Guest guest Posted February 26, 2006 Report Share Posted February 26, 2006 > > how effective is DMPS cream? > That hasn't been studied. Oral DMPS works fine, is less expensive, and less risky. J > thanks again. > janey > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 1, 2006 Report Share Posted March 1, 2006 In a message dated 3/1/2006 1:08:38 PM Eastern Standard Time, beachbodytan2002@... writes: He can't hear the sounds of the letters of a word to try to spell them. He is doing very well with math, science, social studies. Thanks for reading. - Rose You should look at Dyslexia. You teach people with dyslexia in particular ways because they do not hear the individual sounds, cannot break words apart or put them together, cannot read fluently, etc. He may not need all that reading tutoring if you have a specific program being used such as orton gillingham. Just " general reading help " may not be good enough. More of the same that isn't working isn't a good solution. Roxanna ô¿ô Don't take life too seriously; No one gets out alive. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 1, 2006 Report Share Posted March 1, 2006 Dyslexia should be diagnosed by a reading specialist, not an OT. Orton-Gillingham is an approach used to teach children with dyslexia. Pete , a very well known special education lawyer, starts out his boot camps with the story of how he had SEVERE dyslexia as a child and was lucky enough to have parents who were ahead of their time. He was tutuored by one of the original founders of the Orton-Gillingham approach and he grew up to be a lawyer. _What is the Orton-Gillingham Approach?_ (http://www.ortonacademy.org/approach.html) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 1, 2006 Report Share Posted March 1, 2006 Yes, Roxanna! that is exactly what I've been telling the school. instead they give me more strategies to do with him. " It's not working " !!!! They gave him an O.T. eval and she said its not dyslexia & when she asked him to copy something she said he did o.k. (I'm not satisfied with that). Is there an outside place I can take him to to test him for dyslexia?. I'm waiting for Faxton to call us back. should I ask the speech therapist to test him for dyslexia? if its that, at least we would have another way of teaching him. Who should I ask to test him for dyslexia? please don't say the school. Should I also take him for a hearing test? if yes, what kind? He can hear. is there a special hearing test that he can take? What is Orton Gillingham? I do know that more of the same thing is not going to work. It hasn't worked yet. he can't read fluently but learned to memorize a story by looking at the pictures which can fool the teacher into thinking he can read. but, give him a new book, he reads like a pre-k. any advise I will try! I'm going to look into " orton gillingham " I've never heard of this but I will find out anything I can & try it. thank you - Rose kneeleee@... wrote: In a message dated 3/1/2006 1:08:38 PM Eastern Standard Time, beachbodytan2002@... writes: He can't hear the sounds of the letters of a word to try to spell them. He is doing very well with math, science, social studies. Thanks for reading. - Rose You should look at Dyslexia. You teach people with dyslexia in particular ways because they do not hear the individual sounds, cannot break words apart or put them together, cannot read fluently, etc. He may not need all that reading tutoring if you have a specific program being used such as orton gillingham. Just " general reading help " may not be good enough. More of the same that isn't working isn't a good solution. Roxanna ô¿ô Don't take life too seriously; No one gets out alive. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 1, 2006 Report Share Posted March 1, 2006 > > I'm going to look into " orton gillingham " I've never heard of this but I will find out anything I can & try it. thank you - Rose > Hi Rose Orton Gillingham is a multi-modal structured method of teaching reading. It focuses on teaching the sound/symbol correspondences in a very systematic fashion and has been proven to be very successful with individuals who have difficulty learning to read. Your schoold district ought to be able to help you with getting this kind of help for your son. The LD resource teacher can do the kind of testing that would highlight this kind of problem - there are many standardized tests of reading achievement that would document a reading difficulty. Hope this was of some help. Trish Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 1, 2006 Report Share Posted March 1, 2006 This was very helpful. Thank you drexel459 <trish459@...