Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS)


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Old 06-02-2007, 09:24 PM #1
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Hey

Desi - Thankyou so much for your sweet words. Thanks everyone! you have been awesome.

I am having such a bad day today - I am so frustrated and fed up. I got dropped twice again today. I don't know what is happening to my body and I hate it. The "paralysis" is getting worse and my arms are dying more and more. It has got to a point where they are so weak I can barely even press the "on" button on my computer let alone lift my arms from under the duvet or if they fall off the armrests on my wheelchair. I don't know. I hate it.

I am supposed to be at a Ball at the moment - but instead I am stuck in stupid bed, in stupidly evily huge amounts of pain, and I can't do this sort of thing anymore. I'm flat in bed in tears - all my friends are out at the ball partying. I told them to go - they said they were happy to stay, but I have NO choice about living with this disease - they do - and I won't let it ruin my friendships. It's just so so so isolating. Especially as today has been so bad that I just want to be able to get my mates to make hot apple juice with lemon, honey and ginger and then curl up in bed and gossip about something that isn't pain or just sit outside and swap ideas or jokes or just anything that is a distraction from THIS.

I don't know how much longer I can handle this. I am 21. I am at uni. And I guess another thing is that I have just realised how much worse I have got functionally/ physically in the year I have been at university.

It's so so hard and I just hate this so much. But there is no cure but persistence and time and things will improve.

Thanks so much for letting me vent.

Love

Frogga xxxxxxxxx
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Old 06-02-2007, 10:03 PM #2
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Hey there Miss Smartypants - on the other hand...you did get through the exam, which you make light of, but I'm sure - no, I know - that took a tremendous amount of will power, energy and determination. It's the spoon thing again - you used them all up on that, now you need a rest.

But you did really well, I'm sure you will get the .... just lie back and remember YOU *did that*. You need a quiet but engrossing film to watch, take your mind off that ball. Hey, they'll all have horrible hangovers tomorrow and you won't.

Oh yeah, make sure you're battoned down when they lurch in later completely wellied...at least there'll be tons of gossip tomorrow,
xxxxx all the best
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Old 06-03-2007, 12:18 AM #3
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I will sit by your bedside tonight, very quietly. Your victory in finishing out this term is far greater than the study efforts of all those other students put together. I am sorry about the price your body is extracting for this win.
And I am so proud of you for finishing out this term, and this year. You proved your mum quite wrong, didn't you.
Brava! Brava! Brava!
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Old 06-08-2007, 12:20 AM #4
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Dear Frogga,
Boy, you are really having a bad day. I know the toilet thing can be tough to do properly especially if your balance is off. Maybe you could get some type of commode toilet to keep in your bedroom and just hang in there until your balance gets back.I had Lidocaine IV done in June 2006 and I couldn't even lift my head off the pillow because later I fainted and could not leave my bed for 5 days. I used a comode and I hated it but it was the best thing for me to do since everytime I got up I would start to pass out because my blood pressure was too low. I am on the waiting list at the doctors for the Ketamine IV in-patient procedure,which I hear is supposed to be much toughier than the Lidocaine procedure. Are the pills you take now a follow-up to the Ketamine IV treatment you had previously?? Just curious so I know what to look for when I get it done within the next 6 months to a year.

I feel for you being in bed so much because I have just spent about 2 1/2 years in bed too. I've just learned that I can't do a thing about it so I make the best out of everything. I find humor and prayers get me through this RSD nightmare. You have to keep your mind focused on getting better and being stronger. I now say to heck with everyone else and do the best I can each day. Sure there are days I want to jump off a bridge from the pain...but there are no bridges around here and I can't even drive a car to get there:.) So, I keep moving on. I pray that your days are getting better as I pray for everyone on this web site.
Take care,
Kathy d.
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Old 06-26-2007, 10:34 AM #5
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Quote:
Originally Posted by frogga View Post
Hiya,

Sorry I have been away for a bit. I have been having a horrific time with the RSD at the moment and that has culminated with today's (Mondays) nightmare of a day.

My pain levels have been really up lately, and I have also lost more mobility and am now hoist dependent for transfers (apart from the rugby guys , who just pick me up like a baby). I rang my GP 10 days ago in hysterics of pain and he agreed to increase my ketamine to 25mg 4 times a day (as well as my other stuff).

However, over the last day or two I have become far floppier and paralysis has kicked in. (hahaha, unfortunatly only the bad bits not the good bits - so I can still feel EVIL pain). I now can't feel anything but pain from my feet up to my chest and can't move from chest down. I am breathless and have pain on breathing.

Basically, it now turns the ketamine shouldn't have been increased. This happened 10 days ago and because of the half life I apparently now have an almost toxic dose of ketamine in my blood and the only reason I am alive is because I have RSD. Bizzare hey? (as it's a general anesthetic at high long term doses, especially when mixed with other things - but because of the pain...). The drs have been trying to push me into hospital, but I'm a stubborn sod and refuse to go in - though I have been told if I deterioate any more I will be straight in there.

It took 5 hours this morning to get any movement at all in my body, and that was after several hours of passive movements from Becks (my carer) as I couldn't even control my wheelchair, use my environmental controls or anything and even then the movement was just enough to control my wheelchair. And, I have gone totally floppy. Even in full tilt in my wheelchair my head is falling off the headrest and doing exorcist movements if bumped at all...(difficult if you live in Bath!)

