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@keiths-dolls
Doll reviews, thrift/charity shop overviews and general rambling about toys and similar nonsense.
New review. I took pictures despite exhaustion. Go me!

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doctor was about as pointless as I anticipated. He thinks it's carpal tunnel as a result of my stupid dinosaur wrists when I sleep. Like my mother, i sleep with my hands curled up like a t rex against my chest and because we're both hypermobile, this results in overextention of things that shouldn't bend that way. Usually I have a cuddly toy to hug that stops me doing this, but I probably was doing it without noticing while we were away which made existing damage (it was already sore) worse and now the thumb is numb as well as painful. He thinks it's compression of the nerve in the wrist causing the numbness and likely compression of the tendon causing inflamation and pain. He told me to sleep wearing a wrist brace but that was about it.
so not very helpful.
I did mention that I do keep injuring myself in my sleep because my joints are so unstable and please could they figure out who to refer me to for this because it's getting to be a major issue. He said he'd chase up neurology who were looking at my numb patches and then ghosted me earlier in the year (who the hell knows what happened) but I don't hold much hope there.
I don't think neurology is the correct department anyway. And that's the big problem, nobody seems to know what department hypermobility should go to. Presumably it should be muscoskeletal but they lost my last fucking referral for my injured elbow and then sent me in circles when I phoned about it so I got annoyed and gave up.
honestly referrals are just fucked right now. The NHS doesn't have enough money or staff and shit keeps getting lost. It's become increasingly difficult to even get an appointment in the first place, let alone have them do any follow up.
But I keep hurting myself in my sleep and I keep having bits of me go numb and never resolve. There's every chance my thumb never regains full sensation, just like my knee, my toe and other of my fingers never did.
I keep getting pain in my feet becuase I put weight down and the bones literally MOVE. I feel them move, it's gross and it's painful. Sometimes they immediately return to where they should be, sometimes something ends up where it shouldn't and there's a sharp pain til I shake the shit out of my foot and force things to shift. Sometimes it still hurts for several hours after.
I'm fucking tired of it.
my thumb is really painful.
I don't know if I mentioned i'd injured it. I think I slept in such a way I moved it wrong and tore something. Anyway, it's been hurting for days and now it's also going numb. So it hurts inside, but the skin on the outside is numb. my thumbnail - numb. The side and top of thumb on one side - numb. Probably like 60% of the whole digit is numb.
but also searing pain.
It feels tight when I move it, like the ligaments or whatever are too tight. and it's a searing burning pain that appears to now be unrelated to movement. Previously it was when I moved it a certain way, now it's just constant.
if I touch it, it sears worse.
but yeah.
bit concerned about the numbness because that suggests nerve damage.
How can you do so much damage to a finger without any trauma? I just don't get why this keeps happening. My joints are so unstable that I can, while sleeping, completely cripple myself and that's terrifying.
well fuck. My legs don't want to respond to me. it's not that they hurt or are heavy, they just flat out don't respond. I was walking back to the door and then just... stopped and couldn't will them to move. I could stand, but I couldn't will my legs to step forward.
wtf? I assume this is a cfs thing but I can't recall having this happen before. I've had "i can't lift my arms/have no strength in my arms to even lift a glass" but i've not have my legs just stop responding.
it's like when I can't form words, the words are there but somewhere along the way there's a block and they can't come out.
I think i'm going to try not to move around more than strictly neccisary today. I have my computer set up, I have music, I don't need to get up. Husband can help me up the stairs if I need to pee.
But damn.
I looked into PIP/DLA earlier but they make it really difficult to even get the form. I can't do it online, I have to write a letter and ask for a form to be mailed to me which is fucking ridiculous.
I went to do that, my brain stopped working and I couldn't.
But I do think I really should claim it because when i'm having an attack I can't feed myself, I struggle to shower and clean myself and I need help getting up the stairs.
On a good day i'm just achy. On a bad day I can't even fucking walk or speak.
But i'll need to wait til I have the energy for the nonsense and have help filling it all in. I think they make it intentionally difficult honestly, out of spite. Every other benefit you can claim online or get the forms from the post office, there's no reason to make disabled people write a fucking letter asking for a form.
My head hurts. I feel stuffed up as if I have a cold. This is typical of my fatigue, but I could do without my legs refusing to work.
I'm not even tired, I just feel SICK and my body isn't functioning right.
