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Naomi
United Kingdom
Приєднався 6 січ 2018
Hi, I'm Naomi and this is my UA-cam channel!
I make videos on lots of things from book and product reviews, lifestyle, wellbeing, makeup, hair, crafting and my new home - check out the different playlists for everything.
I also have M.E. and Ehlers-Danlos Syndrome so I also make videos on living with disabilities, disability products, chatty videos about disability, collabs and more.
There’s also a lot more content over on my blog www.agirlcallednaomi.com
Custom Reveal Wheel card
Custom made card for a customer. I sell handmade cards to fundraise for M.E. charities. #CardMaking
Переглядів: 23
Відео
My skincare routine [CC]
Переглядів 9828 днів тому
Going through my skincare routine. Daily I use the Elimis Superfood Gel Cleanser and Elemis Refreshing Ginseng Toner along with reusable bamboo wash pads. I did also use the Pixi Clarifying Cleanser and the Magnitone electric facial cleanser. The charge on this lasts a while and if you look after the brush heads they don’t need replacing frequently too. Once a week I use the Elimis Rose Exfolia...
Disability aid: Adapted scissors [CC]
Переглядів 362 місяці тому
These are my adapted scissors. I find them easier to use especially on days when my EDS is affecting my hands more or I’m experiencing more neuropathy and spasms in my hands. The brand is Fiskers and I bought them from Amazon. As you can see the design is very different to traditional scissors and they’d be helpful to people with a wide range of different symptoms, illnesses or disabilities. Th...
Disability aid: Pill popper [CC]
Переглядів 392 місяці тому
This is just a short video reviewing one of my aids that I find really helpful. It cost me £3.99 for two of these from Amazon It’s a great aid to have if you struggle with popping pill packets which covers so many different symptoms, chronic illnesses and disabilities from EDS, MS, peripheral neuropathy, arthritis, muscle spasms, quadriplegia, Cerebral Palsy and more. The pill popper is designe...
About Naomi’s Cards For M.E. [CC]
Переглядів 312 місяці тому
A video chatting about my Cards For M.E. project, the charity I’m currently supporting and what creativity means to me when it comes to to chronic illness. You can buy my cards over on instagram or Facebook.
Organising my makeup #BeforeAndAfter #makeup #organisation
Переглядів 1476 місяців тому
I love watching organisation videos so when I got my first proper make up mirror in my new home I thought it was about time I had a sort out and re organisation of my makeup and makeup supplies and film it for others out there who like organisation videos. Edit: the makeup brush sponge cleanser is actually by Real Techniques #makeup #organisation
2024: the start to a new year [CC]
Переглядів 678 місяців тому
My obligatory new year video. Last year saw a huge change for me as I got my own home! That obviously wasn’t in my plans at the start of 2023 so a lot of last year’s plans didn’t happen as moving into my own home has taken a huge toll on my health and I’m still settling in and my health still isn’t the same pre house move. My new home is much much better for me and my needs though, just simple ...
1SE 2023
Переглядів 558 місяців тому
My 1 Second Everyday video for 2023 #1SE23 #1SecondEveryday #2023
Day in my Life Vlog: Christmas Eve [CC]
Переглядів 908 місяців тому
I thought I’d do a vlog as something different and take you through my day. A lot of my day evolves around my health and my symptoms like it takes me a while to be able to fully sit up in bed in the morning, or I do my bedtime routine early before I get too tired. I’m grateful I’m able to spend time outside my bedroom but I’m still restricted and I still spend most of my time in bed but since m...
Vlogmas: Christmas baking fun
Переглядів 258 місяців тому
CC note: I’ve tried really hard uploading this video a few times but each time I’ve not been able to add CC to this particular video like I normally do with my videos. Apologies for this. If you do require CC please comment on the video and I will try and come up with a a transcript or something for you. I understand how important CC are as a user of CC myself and I’m also aware that UA-cam’s a...
