Guest guest Posted August 23, 2004 Report Share Posted August 23, 2004 Hi Pattie, Welcome to our group. >>>>I've been reading the posts frequently and have gone through the files. I started the diet and am adhering to it strictly, except that I am still eating organic plain yogurt. ===>Well done for starting the diet Pattie. As Robin mentioned it would be better to make your own yogurt if you are having commercial made. Commercial yogurt lacks proper fats (the higher the fat content the lower the lactose/sugars), often does not contain proper bacterial cultures and is much higher in lactose because they do not culture it long enough. >>>>I am also in the process of weaning off coffee. I refuse to do this cold turkey because I have tried it before and got skull shattering migraines. ===>I hear ya. I went off coffee recently but I weaned myself gradually. But the weekend I stopped I got a horrible migraine for about 18 hours - thank goodness it was the weekend. I just prayed it wouldn't last long, which it didn't. Like Zack suggested maybe having pau d'arco tea would help you wean - it helped me a lot. >>>>I'm how quickly die off might begin to occur, because other than the vaginal itching, (which was not impacted at all by any of the > suggestions I received) and two itchy spots on my arm, I feel great! ===>Like Robin says you might not have die-off symptoms on the diet and that's a good thing. You could probably start on the antifungals and probiotics sooner than others. > The VYI seems to be calming down, but the outside skin is still very itchy. For your itching have you tried coconut oil applied directly? It is an antifungal too and very soothing. It is important to alternate antifungal treatment with probiotic treatment for vaginal yeast. You could also make antifungal and probiotic creams by mixing powders in pure cold cream and applying them directly. Also try epsom salts baths. >>>>Also, is there any problem with using a topical benydryl to control itching? ===>It is better to try a more natural treatment first. Use benydryl only for emergencies like when you are attending an important function. Bee Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 25, 2004 Report Share Posted August 25, 2004 Hi and welcome to the group!!! Isn't it amazing how many hoops we sometimes have to go through to get a correct diagnosis? ~hugs~ Repeat after me… " Not all Psychologists are created equally… nor do they all understand Aspergers! " At least you did get the school to do evaluations over the summer and now are in a position to get appropriate care! On my son's team (which changes from year to year) I have every professional that is currently working with my son. That has included his OT therapist, his PT therapist, the facilitator of his social skills group, his counselor, the psychologist, the school professionals working with him, as well as any extracurricular leaders that have an interest in his educational wellbeing. Many volunteered or were more than happy to be involved. Those that couldn't attend a meeting wrote letters containing their observations and concerns, which were then taken into account during the meetings. Congratulations to a good start to the year!!! Often the starts and " newness " is the hardest time for our kiddos, so perhaps he will have an excellent year!!! ~hugs~ Tyler has had a lot of help with social skills and pragmatics. Though he isn't quite " up there with the NTs " , he can hold his own now. Kids 3-5 years younger than he is adore him, looking up to him, and often feel he understands them better than the adults and peers surrounding them. (great improvement!) Though he is a bit behind, he is advancing and eventually (probably as an adult) will catch up to his peer group. Tyler was in a social skills group twice a week for three years. He also had training 4 days a week on boundaries and respectful behavior through martial arts training with an instructor who had a degree in not only martial arts but also in child psychology (and understands AS very well!!!) This training went on for almost four years. Currently, he is on break from both, but has learned to take social cues from the adults around him (we have definite signals we can give him that other kids don't seem to pick up on) and he is able to be involved in a wide variety of activities independently… It is my hope that eventually, he won't need the cues from the adults, but can then take the more subtle cues from his peers as well… As far as elastic waist pants… No worries!!! ~grins~ If he is still needing them when he gets that big, you buy the inseam to fit and the waist about 4 inches too big. Then you take your sewing machine and insert your own elastic into the back. With long shirts being the ongoing thing for high schoolers, no one will be any the wiser that he has an expandable waistband!!! I have had to do this for kids before and have wondered if it wouldn't be more comfortable for me (I don't really like the look of elastic, but it sure seems like it would be more comfortable!!!) Good luck, and again… WELCOME!!! ~hugs~ Rabecca Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 25, 2004 Report Share Posted August 25, 2004 > Thanks for your response Rabecca! , I'm at the same point as you so I also appreciate Rabecca's response! My son is 5 and starting kindergarten soon. I'm worried. He's extremely smart ... I was thinking as were many of my friends that perphaps he is gifted. I think he's just really bright and because he can concentrate and focus so well and has an obsession with numbers and letters, he can appear gifted. He's certainliy my little gift