I'm really worried about money. Husband lost his job in June and his last payment came through the end of the month. So July we've had only universal credit and my carers allowance coming in. We're down to £3k, from about £9k when he WAS working.
and i'm fucking terrified.
the cost of food is going up because of the drought, the kids are getting older and eating more, electricity and water prices are going up and we just don't get enough in to pay for anything.
we may have to start charging eldest "rent" because he does get a student loan, but he's living with us so we're still paying for his water and electricity use and all his food but because he's now an "adult", we don't get any child benefit or anything to pay toward that.
but yeah, in 6 weeks we've eaten through our savings.
the holiday we just did was not expensive, it was our yearly "leave the house so the landlord can do some work on the property" thing. It's not like we just jetted off to disney or something.
and that wouldn't usually wipe out everything. The problem is there's nothing coming IN but the same outgoing costs, costs that are about to increase.
i'm really really worried.
It's the school holidays too which is the most expensive part of the year because everyone's home.
Might be time to start claiming disability, but the energy required to go through all that shit just... eugh.

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beautiful feral pigeon. ive never seen a spotted one. it was even prettier irl, the spots are more crescents and so evenly distributed. stunning bird.
on our way home
it wasn't too stressful after a brief argument with husband about trains. i made the mistake of suggesting the 5.22 train even though we could take any train at any time. but once a time has been decided it sets in stone for him and then he gets pretty grumpy and short with everyone. ahh autistic black and white thinking. our dinner took longer than expected and we would have been really rushing so he finally conceeded the hour later train meant less stress.
i always book open tickets so we can avoid stress. it never works though, he stresses regardless.
but i did get to mooch around and explore a little more than last year which was nice.
i am exhausted though. this yearly holiday isn't a break for me, its really for the kids so i push myself to have things to do every day. ive pushed all week, ignoring the fatigue, the pain in my limbs, the headaches because making these memories is important to me and if we're spending all this money, damnit I'm making the most of every moment.
i got to rest a little at the inlaws because the kids could explore. but then we did the show and that was exhausting and because we don't drive, we have walked a LOT this whole time.
i will suffer for this.
but its the school holidays and the kids are old enough i don't need to get out of bed to care for them. they can feed and clothe themselves. so i will just sleep...
once we have returned all the kitchen to order and my dolls are back on their shelf. my mother decided to redo the hall floor so moved my stuff and im not overly happy about it. she better not have lost anything.
next year hopefully we won't have building work, so we don't come home to chaos.
bees, and vikings and chickens. also tractors and pigeons and goats and cows and sheep.and dogs
so many dogs to pet.
goats were more interested in their hay but i pet them.
i did not get to pet the chickens i wanted to so bad. and the pigeons. there was one really friendly one who kept pushing its head towards me and i wanted tp scritch it soooo bad.
kiddo was grumpy and wouldn't let me stay too long in the bird tent, i was too excited about all the birds.
fil won awards for his honey again so that was cool. he made mead for the first time and came 3rd. dry mead tastes like wine, which i never knew. only mead I've had previously was sweet mead which is really sugary.
exhausted now.
lusted after a massive ride on mower that was £13000. fil also desired it. lol.
kids got to mess around on stationary tractors.
i got a teensy tiny Jesus figure and a bunch of other free swag too. whoo swag! tractor swag!
The whole concept of migraine triggers is just perfectly suited for making disabled people who are already suffering waste time & energy obsessing over every single thing they do every day, especially their diets, and to then blame themselves for their attack like their problem is a lack of discipline & willpower and not the fact that they have a chronic illness. If you get migraines, that isn't because your lifestyle & diet isn't sufficiently optimized, it's because you have a migraine disorder.
My neurologist didn't waste any time trying to get me to identify triggers and just got me on the right meds as soon as she could and I'm so glad she never made me feel like it was somehow my fault.
I'm now finally on a preventative that works for me & I literally don't do anything differently but I went from having daily migraines to sometimes not having a single one for over a week. I could do & consume every supposed trigger & still not get a migraine, when before the medication, I could do everything "right" every day for a week & still get a migraine every single day.
It's always like it's a medical disorder that causes your body to react badly to certain normal daily things & the goal should be to make it do that less, not to find ways to totally avoid all those normal daily things.
Yeah...they're caused by migraine disorders. Because people without them don't get migraines on a regular basis.
The chocolate advice is probably bullshit too. Unless you specifically identify it as something that makes your migraines worse (unlikely), it's way more likely to just be a common craving people have during the prodrome phase before the pain starts. If it's your body signaling you that it wants chocolate, there's no reason not to eat it.
Also, my neurologist said if you take triptans, take them during the headache phase immediately when it starts, not during the aura.
