Guest guest Posted August 29, 2007 Report Share Posted August 29, 2007 They are definitely still in business. Try: www.sundancerebounders.com When you get on that page, there are different ones you can click on. Ours is the 50 " mega soft. Let me know if that works. Rhoda Re: Trampolines > > My kids love it. They used it so much that I ended up > having to replace it again seven months later. I just > replaced it on August 18th (my son's birthday). It is > in the middle of the family room and they take turns > jumping to music on the television. I will never go > another winter again without one. > > All the best, > > Jill > > __________________________________________________________Ready for > the edge of your seat? > Check out tonight's top picks on TV. > http://tv./ > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 29, 2007 Report Share Posted August 29, 2007 Hi , My sister-in-law with CFS (or is it CFIDS?) has breathing difficulties. It scares me at times when I see her or talk to her on the phone. On another topic.... I was wondering, I know of a mother (from an autism group) that had child on the spectrum and she suspects that her child is suffering from CFS as well. Would you mind if I gave her your email address? I think you will be very helpful to her. Thanks, Jill ________________________________________________________________________________\ ____ Moody friends. Drama queens. Your life? Nope! - their life, your story. Play Sims Stories at Games. http://sims./ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 29, 2007 Report Share Posted August 29, 2007 Thanks!! On Aug 29, 2007, at 9:47 AM, Rhoda Boyd wrote: > They are definitely still in business. Try: > > www.sundancerebounders.com > > When you get on that page, there are different ones you can click > on. Ours is the 50 " mega soft. > > Let me know if that works. > > Rhoda > Re: Trampolines > > > > My kids love it. They used it so much that I ended up > > having to replace it again seven months later. I just > > replaced it on August 18th (my son's birthday). It is > > in the middle of the family room and they take turns > > jumping to music on the television. I will never go > > another winter again without one. > > > > All the best, > > > > Jill > > > > __________________________________________________________Ready for > > the edge of your seat? > > Check out tonight's top picks on TV. > > http://tv./ > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 29, 2007 Report Share Posted August 29, 2007 Good OTRs who are trained in sensory integration/regulation issues can be very helpful in identifying what to do to get the necessary input--and when...and how...and teaching the kids to start to recognize these needs and how they can go about getting their needs met. Respirtatory dysregulation could be considered a type of sensory regulation issue, I would think ann On 8/29/07, <thecolemans4@...> wrote: > > No he sure isn't. I sometimes think briefly of that, > but it quickly escapes my mind. But he does love deep > proprioceptive input - squishing, deep pressure, etc. > He doesn't particularly show that many signs, though, > of sensory problems that stand out as classic to me > ... but then, he did last year - tepid water was > 'hot', any little bump 'hurt'... while he was deep in > CFIDS. > > I was thinking that it is dysautonomia, though. > That's one of the things trampolines can help regulate > from what I read. He has this breathing dysregulation > too (which I think can be part of the symptom but I > haven't looked it up lately) - sighs and 'gasps' and > stuff, and it comes and goes without obvious triggers. > I know he's going to have a rough time when I hear > him start doing this. It's not anxiety that I can > tell, though I do think he's more anxious and > irritable when it's happening. > > I wouldn't be surprised if dysautonomia and sensory > dysregulation go together or are one and the same. > > Thanks for the suggestion... > > > --- Ann Osterling <aosterling@... <aosterling%40gmail.com>> wrote: > > > Is working with an OT for sensory > > integration/self-regulation > > issues? Use of deep pressure, as you can get from a > > trampoline, can be a > > very effective way of improving regulation, > > attention, alertness, etc. If > > this is working, you may want to see if an OT who is > > trained in sensory > > regulation issues is available to help you identify > > additional ways to > > achieve this improvement. Isn't it great that the > > teacher saw such a > > difference? > > ann > > > > > > On 8/28/07, <thecolemans4@...<thecolemans4%40> > > > > wrote: > > > > > > Hi - > > > > > > I think I've mentioned this before, but want to > > share > > > w/you all again. > > > > > > After reading Dr Klimas talking about rebounders > > for > > > CFIDS, I had bought the boys a trampoline > > (w/enclosure > > > of course) to see if it helped w/his CFS > > last > > > year. It did. > > > > > > I think I also mentioned it seems to make him > > sharper > > > and brighter mentally. He had been having some > > good > > > days at school, then last week regressed pretty > > badly. > > > Yesterday we had a call from the teacher and a > > long > > > note (and you could pick up her frustration). > > Today > > > she called to ask what we had done or said because > > he > > > was sooo much better today ... very on task, > > hearing > > > directions immediately, etc ... The only thing > > > different was he had spent at least 1/2 an hour on > > the > > > trampoline last night