I’m Madison Perea, an AVM Survivor since May 17, 2014. I Want to share my story and my struggles in life emotionally and physically. #avm #avmsurvivor #stroke #mystory #disabled
Hi Madison. My son Matthew is 36 and he had a ruptured AVM too this morning. He is in ICU and they aren’t very hopeful. I have hope but I need to be patient and thank you for sharing this because he needs time to heal. I hope he wakes up like you did. He is so loved and too young. Keep kicking butt. God bless you. Sara
i had an avm rupture in 2016 and i've developed really severe ptsd from the whole experience. thank you for sharing your story, i've felt so alone in this and it's nice to see someone else who can relate to my struggles. when you said when you woke up you couldn't talk and all you could do was cry...ouch, i relate so hard. you are a warrior.
Hi sasha belcher ! If you don’t mind me asking, how are you doing today? I can already tell that you are strong because YOU made yourself strong enough to get out of the wheelchair!
Saw your story before and found you here! So thankful to see how much progress you have made! I really think you’ll be a cheerleader again someday, keep making video ❤️
I had an AVM when I was 11 on my left side, you have great movement in your arm, that is so awesome. I used one of those leg braces for years. you are doing so great!!!
Hey just know you're not alone! i had problems with my large pelvic AVM since birth, started bleeding internally and didnt get help until i was 18. left my senior year early for surgery and have never been the same. still have trouble with any sort of bowel function, and im going back for new growths and symptoms as of today. keep in touch! lots of support groups on Facebook and such!
Mine ruptured when I was working out with marine recruiters. I don’t remember getting a headache or loosing feeling I just remember getting really dizzy and I guess I passed out. I was rushed to the hospital and they performed emergency surgery. Strokes caused me to lose my left peripheral (hopefully temporary, that’s what I’m told anyways) While I was in the hospital doing pt ot and st every time I stood up I’d get dizzy and that’s gone (thankfully) so I can stand up and not get really dizzy. But I also stayed in the hospital for two-ish months. I was lucky enough to only have problems with my peripheral not my speech or any limbs. God was watching out for people like you and me on those days.
@@lrmcdaleno3301 I am still kicking. It seems I'm too old for anything to be done. I still feel fine and my avm is stable. I turned 59 in December. Yay
@@jamesrandall1915❤️ 59 wow ! Happy to hear your still kicking 😎💪🏼Thank you for answer .. asking because I had this mri and mra and happens that they found avm ,I had this angiogram done last week and next appointment is on feb 23th .. to see exactly what kind of avm I have .. I’m 36 btw and little scared too 💔
I'll say a little prayer for ya. You're young, they can help yoy. 😁 keep me posted. Thank you for the response. You are the first person to actually "talk to me. Be brave. It'll be alright. Later, J.R.
This is really for everyone out there that wants to talk with others that are dealing with an AVM. There is a website called www.avmsurvivors.org you can go there and read other story’s of people like us that have had an AVM or are now dealing with one. It’s a good group to chat with or see others that have gone or are dealing with a AVM.
Hello Madi. I hope you are doing well today? My name is Eddie Price and I am from Wayne County, North Carolina with a 28578 zip code. Would you believe that I had an AVM with a Subarachnoid Hemorrhage in the Occipital ( in the Left Posterior (Back of the Head ). This was back in the year of 1978. December 19, 1978 I was 20 years old that year. I went through 8 hours of Surgery on that day. My Neurosurgeon told me and my family that I was a miracle. Plus if I continue to improve that I would be a miracle for sure. Guess what I have been one ever since. Now that was a gift from God. I hope and pray for you the same and even more. Please listen to me you can do anything you want to. Just know your limitations. Please just know your limitations. That's all.
You are an inspiration Madison. How long did it take you to talk? My brother had a ruptured AVM and has an aphasia. He has a problem expressing himself and can talk only few words and not sentences.
Hi Madison, i gotta ask, are you hemiplegic after the rupture? If you are, have you regained your movements back especially on your fingers and wrists? I had a rupture in 2016 and im still struggling to move my fingers and wrists on my effected side
Had my brain AVM rupture back in 2000. Had just reached the age of 10 when the bleed happened. Was taken to the hospital flatlined for a bit had emergency surgery to stop the bleed and then was air lifted to children’s hospital in St.Louis. Had to wait for the swelling to go down until they could do my surgeries. Ended up having 4. The reason why is because of the rupture. My doctors said it was like a bomb went off in my brain and there were 4 spots in different locations from my bleed.
