@gamingdocmbbs: donations to MND assosiation. or am ALS research charity in America #ALS #mnd

GamingDoctor
GamingDoctor
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Wednesday 02 September 2026 13:36:38 GMT
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londonunrushed
Thelondonedit | Londonunrushed :
ALS and Prion Diseases scare me
2026-09-02 14:24:56
86
secret.jellycat.l
Secret Jellycat Lover! :
My dad past 24 yrs ago of Motor Neurone Disease, always scared it's hereditary 😳
2026-09-02 13:44:51
39
lisalotz499
lisalotz499 :
I'm so pissed 😡 that I have it 😭
2026-09-02 15:20:58
66
kingsmoo
Stack :
i think they biggest thing that scares me is the life expectancy but Steven hawking survived 50 years. how???????
2026-09-03 00:50:13
30
ambergray2023
Amber Gray :
I also commented on yesterdays video. My mother is in her final days. Thank you SO much for this explanation. In all the reading and all the visits to the neurologist, no one has EVER explained it like this. My mother will be donating her brain and spinal cord to the Brain Endowment Bank in Florida for research. I hope so much that her brain makes a difference.
2026-09-02 14:31:15
258
ecliptic.cos
laur ☾ :
i am a molecular biologist who is super passionate about science communication. i am binging your videos!! you explain concepts so well because you break them down into extremely digestible pieces. this is a masterclass in accessibility!
2026-09-02 14:47:21
92
chixynuggies
Chicky Nuggies :
My mom has ALS and it’s tearing our heart to pieces. She was a pianist and now she’s completely paralyzed and can’t even talk. I spent my entire life savings on giving her one last vacation last year, but even then she needed help raising her arms and her legs were paralyzed
2026-09-03 03:04:50
52
hatari91
Arslan Ashraf :
My mum passed away due to mnd - this was in 2020
2026-09-13 17:54:37
0
robin8322
🌾🌷🌿Robin🌾🌷🌿 :
My husband was diagnosed August 11th 2025 with ALS 😞
2026-09-02 17:31:18
31
claire.small19
Claire Small :
I have MND - but a form called SOD1 which the incredible researchers of the world have found a treatment for (not a cure but it massively slows progression) it’s is called tofersen and i have it monthly via lumbar puncture. It’s currently not been licensed by NICE so it is a postcode lottery whether you can get it - I’m one of the very lucky few who can receive it. But it’s money that people donated that funded this research and therefore saved my life, I was diagnosed at 37 with two young children. So THANK YOU for raising awareness of this evil disease to get more funding to save others like me.
2026-09-02 18:54:27
103
_galega.__
Sónia Santos :
January 2015 I was diagnosed with Amyotrophic Lateral Sclerosis. It’s not an easy diagnosis to accept, but I have learned to live with resilience, perseverance, and optimism. I live one day at a time and make the most of every opportunity life gives me, with the joy that defines me so well!!
2026-09-10 22:56:30
5
tinariesberggehling
Tina :
I am an RT and this is totally an observation…all of the ALS pts I have treated are highly educated and smart people, professionals. Military and teachers especially.
2026-09-02 21:29:14
19
lazulitetea
Lazulite Tea :
I have a sister disease issue (upper motor only, not ALS but not MS) and "because fuck you that's why" has been something I've been saying the past year when people ask why it happened to me
2026-09-02 14:26:05
39
patriotmom13
Patriotmom13 :
Also gene mutation like C9ORF72 and SOD-1 and about 40 more
2026-09-02 21:26:00
6
2tempikxm
2TempiKXM :
We lost my bother to ALS. He was 59 and the strongest man I ever knew. it took him in 3 years. The day before he died, the was out in the street on his motorized wheelchair racing the neighborhood kids. He asked if his ALS could have been related to the concussions he got as a high school and college athlete. At the time, the doctors said no.
2026-09-02 22:20:51
17
calliemcphersonnichols
Callie🖤 :
I have stiff man syndrome. It’s terrible.
2026-09-02 21:34:58
0
j7_vfx
j7_vfx :
I've been suffering from FND after a stroke a few years back. i had a noticable drop in muscle mass and weakness after the stroke. The neurological pain has been intense, it feels like 1000 needles flowing through the nerves on bad days as well as random tremors and memory issues.. but I'm thankfully managing through medication. funny enough not many people know if these neurological conditions. there should be more awareness for these conditions
2026-09-02 22:49:05
7
katundrakat
Kathryn :
My mom had no other health conditions and when she was diagnosed in her 60s. She lived six years , it was all terrible.
2026-09-02 19:42:49
6
yoloswag420xd
Chipstutte :
Als is terryfing
2026-09-02 13:41:18
9
zacprocyon
Zac From Space :
nature doesn't care who it takes out. it's so unfair.
2026-09-02 14:37:24
9
bobbybobbob264
Bobbyyyyyygirllyyybob :
100% done justice as someone who lost there dad to MND / ALS 💙 thank you for talking about it ♥️♥️♥️
2026-09-02 13:42:31
9
nanathealien
Joana Nathis :
can you speak about MS? My best friend has it at 25 y.o. and I have no idea how to support her or help
2026-09-09 23:41:25
0
gebles2vw
bgdefxt :
can my gallstones still be dissolved? i have 5mm. i don't want to get a surgery 😭
2026-09-06 14:18:27
1
moma_earth
Cody bear :
What do you mean by prion??
2026-09-04 02:32:54
0
mitrinapye
Nurse :
I want to thank you for your educational videos. When I was a new nurse I worked at Henry Ford Hospital in Detroit. They were on the cutting edge and I was constantly learning. My skills and knowledge grew at a fast pace. Now I’m at a different hospital. The learning opportunities aren’t there. I’m 63 now and am still fascinated with the why and how. Your style of teaching makes everything so clear. That is the highest evidence of intelligence. Take a difficult subject and find an effective way to teach it.
2026-09-06 14:39:12
3
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