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Old 09-25-2013, 08:08 PM   #1
KPeveler
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Ehlers Danlos Syndrome Thread

Calling all Zebras!

There seems to be a lot of us with EDS here on the DISboards, and just as there are threads for people with fibromyalgia or thyroid problems, I figured we could do with our own general thread. It is nice to meet others with the same condition, ask questions, and just get to talk even vent to others who understand what we are going through.

I am Katy, I live in Anaheim, CA (for now) and I have EDS: Hypermobility Type (HEDS, or under the old system, EDS Type 3/EDS3)


I also have a host of secondary conditions, including POTS/**, GI problems, and neuro damage and problems due to laxity in my spine. I probably have a tethered cord. I also have a neck fusion from C2-Occipital (skull). So I literally have my head screwed on straight. Before that, it was so loose my doctor was shocked I was not dead or a quadriplegic. There is some residual damage there too. I use a wheelchair full time when I leave the house.

I live down the street from Disneyland, so I go often. I am learning ASL. I have one small, very dumb but very sweet, kitty.

So that is me!

So if any other people with EDS, any type, around want to chime in, introduce yourself, just say hi, ask a question, anything, please join in! Welcome to the EDS thread!
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Old 09-30-2013, 04:33 PM   #2
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I was hesitant to post to this thread, because I'm not diagnosed with EDS yet, but I definitely have either EDS or something very similar. I saw a geneticist about a month ago who wants to rule out a bunch of other stuff first (she's very thorough, and I foresee myself showing up in a journal someday :P).

So, yeah, that's me. Hi.
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Old 10-15-2013, 07:47 AM   #3
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I suppose I should add my info.

I posted a thread some time ago asking about EDS in regards to my 13 year old DD. I had a couple doctors tell me she does not have EDS. Her Physical Therapist was great about encouraging me to continue finding answers as she continued to help DD13 with her pain and recurring injuries. Her PT was thinking recently that she has JRA. Her primary doctor researched rheumatologists who have good histories of really investigating her kinds of problems, especially when the symptoms aren't a perfect fit for any one particular diagnosis. We just saw the new rheumatologist this past Friday and she is very confident that DD13 DOES have EDS type III with POTS. She said that DD13 doesn't fit a nice little checklist for EDS but most definitely has it. I have to call later today to book an appointment with a cardiac geneticist just to make sure she doesn't have anything serious going on but the rheumatologist considers this something we're doing just to rule it out as opposed to thinking it's a likelihood (and I'm letting myself believe her).

My 15yo daughter was given a tentative EDS type III diagnosis last year but in her case she doesn't have any kind of negative symptoms from it as far as we can tell. She's just unbelievably flexible. I suspect she may have POTS issues going on but it seems as though she hasn't had any of her little dizziness episodes in quite some time so I'm hoping that now that she hasn't grown in over 2 years that it may be settling down or even going away (I've read that happens).

Anyway, DD13's issues involve a lot of pain in her feet, ankles and knees. She has custom orthotics for her feet since she basically walks on the inside of her feet without them (her ankles collapse inward and her feet are completely flat) and this helps a lot with the ankle and knee pain since it at least keeps her properly aligned. It's pretty rare for her to get any pain in her arms but she is prone to pain in the upper half of her back, her neck, and the base of her head. This back, neck, and head pain had eased up quite a bit when she went gluten free but it's back again. It also seems to only be bad when her GI symptoms are bad so I think it's more GI than EDS related but then again I've also been reading of ties between POTS and GI issues so I really don't know which direction to look. I think I need to focus on one thing at a time.

Anyway, that's us.
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February 2014 AKL: me, DH, DD15, DD13 * July 2013 DL offsite (Tropicana): me, DH, DD15, DD12, DSD30, DSSil * February 2013 WDW Poly: me, DH, DD14, DD12
August 2012 WDW FW Cabin & AoA Nemo: me, DH, DD14, DD12, DD12's BFF11 * February 2012 WDW Poly CL: me, DH, DD14, DD11 * August 2011 WDW YC: me, DH, DD13, DD11
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December 2009 WDW POFQ: me, DH, DD11, DD9 * February 2009 WDW Pop: me, DH, DD11, DD8 * August 2008 WDW SSR: me, DH, DSD25, DSD24, DD10, DD8
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January 1994 WDW offsite: me, DH, DSD11, DSD9 * January 1992 WDW offsite: me, DH, DSD9, DSD7
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Old 10-15-2013, 07:24 PM   #4
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Quote:
Originally Posted by utterrandomness View Post
I was hesitant to post to this thread, because I'm not diagnosed with EDS yet, but I definitely have either EDS or something very similar. I saw a geneticist about a month ago who wants to rule out a bunch of other stuff first (she's very thorough, and I foresee myself showing up in a journal someday :P).