Vlogmas: Christmas Angels, my strange story [CC]
Переглядів 278 місяців тому
This is a little video of something strange that happened this year with my Christmas Angels card that I received from the project that the charity Action for M.E. runs at Christmas. I talk a little about the project in the video. If you’re wondering about Spoon Theory check out this blog post I wrote explaining what it is: www.agirlcallednaomi.com/2018/01/whats-with-spoons.html #vlogmas #chari...
Vlogmas: My Christmas tree [CC]
Переглядів 308 місяців тому
This is my second Vlogmas video. This time I’m sharing the palaver I had with the electronics with my new Christmas tree and how I was finally able to get my dream tree. I plan on buying more tree ornaments as the years go by. 0:00 Into 1:42 Not-so-simple tree building 3:12 My decorated tree #Vlogmas #ChristmasTree #TreeDecoration
Vlogmas: Intro, wrapping and organising tips [CC]
Переглядів 418 місяців тому
Vlogmas: Intro, wrapping and organising tips [CC]
FFORA bags: look inside! | Wheelchair accessories [CC]
Переглядів 278Рік тому
FFORA bags: look inside! | Wheelchair accessories [CC]
2022 look back and 2023 projects and plans [CC]
Переглядів 91Рік тому
2022 look back and 2023 projects and plans [CC]
Vlogmas: Easy Christmas tree handmade card tutorial [CC]
Переглядів 18Рік тому
Vlogmas: Easy Christmas tree handmade card tutorial [CC]
3.12.22 - Vlogmas Vlog: A very exciting parcel and a crafty afternoon [CC]
Переглядів 28Рік тому
3.12.22 - Vlogmas Vlog: A very exciting parcel and a crafty afternoon [CC]
1.12.22 ~ Vlogging Vlogmas: Explaining how Vlogmas will work and vlogging my day [CC]
Переглядів 34Рік тому
1.12.22 ~ Vlogging Vlogmas: Explaining how Vlogmas will work and vlogging my day [CC]
Creative mail creations | Rosie's letter to me and my creative reply 📮 [CC]
Переглядів 412 роки тому
Creative mail creations | Rosie's letter to me and my creative reply 📮 [CC]
Thank you so much. Watching this tonight while laying on an ice pack on the floor while I’m waiting for something in the oven.
Bonjour, Cool la vidéo de présentation. Je trouve ces sacs super bien. Mais comment faire pour le commander depuis la France. Merci
Sorry to jump on two years late but thanks so much for this video. Do you get your PA funded but social care? I'm 26 with chronic illnesses and always up for a chat if you want ☺️
I hope this doesn't offend you, but you sound like the British version of Gayle from Bob's Burgers. Bob's burgers is one of my favorite television shows and I love Gayle!
Thank you for your comments on flexifoot. I am about to return my NHS crutches after a repair to a broken ankle but want my own single crutch for work for a while.
are you aware that your blog is....not..secure...mark
This is very brave of you to spend so much time explaining this. Thank you. Have you had your B12 levels tested and have you thought of having b12 injections? How are you now, I realise you published this ages ago?
thank you so much for sharing this. i am the same age as you and have had a nightmare with carer agencies but thankfully finally got social services to fund a PA! this has been a really helpful insight to what support from a good PA can look like. I know how vulnerable it can feel to be open publicly about the realities of living with health conditions and needing support to maintain a good quality of life so I really appreciate you making this video and sharing it with us. This has helped me more than I feel I can put into words. I feel very hopeful now about what life can look like once my PA starts working with me <3 thank you!
Hi there, I’m so glad this video was helpful to you and has given you hope for hopefully a better life once your PA starts and you start to build up that professional relationship with your PA. Diane who’s in this video has been with me over 3 years now, almost 4 probably (!) and we get on so so well and we have a good routine going and she’s very attuned to my needs and she just loves her job. It will be hard at first for both you and your PA but the great thing about PAs is you have someone who is supporting you constantly so you see each other regularly so you have that time to establish a routine and relationship as opposed to agency carers. There’s such a shortage of PAs; I’m really struggling to find extra PAs to join my team so I’m using agency carers to fill the gaps so I know the difference in care. I made this video more to highlight and raise awareness of just the variety in what a PA can do to support someone and enable them to live out their life as well as the relationship that you build up with your PA. I really appreciate your comment it was lovely to read and all the best, Naomi
Lovely to spend the day with you 🥰🎄
thank you - would you like to see more DIML vlogs like this when I’m well enough to film them?