Then in the evening...I was in the kitchen with some of my friends and nobody had bothered to strap me into my wheelchair properly (as I was in a high angle of tilt and thus leaning backwards about 30 degrees). I slipped to the side trying to move closer to one of my friends, Nick, and fell sideways out of my wheelchair straight onto my head on the floor. I then don't remember what happened, but apparently ended up in a form of floppy headstand and forward roll ending up smacking into a cupboard. It hurt SO much. I just didn't know what to do!!! Ended up having to get my carer to come and hoist me off the floor whilst I had hysterics. We decided I really should give up on today and just get into bed and I went into the bathroom (with my carer outside the door). And. Fell off the toilet and managed to get both my arms caught so I couldn't move an inch as I was trapped between support bars, wheelchair and door. My carer ended up having to break into the bathroom, and as soon as she moved the wheelchair I passed out on the floor. So had to be rescued (again) by my carer and friends.

I'm scared I will end up in hospital. I know if I tell my doctor that I fell and landed on my head and damaged my neck again then I will be straight in hospital but I just can't handle it. Life is painful enough without being in hospital (and I have an exam on Thursday). I also fear that the paralysis is spreading and I am having more problems breathing (though this may be due to increased pain).

It hurts so much - I have so much else to deal with at the moment - I just can't handle this much pain etc with all the other symptoms and just generally with exams etc. AND, I refuse to ask for special consideration with my exam (eg that pain/ falls etc on top of having RSD are destroying my chances of a first this year) because I don't want to take "advantage" of being ill.

Ok. update - Tues morning. Well, I have managed to be out of hospital, breathing is still partially compromised, mega mega pain, totally floppy, fell headfirst off the toilet again - looks like will have to accept using sling in the toilet as well which I am VERY anti. Having to be in bed because I just can't sit up and have had to have my cot bars bolstered because my fitting spasms have kicked in. Oh, and my left side has gone really really bad. My neck is so so painful and I....

I'm just so fed up with all of this. It just feels so unfair - and I know that there is absoloutly nothing I can do and nothing the drs can do to help. The only thing I can do to help is either a) reduce the ketamine dose - but, it's the only pain killer that helps or b) accept that I will not even be able to be in the toilet on my own. Life sucks, I just am so fed up and don't know what to do. It's bad enough being at uni - I love it - but the jealousy of all these people who are pain free, who can walk, who can be themselves and don't have to rely on others for the stupidest things - just is so hard to deal with.

Sorry for the moan I'm just so fed up

Love ya

Frogga xxxxxxxxxxxxxxx
I will tell you that this all sounds just like Brooke... She falls off the toilet and out of the w/c.. YOU 2 really are goin through the same and I am praying for you also each day... I wish Brooke could get on the ketamine... She is two young to see Dr. Schwartman yet.. Nobody under 18... Its totally not far to anyone... God Bless you...
Betsy Ann
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Old 06-26-2007, 05:42 PM #6
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you know, girl, i think i'm feeling good enough to come over there and take care of you. i can stop and pick up molly on the way. hey - i used to be a travel agent! i can get us there for next to nuthin. and, i'll have you know, i am a wonderful cook (i just don't eat what i cook) and i will bring my guitar - if you can get a piano in there i can do music therapy with you.

i think i will write a song about all of you on here...

love you!
ang
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Old 06-27-2007, 06:02 AM #7
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I am NOT feeling well enough to go, but I'm going anyway! The rest of you can handle the care part... I am going so I can give her family an "attitude adjustment", if ya know what I mean.
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Old 06-27-2007, 08:19 AM #8
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WOOHOO!! house party at mine a go go then! Don't worry Rogue, I will make Molly, S and unrouley do the cleaning before you arrive so you can't pick up too many infections from any of the babies (2 dogs, 4 cats), but I have a spare hospital bed - though we may end up top to tailing! Molls, I'm sorry that you will have to let unrouley cook! I don't really eat properly since the RSD either.. (sending you a virtual bone to knaw on).

Allen, are you still up for it? Anyone else fancy a quick trip across here?

Mollsy - S was right about the maternal ballet dancing - she believes if we don't do it then my joints will fuse. She doesn't get they ARE fused and will not understand why they can't be bent back. Mum gets so frustrated she has been known to jump onto my legs to try and get them moving - I swear she took lessons from that nurse who created the heat treatment for polio (to reduce deformities through use of heat and strength by trying to break the spasm and then keep in the correct position).

And hey, if any of you need nursing care, I have mum AND Char and they are as bad as each other for dealing with RSD.

See you all soon!!

Love ya

Froggsy xxxxxxxxxxxxx
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Old 06-27-2007, 09:51 PM #9
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Smile Mad Mums, RSD Bibliography, Perfection enemy of the good?

I'm speechless. This is a rare occurrence...
I am a former ballet dancer [as you might guess by my avatar] and I do solemnly swear that it is NOT supposed to involve Mad Mums pouncing up and down and twirling unbendable bits. [you're supposed to do that to yourself, for Love Of Art! Ergo, in ballet masochism is OK, but sadism is not.]
About the ketamine pump... I will look in my unwieldy article database to see if there's anything... Speaking of my database; do you think I should just post my outsized RSD bibliography in the Resources section of Neurotalk RSD and let folks read through it (with Abstracts)? I keep fiddling with the Biblio trying to make it perfectly searchable with Index, Table of Contents, etc... but maybe I should just post it as is? it's rather excessive: about 900 medical/ scientific articles. but maybe perfection is the enemy of the good and i should just get it all out there to you?
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