So, yeah, that's me. Hi.
No problem - I actually first heard of and figured out I had EDS right here on the DIS! I just know there are a lot of us, and I figured at least now we have one thread if we have general questions or whatever. That and it is nice to know there really are a lot of zebras out there!
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Old 11-03-2013, 01:23 PM   #5
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Quote:
Originally Posted by clanmcculloch View Post
I suppose I should add my info.

I posted a thread some time ago asking about EDS in regards to my 13 year old DD. I had a couple doctors tell me she does not have EDS. Her Physical Therapist was great about encouraging me to continue finding answers as she continued to help DD13 with her pain and recurring injuries. Her PT was thinking recently that she has JRA. Her primary doctor researched rheumatologists who have good histories of really investigating her kinds of problems, especially when the symptoms aren't a perfect fit for any one particular diagnosis. We just saw the new rheumatologist this past Friday and she is very confident that DD13 DOES have EDS type III with POTS. She said that DD13 doesn't fit a nice little checklist for EDS but most definitely has it. I have to call later today to book an appointment with a cardiac geneticist just to make sure she doesn't have anything serious going on but the rheumatologist considers this something we're doing just to rule it out as opposed to thinking it's a likelihood (and I'm letting myself believe her).

My 15yo daughter was given a tentative EDS type III diagnosis last year but in her case she doesn't have any kind of negative symptoms from it as far as we can tell. She's just unbelievably flexible. I suspect she may have POTS issues going on but it seems as though she hasn't had any of her little dizziness episodes in quite some time so I'm hoping that now that she hasn't grown in over 2 years that it may be settling down or even going away (I've read that happens).

Anyway, DD13's issues involve a lot of pain in her feet, ankles and knees. She has custom orthotics for her feet since she basically walks on the inside of her feet without them (her ankles collapse inward and her feet are completely flat) and this helps a lot with the ankle and knee pain since it at least keeps her properly aligned. It's pretty rare for her to get any pain in her arms but she is prone to pain in the upper half of her back, her neck, and the base of her head. This back, neck, and head pain had eased up quite a bit when she went gluten free but it's back again. It also seems to only be bad when her GI symptoms are bad so I think it's more GI than EDS related but then again I've also been reading of ties between POTS and GI issues so I really don't know which direction to look. I think I need to focus on one thing at a time.

Anyway, that's us.

Ah, diagnoses have been given since. Congrats, I guess?

DD13, if not done recently already, have her feet and most importantly alligment during usage looked at. She wouldn't be the first (or last) where the ankle issue might already have a contributor in improper alligment within the feet. Easy enough to adress, but you do need to be aware about it first.

As far as the cardiac side; no need to tell yourself anything. I know the scary stories stick much more than the others, but they are not the norm. Cardiac issues to such an extend it becomes anything other but innocent are rare. Some issues aren't that uncommon and while the symptoms can be an issue, the most important thing is that they are innocent. And let's face it, the not innocent is what worries when just hearing a word cardiac, let alone when reading some of the stuff about vascular eds.


DD15; let's also not forget her being a teenage girl. It's not uncommon for girls in their teens to have a period of easy fainting etc. Maybe time will reveal her to be one of those girls.
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Does it really work that way? Doors closing, windows opening, can you really allways count on that? I'll just continue to wish, hope and pray to make sure. Knock on wood, one, twice and trice. Still can't believe it, I really get to visit Mickey again..........


Always keep wishing, dreaming and hoping.

Beyond greatfull for so many WDW trips, dear friendship and even a dlrp wish trip in october 2014 to close the Disney chapter. Lifes come and go, memories last for ever.
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Old 11-12-2013, 03:05 PM   #6
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Quote:
Originally Posted by goofieslonglostsis View Post
Ah, diagnoses have been given since. Congrats, I guess?

DD13, if not done recently already, have her feet and most importantly alligment during usage looked at. She wouldn't be the first (or last) where the ankle issue might already have a contributor in improper alligment within the feet. Easy enough to adress, but you do need to be aware about it first.