Your Christmas tree is gorgeous! I love the ballet themed ornaments🎄and I felt so happy seeing my Christmas card to you on your window sill ☺️
thank you and thanks for the card x
I love this! 🦓 ♿️ xx
thanks ☺️
Thank you for sharing! I definitely need to get some fairy lights now too 😍😍😍
I love fairy lights!
Your home is lovely.I would love a bungalow of my own one day x
thanks, I hope you get your bungalow one day
I would be in heaven In your craft corner- it’s incredible!! Lovely to see you have a dedicated space to create now🥰
thank you yes it is lovely to have a little dedicated craft space
Thank you, Naomi. I'm considering a career change and am considering becoming a PA. Thank you so much for your honesty and opening up. Bright blessings.
That’s great! I’m glad you loved my video and you’re considering becoming a PA it really is such a rewarding and fun job. My PAs love coming to work and we have a great working relationship. There’s also such a shortage of PAs; I’ve been desperately looking for more PAs for a long time but there’s just so few people out there. I’m sure you’ll be an asset to the profession!
Very well done, my dear!❤
Thank you so much!
I’m a new subscriber. Wish I had your confidence to do one. 💕☺️ I've just ordered a thrift bag to send some stuff off.
thank you, it’s my first and only fashion video.
Can you please do your wheelchair review folding
Could you please expand on what you mean by this please? Naomi
I got FND after my second vaccine Astra Zeneca
Oh no, I’m really sorry to hear that. I’ve never heard of that happening before. I hope you’re recovering well.
Thank you for your bravery and generosity in coming forward and sharing your experience and symptoms. I think through people like you, showing so much courage, the understanding of FND will increase! I too have FND and share some of your symptoms, you explained everything in your video very well! Thank You for sharing!
Hi Milly, thank you so much for your lovely comment what you’ve written is so so kind and has really made my day. It takes a lot for me to open up about FND because people assume it’s all in our head rather than it being a neurological illness. But on the other hand I firmly believe that it’s only through talking about it and sharing that awareness of FND and the true nature of the condition can be raised. Hopefully the more FND is talked about the more people will understand it. Also thank you for watching my video. Naomi
@@AGirlCalledNaomi I agree with you completely and believe the same thing! The sigma and prejudice against sufferers of FND is appalling, it’s like the poor cousin of disability nobody wants, yet for so many people it’s the factual reality of daily life. The part you are bravely playing is addressing this stigma and championing so many hidden suffers, is amazing and inspiring, I hope you feel some pride and achievement in that! My career was (I say was, as 2 years ago I gave it up, unable to cope) in communication, PR and brand management, I feel more inspired today than every before to join you and do what I can to help address the stigma, bring true awareness and promote education of this disorder. It’s time the world understood the real FND, not the heavy Freudian misconceptions we all still fight to lift off us everyday! You are an inspiring person Naomi, keep going one moment at a time and rest well! Xx
Thank you Milly. I want to be brave enough to talk more about FND especially after the experiences I’ve had from health care professionals. Do you have any suggestions for videos I could make on the topic of FND?
@@AGirlCalledNaomi I’ve just liked your Instagram page, so will send you a message 🙂 I would always say, talk about things that you feel passionate about and want others to understand about FND, maybe tackle some of the preconceptions people have? Sometimes it’s really good to just ask questions too, and communicate what you’ve learnt about some of the questions you once had, maybe when you were diagnosed for example 😊 I think you are doing a fantastic job of talking about FND and ME!
@@millymay0025 thank you so much that’s really kind of you. I’ll take that advice on board and think how I can make a video about FND as I know I don’t have many and haven’t done any for a while.
I just subscribed today and all the clips I've watched have been helpful!
