hannahgouldingg
Region: GB
Wednesday 01 July 2026 14:38:36 GMT
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Rhialy5 :
“Are you better yet?” Is the most common question I get asked. Oh and “so what are you doing about it?” ☹️
2026-07-02 10:43:46
92
Mullers03 :
Anyone with mecfs seeing this try the Perrin technique it’s helped me go from sever to almost symptom free 🫶🏻
2026-07-01 22:33:48
2
ChroniclesofME💜 :
Best thing to use its proper clinical name on ME it’s the name Cfs that creates so much stigma for us speaking as a sufferer from 20 years and lack of support and understanding thank you for raising awareness of what we go through 💜
2026-07-01 22:59:55
67
enomanika :
reminder that whilst ME/CFS can be invisible for one person it is not invisible for all people ❤️
2026-07-02 12:12:01
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Adina ❤️🦋 :
i live with chronic fatigue dince 2020. it is like a horror movie
2026-07-01 15:36:32
18
user7616538105201 :
What was it like having this? I have pots and I’m trying to figure out if i have me cfs as well.
2026-07-03 23:50:28
1
krapa75 :
Are u healed ? ‘Cause I still don’t understand if it is possible or not! I got my diagnosis in novembre and all the doctors said me there is no cure! I live in constant pain! Before I was a sporty woman, now I’m housebound since 7 months😫
2026-07-11 15:59:09
1
hannahgouldingg :
Just to clarify - M.E is the preferred term for this! For the purpose of this video, for the on screen title, I went with the name that most people recognise it as on socials. But to raise more awareness… it is called ME
2026-07-05 00:53:53
7
Swayonline :
Thank you for raising awareness. I get too tired to eat. Chewing just feels too much. It’s hard to explain that to anyone. Gravity feels so strong I can’t move 🙈
2026-07-08 13:23:10
2
yourgirlcharl_ :
Thankyou for sharing this ! Is there anything that helped you improve would you say your fully recovered now ? Xx
2026-07-01 22:23:31
6
GriMsWife 🇬🇧📚🍉🏳️🌈AuDHD :
I think this is why I just get 4 hours as it doesn’t matter if I have 4 or 12 I feel the same :/ rather doom scroll and rest
2026-07-02 22:40:26
20
Sophie Drewicz | Photographer :
I’ve had M.E since 2007. It’s so physically and mentally draining. 😴😪
2026-07-02 23:42:10
2
Kirsty Shead :
i have this its awful 😖 it robs ur life !!!!!!
2026-07-09 18:20:45
7
bee! :
ME is such an awful condition to live with :( i hate that so many people don't believe me, or think that since i'm young i can't be this ill!
2026-07-04 00:42:47
8
Debz :
Mine was triggered by glandular fever too. I’m still unwell but would say I’m mild at the moment
2026-07-01 21:02:08
1
Bronwyn :
ME is so awful, i wouldn’t wish it on my worst enemy. I’m 25 and have been diagnosed since 14 ❤️🩹
2026-07-02 16:12:58
26
claire hardy & pipes 🐶 :
I find the pain is something u get use to ! But fatigue isn’t 12years 28 when diagnosed , I think I explain this what you have everyday coz I do work n mask xxx
2026-07-02 19:15:59
11
Larissaummyahya 🍉 :
I feel like I might have this / what test did you do?
2026-07-02 16:49:02
1
Lisa Gothika :
Ive been diagnosed for 11 yrs and no one understands
2026-07-02 20:05:30
6
becky_belle94 :
Would really appreciate it if you could do this video while calling it M.E (people hear chronic fatigue and think tired 😅)
2026-07-03 22:23:30
8
🤎✨Krystalou✨🤎 :
My daughter 13 and been diagnosed 😔 shes also adhd. Asd, POTS , hyper mobility, now been referred to metabolics . She misses out on so much including having to home school. And hour out of house and she has to go back. Its so hard when people dont understand x
2026-07-01 18:08:01
1
Ashling Curran :
It’s been over a year now. I’m so hopeful to get my life back
2026-07-01 20:03:37
2
Kel :
Is this related , my daughters got it she did sports day on Monday didn’t do that much but her legs are still really aching , could this be related .
2026-07-02 06:25:35
2
jo.radbourne :
But why do I always feel better on holiday 🫠
2026-07-13 14:57:53
2
Amy:) :
My manager said to me yesterday “don’t let your body get confused with it just being a hot day and not your fatigue” I was about to cry because I was so tired.
2026-07-10 22:06:17
1
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