for the first time in a > > week. > > > > > > That thing is cool. This isn't a proven hypothesis > > > here, but it really does seem to increase his > > focus a > > > great deal. > > > > > > So anyway - I'm throwing that one out there again. > > I > > > would love to know if anyone else has had this > > > experience too. > > > > > > Later- > > > > > > > > > > > > __________________________________________________________ > > > Choose the right car based on your needs. Check > > out Autos new Car > > > Finder tool. > > > http://autos./carfinder/ > > > > > > > > > > > > [Non-text portions of this message have been > > removed] > > > > > > __________________________________________________________ > Moody friends. Drama queens. Your life? Nope! - their life, your story. > Play Sims Stories at Games. > http://sims./ > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 9, 2011 Report Share Posted August 9, 2011 >2a. Re: White water rafting > Posted by: " " christinejones51@... christinejones333 > Date: Mon Aug 8, 2011 8:28 am ((PDT)) > >Oh, sorry to butt in on a different subject but I just bought a 'family' >trampoline.... Is that a big no no for my achon daughter? My daughter has had >decompression surgery. Lailou is nearly 4. Any further advice most welcome. > , the Medical Advisory Board docs told me to stay away from trampolines. Given the achon spine, landing on our back/neck the wrong way, or, a fall on the metal or off the trampoline could cause serious injury. We used the trampoline in gym when I was in junior high school (35-40 years ago) and I never had a problem, but once I was told not to use it by the doctors, I stopped. The chances of anything bad happening probably weren't real real high, but given what could happen (paralysis, spinal damage, etc) my thinking was " why take the risk? " . Digest Number 5003 > >There are 9 messages in this issue. > >Topics in this digest: > >1a. ear infections and ear tubes > From: candilux_tade >1b. Re: ear infections and ear tubes > From: Casey Hubelbank > >2a. Re: White water rafting > From: >2b. Re: White water rafting > From: My Email > >3a. Re: Knee docs around DeKalb, IL? > From: Tolliver >3b. Knee docs around DeKalb, IL? > From: Tolliver > >4. UPCOMING EVENTS,REMINDERS,NOTICES FROM CHAPTER 13 D4 > From: Michele Charbonneau > >5. UPCOMING EVENTS,REMINDERS,NOTICES FROM CHAPTER 13 D4þ > From: Michele Charbonneau > >6. loan or grant > From: Ebarb > > >Messages >________________________________________________________________________ >1a. ear infections and ear tubes > Posted by: " candilux_tade " canditorres@... candilux_tade > Date: Mon Aug 8, 2011 8:28 am ((PDT)) > >Hi everyone, >I am new in the group, and still not sure how it works... I have a question, and i would love some help. My nephew is 6 Y.O. he has achondroplasia and he suffered from several ear infections.. After a while, the doctor recommended ear tubes to drain his ears. They worked wonderfully, he could hear better and no more infections!! and after a while they came out. Now, he has lost some hearing.. ( not sure if this is permanent) and the doctor wants to treat the ear infections with more meds.. but there is some concern about putting new tubes ( more permanent ones). My question is.. have you gone through something similar?? any suggestions or comments?? is it worthwhile to put the ear tubes?? >Thanks for your help!!!!!! ;-) > > > > > > >Messages in this topic (2) >________________________________________________________________________ >1b. Re: ear infections and ear tubes > Posted by: " Casey Hubelbank " caseyhubelbank@... caseyhubelbank@... > Date: Mon Aug 8, 2011 9:08 am ((PDT)) > >Hello, > > As this will be an ongoing issue, you would probably want to look into >permanent T-Tubes in the ears. Replacing tubes every couple of years will >lead to significant scaring which will lead to hearing loss. Doing it once >with the t-tubes will last several years. I had them for 15-20 years. I can >tell you that it was absolutely necessary in my case. In the past couple >of years they have come out. I haven't had an infection yet so it seems as >though I have grown out of them at this point. I went snorkling for the >first time a couple months ago and loved it. My wife (also in her 30's) on >the other hand who also had them for a similar amount of time and also >currently lost them, has had some minor infections over the past couple of >years easily treated with drops and antibiotics. (nothing like we had when >we were kids) > >-Casey > > > > > >On Sun, Jul 31, 2011 at 10:35 PM, candilux_tade <canditorres@...>wrote: > >> ** >> >> >> Hi everyone, >> I am new in the group, and still not sure how it works... I have a >> question, and i would love some help. My nephew is 6 Y.O. he has >> achondroplasia and he suffered from several ear infections.. After a while, >> the doctor recommended ear tubes to drain his ears. They worked wonderfully, >> he could hear better and no more infections!! and after a while they came >> out. Now, he has lost some hearing.. ( not sure if this is permanent) and >> the doctor wants to treat the ear infections with more meds.. but there is >> some concern about putting new tubes ( more permanent ones). My question >> is.. have you gone through something similar?? any suggestions or comments?? >> is it worthwhile to put the ear tubes?? >> Thanks for your help!!!!!! ;-) >> >> >> > > > Quote Link to comment Share on other sites More sharing options...
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