Hi there, I’m so glad to hear that! Naomi :)
It feels like my circle isn’t building up into a cylinder shape on the sides and is just getting wider. Any clue what I’m doing wrong?
Hi Megan. I’m really sorry for my very delayed reply. Once you’ve built the base you need to stop increasing your stitches and just take out your stitch marker and work a single stitch in each space going round and round building up the sides of your can cosy to your desired hight. Hope that helps and works for you. Please do reply if you get stuck and I will respond much much quicker next time! Naomi
Does ME affect fertility in women's health? Perhaps in the severe ME cases?
Hi, a good question; not one I'd given much thought as I've never been interested in having children myself. I've always preferred to foster/adopt. This was even way before I ever became unwell so the topic has never made me think much. I do have fertility issues but the cause is unknown. I do know of one person who has severe M.E who has a child Jessica Taylor-Bearman (she's written two books on her story of living with the condition). On reading your comment I did some research and there was some mixed results. I always try to go for reputable sources of information so I've found this leaflet from the M.E Association (I'm not sure if you're in the UK or not) but it's not too long like the other link I was going to include: meassociation.org.uk/wp-content/uploads/pregnancy.pdf - Hope I have been of some help. Please do keep the conversation going it is so important to help raise awareness and understanding. Naomi EDIT: I would guess that like with any condition things vary depending on how the illness affects you so I would guess and from the little bit of research that I did that fertility both in getting pregnant (was difficult for men and women with severe M.E) and carrying a baby for women was more difficult for those with the more severe spectrum end of M.E/CFS.
@@AGirlCalledNaomi Thanks for your perspective on this issue. I did know someone with ME that believe fertility issue is related with the condition. I am from the UK and just round the corner to yours actually. I've not heard complaints from Men with ME regarding their fertility, but I do think as you are an advocate for ME, it's an important area of research you can put forward to the ME associations to consider exploring. I'm on your facebook page aswell and keeping up with your posts. kudos
Thanks for this video.I literally got fed up of buying replacement crutch foot pads. They worn out every couple of weeks. This video explains why they worn out because we walk at an angle. Now I know flexifoot exist and I'm going to order some. Thanks
Hi there. I’m so glad that this video was so helpful to you. Another positive I feel is that unlike many disability products the FlexyFoot ferrules are a fairly good price especially for something designed so well. I hope that they work out better for you. Since I started using FlexyFoot ferrules I’m more steady so I feel more confident when I’m walking with my crutches. You’ll have to let me know how you find them after you’ve started using them. Naomi
Thank you its very helpfool . You a star !
Happy Birthday Naomi 🥳 I’m glad you had a lovely day!
Hi Susanna, thank you very much for your kind words. Naomi
Hi Naomi, I just saw the article about you in the MEA magazine and was pretty sure I recognised your photo… so I also checked out your UA-cam channel! I moved away a year ago but would love to be in touch with you again if you’re interested - please look me up on Facebook if you would like to reconnect :) x
Hi Susanna, it’s lovely to hear from you. Yes I did do an article for the MEA. Thank you for checking my channel out, any support for it is much appreciated. It’s my little project, I do disability videos but also craft tutorials, makeup, product and book reviews etc - basically me summed up into a little UA-cam channel. I used to post regularly but due to my health I had to reduce to just post when I’m able to. Unfortunately I’m not on Facebook to be able to reconnect back with you.
New subscriber! This means so so much. Thank you for your detailed and thoughtful review. 💜
Hi Hannah, thank you so much for your comment and subscription. I love your channel too and you've helped me find some amazing books (plus the ones you've put up on your Good Reads). You've also helped me enjoy poetry. My current reading book is 163 Days which I'm really enjoying and I'm going to review it on my channel once I've finished it. I do find reading difficult but the format of 163 Days makes it a really easy book to read. I hope you are as well as possible. Naomi x
Cheers, the info is much appreciated !
You're more than welcome and I'm glad the information was of help - I aim to help people know what products are out there.
Looks so cool! I made one of these for my sister years ago, but yours looks way better than mine did.
