Guest guest Posted August 8, 2006 Report Share Posted August 8, 2006 Well, you're in luck. There are automated systems available you can purchase that allow you to control things around your house by computer, and, i suppose, by portable remote control. They cost quite a bit of money obviously, due to all the wiring and other things the electricians and custom installers would have to do. I don't know about any mounts for camcorders specifically designed for a wheelchair but well, you could always duct tape a camcorder to one of your wheelchair arms, LOL. On 8/5/06, loki200673 <loki200673@...> wrote: > > My cousin had a highschool project to make a movie. This got me > thinkng, " boy, that sounds like fun. " Now, I have SMA II, and very > little movement, but I'd like to try this. Does anybody have any info > on camcorders, mounts to put it on my wheelchair, or adaptive > equipment that could help me out? > I'm also interested in technology to help me around the house. > Especially things that make it easier to operate tv, vcr, dvd, lights, > etc. > > Mike > loki200673@... <loki200673%40> > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 11, 2006 Report Share Posted August 11, 2006 Hey Larry, I have 2 handy pages on the HDI I keep on file from Yeoman's book on outcomes assessment. Send your fax # and I'll send it over. He mentions no criteria for judging the emotional/functional score but does give references to establish ranges of impact on the overall score. W. Snell, D.C. Hawthorne Wellness Center 3942 SE Hawthorne Blvd. Portland, OR 97214 Ph. 503-235-5484 Fax 503-235-3956 drpsnell.chiroweb.com >From: " Larry Oliver, DC " <dro@...> > " Chiro ListServe " < > >Subject: (unknown) >Date: Fri, 11 Aug 2006 11:56:02 -0700 > >Your wisdom is needed: We came across a Headache Disability Index >questionnaire. When scored it gives a percent of emotional and percent of >functional, the two equaling 100%. It is not clear to me how to interpret >those percentages. Does a functional score greater than 50% mean it is >more >of a functional problem? I appreciate your knowledge. Thanks. > >BTW if found it at www.clinicalhealthservices.com ><http://www.clinicalhealthservices.com/> . It can be scored on-line with a >nice printed report. > >Larry L. Oliver, DC >408 NW 7th >Corvallis, OR 97330 >dro@... >541-757-9933 > >The information contained in this electronic message may contain protected >health information which is confidential under applicable law and is >intended only for the use of the individual or entity named above. If the >recipient of the message is not the intended recipient, you are hereby >notified that any dissemination, copying or disclosure of this >communication >is strictly prohibited. If you have received the communication in error, >please notify Heresco Chiropractic & Associates, 408 NW 7th St, Corvallis, >OR 97330, 541-757-9933 and purge the communication immediately without >making any copy or distribution > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 7, 2006 Report Share Posted September 7, 2006 I just wanted to add that my son does have a one on one aide and he is in 1st grade- I wouldn't have it any other way. He gets his space but he also has the help right there when he needs it. I personally would rather her assist than another child who may or may not have a cold. I think with some of the kids, limiting the exposure to more germs is important- at least with my son I feel that it is. It has also helped him transition into school- he is used to having me near and he didn't want to go to school until I told him there would be someone helping him when he needed it. He was homebound for Kindergarten. Hopefully, the need of her being so close can dissipate and Brett can rely more on friends. His school has been phenomenal with all of our requests and gone the extra mile in every way possible- I feel very lucky! Kristal Mom to Brett- SMA II- 6-1/2 years old Visit Brett's website at: http://www.our-sma-angels.com/brett/index.htm Learn more about SMA: www.fsma.org www.smasupport.com (unknown) Thanks to all who gave info on my earlier post. I will get busy with calling and letters. This isnt a problem that has just started. I have fought with this school since PreK. I do know that If we were in a different county we wouldnt be having these problems. But we arent looking to move, and its the county and the schools responsiblility to accomodate to Zack and the other children. The buddy system gets old. He has tons of friends, but most ten year old children dont get the responsibility thing like they should. So even with them helping, the class is still waiting on him. Zack does speak his mind to us and tells us what he thinks and wants. He is so very much main streamed in every way possible. And there have been times where the friend was with him opening doors for him, but take off and decide they are done so thats leaves him where? I have looked at this from all different ways. Im not asking for someone to sit on top of him, just be there when he needs them. Its just our school system here. Didnt have this problem with the school when we moved away for a short time. Once again thanks a bunch and anything helps. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 7, 2006 Report Share Posted September 7, 2006 Very nice!!! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 7, 2006 Report Share Posted September 7, 2006 Bekka's soap sounds wonderful how can one get the receipe? Carol (unknown) This was suppose to be the infamous soap cake that Bekka makes.....but I tweaked her original recipe and add a couple of different oils and used my log mold. If you haven't tried Bekka's soap cake recipe you are really missing out on a rich creamy soap. The half n half with the addition of silk gives this soap it's rich creamy texture.........awesome!!! This soap is actually colored with pink oxide. http://www.flickr.com/photos/51707978@N00/ __________________________________________________________ Search from any web page with powerful protection. Get the FREE Windows Live Toolbar Today! http://get.live.com/toolbar/overview Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 7, 2006 Report Share Posted September 7, 2006 Wow, I'm really shocked by how many SMA kids have one-on-one assistance at school. This is actually common practice now? I'm only 22, it hasn't been long at ALL since I graduated, and I definitely never had nor wanted that kind of help as a kid. I had an aid to help me in the bathroom at a scheduled time, but that was all. The other kids would help me open doors and get books out of my backpack. I don't think I needed much help beyond that. And I never had an assigned buddy system, it was always just whoever was around at the time. My friends, the people I sat by, whatever. The kids never minded helping, usually they thought it was fun. And I learned how to ask for things politely and show appropriate appreciation. I wouldn't have had it any other way. I was such a painfully shy child; asking peers for help and explaining my needs helped me to develop some badly needed assertiveness. Besides, I eventually was able to leave home and go to college, where there definitely isn't anybody following me around all day at my beck and call. I'm glad I learned early on to rely on myself and the kindness of whoever happens to be around. If this is the trend for SMA kids now, I have to wonder where the funding and staffing are coming from. I've just started my student teaching in the special ed department of a local high school, and all I ever hear about is all the cuts they've made to save money. The resource rooms don't have any para eds, the self contained unit is full so kids get placed inappropriately, the secretaries who used to handle paperwork are gone, the classes don't have textbooks, the teachers have way more students in their classes than state law allows... I just hear nonstop stories about kids and teachers that aren't having their needs met because of fundingcuts, it surprises me that there are so many stories of SMA kids with the opposite experience. Just interesting is all. e Re: (unknown) I just wanted to add that my son does have a one on one aide and he is in 1st grade- I wouldn't have it any other way. He gets his space but he also has the help right there when he needs it. I personally would rather her assist than another child who may or may not have a cold. I think with some of the kids, limiting the exposure to more germs is important- at least with my son I feel that it is. It has also helped him transition into school- he is used to having me near and he didn't want to go to school until I told him there would be someone helping him when he needed it. He was homebound for Kindergarten. Hopefully, the need of her being so close can dissipate and Brett can rely more on friends. His school has been phenomenal with all of our requests and gone the extra mile in every way possible- I feel very lucky! Kristal Mom to Brett- SMA II- 6-1/2 years old Visit Brett's website at: http://www.our-sma-angels.com/brett/index.htm Learn more about SMA: www.fsma.org www.smasupport.com (unknown) Thanks to all who gave info on my earlier post. I will get busy with calling and letters. This isnt a problem that has just started. I have fought with this school since PreK. I do know that If we were in a different county we wouldnt be having these problems. But we arent looking to move, and its the county and the schools responsiblility