after almost 4 years with dropfoot, and its still just my legs just like you. I live in Denmark
It killed my dad and youngest brother
If newly diagnosed with ALS and just starting to show symptoms I would think medication that will halt or reverse would be fabulous. It is heart wrenching to know it failed for patients who were in further decline. Keep working on something for them, but that one medication should pass and be given to those just diagnosed.
I am so sorry
Is there a medicine ??
@@RobdeKlerk-qg6lc I heard they were waiting on something from the FDA, I am not sure if there is or isn’t. Truth be told not enough resources are spent on finding a cure or a medication to slow the progression significantly. Right now I believe the only approved medications they have will possibly extend life approx 6 moths. 25 years ago the approved or medication in trials possibly extended life by 3 months. Not much progress in 25.
@@luzperez5251 I do not have ALS my cousin, she is 52 was recently diagnosed and she has Bulbar ALS, it is more aggressive as it starts with having problems swallowing and slurred speech, the other starts in the limbs. As I said in my initial comment, this disease is heartbreaking and little to no hope for those diagnosed, it’s terminal.
She is so pretty ❤😢
So if she was ugly you wouldn't care basically
Brook you're a inspiration a quick question for you. Have you thought of stem cell to help or is that something possible. Just a nugget to ask you in my prayers ❤❤❤❤
There is no evidence that stem cell treatments do anything for MND. There are clinics who offer it and make all kinds of claims, but they are nothing but money-grabbing scammers.
I have heard about people developing ig after lyme disease . I have had lyme and lots of strange neurogical symptoms so did a bjt of googling . Not saying that it is the case here. Of course not, but it is worth considering.
The 25 year old one put me in the hospital with sky rocketing blood pressure. I'm doing fine with the next one. Number newest is digusting!!! Tastes like grapefruit rinds ground up in a drink. Plus diarrhea after consumption...no way to live.
Prayers go out to you. Stay in the moment, and talk to Jesus, every day. He will become your best friend.
If your god is real , they're responsible for this
If god exists, why do good people get struck down with illnesses like this? But the worst type of people live a long healthy life?
There is no GOD...trust me. I used to believe there was but it's all nonsense. It was something that was created to keep people on the straight and narrow. And probably to help people with the fear of dying.
God is an imaginary friend for grown-ups. Snap out of it, just like all of the thousands of other gods man has invented, the god of the bible does not exist.
ALS its like expiration date on human beeing. Its a gift, not so many ppl knows when they are suppose to die.
Tell that to Als victims.
A gift? That's one gift I wouldn't want😢
Sure. Nothing like a gift that destroys you day by day and makes life horrifying to try to live through to the end. If you think it is a gift, I wish you the luck of having it bestowed upon you.