This isn't just my opinion btw, it's the current state of migraine research that shows that a) evidence for the belief that specific foods can trigger an entire migraine in someone who would've otherwise not had it is just not there and b) people are prone to misidentifying "triggers" and c) some "common triggers" have been shown in research to have protective qualities against migraines in some people and finally, d) the most up to date approach is to, instead of chasing possible triggers, raise your migraine threshold, which for some people can be achieved only with medication, but stuff like exercise & a nutritious diet could possibly also help you become more resistant too, once your threshold has been raised enough that you have the spoons for it, that is.
Learn more about how “triggers” may actually be signs of migraine prodrome and why identifying migraine triggers is not always easy.
Sometimes when people attempt to carefully track and avoid all their triggers, it creates a sense of guilt. When we think about it this way, the burden is on the person with migraine to avoid their triggers, and people may feel that if they experience an attack, it’s because of their own behavior. “Many times it is just the disease,” says Dr. Halker Singh. “This is the unpredictable nature of migraine. I think we carry enough on our shoulders as it is without the added stigma or guilt [around triggers].” Instead, we can shift to a healthier conversation about awareness in migraine management by learning to recognize prodrome symptoms and early signs of a migraine attack. This puts the focus on a deeper, more personalized understanding of each individual’s own unique experience with migraine. “I think making that shift is a little bit freeing and allows us to separate ourselves from migraine,” says Dr. Halker Singh. “My personal relationship with my migraine changes a little bit—I can separate from my own guilt and say, ‘OK, this is happening, what can I do about it?’” This kind of shift enables someone with migraine to focus more on self-care and addressing what their body needs in the moment during an attack.
New research reveals that 82% of suspected migraine triggers may be false. Learn how science is challenging traditional beliefs about migrai
Your diet can sometimes impact your migraine. Learn which foods are suspected triggers and how to adjust what you eat to help prevent or rel
One study compared headache activity between two groups of people living with migraine while they followed different diets. One diet eliminated foods commonly thought to trigger migraine attacks, and the other diet required patients to eat those same foods. Interestingly, headache frequency improved on both diets. This suggests that particular foods are not likely to trigger an attack, but rather that following a consistent, healthy diet may itself be therapeutic. In other words, feeling that you have control over your headaches may improve your headache symptoms. It also suggests that no single food is a trigger for all people living with migraine.
There's lots of people in the tags going well my dad's uncles grandma cut X out of her diet & it cured her migraines.
If you're a chronic migraine haver please please learn to ignore all of that. There's always going to be people claiming that doing keto/paleo/gluten-free or cutting out seed oils/sugar/MSG and taking 15 different supplements cured their chronic illness and migraine is much the same. I'm not saying they're lying, they can absolutely believe that's what happened but it doesn't mean any of that is going to work for you nor do you have to try it.
I had some of my worst most painful headaches while on strong painkillers, at the hospital, eating only bland low sodium vegan hospital food and getting fluids straight into my veins because apparently, the stress of surgery & recovery made my migraine disorder worse. Despite me being on Emgality. That's just what being chronically ill is like sometimes, there's not much you can do. Some of us can't self-optimize ourselves out of it, despite what every armchair neurologist & dietitian seems to think.
Sometimes the stress of constant headaches & migraines is what's causing your migraines because it's an evil disorder.
I know I do this all the time, but. Some people may read this and think, hey, wait, my migraines DO have a specific trigger and it's alcohol. I know alcohol is my migraine trigger because the pain comes on in about 30 seconds.
Hi. I love you. You have cluster headache. You don't have migraine. You have cluster headache. Look it up. I love you.
my triggers are heat and hormones. i can't control the weather and only going on cross sex hormones solved the hormone trigger. these aren't things i canjust discipline away ffs.
paaaiiin.
i think one of my pills got stuck in my throat, dissolved and is now burning me. drinking didn't ease it, eating doesn't help. it burns so bad

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surf shop came in clutch. got a short sleeved rash guard in a size up so its more comfortable and shorts.
pool was nice enough but im allergic to something they use in pools, i always get asthmatic just being near the pool. this was a salt water pool so its not chlorine, its something else.
middle kiddo also dunked me so i had a headache from water in sinus and was having trouble breathing for a while.
kids had fun, except eldest who pyched himself out of going on the slides and was beating himself up about it. poor kids really does get into his own head a lot.
got an uber back to the air b&b and the driver warned us to avoid the area we.walked through on Monday. he was all "that's where they put the dregs of society" but its just poor, poor areas are rough and dirty and a bit dangerous because they're poor, the people there aren't inherently terrible people or something. i already noticed it was an estate, the humping dogs, burned mattresses and shit everywhere was a good clue. but.i don't think these people are "dregs", that's implying some moral failing rather than simply a shitty situation. some of tḥe kindest people I've met have been estate folk.