to accomodate to Zack and the other children. The buddy system gets old. He has tons of friends, but most ten year old children dont get the responsibility thing like they should. So even with them helping, the class is still waiting on him. Zack does speak his mind to us and tells us what he thinks and wants. He is so very much main streamed in every way possible. And there have been times where the friend was with him opening doors for him, but take off and decide they are done so thats leaves him where? I have looked at this from all different ways. Im not asking for someone to sit on top of him, just be there when he needs them. Its just our school system here. Didnt have this problem with the school when we moved away for a short time. Once again thanks a bunch and anything helps. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 8, 2006 Report Share Posted September 8, 2006 In a message dated 9/9/2006 12:05:11 A.M. Eastern Standard Time, herdqueen13@... writes: Hi, my name is Susie.I'm new to soapmaking and would enjoy picking your brains! LOL I would like to start making and selling soaps for a little extra income. Any help would be most appreciated ~~~~~~~~~~~~~~~~~~~~~~~ Hi and welcome, Susie. Please take my comments in the helpful light I mean them in. Good soapmakers invariably make soap for quite awhile before selling it because there is so much to learn about making good soap. So, go ahead and begin making soap with an eye toward selling in the future, but if you want to make money now, you might look for something else. In addition, start learning about what it would take for you to start a business. It's not as easy as it looks! Beth _www.soapandgarden.com_ (http://www.soapandgarden.com/) www.saponifier.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 9, 2006 Report Share Posted September 9, 2006 yes it took my son who is 12 from 1 and a half til 9 yrs old to get the dianosis of pdd i had to fight at the school and take him from one dr to another trying to get it figured out what makes it worse is i still get people asking are you sure this is the right diagnosis it drives me nuts ,my 10 yr old his diagnosis keeops changing becus he makes more eye contact and can talk to drs they think maybe he isnt pdd but yet the teachers( autistic support) in the classes he is in say he shows the classis symptoms of the pdd autistic child it is very nerve racking he was dignosed at the a yr after his brother so he was 8 we battled trying to find out since he was 4.stick to it and if you dont feel it is accurate or there is something more dont be afraid to voice your objections and change drs . good luck to u dawn greenwood-osullivan <hex_1970@...> wrote: Hi, I am new to the group and the reason I have joined is because of my 4 year old son. Our family are new to aspergers and as yet are waiting to get our diagnosis in writing, he was diagnosed verbally in January after a year or so of trying to find out what was wrong. I am now teaching him at home as he did not settle into nursery and was bullied. He is bullied a lot even here by friends of his siblings. I was wondering if anyone else had found it so hard to get a diagonosis in writing. Our son has a mild form of aspergers, but I am finding he is getting worse as he gets older especially with his anger and obsessive behaviour. All new "The new Interface is stunning in its simplicity and ease of use." - PC Magazine Hosted by Sparkle Tags vickie Messenger with Voice. Make PC-to-Phone Calls to the US (and 30+ countries) for 2¢/min or less. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 9, 2006 Report Share Posted September 9, 2006 Hi and welcome to the group: I am new here as well. My 4-year old daughter is on the spectrum. We did not have any trouble getting a dx on paper, in fact just the opposite was true for us. has had since she was little a feeding disorder and that is what prompted the docs to look deeper into all her behaviors and dx her as being on the spectrum. We weren't even looking for a dx except for someone to help us help her to eat nutritious food. They asked if they could test her for autism and I agreed thinking nothing would come of it, but then they said she has many of the signs. After talking to the doc about it, I guess she always did display signs and I always knew she was wired differently than my other kids. I hope that you can get your written dx soon and get the help your little one needs. Good luck and again, welcome to the group. TERIMommy to 5, 10 HH, le, 8 HH, Brittany, 5 HH; , 4 HH, Autistic, feeding disorder; , forever 18 months, 13 days HLHS (Modified Norwood with Sano shunt; coarctation; Glenn & tricuspid valve repair, g-tube; became an Angel 6-22-06--I love you baby