As far as the cardiac side; no need to tell yourself anything. I know the scary stories stick much more than the others, but they are not the norm. Cardiac issues to such an extend it becomes anything other but innocent are rare. Some issues aren't that uncommon and while the symptoms can be an issue, the most important thing is that they are innocent. And let's face it, the not innocent is what worries when just hearing a word cardiac, let alone when reading some of the stuff about vascular eds.


DD15; let's also not forget her being a teenage girl. It's not uncommon for girls in their teens to have a period of easy fainting etc. Maybe time will reveal her to be one of those girls.
I guess congrats? LOL It is a big help to at least have a direction to focus on. You really have been a LOT of help. I can't express enough how much all the info you've given me since I began this journey has helped, including with perspective (maybe especially with perspective?).

I realize that the serious cardiac issues are rare and she has no signs pointing to the likelihood of her having them so really I'm not stressing that at all. I haven't spent any time researching it which tells me I really am pretty relaxed about the possibility of it being something we need to worry about (in case you haven't noticed, my coping strategy for these things is research).

She definitely has problems involving alignment from her flat feet which causes some of her pain. Over the weekend she doesn't wear her orthotics which are what keep her properly aligned and by the end of the weekend her ankles and knees are in pain. No, that doesn't convince her to wear them. She likes being bare foot too much. She's a teenager. Sigh......

So far no fainting. Her PT has her keeping a journal of what she's doing when she suddenly feels dizzy so that she can be more aware of what movements cause it. So far there are some very clear patterns to which movements cause it which is good so she can be more cautious when doing those movements.

Thanks again!
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Multi-Allergy & Autism Dining Reviews: February 2014 * DL & LA July 2013 * February 2013 * August 2012 * February 2012 * August 2011 * August 2010


February 2014 AKL: me, DH, DD15, DD13 * July 2013 DL offsite (Tropicana): me, DH, DD15, DD12, DSD30, DSSil * February 2013 WDW Poly: me, DH, DD14, DD12
August 2012 WDW FW Cabin & AoA Nemo: me, DH, DD14, DD12, DD12's BFF11 * February 2012 WDW Poly CL: me, DH, DD14, DD11 * August 2011 WDW YC: me, DH, DD13, DD11
February 2011 WDW Poly CL: me, DH, DD13, DD10, DSD28, DSSil * August 2010 WDW POFQ & Poly CL: me, DH, DD12, DD10 * June 2010 WDW Pop: me, DH, DD12, DD9
December 2009 WDW POFQ: me, DH, DD11, DD9 * February 2009 WDW Pop: me, DH, DD11, DD8 * August 2008 WDW SSR: me, DH, DSD25, DSD24, DD10, DD8
September 2007 WDW Pop: me, DH, DD9, DD7 * April 2002 DLR offsite: me, DH, DSD19, DSD17, DD4, DD1.5 * June 2000 DLR offsite: me(pregnant), DH, DSD17, DSD15, DD2
January 1994 WDW offsite: me, DH, DSD11, DSD9 * January 1992 WDW offsite: me, DH, DSD9, DSD7
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Old 11-13-2013, 09:29 AM   #7
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Quote:
Originally Posted by clanmcculloch View Post
I guess congrats? LOL It is a big help to at least have a direction to focus on. You really have been a LOT of help. I can't express enough how much all the info you've given me since I began this journey has helped, including with perspective (maybe especially with perspective?).
You are SO welcome. I've never forgotten the warm bath I slid into when visiting the Dutch marfan board. Back than gp suspected me of marfan, so off I went to read up. It felt kinda fitting but not that eureka-fitting. They were the once that instinctively knew it would be connective tissue disorder and question would just be which. Through them I found eds, through them I learned where to get my info, through them diagnosis would follow. Paying it forward is easy enough to do, but can be so all important which these types of conditions that are too unknown within the medical profession.

I'm not always that great with the touchie-feelie so to say but do have real talents when it comes to knowledge gathering, processing, advocating, relating issues to gouvernment etc. and through my own life with eds have found that this is my statement in life to use that in order to try and pave the road for others just a little bit, whether it being eds-specific or more general in legislation. So when reading a topic like yours, it's a must to respond.


Quote:
I realize that the serious cardiac issues are rare and she has no signs pointing to the likelihood of her having them so really I'm not stressing that at all. I haven't spent any time researching it which tells me I really am pretty relaxed about the possibility of it being something we need to worry about (in case you haven't noticed, my coping strategy for these things is research).
Grin, we all need our strategies.