Thank you Fuschia! This was my first attempt, it was a bit wonky but I always feel that it looks more handmade that way. - Do you think it would be good of I did a video tutorial on how to make one of these? I've had a lot of views on this video which is so lovely.
😻😻😻
Thanks for the info about the ferrules!
You’re welcome. I’d totally recommend them. After using them for a while now I can notice the difference and how much better and more stable I am with the Flexy Foot ferrules.
Hi Naomi! 😻😻😻
Thank you for sharing this vlog Naomi. It is very important to raise awareness of ME/CFS and to show the care people who are severely affected require to manage daily activities of living. I can imagine how vulnerable you may have felt sharing this on UA-cam, however, please know you've done remarkably well and have truly shown the reality of ME/CFS - Emma
Hi Emma. Thank you so much for your comment, what you’ve written means a lot as when I was editing I did feel so vulnerable seeing things like needing support to get a bath etc. However this is the reality of what having severe M.E is like and I'm glad that you feel that it's helped raise a little bi of awareness into how M.E can affect people like myself. I kept this video focused on how Diane supports and enables me, so when we went out for a coffee what I didn't show is how that trip out left me feeling utterly crashed that evening. I also like in this video how the relationship I have with Diane shines through like how Diane jokes about how I always over scrub my face or our conversation in the car about liking egg mayo. When you spend so much time with someone like a PA it’s so important that there’s a positive professional working relationship and Diane and I get on so well and can have a laugh but at the same time there’s a seriousness such as when I become unwell and I need Diane to step in and take over.
I used to read a lot of dystopian fiction as a teenager. I will research this book..thanks
You're welcome, I'm glad you liked my first book review and you've found a new book to try. I really did love this book once I got into it. The sequel to this book is 'The boy of the bridge' so I've got that on my list of books to listen to. Let me know your thoughts on this book once you've read/listened to it as I've love to hear your thoughts and take on the book.
Thanks for sharing this Naomi. I appreciate that it took a lot for you to share this. I am currently awaiting my pip decision so this was useful to help me think what I could spend the money on to make my life easier.
Hi Sarah, thank your comment, what you've written is such appreciated. I really hope you do get your PIP and I'm happy to offer any advice or support if you wish. My email is hello@agirlcallednaomi.com if you wish to contact me. PIP defiantly helps to cover the extra costs as being disabled/chronically ill does get quite expensive and before I got my care package it helped me to pay for care and now it helps me pay for my care contribution payment along with everything else.
@@AGirlCalledNaomi I heard this week I got my pip for 3 years at higher rate mobility and higher rate daily living. I was so overwhelmed as I'd heard such horror stories of people having to fight for a year or two to get anything. Now I just need to think best how to spend it. As I'm self employed I think for the moment I'm going to use it so I can allow myself hours / days off.
@@sarahgibbons9737 Hi Sarah, I'm really glad that you've been awarded PIP it really does help to cover the extra costs of having a chronic illness/disability and it's there for people to use however they wish in whatever way will help and support their needs best as everyone is unique even two people with the same diagnosis. I'm also glad that you didn't incur the difficulties a lot of people do face to get PIP especially when you have lesser understood diagnosis' like M.E/CFS.
Great vlog. I'm sure it will be good for others who are wondering about direct payments or some of the things they can have help with. I don't know if this is helpful to you or anyone reading this but this is the technique my PAs and I use for my compression socks just imagine it with someone putting it on instead of like in the video where the person is putting it on themself. I mostlt use nhs ones as I find it easier to put those on but I do have a few pairs of interesting ones including dinosaur ones ua-cam.com/video/Lf_MlNi9tb0/v-deo.html
It's lovely to see Diane after hearing about her and how she's made such an improvement to your quality of life x
I’ll be sure to let Diane know :) when editing I felt quite vulnerable showing that I need help with things like getting a bath but I wanted to help raise awareness of how important people like Diane are. PA’s and carers and unpaid carers too are not recognised for the wonderful work they do to change and enable people’s lives. I definitely think both paid and unpaid carers deserve to earn more for what they do. I find it Absurd that there’s people on a supermarket checkout earning more especially when it comes to carers allowance which when working out their hourly rate income is less than minimum wage! I know this video was much requested and even chased up asking me when I would be sharing it so I pushed myself to film, edit, upload and add subtitles to get it shared on time so I’m now having a quiet weekend as it was a massive challenge to do all that. I also have another video in the making to share how challenging it is to be a UA-camr with M.E and other illnesses just so people understand that I love my channel but equally it is so hard especially when people are chasing me up asking when I’ll be sharing certain videos.