girl--Always & Forever))carepage name: Girlhttp://www.carepages.com/Login?seed=844556http://www.babiesonline.com/babies/p/peanutbutter5/http://knightfamily-adventures.blogspot.com/ (unknown) Hi, I am new to the group and the reason I have joined is because of my 4 year old son. Our family are new to aspergers and as yet are waiting to get our diagnosis in writing, he was diagnosed verbally in January after a year or so of trying to find out what was wrong. I am now teaching him at home as he did not settle into nursery and was bullied. He is bullied a lot even here by friends of his siblings. I was wondering if anyone else had found it so hard to get a diagonosis in writing. Our son has a mild form of aspergers, but I am finding he is getting worse as he gets older especially with his anger and obsessive behaviour. All new "The new Interface is stunning in its simplicity and ease of use." - PC Magazine Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 10, 2006 Report Share Posted September 10, 2006 Dawn check out this group HomeschoolingAspies it is for home schooling Aspie kids and you may get lots of advice, I home school my DS currently and did last year for 5th grade and this year 6th grade. there is also a book I recommend you check out "Homeschooling the child with Asperger Syndrome" by Lise Pyles the isbn# 1-84310-761-9 from JKP.com I would also recommend you find a social skills group ASAP to help him identify the bulling and to give him the skills to deal with it and lots of other things a good social skills therapy is worth its weight in gold :-) I love my sons therapist and she has helped him grow so much and handle things that I did not think were possible. 4 is young but if you state where you are maybe someone can recommend a good developmental pediatrician to help you work out a diagnosis. for insurance purposes and to get any state help its necessary. email me off list if you want Greta -----Original Message-----From: Autism and Aspergers Treatment [mailto:Autism and Aspergers Treatment ]On Behalf Of dawn greenwood-osullivanSent: Friday, September 08, 2006 3:30 AMAutism and Aspergers Treatment Subject: (unknown) Hi, I am new to the group and the reason I have joined is because of my 4 year old son. Our family are new to aspergers and as yet are waiting to get our diagnosis in writing, he was diagnosed verbally in January after a year or so of trying to find out what was wrong. I am now teaching him at home as he did not settle into nursery and was bullied. He is bullied a lot even here by friends of his siblings. I was wondering if anyone else had found it so hard to get a diagonosis in writing. Our son has a mild form of aspergers, but I am finding he is getting worse as he gets older especially with his anger and obsessive behaviour. All new "The new Interface is stunning in its simplicity and ease of use." - PC Magazine Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 11, 2006 Report Share Posted September 11, 2006 Hi Felicia, How long did it take for the cimetidine to start working for Blake? just curious how different it is from child to child. Thanks, Gretchen, 13 (waiting for test results....????) Felicia Olson <co_olson@...> wrote: Hello All, I have not posted in a while, I do read all the posts and I am sorry to hear of all the families that are struggling with the fevers and other symptoms. I would love to hear more on the conference since we were unable to attend. My son Blake 3, has been on Cimetidine for nearly a year now and fever free, knock on wood!! God Bless to All, Felicia Blake 3, Caitlin, 10 Alec, 1 , CO --------------------------------- Get your email and more, right on the new .com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 13, 2006 Report Share Posted September 13, 2006 wrote: > somethng's not right with > the way this stuff's posting If by that you mean in email the menu on the right sometimes covers up part of the text, I agree. I hate that menu. I don't use it but I have to fight it to edit the messages when I reply. notan Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 15, 2006 Report Share Posted September 15, 2006 OHMIGOSH!!!! How funny is that! Loree SORT OF reminds me of the time that I was in a huge line at Target and grabbed me in the crotch and said, " yea mommy, dry!! " Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 15, 2006 Report Share Posted September 15, 2006 lol!!! SORT OF reminds me of the time that I was in a huge line at Target and grabbed me in the crotch and said, " yea mommy, dry!! " kym Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 15, 2006 Report Share Posted September 15, 2006 Hi Sharon and others! Sharon's post reminded me of something my daughter's speech therapist told me