this hill we are on, though it has amazing views, is a slum because until the 80s the ground was literally poisoned by the copper works and nothing could grow. where do you build your slums? on toxic ground nobody wants or can use.
im tired though. we did a fair bit today. lost the kids from about an hour to the retro game store lol. i knew they'd enjoy it, but i didn't think they would agonisingly paw through the whole collection. lol. they are such bloody nerds.
patty pal is a terrifying doll. the giant princesses looming were pretty intimidating too.
cool to see some bratz, though none took my fancy.
im trying to take photos this holiday because i often forget. its day 2 and im exhausted.
we climbed a hill day one. explored a beach and found a ruined pump house in the woods day 2.
today the kids want to go swimming at the waterpark.
they are probably old enough i can trust them to leave my line of sight but i always get paranoid around water. so long as they remain in their depth they should be fine, there's life guards and its aimed at families. but its still sttessful for me.
first i need to obtain a swimsuit. i couldn't find mine before we left, i havnt gone swimming in s few years so god know where it is. and i can't wear a t or shorts bra so ill need to buy a top too. bah. there's a stuff shop that hopefully will have what i need. its a pain in the arse though. this is why i don't go swinming, i have to wear things that make me overheat or out me and could endanger me. it fucking sucks.
the things i do for the love of these kids
im going to struggle if i keep up this level of activity, but what else can i do? i don't like saying no when it comes to "lets explore the outdoors" you know? but i don't want them going up that hill again without an adult, there's some iffy people around and there's a lot of large drops and literal cliffs. (see photo) so ill likely be dragged back up there later. youngest wants to see the relay towers.
i so wish husband would take over for a bit but hes grumpy and not being that helpful. hes also not as indulgant of exploration as i am so wouldn't let the kids poke around ruins and stuff.
i fell into some brambles yesterday and i sublocated my thumb dragging the suitcase so i kinda hurt. ho hum.
in Wales. took kids on a walk up a hill. met a horse. found a definitely haunted ruined house surrounded by woods and barbed wire.
gonna have to go back, get past the barbed wire and hopefully not get cursed.
So uh.. oxfam... i'm pretty sure that's not a children's book....
finally got to go to trans pride. so many people, it was incredible how many people turned up.
and i met the pride mando again. she's awesome.

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On the one hand, kinda disappointed I don't love any of the SDCC monster high reveals but on the other, my bank balance is relieved.
others will of course love the offerings, but I have never been a huge fan of the movie tie in dolls anyway. They aren't my vibe. I don't give a shit about the Living Dead Doll presents line either for the same reason. I don't feel a need for a doll cosplaying a gender bent version of a character from a horror movie. That's some people's jam, it's not mine.
But I do kinda want those universal girls. The trio are really basic in many ways, they feel like they're lacking something, but that's I think what appeals to me about them. I itch to restyle them, to play with the potential I see.
But i'm not even sure they'll be sold over here.
I do hope we see some g3 stuff, I want more playline stuff to get excited about.
I mean I don't have the energy right now, but I keep thinking about a destash. My lack of space stresses me out and the knowledge that I have so much stuff just in boxes all over the place fills me with guilt about buying NEW things.
so i'm thinking I need to set aside time to just do a big destash. Because I have a lot of dolls I only have because "rare" or because "interesting at the time" or whatever.
I think the first lot will be my Bratz girls. I have a LOT of them and I think I need to really strictly curate that collection to only the ones I find particularly special.
So that'll be the first step. The Bratz.
then I will have another look into the "everything else" category. I should destash a lot of rainbow high too but they're not really worth anything right now so that's a lot of work for not much gain. I'll keep the ones I really love and keep the clothing because that was always the main draw for a lot of them, the clothes. I love me some well made doll clothing.
I do have a lot of somewhat obscure and random dolls about but none of them have much intrinsic value and they don't take up that much space, not like the bratz, omg and rainbow highs who take up multiple boxes. THOSE are the ones I need to rationalise down to a single box if not fewer. Much like with Rainbow High, the main draw for OMG was the hair and clothing, I enjoyed the funky variation in their styles though I never really warmed to their faces. So i'll keep a couple but I think the majority need to be rehomed honestly. I'll probably steal their clothes too, they fit a fair few other dolls.
But yeah, it's a LOT of work. I'll probably do the low value stuff in bundles to make it worth my time.
Because right now a big thing stopping me from deboxing stuff is that I have nowhere to PUT the doll once I debox them. So I have a pile of doll boxes and it's stressing me.
It's like, why am I spending money on things I can't enjoy because I have no space for them?
so yeah, I need to MAKE space.