Georgina when you’re talking sometimes it’s like listening to ASMR your voice with the soft english accent is relaxing even though you are talking about your serious issues . I hope at some point we get some relief chronic illnesses are tough.😞
Oh man I'm so sorry that the difference is so small but even if I can help in the tiniest way then it's worth my time. I watched 30. I really hope that helps even if it's in the littlest way.
Ally!!! Omg that’s SO kind! But I genuinely would rather you spend your time on things for you, life is too short for ads, I find even the 10 sec non-skippable ones annoying 🙈
Lol ur right ads r annoying but don't worry I just put aside the phone and let it play while I rest like usual so it's not that annoying it's the least I can do honestly
Do your fingers always pop and crack? I always feel the need to crack my fingers and joints. I’m looking into EDS and hyper mobility. I have a lot of pain in my legs, ankles,neck, fingers,wrists,and shoulders. My joints (that I know of) haven’t dislocated, I just want to constantly pop my joints or I want someone to yank my fingers and arms because that sounds like it would feel good, I know that’s weird, I would never have someone yank my arms and fingers, it just sounds like it would bring relief!😆
No, but it was a specialist for hand & wrist deformities, since I’ve reached that point. general physios are mainly just are trained to teach exercises & stuff like that. In addition to the hand therapy I discussed here, I had 2 great physios for my EDS related problems, & 1 who was absolutely terrible. none of those 3 supplied braces or supports or anything, they just taught me exercises & how to use KT tape and resistance bands. 1 of those 3 was knowledgable about EDS, 1 didn’t believe in it, & the 3rd was able to adapt the exercises & taping methods for me, & that course of treatment was as successful as it could be, despite her not having prior knowledge
Sorry, it looks like the premiering comments will be lost, so I have tried to turn the premiere off but I’m not sure if it will work!
Great video, thanks!
Georgina when you’re talking sometimes it’s like listening to ASMR your voice with the soft english accent is relaxing even though you are talking about your serious issues . I hope at some point we get some relief chronic illnesses are tough.😞
Hope me watching and not skipping ads helps. Would normally never do this for any other UA-camr but you deserve the best. Great video btw!
You're the best, thank you! But honestly, please don’t worry about that- the difference it makes is so small that your time is much more valuable 💙
Oh man I'm so sorry that the difference is so small but even if I can help in the tiniest way then it's worth my time. I watched 30. I really hope that helps even if it's in the littlest way.
Ally!!! Omg that’s SO kind! But I genuinely would rather you spend your time on things for you, life is too short for ads, I find even the 10 sec non-skippable ones annoying 🙈
Lol ur right ads r annoying but don't worry I just put aside the phone and let it play while I rest like usual so it's not that annoying it's the least I can do honestly
P r o m o s m 😋
okay cool, glad it went through! deleted the earlier comment so your comment section isn't cluttered with ko-fi related stuff.
Thank you! ☺️
Do your fingers always pop and crack? I always feel the need to crack my fingers and joints. I’m looking into EDS and hyper mobility. I have a lot of pain in my legs, ankles,neck, fingers,wrists,and shoulders. My joints (that I know of) haven’t dislocated, I just want to constantly pop my joints or I want someone to yank my fingers and arms because that sounds like it would feel good, I know that’s weird, I would never have someone yank my arms and fingers, it just sounds like it would bring relief!😆
I wouldn’t be able to say just from that, you’d have to see a rheumatologist in person 🫶🏽
@@GeorginasJourneyJust thought I’d tell you, I just got diagnosed with EDS by my neurologist today; along with small fiber neuropathy. 😊
Hey. I've noticed that I have been receiving a lot of your videos. I hope your are doing well. I'm worried about you. Please take care.
What do you mean? What do you mean you’ve been receiving a lot of my videos and you’re worried?
I posted this video 13 days ago & no actual videos since, just shorts that are a few seconds long each
Was it a specific physiotherapist for eds? My physiotherapist is very vague & dismissive (re foot injury). I'm looking into eds assessment
No, but it was a specialist for hand & wrist deformities, since I’ve reached that point. general physios are mainly just are trained to teach exercises & stuff like that. In addition to the hand therapy I discussed here, I had 2 great physios for my EDS related problems, & 1 who was absolutely terrible. none of those 3 supplied braces or supports or anything, they just taught me exercises & how to use KT tape and resistance bands. 1 of those 3 was knowledgable about EDS, 1 didn’t believe in it, & the 3rd was able to adapt the exercises & taping methods for me, & that course of treatment was as successful as it could be, despite her not having prior knowledge
@@GeorginasJourney it's a flipping nightmare trying to get bespoke care/referrals
Any updates on your thyroid?
There won’t be any updates really as nhs have chosen to just leave it as it is, not even follow up scans to see how much it grows or monitor it
@@GeorginasJourney Thank you! Big Hugs