years ago. The therapist has a beautiful voice and she sings songs to the kids all of the time to help them with their speech. She was so happy, at first, when a mom of a little boy with DS called and said that he started singing one of the songs at Wal-Mart while they were out shopping. Then the mom said, " PLEASE! Don't ever sing that song to my son again! " Apparently he was singing the song (quite loudly), " Where is Thumbkin? " very loudly, and was pronouncing the " th " as an " f " . Pretty funny! Terri Sharon wrote: > > Okay, I have been laughing about this one. I can just see her doing it. > > When was 18 months, was 5. I was cooking dinner, > kept trying to get my attention saying " poo poo " . Finally I > turned around, and had poop all up her back and front, oozing > out her diaper to the floor, and of course, smeared on the floor where > she had stepping in it. In my kitchen. I remember just sliding to the > floor, shaking my head and I said " Oh sh** " . (Now I honestly > don't curse, I am fairly strict about that, but this was one of those > times.) then sat down, shaking her head, and clear as a bell > said " Oh sh** " . I thought, oh great, the speech therapy is > working, can't understand half of the other stuff she says, but she > got that one out loud and clear. > Isn't it fun?!?!?!? > > Sharon H. > Mom to , (15, DS) and , (11) > South Carolina > > " Be kinder than necessary, for everyone you meet is fighting some kind > of battle. " > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 18, 2006 Report Share Posted September 18, 2006 You'll need to take the PCAT, get admitted into Pharmacy School, and make it through the 4 year program. Della On 9/18/06, ronald aguilar <ronrhon27@...> wrote: > I you're curently a pharmacy tech, and you wanted to continue your education as a pharmacist what do i need to take and how long? > > thanks, > ronald > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 18, 2006 Report Share Posted September 18, 2006 Hi Della, Isn't it 6 years now? I thought all the pharmacy schools discarded the traditional BS degree in favor of the PharmD? Or are you assuming he finished his first 2 years? Thanks, -- Life should not be a journey to the grave with the intention of arriving safely in an attractive and well-preserved body, but rather to skid in sideways, champagne in one hand, strawberries in the other, body thoroughly used up, totally worn out and screaming " WOO HOO - what a ride! " -------------- Original message -------------- From: Della <dhengel@...> You'll need to take the PCAT, get admitted into Pharmacy School, and make it through the 4 year program. Della On 9/18/06, ronald aguilar <ronrhon27@...> wrote: > I you're curently a pharmacy tech, and you wanted to continue your education as a pharmacist what do i need to take and how long? > > thanks, > ronald > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 18, 2006 Report Share Posted September 18, 2006 Hi and welcome...I had implants almost 3 years..saline. I just had them removed last Tuesday after being sick and not knowing why for over 2 years....read on ...it's your implants...no Ps will tell you but read here and go to www.explantation.com and read the stories there you'll know you are not alone. Good Luck. Where do you live ? karen Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 18, 2006 Report Share Posted September 18, 2006 Hi Maritza, Where are you? It sounds like you are having typical problems from implants. What can we do to help you? Lynda At 05:09 PM 9/18/2006, you wrote: >Hi, my name is maritza perez, >i just went into this web site becouse for the >past month i've been very ill, i had my >surgery about 1year ago and i have been >notecing my left implant has been deflating >alot, i read the web site about the >complacations of leaking implants, to my >surpriced i now know that it was not my >imagination as to why i have been so, so ill my >back has been hurting me a great deal specialy >the middle uppper back it goes all the way up to >the back of my neck, been having a flu like >symptoms having a dry cough that does not go >away, head aches, muscle ache and last but not >least my right leg has been hurting me all the >way to my ankle and the buttom of my foot. been >going to my physician which tells my it's just a >muscle spasm to the er thinking it was my hurt >because my left arm gets numb am also i have >been itchy every where, now my head has been >itchy like crazy and no one knows what is wrong >with me, please help am going crazy. > >__________________________________________________ > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 18, 2006 Report Share Posted September 18, 2006 > > >Hi, my name is maritza perez, > >i just went into this