Random Stuff I Can’t Think of a Title For

It feels strange that I’ll only be 26 for two more days. On Tuesday I turn 27. This is the first year I’ve felt like I’ve not really done anything of note- I got more ill and have spent more than half of it completely bed bound, but I’ve not been anywhere interesting, or done much.

Not sure what I’ll be doing on Tuesday. Have decided to get a nice takeaway that evening- either Lebanese or Sushi. I also want a birthday cake. Having a birthday cake is very important to me, especially since on my 16th birthday I didn’t get any (and I’d had two GCSE exams that day so my birthday being pretty much ignored didn’t make me feel better). Birthday cake is one of my favourite foods, especially with lots of nice icing.

I was torn between buying a new television or a new monitor (I’d saved a bit of money and got a refund from a cheap telly I tried and ended up not being as described- don’t say there’s a DVD drive if there isn’t!). I’ve ended up buying a 24″ Dell monitor, with a resolution of 1920×1200. I don’t like 16:9 resolution for my monitor (I need the extra height) and trying to find a 16:10 monitor these days is really difficult. This one has excellent reviews and I’ve bought a very good used version from Amazon to save about £40 on the new price, as it working is the most important thing to me. I’ll get the television in the future, probably around the time I get a Virgin box in my room (I’m well enough to watch stuff now and the streamed stuff isn’t quite as good as what I can get through the box). The new monitor will help me play World of Warcraft better and will make things a bit easier to see, so I’m looking forward to it. I could use the old monitor as a television temporarily (it has speakers and a HDMI connection) though I’m not sure I’ll be able to see it properly at a distance with my eyesight as screwy as it is.

My health has been variable. Had a good few days when it was really warm, then started going downhill a bit with lots of pain and mood swings and stuff. Was worried it was a relapse but it turns out I was about to start my period. First one that Johan has had to help me with (I have a Mirena coil which means I only rarely get periods- can go months or years without one) and he didn’t know what it was at first đŸ˜› Luckily as I’m wearing pads anyway it wasn’t really any extra work for him. Seems to be nearly over so hopefully my body will settle down again, as I was enjoying not needing as many painkillers and hate being all moody.

The incontinence pads the NHS provided me aren’t absorbent enough. I think my urinary retention over the past year has stretched my bladder, as when it completely empties there is a lot of liquid- over a litre at a time. It’s rare I can get it to empty completely (have loads of issues with it) but when it does it was too much for those pads to deal with. Luckily I still have plenty of the ones I bought myself which can handle my bladder emptying, so am using them again until it’s sorted. Unfortunately my carer wasn’t able to explain to the district nurses the situation properly (I said we needed to change for more absorbent ones- she said I wanted to order more), so the district nurse said we’d contacted the wrong people and that I need another assessment as I think she didn’t know I’d just had one) so I’m going to ask the GP to sort it, if I ever see her.

It’s frustrating when I word things very carefully to make sure what I need is really clear and then people reword it to something that doesn’t mean the same thing at all. Happens all the time and means things end up harder than they should be. I’m not blaming the carer for this- she didn’t know that her wording wouldn’t work or that it was an issue for me, but it’s still frustrating anyway.

I have finished playing Katawa Shoujo (a romance visual novel set in a school for the disabled in Japan). My favourite route was probably Hanako’s, though I enjoyed all of them except maybe Shizune’s. Shizune is too manipulative and it brought up some bad memories. I sometimes got really frustrated with Hisao, the main character, as he often acted in ways that were too different from how I’d act. It was really enjoyable and I liked it a lot. It does contain sex scenes but they can be turned off (I still wouldn’t recommend it for kids though). I thought the portrayal of disability was pretty realistic, and I related a lot to Hanako, Rin and Emi (I have aspects of all of them, though Rin thinks closest to how I do).

I’ve also caught up with My Little Pony: Friendship is Magic. I enjoyed season 3, but felt the ending was too rushed and confusing. It should have been split into two episodes. I don’t mind the outcome too much, but would have preferred more explanation. I’m interested in Equestria Girls which is coming out today in the US, so might have to see that when I can.

Still nothing from the OT or a social worker yet. I’m frustrated that I’m doing so well in some ways, but I’m stuck in bed because I’m waiting for an assessment. It’s not safe for me to transfer without a hoist and I’ve fallen too many times now to risk it again. I also want to rearrange my powerchair assessment but I can’t do that until I know when I’ll be able to get out of bed again.