Quote:
She definitely has problems involving alignment from her flat feet which causes some of her pain. Over the weekend she doesn't wear her orthotics which are what keep her properly aligned and by the end of the weekend her ankles and knees are in pain. No, that doesn't convince her to wear them. She likes being bare foot too much. She's a teenager. Sigh......
A teen and a girl, most interesting combination. If she can see the link, discuss the possible long term issues, like not so easily pain relieve when wearing later on etc. Obviously she's still a child and will need guidance and can't (shouldn't) take 100% responsibility, but making her part responsible imho is a good thing. Just like you are raising her for daily adult life, you are also raising her to eventually manage her health, which includes making decisions like this, overseeing consequences and going the right path for her short and long term.

If it's pure esthetics; more and more can be done these days, but can take quite some shopping around. Whether it being insoles that are made in such a way they will fit most shoes right upto full orthopedic shoes that, where possible will now be made to mimic that shoe the child (or adult) loves the look of. Unfortunately $$ can be an issue, esp. making orthopedic shoes have nicer looks can add up and most plans do not cover the esthetic part of the bill (if already covering the medical costs). But if technically and financially possible, it might be a subject worth putting on the table with her.

Same goes for more aids, money and the right dealer can make the world go round when it comes to it not just being functional but also esthetically looking more attractive.

Quote:
So far no fainting. Her PT has her keeping a journal of what she's doing when she suddenly feels dizzy so that she can be more aware of what movements cause it. So far there are some very clear patterns to which movements cause it which is good so she can be more cautious when doing those movements.

Thanks again!
Sounds good! If amongst those moments are the going from sit to standing, from flat to sit etc. there could be a mild issue of pots in there. Good thing though, that as you said can be very managable with awareness and alternating behaviour like moving a bit slower or for instance having a bite to eat before getting up out of bed in the morning.

PT journaling; smart cookie! It's consuming, but also journaling her food, activities and pain levels can add to the info. All those can add to (feeling like) fainting or reducing it.
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Does it really work that way? Doors closing, windows opening, can you really allways count on that? I'll just continue to wish, hope and pray to make sure. Knock on wood, one, twice and trice. Still can't believe it, I really get to visit Mickey again..........


Always keep wishing, dreaming and hoping.

Beyond greatfull for so many WDW trips, dear friendship and even a dlrp wish trip in october 2014 to close the Disney chapter. Lifes come and go, memories last for ever.
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Old 11-27-2013, 04:30 PM   #8
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Glad to find this thread, I don't have it myself but I have a ton of friends I made on Instagram with it. Support for you all from me!
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Old 11-28-2013, 05:15 PM   #9
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Hi, there!

Single Mom with 3 kids. My oldest (DS13) was diagnosed with EDS (hypermobility) earlier this year and the geneticist 'unofficially' diagnosed me as well while we were there (no insurance, but have been having issues since I was a kid that no one picked up on). My other two children, DS5 and DD11 are going to see him in a few weeks. I'm so glad we can finally put one.. and one... and one... and one together as far as all the health issues are concerned.

Don't have time to type much today, but wanted to say hello!

Happy Thanksgiving!!!
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Old 12-15-2013, 12:23 PM   #10
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I don't think I noticed this board before! I'm another EDSer, with hypermobility type. I have what the geneticist called "some classical crossover", as my skin and small joints are involved. The only joint I have that is "normal" is my right elbow.

I don't post often and when I do they tend to be short (hands are one of my worst areas) but I'm on the DIS reading quite often. I would love it if this thread would stay going

ETA....come to think of it, the right elbow IS hypermobile, so I guess it's not normal. But it doesn't cause me pain or dysfunction yet!
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Old 12-15-2013, 03:36 PM   #11
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I realized I hadn't posted here so I might as well, although I'm generally fairly open about having EDS. I have hypermobility type, but some features from the other types. While I have all sorts of instability/other EDS issues, my real limiting factors are having severe fatigue and pain. Everything else I can work around.

Of relatively typical co-morbid conditions I have: dysautonomia (not typed), GI problems, Chiari Malformation (had decompression surgery), occult tethered cord syndrome (had detethering surgery), probably a mast cell disorder, intercranial hypertension, cervical instability (fused C2->skull, but have lower instability that we'll have to correct at some point), and other things I'm not remembering.

Not directly related, I have learning disabilities mainly centering on executive functioning deficits (mine is almost like non-verbal learningly disability, but not quite). I only mention that because I know quite a few EDSers who have conditions relating to executive functioning difficulties (autism, ADHD, NVLD, etc.). It's been a high enough percentage that I really wonder if there's something linking them.