web site becouse for the > >past month i've been very ill, i had my > >surgery about 1year ago and i have been > >notecing my left implant has been deflating > >alot, i read the web site about the > >complacations of leaking implants, to my > >surpriced i now know that it was not my > >imagination as to why i have been so, so ill my > >back has been hurting me a great deal specialy > >the middle uppper back it goes all the way up to > >the back of my neck, been having a flu like > >symptoms having a dry cough that does not go > >away, head aches, muscle ache and last but not > >least my right leg has been hurting me all the > >way to my ankle and the buttom of my foot. been > >going to my physician which tells my it's just a > >muscle spasm to the er thinking it was my hurt > >because my left arm gets numb am also i have > >been itchy every where, now my head has been > >itchy like crazy and no one knows what is wrong > >with me, please help am going crazy. > > > >__________________________________________________ > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 18, 2006 Report Share Posted September 18, 2006 My dear Maritza, No, you are not going crazy, the symptoms you are suffering from are identicle to alot of other women who have come here looking for answeres. This includes myself. I came here last December looking for reasons for all my physical symptoms. I was so sick, and was told by a couple of doctors that it was all in my head. I was explanted in February. I have seen some improvement in my health, however, I still struggle with Chronic Fatigue and Fibromayalgia. We have many knowledgable women here who can help you understand what is going on inside your body. Keep coming and posting, we are here to care for you. Have a good night, maritza perez <maritza_perez9@...> wrote: Hi, my name is maritza perez, i just went into this web site becouse for the past month i've been very ill, i had my surgery about 1year ago and i have been notecing my left implant has been deflating alot, i read the web site about the complacations of leaking implants, to my surpriced i now know that it was not my imagination as to why i have been so, so ill my back has been hurting me a great deal specialy the middle uppper back it goes all the way up to the back of my neck, been having a flu like symptoms having a dry cough that does not go away, head aches, muscle ache and last but not least my right leg has been hurting me all the way to my ankle and the buttom of my foot. been going to my physician which tells my it's just a muscle spasm to the er thinking it was my hurt because my left arm gets numb am also i have been itchy every where, now my head has been itchy like crazy and no one knows what is wrong with me, please help am going crazy. __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 18, 2006 Report Share Posted September 18, 2006 Hi , Your letter just made me think of something. Have you been checked for Epstein Barr Virus? If not, you might want to have a blood test for it. If you are positive, anti-viral supplements can help you beat your chronic fatigue and fibro symptoms. My son and I are both EBV positive. Kenda > No, you are not going crazy, the symptoms you are suffering from are > identicle to alot of other women who have come here looking for answeres. > This includes myself. I came here last December looking for reasons for all > my physical symptoms. I was so sick, and was told by a couple of doctors that > it was all in my head. I was explanted in February. I have seen some > improvement in my health, however, I still struggle with Chronic Fatigue and > Fibromayalgia. We have many knowledgable women here who can help you > understand what is going on inside your body. Keep coming and posting, we are > here to care for you. > > Have a good night, > > > > maritza perez <maritza_perez9@...> wrote: > Hi, my name is maritza perez, > i just went into this web site becouse for the past month i've been very > ill, i had my surgery about 1year ago and i have been notecing my left > implant has been deflating alot, i read the web site about the complacations > of leaking implants, to my surpriced i now know that it was not my imagination > as to why i have been so, so ill my back has been hurting me a great deal > specialy the middle uppper back it goes all the way up to the back of my neck, > been having a flu like symptoms having a dry cough that does not go away, head > aches, muscle ache and last but not least my right leg has been hurting me all > the way to my ankle and the buttom of my foot. been going to my physician > which tells my it's just a muscle spasm to the er thinking it was my hurt > because my left arm gets numb am also i have been itchy every