This is brilliant.
Thanks so much Chlo
Hey. What happened to your a day with my PA vlog? I was really looking forward to that. Thank you for your video though. I never use disabled with people I know, despite fitting the criteria. Mainly because I feel people wouldn't even think of me as coming under this label, mainly because I don't actually share things about my condition. So I feel they'd just think I'm attention seeking if I ever were to call myself disabled, so i don't. I know it's sad in a way. But sadly life isn't so kind to things they can't physically see. It's far harder to understand something that isn't displayed on full view. So people are less sympathetic & believing. This is how I feel anyway.
Hi there, thank you for sharing your thoughts on the topic of this video. I haven't forgotten about the video on what I get up to with my PA and I will try and get round to filming it when I can. I'm really glad to hear that it's a video you're looking forward to watching. Things have just been a bit challenging for me lately as my health hasn't been too great and I've been waiting and trying to get a date for my surgery. so I've just been using videos I made a while back. I hope to be well enough to film soon but as I'm sure that as someone who also has chronic health issues you can relate to how challenging it is to run a UA-cam channel. I love my channel but it takes up a lot of my time and energy to film, edit the footage, upload it to UA-cam then add subtitles also which I do to increase accessibility. I haven't forgotten about the PA vlog and I hope to film it when I'm able to.
Hi there, just an update for you. I wanted to film my PA vlog when there was some variety to show the wide range of ways in which my PA supports me so as I have a hospital appointment this week I've started my PA vlog which I'm filming over the course of a week so I can show the many different ways my PA supports me.
😻😻😻 Thank you! Xx
If you make this card I'd love to see a photo of your creation and how you've adapted the card's design. You can share a photo over on IG - @agirlcallednaomi_blog or you can email me a photo - hello@agirlcallednaomi.com. Let me know if you're happy for me to share the photo plus with your name or if you'd prefer to be anonymous.
Thank you for sharing! So many people don't realise how long we have to "save up" for just to do Christmas. Many people don't realise how much energy it takes/how overwhelming it is to just being around people ❤❤❤
You're welcome. It seemed a bit much to talk about all my illnesses and how each one affects me so I just focussed on M.E for this video as I think that one can be the hardest at Christmas due to how little energy I have and the hypersensitivity though obviously dealing with a seizure and as a result badly dislocating a few joints on Christmas Day also isn't that much fun either! But yes as I type I'm reaching for my noise cancelling ear plugs as my some of my stepmum's family have just arrived and I'm tired and finding the noise a bit painful so I'm staying upstairs (plus I'm terrified of covid). But yes totally, people don't understand how EVERYTHING uses energy even just travelling in a car or holding a conversation but also how M.E has many other aspects and symptoms especially when you have severe M.E.
I'm so sad about these, I feel people only see them as a mask exemption lanyard now. I was actually told by a train officer it was great I was wearing one, because many people don't and still don't wear a mask; and then went on to ask why I was wearing a mask though 😏 I had to tell him that it actually represents a hidden disability. Quite sad really. The point of them i find had been overshadowed
I totally totally agree with you! It's losing it's meaning first like you said during the pandemic people where just buying them as they didn't want to wear a mask and now people like the design of them so companies are designing and selling their versions of a sunflower lanyard. I feel it all could have been stopped if Hidden Disabilities and places like supermarkets who offer free lanyards asked for evidence of disability when people where purchasing them plus they're so cheap it to buy it doesn't put off people who want to evade wearing a mask. I made this video originally to highlight the real reason behind the lanyards but now it's loosing it's meaning. I still find in some places that they understand they're for hidden disabilities and you would have thought transport staff would be aware that they highlight hidden disabilities - that's the point of them it shouldn't be vice versa. Also thank you for watching some of my videos and commenting. It's nice to hear from people who watch my videos.