> wrote: > > I'm going to look into " orton gillingham " I've never heard of this but I will find out anything I can & try it. thank you - Rose > Hi Rose Orton Gillingham is a multi-modal structured method of teaching reading. It focuses on teaching the sound/symbol correspondences in a very systematic fashion and has been proven to be very successful with individuals who have difficulty learning to read. Your schoold district ought to be able to help you with getting this kind of help for your son. The LD resource teacher can do the kind of testing that would highlight this kind of problem - there are many standardized tests of reading achievement that would document a reading difficulty. Hope this was of some help. Trish Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 1, 2006 Report Share Posted March 1, 2006 Awesome information!. He is finally in a reading resource program at school. I knew I had to do something because everything I'm already doing is not working. so, Faxton Hospital got back to me. listened to my concerns about my son and said I need to have him come in for a Central authorial processing testing with a hearing test. that is part 1. next: while this is being done I will also get a reading specialist to evaluate him to test him for dyslexia, and I will mention about Orton-Gillingham. thanks to the support of everyone in this group. I can explain my concerns about my son and Know what to ask for and give - mention " Orton-Gillingham. " WOW!!! it does help when a person knows what to ask for because they(the school) sure do offer. Big thanks and hugs to you all!! I now feel by the time school is over my son will be able to read, write & spell. ( I will post it when he does).. - Rose ppanda65@... wrote: Dyslexia should be diagnosed by a reading specialist, not an OT. Orton-Gillingham is an approach used to teach children with dyslexia. Pete , a very well known special education lawyer, starts out his boot camps with the story of how he had SEVERE dyslexia as a child and was lucky enough to have parents who were ahead of their time. He was tutuored by one of the original founders of the Orton-Gillingham approach and he grew up to be a lawyer. _What is the Orton-Gillingham Approach?_ (http://www.ortonacademy.org/approach.html) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 14, 2006 Report Share Posted April 14, 2006 Hello Willow my daughter also had bad eczema. We just used the aveeno products on her. We made the oatmeal stuff into a paste and put it on her little noggin. Learned that trick from and it worked great. Your ped can write you an Rx for the band, you do NOT have to see a specialist if you want to save yourself some time. Sandy Willow's Mom (6-2-2003) Torticollis resolved (02-2004) Cranio Germany Grad (02-2004) www.geocities.com/samipa74/Willow_Lanette.html www.palmerfamily.armedforcesfamilies.com www.drmy.net/spalmer > > When you babies got their bands, were they really > uncomfortable and what were any skin reactions they > had. Logan already has severe eczema so I'm wondering > if he had to get one, how he would react to it, on the > plus side I guess he couldn't scratch his head anymore > > P.S. I emailed my ped about the referral to the neuro > > -Oregon > mom to alyssa former 30 weeker now 7 > kaelyn full term now 5 and > Logan 33 weeker now 7 months(may need banding) > > __________________________________________________ > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 14, 2006 Report Share Posted April 14, 2006 Logan has state paid insurance so I'm not sure if I can go straight for the band. I don't mind the referral. My ped is pretty quick about getting things done so hopefully it will be quick. thanks for all the help. I'll let you know what she says. heather-oregon mom to alyssa former 30 weeker now 7 kaelyn full term now 5 and logan 33 weeker now 7 1/2 months (may need banding) --- Sandy <samipa74@...> wrote: > Hello > Willow my daughter also had bad eczema. We just > used the aveeno > products on her. We made the oatmeal stuff into a > paste and put it > on her little noggin. Learned that trick from > and it worked > great. > Your ped can write you an Rx for the band, you do > NOT have to see a > specialist if you want to save yourself some time. > Sandy Willow's Mom (6-2-2003) > Torticollis resolved (02-2004) > Cranio Germany Grad (02-2004) > www.geocities.com/samipa74/Willow_Lanette.html > www.palmerfamily.armedforcesfamilies.com > www.drmy.net/spalmer > > > > > > > When you babies got their bands, were they really > > uncomfortable and what were any skin reactions > they > > had. Logan already has severe eczema so I'm > wondering > > if he had to get one, how he would react to it, on > the > > plus side I guess he couldn't scratch his head > anymore > > > > P.S. I emailed my ped about the referral to the > neuro > > > > -Oregon > > mom to alyssa former 30 weeker now 7 > > kaelyn full term now 5 and > > Logan 33 weeker now 7 months(may need banding) > > > > __________________________________________________ > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 15, 2006 Report Share Posted April 15, 2006 Fortunatley my son didn't have any skin