I use a walker indoors and wheelchair outdoors. I started out with a manual wheelchair, but now I mostly use a powerchair because I ruined my, already bad, shoulders with the manual chair (bought 5 1/2 years before I got my EDS diagnosis).
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Old 12-20-2013, 05:33 PM   #12
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Originally Posted by WheeledTraveler View Post

Not directly related, I have learning disabilities mainly centering on executive functioning deficits (mine is almost like non-verbal learningly disability, but not quite). I only mention that because I know quite a few EDSers who have conditions relating to executive functioning difficulties (autism, ADHD, NVLD, etc.). It's been a high enough percentage that I really wonder if there's something linking them.

I'm one of those that have started to think that as well. Both my boys are on the spectrum, SPD, ADHD as well)
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Oct 2013 - Old Key West and POP!
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Old 12-20-2013, 10:46 PM   #13
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Quote:
Originally Posted by WheeledTraveler
I realized I hadn't posted here so I might as well, although I'm generally fairly open about having EDS. I have hypermobility type, but some features from the other types. While I have all sorts of instability/other EDS issues, my real limiting factors are having severe fatigue and pain. Everything else I can work around.

Of relatively typical co-morbid conditions I have: dysautonomia (not typed), GI problems, Chiari Malformation (had decompression surgery), occult tethered cord syndrome (had detethering surgery), probably a mast cell disorder, intercranial hypertension, cervical instability (fused C2->skull, but have lower instability that we'll have to correct at some point), and other things I'm not remembering.

Not directly related, I have learning disabilities mainly centering on executive functioning deficits (mine is almost like non-verbal learningly disability, but not quite). I only mention that because I know quite a few EDSers who have conditions relating to executive functioning difficulties (autism, ADHD, NVLD, etc.). It's been a high enough percentage that I really wonder if there's something linking them.

I use a walker indoors and wheelchair outdoors. I started out with a manual wheelchair, but now I mostly use a powerchair because I ruined my, already bad, shoulders with the manual chair (bought 5 1/2 years before I got my EDS diagnosis).
I am another with ADHD, sensory issues, and social issues relating to body language and other non-verbal queues. I also have anxiety that manifests in a variety of ways.

I believe that there is a type of spectrum disorder which is not something like a combination of ADHD/ADD, sensory processing disorder, non-verbal learning disorder, anxiety, and autism/Asperger's qualities. I do not fit into any "box" nicely and I believe that when you have this many diagnoses with overlapping symptoms, there is often an unknown, undefined, or as yet undiagnosed disorder.

A friend of mine doing research into the genetics of anxiety and its overlap with other genetic disorders said there is evidence one gene connected to some types of anxiety is on the same gene as the one where hypermobility is found. I will try to find the studies she sent me abd post them here.

I too use a wheelchair for any distance more than around the house. I use a manual chair. I have a powerchair but I hate it. It is not well fitted to me and I find the shock absorbers are not as good as the vibration reduction I get from my manual chair!

I am looking at getting an addition for my manual chair like Wijit wheels. They are lever driven wheels which allow better pushing with less shoulder stress (it is more like a push up motion rather than traditional wheeling, plus a host of other benefits). I much prefer manual chairs to other options.

Anyone else (other than WheeledTraveler) who has had neck problems?

Also, has anyone ever heard of or experienced hearing loss as part of EDS?
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Old 12-22-2013, 02:54 PM   #14
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I do know a couple people with hearing loss and EDS. One isn't actually EDS diagnosed yet, but since they couldn't find any cause for the loss when it started, I wouldn't be surprised if it was EDS related (tbh, when I first suggested she look into EDS as an explanation for her overall medical problems, the hearing loss was one of my clues). The other I'm not sure about, but I've had it in my head for years that hers was also EDS related.

I have a friend with osteogenesis imperfecta (better known as "brittle bone disease"), another genetic collagen disorder, who also has hearing issues. I think hers relate to the **. I don't know, though, whether hers would be bone problems or hypermobility (yes, people with ** are often hypermobile in joints that aren't effected by a nearby bone breaking).
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Old 12-22-2013, 04:28 PM   #15
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So far my only neck problems are from vertebrae subluxing from muscle spasms pulling them out of place. My PT Is pretty good at gently getting them back into place. If only they would stay that way! I do have stenosis but it's not causing any issues.

I have a lightweight transport chair my husband pushes me in for long distances or when my hip is out. I don't have the ability to push a wheelchair, so around the house I use a rollator and scooch around with my feet when needed.
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