My hair is annoying me. It’s a few inches long now and sticks out everywhere. I can’t get it to behave. I think I want to shave it all off as I much preferred it shorter and I’m still not able to look after it properly (touch makes me really ill). My noise sensitivity isn’t as bad now and I can be more upright than before so I’m hoping that I’ll be able to get it done soon if I wear earplugs and things.

We watched the Sony presentation at E3 online, and have decided to get a Playstation 4. Johan has put in a preorder and I’ll be buying it for his Christmas/birthday present. It looks really good, and the price is lower than we were expecting. It’s the first console we’ve been so impressed by we want it as soon as it comes out. Will mean a bit of saving but not too much and it’ll be easily doable. Being bed bound has its uses. (The main reason I don’t just buy a hoist and things is I don’t know what ones to get without an assessment first- I’d be quite happy to buy what I need if I knew what it was I was meant to be getting. There’s also the problem of sorting out maintenance and stuff like that, where if I stick with NHS or Social Services they are responsible for it all.)

Hopefully I’ll hear something from someone soon. I’m starting to get bored in bed- I have been here nearly constantly since November so I think that’s understandable. If it does look like it’ll be loads longer then getting a television and things will at least make it more bearable. I’m happy that I’m nowhere near as ill as I have been- severe ME beats very severe ME any day đŸ˜›

Twilight Sparkle is Favourite Pony

Danni wearing purple wig with pink at the front, surrounded by penguins.

I really like this photo of myself. Yesterday (Tuesday) I finally wore my wig, and I love it. I also got dressed and had my hair washed (took wig off for that). Had the best day I’d had in months so very happy. Bullet points for easiness.

  • I have a Tumblr now. Tumblr is cool. I’m at http://dannithepurplepenguin.tumblr.com/(Dannilion was taken) and I’m slowly figuring it out.
  • Still not spending much time on Twitter or Facebook. They are overwhelming. That is frustrating.
  • Spending lots and lots of time in World of Warcraft. Brilliant distraction.
  • Tiarna (my Gnome Mage) is now level 90. I now have two characters at level cap.
  • I saw the CFS team again. They are going to continue visiting me at home as long as I find it helpful. That is reassuring.
  • I need to see the GP again about stuff. Still getting kidney pain even though I’d been on antibiotics for the infection.
  • I have NHS incontinence pads/adult nappies now. First got sent the small which are tiny. Now have the medium which are too big but usable. Gateshead use Molicare, which are actually decent.
  • Still no sign of the OT. I wanna get out of bed!
  • Social services sent out a not-social worker to do my care review. Not-social worker quickly realised we need a full care review, not a quick “everything’s fine, sign here” as he was expecting. He said he’s going to yell at people for us. Made it clear we’re not coping.
  • Fortijuice seemed to help at first when mixed with lemonade, but then they made nausea really really bad. Need to contact dietician as I’m meant to be having three a day.
  • Eating has improved a bit, and I’ve gained some weight back, but food digestion seems broken. I’m bringing up food I ate over 12 hours later. And it’s still identifiable. And not nice at all. It’s also causing constipation.
  • My emotions have been all over the place for no apparent reason, though my mood overall has been good. Feels weird and frustrating, but it’s probably an M.E. thing.
  • My anxiety is still really bad. Still having panic attacks over things like the doorbell. Need to speak to GP about it as I have a solution (small quantities of benzos) but need to see if she’ll agree.
  • Am in ESA Support Group. That is a relief. Didn’t need a work capability assessment or anything.
  • Currently have Vicky and a new friend, Duck, staying over. This is nice. Duck is from Israel and is a big geek (and autistic).
  • Johan bought a bike. Then discovered he can’t ride up hills. We live in a very hilly area, halfway up a steep hill. We’re trying to figure out a solution.
  • The 24 hour Tesco has reopened. Johan can go there when it’s quiet (so late at night).
  • I need to catch up on Ponies and Doctor Who. Just need to have the right type of brainpower. I’m getting there though đŸ™‚
  • I have a grade 1 (least serious) bedsore on my bum. Need to keep an eye on it as I don’t want the skin breaking. It hurts (and has done for a couple of days). I really need a profiling bed.
  • I think I’m finally accepting that I’m severely disabled. Still don’t feel it though. Just means I now get surprised when people do things that are easy for those who aren’t severely physically disabled to do that I struggle with or can’t do at all.
  • Dairy Milk Marvellous Creations Jelly Popping Candy Shells is the best chocolate. And seems really hard to get around here.