Wow Yoehon John ! I can’t believe 10 years old. You are strong! Especially to flatline then come back. I was only in a-comma for 2 weeks. They told my dad that I wasn’t to survive the first night. But look at us now, stronger than ever!
Was also in a-comma for 2 weeks. Woke up blind and paralyzed on my right side. Was able to see after 2 weeks once the swelling had gone down. Had a lot of therapy done even after my surgeries. On in to high school did sports. Track and golf. One funny thing about in track. My friends would joke about how they could tell I was behind them when running. My right foot runs flat. I don’t really have as much control with it because of the brain damage. But at least my left is normal.
We are caregivers of our granddaughter. She had her AVM rupture with subsequent bleeding at age 9 in December 2000. She is now 33 years old and lives in her own apartment. She does have supports because of the common consequences from brain injury, especially to the frontal cortex and limbic system. It is important for caregivers to learn as much as possible so they can advocate and communicate if the survivor has difficulty do that for themselves. I am very happy Madison is communicating so well. Every person who has survived any type of brain impact has their own individual story. They want understanding, respect, patience, and support. The world has learned so much more about the brain since 2000. The procedures for dealing with an AVM in the brain has really advanced.
Hi Madison. My son Matthew is 36 and he had a ruptured AVM too this morning. He is in ICU and they aren’t very hopeful. I have hope but I need to be patient and thank you for sharing this because he needs time to heal. I hope he wakes up like you did. He is so loved and too young. Keep kicking butt. God bless you. Sara
Mine ruptured at work I had a seizure and they took it
Out I’m alive and back to normal at about 98% one year later keep fighting don’t stop !
I just had one rupture in February while 19 weeks pregnant we both made it thank God 🙌🏼🙌🏼🙌🏼 I am happy you made it 🙌🏼🙌🏼🙏🏼🙏🏼🙏🏼♥️♥️♥️♥️♥️
Hey me too,in 2014
To help with memory make sure you keep all your things together at all times. Thats whats helped me with memory
Had a avm rupture in July ..... getting stronger everyday!!!!! You got this be strong !!!
i had an avm rupture in 2016 and i've developed really severe ptsd from the whole experience. thank you for sharing your story, i've felt so alone in this and it's nice to see someone else who can relate to my struggles. when you said when you woke up you couldn't talk and all you could do was cry...ouch, i relate so hard. you are a warrior.
It’s been a year from mine and Im struggling with ptsd
My son had avm rupture and is making a miracle like recovery. Stay strong.
I am an AVM survivor too.
I had an AVM rupture in my cerebellum 3 yrs ago that left me in a wheelchair for about 8 mos, but I’m getting stronger everyday!
Hi sasha belcher ! If you don’t mind me asking, how are you doing today? I can already tell that you are strong because YOU made yourself strong enough to get out of the wheelchair!
Saw your story before and found you here! So thankful to see how much progress you have made! I really think you’ll be a cheerleader again someday, keep making video ❤️
Great video!! Keep up the good content!! 💚♥️💚♥️
I had an AVM when I was 11 on my left side, you have great movement in your arm, that is so awesome. I used one of those leg braces for years. you are doing so great!!!
Hi General Tso . Wow 11 years old. I couldn’t imagine, I was 19 and I thought that was tough. You are a fighter.
Thank you!
Kick ass and be a beast! Your awsome #first
Hey just know you're not alone! i had problems with my large pelvic AVM since birth, started bleeding internally and didnt get help until i was 18. left my senior year early for surgery and have never been the same. still have trouble with any sort of bowel function, and im going back for new growths and symptoms as of today. keep in touch! lots of support groups on Facebook and such!
Go girl...so proud of you..:) xx
Mine ruptured when I was working out with marine recruiters. I don’t remember getting a headache or loosing feeling I just remember getting really dizzy and I guess I passed out. I was rushed to the hospital and they performed emergency surgery. Strokes caused me to lose my left peripheral (hopefully temporary, that’s what I’m told anyways) While I was in the hospital doing pt ot and st every time I stood up I’d get dizzy and that’s gone (thankfully) so I can stand up and not get really dizzy. But I also stayed in the hospital for two-ish months. I was lucky enough to only have problems with my peripheral not my speech or any limbs. God was watching out for people like you and me on those days.