though! <big grin> I picked him up at school yesterday and he was all alone in the sandbox while ALL the other kids were playing together. They were all kind of loud and running around playing tag so I think he just couldn't handle it. It took him 5 minutes to acknowledge me ... all the other kids were going over to him saying " your mommy is here! " over and over and he just walked in circles looking at the ground. Breaks my heart but I guess I'm lucky that he's not like that always. The rest of the evening alone with me and my 2.5 year old he was engaging and " normal " ... hate to say that since it appears I think he's not! He's a darling and I'm actually quite fascinated by his thought process ... I just see a desperate need to get him some socialization help ... fortunately my cousin works with autistic kids and she's coming over tomorrow night to give me her opinion and hopefully some techniques to use at home to give him a headstart. I'll share whatever I learn with ya! We don't have an official diagnosis yet ... we meet with a neurologist September 7. Sounds like AS thought doesn't it? Kathy Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 25, 2004 Report Share Posted August 25, 2004 Hi Kathy, If possible, you might visit your son at school during recess. When my son was in kindergarten, parents volunteered in the class. i would always stay through recess and help my son socially on the playground. When the other kids at their snack, i would have my son sit with the group. If another kid had a character snack, my son liked I would point it out and saymy son likes Scooby Doo, too. And ask my son to say something about it. Which he would withmy promopting. If other kids said Hi to him, i would point it out to him and suggest that he say hi back. When the kids went to play, I would walk my son other there and have him join in. Still staying with the kids to help him with conversation. The other kids get to know me and they talk more to my son than they otherwise would. I continued to do this through 1st grade. He is doing well now without me. He'll be starting third grade in two weeks. i think this might help your son socially if you are able to go to his school during those social time. Hope this helps. Angels >From: " alexosmommy " <kshear@...> >Reply-Autism and Aspergers Treatment >Autism and Aspergers Treatment >Subject: Re: " New " member with questions >Date: Wed, 25 Aug 2004 16:54:24 -0000 > > > > Thanks for your response Rabecca! > >, > >I'm at the same point as you so I also appreciate Rabecca's >response! My son is 5 and starting kindergarten soon. I'm >worried. He's extremely smart ... I was thinking as were many of >my friends that perphaps he is gifted. I think he's just really >bright and because he can concentrate and focus so well and has an >obsession with numbers and letters, he can appear gifted. He's >certainliy my little gift though! <big grin> > >I picked him up at school yesterday and he was all alone in the >sandbox while ALL the other kids were playing together. They were >all kind of loud and running around playing tag so I think he just >couldn't handle it. It took him 5 minutes to acknowledge me ... all >the other kids were going over to him saying " your mommy is >here! " over and over and he just walked in circles looking at the >ground. Breaks my heart but I guess I'm lucky that he's not like >that always. The rest of the evening alone with me and my 2.5 year >old he was engaging and " normal " ... hate to say that since it >appears I think he's not! He's a darling and I'm actually quite >fascinated by his thought process ... I just see a desperate need to >get him some socialization help ... fortunately my cousin works with >autistic kids and she's coming over tomorrow night to give me her >opinion and hopefully some techniques to use at home to give him a >headstart. I'll share whatever I learn with ya! > >We don't have an official diagnosis yet ... we meet with a >neurologist September 7. Sounds like AS thought doesn't it? > >Kathy > > > > _________________________________________________________________ Express yourself instantly with MSN Messenger! Download today - it's FREE! hthttp://messenger.msn.click-url.com/go/onm00200471ave/direct/01/ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 25, 2004 Report Share Posted August 25, 2004 wrote: > My questions for you today are: > 1. What team of professionals do you guys have for your AS children? > And what do each of them do specifically? I have read about > developmental pediatricians and DAN doctors on the autism list serve I > also joined, but I can't figure out if they relate to an asperger kid. > 2. What have you all done in the way of teaching your AS kids social > skills and pragmatics? My son's biggest issue is out of control > behavior with kids and adults in the school and daycare setting. I long > ago resigned myself to the fact that he would only wear plain t-shirts > and elastic waist pants (though I am wondering how we will clothe him as > he gets to be a teenager!!). > Thanks, I am sure I will have more questions later. When Louie was in school (and for a while thereafter), he had an OT, a PT and an ST. His Physical Therapist helped him with his body sense, especially the sense of his body in space. The Occupational Therapist worked with him on manual skills, coloring, artistic expression, holding the pencil/pen/crayon in other than a primitive manner, things like that. The Speech Therapist helped him not only with enunciation and prosody, but also they did social stories to help him in various social interaction situations. You can find out