I’ve probably missed loads of stuff. Still not great at the whole communication thing but a little better than I was. I want to blog more so I’m hoping this improvement lasts so I’ll have the spoons to do it. We’ll see đŸ™‚

Body Naughty

I wish my body would make some sense sometimes. I can watch Doctor Who and go on computer and play World of Warcraft. This is all yay! I feel okay so long as I don’t try and sit up or be touched.

Not being able to sit up (I keep fainting- highly inconvenient) means I’m stuck in bed (also because we not got a hoist). Not being able to be touched without becoming really ill means I have to be really careful about being washed, dressed, or moved (I can roll and shuffle a bit on the bed, but that’s about it due to muscle weakness and stuff). Also means that there’s very little personal care that my carers can do (if I have too much done, I get really ill for too long so they no want to do that).

Brain hasn’t been working for writing stuff which means no emails, blog posts or tweets for ages. Very annoying.  Still not heard from the OT or Social Services. Still having problems with the neighbours. Missed my second appointment with wheelchair services and looks like I won’t be going until a hoist is sorted. Missed loads of other appointments too, and having to accept that I can only have home visits now as can’t get out.

Bought Desire Z as needed keyboard on phone. Not as easy as tablet to use but much better than trying to type on touchscreen with hands that don’t work properly.

Missed Autism Awareness/Acceptance Day/Month, and ME Awareness Day/Week. Also Blogging against Disabled Disablism Day. I wanted to participate but beyond my capabilities.

Apart from a meltdown caused by missing the wheelchair assessment (I’m pretty desperate now for a wheelchair that fits and works for me) not been too bad on days I’ve  not had a wash or changed clothes or had teeth brushed or anything. If I have, then I really really ill (and for a while afterwards). Trying to manage it in bits. Pad changes are the most I can cope with, and even then if touched too much then make ill. Carers do more touching than Johan which means I do better when he does changes. Too ill to teach carers how to do pad changes properly.

Saw good friend. Didn’t make too ill. Made happy. Was good. Hope to see good friend again soon.

Still think I’d be better at running the country than the present government, even with current brain problems. Least I know who to ask for help and what’s fair.

Sorry blog post broken like body. Hope for proper post as soon as brain works for writing again.

Gorillas: Not As Good As Penguins

Not having the best week ever having acquired some form of infection that was making my temperature keep spiking at over 40C. Luckily it’s no longer doing that (instead hovering at 37.5C- higher than normal but not high) but I’m still rather ill with it, and need to remember not to move my head too much as it feels like it’s full of marbles and I get immense pain when I move it too quickly. Unfortunately Johan was too ill to contact the doctor for me so we don’t know what kind of infection (the wide variety of symptoms I had mean I could have been anything from kidney to gastrointestinal to ear, as I had symptoms of all of them) but it hasn’t killed me.

Cognitively I’m doing terribly. What I’m going to do is link a blog post I read today instead. I think I’ve read the same thing before, but it’s a funny metaphor for illness.

Disability is like having a Gorilla in your house

Phillip the Penguin Says Hello

Another bullet point update post as not doing great.

  • Johan’s legs started working last Thursday as quickly as they stopped. Still no idea what caused it, but he’s better now. He got home on Friday.
  • I stayed at the care home for a couple of days to let him get settled. I got home on Monday.
  • Care home said they’d contact social services for me as we need to speak to them. Not heard since but will give it a few days.
  • I’m really not doing very well. It’s an odd thing- I can do more in some ways (be propped up more, go on puter, watch telly) but a lot of my symptoms are worse and my thinking brain is now very very bad. Not doing things doesn’t make things any better though.
  • I have 2 weeks now to get the ESA50 back. We’ve not started it yet. I won’t be able to help, but we have had an offer of help to fill it in so I have asked Johan to contact them soon about it.
  • I have lots of appointments coming up and no idea when any of them are as they’re not in the calendar. I’m scared.
  • I think I might need some help with my mental health soon. I’m having major issues dealing with things. Not sure what help there is for someone who can’t really hold a conversation though.
  • I visited Johan twice in hospital. The second time he gave me a penguin. His name is Phillip, he is very nice and he has blue feet.
  • Having a specialist profiling bed and an air pressure relieving mattress helped me massively. I’ve had an increase in my pain levels since I got home.
  • I lost more weight while I was in the care home. I’m now underweight by every measure. Johan has lost the contact details for the dietitian.
  • My ability to communicate is getting worse.
  • I’m still mostly happy, and I could be a lot worse.
  • Penguins definitely make me happy.