Omg wow!! This look suits you SO.... MUCH! I almost didn't recognise you! I'm new to your videos so looking back at your past videos, and I really wanted to see what aids you use. So really glad to have found this one
Thank you. I loved having red hair but it was difficult to keep up with colouring it (me and my PA have been searching for hairdressers today as I haven't had it cut in 2 years!) but yes I do love having curled hair too. Again my fringe was a nightmare to maintain so that's grown out too but thank you for you comments on how I look in this video and thank you for checking my videos out and for making the effort to leave a comment as it's lovely to hear from people who are checking my videos out.
Hi, sorry you're struggling. It's not easy. It would be really helpful to see the vlog, but also if you could do a video showing how you go though the process of getting care? As I'm in the UK too & sadly probably need to apply for some support now. Thanks
Hi there, yes I can totally relate to the emotionally difficulty of realising that you're not coping on your own and/or with the support of family and friends. I've have a few requests for the vlog so I'll be doing that. Your suggestion for the other video is a great idea so thank you as I'm always after suggestions and ideas. With my health as much as I love my UA-cam channel I may do your suggestion initially as a blog post (I did sort of talk about my journey from first needing care to where I am now in this video but I can explain more and in order in my blog post) and then one day I may make it into a video also as I know so people find UA-cam more accessible but I do have an accessibility widget on my blog. My blog is www.agirlcallednaomi.com and if you're on Instagram my account is @agirlcallednaomi_blog.
@@AGirlCalledNaomi Oh no sorry I meant the process of getting care as in how to do about accessing it, like how to apply. But I really appreciate you sharing your blog because I would like to take a look. Also it is true that I definitely find UA-cam easier. Great to hear you will be trying the vlog! It will be so interesting to see! Thanks!
@@mayflower2158 Hi, oh okay thanks for clarifying - it's helpful to know what information you wanted and hopefully I can help you out. I'll still plan to do the blog and video as it's a good suggestion of yours. Thank you for checking out my blog and it's good to know that people like yourself find my UA-cam channel more accessible than my blog. I've been blogging for a few years so now I know that I may look back on my blog posts and make some of those old blog posts into videos for my channel - what do you think and looking at my blog have you seen any particular blog posts that you'd like me to make as a video? As well as my blog you can check out my Instagram @agirlcallednaomi_blog as I have other and share other videos there too especially shorter videos.
@@AGirlCalledNaomi Sure! I definitely will! And I'll be more than happy to let you know. It's so lovely that you care about your viewers thoughts & opinions & take time to respond to them fully. So nice! 🥰
@@mayflower2158 Hi there, I've made a little video about how I got care both privately and also the process of having an assessment and getting care from adult social care. I made is as a video as I know you find videos more accessible. Are you on Instagram as I'm planning on adding the video on IGTV as putting it up on UA-cam would mean refilming as it's not great quality plus the editing and adding CC which is all pretty exhausting and time consuming.
😻😻 Potsie here ❤❤
Unfortunately I must welcome you to the PoTS party and whilst fainting isn't that fun standing up too quickly is a perk as you get a high for free!
@@AGirlCalledNaomi 🤣🤣🤣
Thanks for sharing.
Thank you - any other suggestions for videos I'd love to hear them (PS apologies for my late reply to your comment)
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Thank you both for sharing! I also have FND and have tried to explain it from my perspective for some awareness: ua-cam.com/video/OVJmcg4HL0g/v-deo.html
Really struggle with sleep. Thanks for the tips! ❤
You're very welcome - if you have any tips of your own to share I'd love to hear them and I'm sure other would like to hear them too
Get well soon
Thank you, unfortunately feeling like this is pretty much a daily occurrence to one degree or another.