reactions with his docband. He had redmarks from his starbands due to fit issues. I think I have read that some babies eczema gets better after banding and some have some flareups. Haylee mom to andre doc band grad > > When you babies got their bands, were they really > uncomfortable and what were any skin reactions they > had. Logan already has severe eczema so I'm wondering > if he had to get one, how he would react to it, on the > plus side I guess he couldn't scratch his head anymore > > P.S. I emailed my ped about the referral to the neuro > > -Oregon > mom to alyssa former 30 weeker now 7 > kaelyn full term now 5 and > Logan 33 weeker now 7 months(may need banding) > > __________________________________________________ > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 2, 2006 Report Share Posted August 2, 2006 , You could very well run into trouble increasing the Minocin while at the same time reducing the prednisone. If you are still incurring a lot of inflammation, then you need to consider staying on the higher dosage of prednisone until it subsides. If you increase the Minocin, do it slowly, and if in doing so an increase in symptoms occurs, you might want to back down to a lower dose until they subside, then try again. Remission is when symptoms are gone and lab values have returned to normal and remained stable over a period of time determined by your physician. Ethel rheumatic Another question > To group: I have a couple of more questions. I am weaning off of the > prednisone while increasing the Minocin. Is this okay? I am increasing > to 200mg Minocin and I am decreasing my prednisone from 9mg to 8mg and > hoping to decrease 1mg every 2weeks. My other question is...What > constitutes remission? Where do my stats need to be before I am > technically in remission? Do I go by my sed rate and my RA factor? And > is normal 0 and 20? > > > > Thank you, > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 2, 2006 Report Share Posted August 2, 2006 Ethel, Thank you for responding so quickly, this information helps me a lot. I do not hardly have any inflammation at all but if it gets worse with the increase of Minocin, I will increase the prednisone back to 9mg. ________________________________ From: rheumatic [mailto:rheumatic ] On Behalf Of Ethel Snooks Sent: Wednesday, August 02, 2006 11:01 AM rheumatic Subject: Re: rheumatic Another question , You could very well run into trouble increasing the Minocin while at the same time reducing the prednisone. If you are still incurring a lot of inflammation, then you need to consider staying on the higher dosage of prednisone until it subsides. If you increase the Minocin, do it slowly, and if in doing so an increase in symptoms occurs, you might want to back down to a lower dose until they subside, then try again. Remission is when symptoms are gone and lab values have returned to normal and remained stable over a period of time determined by your physician. Ethel rheumatic Another question > To group: I have a couple of more questions. I am weaning off of the > prednisone while increasing the Minocin. Is this okay? I am increasing > to 200mg Minocin and I am decreasing my prednisone from 9mg to 8mg and > hoping to decrease 1mg every 2weeks. My other question is...What > constitutes remission? Where do my stats need to be before I am > technically in remission? Do I go by my sed rate and my RA factor? And > is normal 0 and 20? > > > > Thank you, > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 21, 2006 Report Share Posted August 21, 2006 50/50 i think a biopsy is the same just like TX.that's why i feel that we all choose based on our own feelings and beliefsTim Parsons knoxville,tn 37931 865-588-2465 x107 work www.knoxville1.com How low will we go? Check out Messenger’s low PC-to-Phone call rates. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 3, 2006 Report Share Posted September 3, 2006 Carol – I slept flat on my back for about 8 months and didn’t move from that spot! I was scared to move – Just recently I’m able to sleep on my right side. The doctor didn’t specify how to sleep at all – the drugs made me quite sleepy so I lied pretty still all night. Lorrie From: [mailto: ] On Behalf Of Carol Sent: Sunday, September 03, 2006 6:16 PM Subject: [ ] Another Question The other question I just remembered is: What was the most comfortable sleeping position after revision--side or back? And did your doctor recommend or discourage one or the other? I have been sleeping on my sides since my surgery 32 years ago with a pillow between my legs, and rarely sleep on my back. Just because the back sleeping is too uncomfortable. Carol V (CA) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 3, 2006 Report Share Posted September 3, 2006 Hi Carol V, I think different surgeons recommend different sleeping positions based on the work that is done. I was told all through the hospital stay, to