I just found in march i have an avm im hopin this surgery in may will cure me
I barely survived a ruptured AVM and a really bad stroke when I was 16. My right side was and still is struggling with a lot of stuff.
Just had an AVM removed a few months ago. I understand.
Thank you for your story. I have a large AVM behind my left eye. I'm 58. Very scared. You are very tuff.
How are you now?
@@lrmcdaleno3301 I am still kicking. It seems I'm too old for anything to be done. I still feel fine and my avm is stable. I turned 59 in December. Yay
How old are you?
@@jamesrandall1915❤️ 59 wow ! Happy to hear your still kicking 😎💪🏼Thank you for answer .. asking because I had this mri and mra and happens that they found avm ,I had this angiogram done last week and next appointment is on feb 23th .. to see exactly what kind of avm I have .. I’m 36 btw and little scared too 💔
I'll say a little prayer for ya. You're young, they can help yoy. 😁 keep me posted.
Thank you for the response. You are the first person to actually "talk to me.
Be brave. It'll be alright.
Later, J.R.
This is really for everyone out there that wants to talk with others that are dealing with an AVM. There is a website called www.avmsurvivors.org you can go there and read other story’s of people like us that have had an AVM or are now dealing with one. It’s a good group to chat with or see others that have gone or are dealing with a AVM.
Hello Madi. I hope you are doing well today? My name is Eddie Price and I am from Wayne County, North Carolina with a 28578 zip code. Would you believe that I had an AVM with a Subarachnoid Hemorrhage in the Occipital ( in the Left Posterior (Back of the Head ). This was back in the year of 1978. December 19, 1978 I was 20 years old that year. I went through 8 hours of Surgery on that day. My Neurosurgeon told me and my family that I was a miracle. Plus if I continue to improve that I would be a miracle for sure. Guess what I have been one ever since. Now that was a gift from God. I hope and pray for you the same and even more. Please listen to me you can do anything you want to. Just know your limitations. Please just know your limitations. That's all.
You are an inspiration Madison. How long did it take you to talk? My brother had a ruptured AVM and has an aphasia. He has a problem expressing himself and can talk only few words and not sentences.
how’s he doing now?
Hi Madison, i gotta ask, are you hemiplegic after the rupture? If you are, have you regained your movements back especially on your fingers and wrists? I had a rupture in 2016 and im still struggling to move my fingers and wrists on my effected side
Had my brain AVM rupture back in 2000. Had just reached the age of 10 when the bleed happened. Was taken to the hospital flatlined for a bit had emergency surgery to stop the bleed and then was air lifted to children’s hospital in St.Louis. Had to wait for the swelling to go down until they could do my surgeries. Ended up having 4. The reason why is because of the rupture. My doctors said it was like a bomb went off in my brain and there were 4 spots in different locations from my bleed.
Wow Yoehon John ! I can’t believe 10 years old. You are strong! Especially to flatline then come back. I was only in a-comma for 2 weeks. They told my dad that I wasn’t to survive the first night. But look at us now, stronger than ever!
Was also in a-comma for 2 weeks. Woke up blind and paralyzed on my right side. Was able to see after 2 weeks once the swelling had gone down. Had a lot of therapy done even after my surgeries. On in to high school did sports. Track and golf. One funny thing about in track. My friends would joke about how they could tell I was behind them when running. My right foot runs flat. I don’t really have as much control with it because of the brain damage. But at least my left is normal.
We are caregivers of our granddaughter. She had her AVM rupture with subsequent bleeding at age 9 in December 2000. She is now 33 years old and lives in her own apartment. She does have supports because of the common consequences from brain injury, especially to the frontal cortex and limbic system. It is important for caregivers to learn as much as possible so they can advocate and communicate if the survivor has difficulty do that for themselves.
I am very happy Madison is communicating so well. Every person who has survived any type of brain impact has their own individual story. They want understanding, respect, patience, and support.
The world has learned so much more about the brain since 2000. The procedures for dealing with an AVM in the brain has really advanced.
How long did it take for your short term memory to come back somewhat?