where, now my > head has been itchy like crazy and no one knows what is wrong with me, please > help am going crazy. > __________________________________________________ > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 18, 2006 Report Share Posted September 18, 2006 Mammograms can rupture implants. Possibly there was something growing inside your implant that leaked into your body and is making you ill. You need to have the implants and the scar tissue that formed around them removed, we call it en bloc removal. The doctors you are seeing will not help you with the implant problem. Lynda At 05:40 PM 9/18/2006, you wrote: > > > > > >Hi, my name is maritza perez, > > >i just went into this web site becouse for the > > >past month i've been very ill, i had my > > >surgery about 1year ago and i have been > > >notecing my left implant has been deflating > > >alot, i read the web site about the > > >complacations of leaking implants, to my > > >surpriced i now know that it was not my > > >imagination as to why i have been so, so ill my > > >back has been hurting me a great deal specialy > > >the middle uppper back it goes all the way up to > > >the back of my neck, been having a flu like > > >symptoms having a dry cough that does not go > > >away, head aches, muscle ache and last but not > > >least my right leg has been hurting me all the > > >way to my ankle and the buttom of my foot. been > > >going to my physician which tells my it's just a > > >muscle spasm to the er thinking it was my hurt > > >because my left arm gets numb am also i have > > >been itchy every where, now my head has been > > >itchy like crazy and no one knows what is wrong > > >with me, please help am going crazy. > > > > > >__________________________________________________ > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 18, 2006 Report Share Posted September 18, 2006 Kenda, I don't know if I have been checked or not. I have had so many blood tests and I can't remember the names of any of them, I just know the results all say "normal or negative." I guess I will ask my GP when I see him next. Thanks, Kenda Skaggs <skaggs@...> wrote: Hi ,Your letter just made me think of something. Have you been checked forEpstein Barr Virus? If not, you might want to have a blood test for it. Ifyou are positive, anti-viral supplements can help you beat your chronicfatigue and fibro symptoms. My son and I are both EBV positive.Kenda> No, you are not going crazy, the symptoms you are suffering from are> identicle to alot of other women who have come here looking for answeres.> This includes myself. I came here last December looking for reasons for all> my physical symptoms. I was so sick, and was told by a couple of doctors that> it was all in my head. I was explanted in February. I have seen some> improvement in my health, however, I still struggle with Chronic Fatigue and> Fibromayalgia. We have many knowledgable women here who can help you> understand what is going on inside your body. Keep coming and posting, we are> here to care for you.> > Have a good night,> > > > maritza perez <maritza_perez9 > wrote:> Hi, my name is maritza perez,> i just went into this web site becouse for the past month i've been very> ill, i had my surgery about 1year ago and i have been notecing my left> implant has been deflating alot, i read the web site about the complacations> of leaking implants, to my surpriced i now know that it was not my imagination> as to why i have been so, so ill my back has been hurting me a great deal> specialy the middle uppper back it goes all the way up to the back of my neck,> been having a flu like symptoms having a dry cough that does not go away, head> aches, muscle ache and last but not least my right leg has been hurting me all> the way to my ankle and the buttom of my foot. been going to my physician> which tells my it's just a muscle spasm to the er thinking it was my hurt> because my left arm gets numb am also i have been itchy every where, now my> head has been itchy like crazy and no one knows what is wrong with me, please> help am going crazy.> __________________________________________________> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 18, 2006 Report Share Posted September 18, 2006 Maritza, I think it's your implants. You've got one that's ruptured! You need some good advice, which you can get here, about your options for getting rid of those things. Your symptoms don't sound like breast cancer. You're going to be OK. Keep writing, and pay attention to what info you get here on the list. We've all been through something like what you're going through. Hugs, Quote Link to comment Share on other sites More sharing options...
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