lie on my back only. Occasionally, they would prop me at a 30 degree angle. This went on after I got home for about 3 months. I was told at that point anything goes, what ever is comfortable. The surgeon promoted belly sleeping to stretch gluts but I only last about 2 minutes. I know others are told their sides and sleep like that in the hospital so I suppose it depends on the work done and the surgeon. > > Carol - I slept flat on my back for about 8 months and didn't move from that > spot! I was scared to move - Just recently I'm able to sleep on my right > side. The doctor didn't specify how to sleep at all - the drugs made me > quite sleepy so I lied pretty still all night. > > > > Lorrie > > > > _____ > > From: > [mailto: ] On Behalf Of Carol > Sent: Sunday, September 03, 2006 6:16 PM > > Subject: [ ] Another Question > > > > The other question I just remembered is: What was the most comfortable > sleeping position after revision--side or back? And did your doctor > recommend or discourage one or the other? > > I have been sleeping on my sides since my surgery 32 years ago with a > pillow between my legs, and rarely sleep on my back. Just because the > back sleeping is too uncomfortable. > > Carol V (CA) > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 12, 2006 Report Share Posted September 12, 2006 Jo wrote: > > sorry, i forgot, i was wondering if druing die off when a large number of toxins are being released if this could have an effect on the > strength of the immune system? and if it was therefore better to take > things very gradually ==>Yes, it is better to take things very gradually so you function okay instead of your body being overwhelmed by too many candida toxins being released at one time. And yes, toxins are affecting the strength of the immune system that is why the diet and supplements are so important. I had to be on the diet for 6 mos. before I could take antifungals and even then I was horribly sick (I wasn't working and I was single so I pushed through it, but my mother had to take care of me). > also i am studying nutrition with cnm, and i would like to learn about candidiasis in depth, could u recommend any sources? ==>The main sources I use are two books Copyright 1986: 1) Back to Health: Yeast Control, by Dennis W. Remington, M.D. and Barbara W. Higa, R.D., Publisher: Vitality House International Inc., Provo, Utah, 1986, ISBN 0-912547-03-0. 2) The Yeast Syndrome, by Parks Trowbridge, M.D. and Morton , D.P.M., Publisher: Bantam Books, 1986, ISBN 0-553-26269-0. Bee Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 9, 2006 Report Share Posted December 9, 2006 I had to give blood before my hip replacement. I had to give three units and the Dr. forgot to tell me until a month before surgery so we had to forget/ignore the usual rules about giving blood. After the third unit I was a little green around the edges for a while but I’m glad I gave because I needed all three units. I’m not a true “bleeder” but I do bleed more that most people during surgery. I tried to tell my back surgeon about this but he didn’t listen very well. He will the next time! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 9, 2006 Report Share Posted December 9, 2006 Lindy, I couldn't. Because of my veins, they can't get more than a fourth of a pint at any one time. I considered having a compatible family member donate, but my doctor said he didn't think it was necessary because blood transfusions from the blood bank are very low risk now with improved and more stringent screening than ever before. Regards, Donnalindy <everyothername.istaken@...> wrote: who asks more questions than moi? lol has anyone here given their own blood prior to the surgery in case you need blood after? or is anyone with a surgery coming up, thinking of doing this? hugs,~ linDUHlou ~RTHR/1/22/2007 Need a quick answer? Get one in minutes from people who know. Ask your question on Answers. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 9, 2006 Report Share Posted December 9, 2006 I gave a pint of blood before my surgery - they wanted me to give 2 pints, but I have very small veins and the Red Cross nurse couldn't find but one vein large enough. As it turned out, I did need two pints after surgery... Judy -- In Joint Replacement , " lindy " <everyothername.istaken@...> wrote: > > who asks more questions than moi? lol > has anyone here given their own blood prior to the surgery in case you need blood after? or is anyone with a surgery coming up, thinking of doing this? > hugs, > ~ linDUHlou ~ > RTHR/1/22/2007 > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 10, 2006 Report Share Posted December 10, 2006 has anyone here given their own blood prior to the surgery in case you need blood after? or is anyone with a surgery coming up, thinking of doing this? >>>> I did for my first & second... third doc said no cuz I was anemic. You can speak 2 your doctor about donations or call the red-cross in your area~ they'll advise you as to the step by step process. Just make sure if your interested in doing so... that you give yourself enough time~ AND CHECK YOUR MEDS if your taking them... some you have to stop taking prior to donating. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 10, 2006 Report Share Posted December 10, 2006 >>>has anyone here given their own blood prior to the surgery in case you need blood after? or is anyone with a surgery coming up, thinking of doing this? >>>> I did for my first & second... third doc said no cuz I was anemic. You can speak 2 your doctor about donations or call the red-cross in your area~ they'll advise you as to the step by step process. Just make sure if your interested in doing so... that you give yourself enough time~ AND CHECK YOUR MEDS if your taking them... some you have to stop taking prior to donating. I've always given 3 units (short units - my veins can't do normal size ones) before each of my replacement and revision surgeries (4 total surgeries). I've used every drop of those too! Felt much better each time afterwards. I'm one of those that runs anemic. My last donation was 6 yrs ago, drawn at our local Hospital and shipped across the State to the Hospital that was doing my surgery. The Hospital doing the surgery made me verify it was my signature on the blood packets, all 3 of them prior to getting wheeled into the operating room. I just wanted to suggest, if you are donating your own blood to use -- don't forget to verify what your Insurance will cover in regards to the donation, who they prefer to draw it etc. Not all Insurance carriers (at least in my experience) cover this the same and may have their own rules/regulations to follow. tanya Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 11, 2006 Report Share Posted December 11, 2006 Now that is great advice Sassy, and one I hadn't heard before - but is pretty obvious now it has been said. I donated my own blood and no one mentioned that to me. I wasn't on anything that had to be stopped, but I wonder if the blood bank would have stopped me if I had, and would they be aware? Valuable information on this group. Well done everyone. Aussie Margaret RTHR 1990 revised 2004 Re: another question (on the subject of storing your own blood) AND CHECK YOUR MEDS if | your taking them... some you have to stop taking prior to donating. | Send instant messages to your online friends http://au.messenger. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 11, 2006 Report Share Posted December 11, 2006 Hi, I gave two pints before my double TKR and boy am I happy I did. As it turns out, I needed to get both back on day #3 post Op. If I hadn't given my own blood I would have needed someone else's. Since it was my own I had no quams about getting both units. If you have a choice give the blood just in case. If not you I'm sure someone else will get good use out of it. Best Regards, Alan B. > > who asks more questions than moi? lol > has anyone here given their own blood prior to the surgery in case you need blood after? or is anyone with a surgery coming up, thinking of doing this? > hugs, > ~ linDUHlou ~ > RTHR/1/22/2007 > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 11, 2006 Report Share Posted December 11, 2006 in one of the books about joint replacement i just read it stated that giving one's own blood doesn't necessarily guarantee that if you need blood you'll get your own . . . that stinks. does anyone know if B Rh Negative is considered rare? hugs,~ linDUHlou ~RTHR/1/22/2007 Hi,I gave two pints before my double TKR and boy am I happy I did. As itturns out, I needed to get both back on day #3 post Op. If I hadn'tgiven my own blood I would have needed someone else's. Since it wasmy own I had no quams about getting both units. If you have a choicegive the blood just in case. If not you I'm sure someone else willget good use out of it. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 11, 2006 Report Share Posted December 11, 2006 I didn't donate my own blood prior to my surgery in August, but my primary physician advised me to do it for my other hip which will be done in January. He said " there is no blood better than your own " . Arianne > > has anyone here given their own blood prior to the surgery in case you need > blood after? or is anyone with a surgery coming up, thinking of doing this? > >>>> I did for my first & second... third doc said no cuz I was anemic. You > can speak 2 your doctor about donations or call the red-cross in your area~ > they'll advise you as to the step by step process. Just make sure if your > interested in doing so... that you give yourself enough time~ AND CHECK YOUR MEDS if > your taking them... some you have to stop taking prior to donating. > Quote Link to comment Share on other sites More sharing options...
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