about social stories online, BTW. That person also worked with his teacher (one of them, anyway( and then later alone on an course of Conversational English that did wonders for his ability to identify and understand idioms and like that. He also had a 1X1 aide since he tended to elope and to also melt down in heavy sensory input situations (like lunch). I'd recommend all three starting out, until you know just where you and your son stand. Annie, who loves ya annie@... -- People are lucky and unlucky not according to what they get absolutely, but according to the ratio between what they get and what they have been led to expect. ~ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 26, 2004 Report Share Posted August 26, 2004 , Tyler had PT to address his muscle problems. It seems, when he was a baby, he had very poor muscle tone. When he began to move, he didn't use all muscle evenly. Some developed and were overused due to being used for functions they were not intended for while others didn't develop and were sitting there basically useless. They strengthened his weak muscles and taught him how to move to better utilize all muscle groups rather than depending upon only a couple. The social skills group was actually organized by a psychologist who had noticed an extremely high population of kiddos on the spectrum at Tyler's grade school. It was run as an " extended curriculum " for those that needed it so that they were not pulled out of class time to participate. Instead, they met after lunch, when most of the kids usually hid from bullies or isolated themselves due to the over stimulation on the playground. The kids treated it as a refuge and none would miss it for the world after the first month (Tyler never wanted to be sick for fear of missing)!!! Tyler turns 14 next month. I was actually led to the program not only by his school counselor but also by his OT. We went in and talked extensively without Tyler before giving it a try. We initially signed him up for 3 months. When he made such tremendous leaps forward, the OT suggested we sign him up for the 3 year program. We did, and he took a bit longer to complete it than some, but complete it he did (and so proud we are!!!) I will privately send you a note I wrote earlier this year that really tells about what we have done, how far he has come, and what made the most differences for us… It is several months old, so probably isn't complete any more, but it is the most comprehensive letter I have probably written!!! ~hugs~ Rabecca Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 26, 2004 Report Share Posted August 26, 2004 Kathy, Doesn't it just break your heart to want him to fit in so badly and for his thought processes and instincts being so contradictory??? I loved and still love listening to Tyler's thought process... and he does WONDERFULLY well with younger children as well as one on one. Yet, in groups, he just doesn't have the " social skills " even yet at almost 14, and that is with lots of intervention. Yet, now that I have Tyler as a Teen and am seeing what other parents are going through, I think I will take my ASPIE and thank my lucky stars!!! Though he has trouble with subtle social cues or picking up on multiple cues or with massive stimulation... he is very bright, happy, fairly well adjusted, and now is back on an even keel emotionally!!! (he had trouble for the first time earlier this summer, which has now been helped with meds) Enjoy your son and his uniqueness... You will find his self esteem really flurishes with it and that you will have less problems than you would otherwise!!! ~hugs~ Rabecca Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 1, 2004 Report Share Posted September 1, 2004 Hi, I read your message and was wondering if you would mind emailing me the letter you wrote that tells of the things you have done and what has worked for you. I have a ten yr. old son. He has come a long way with just my efforts, but I am having major difficulities with his school because of his different needs and there are a few other areas I would like to address with his reactions, behaviors etc. Any information you have would be greatly appreciated. Judy ----Original Message Follows---- From: "rabecca_whalen" <rabeccawhalen@...> Reply-Autism and Aspergers Treatment Autism and Aspergers Treatment Subject: Re: "New" member with questions Date: Thu, 26 Aug 2004 03:52:43 -0000 , Tyler had PT to address his muscle problems. It seems, when he was a baby, he had very poor muscle tone. When he began to move, he didn't use all muscle evenly. Some developed and were overused due to being used for functions they were not intended for while others didn't develop and were sitting there basically useless. They strengthened his weak muscles and taught him how to move to better utilize all muscle groups rather than depending upon only a couple. The social skills group was actually organized by a psychologist who had noticed an extremely high population of kiddos on the spectrum at Tyler's grade school. It was run as an " extended curriculum " for those that needed it so that they were not pulled out of class time to participate. Instead, they met after lunch, when most of the kids usually hid from bullies or isolated themselves due to the over stimulation on the playground. The kids treated it as a refuge and none would miss it for the world after the first month (Tyler never wanted to be sick for fear of missing)!!! Tyler turns 14 next month. I was actually led to the program not only by his school counselor but also by his OT. We went in and talked extensively without Tyler before giving it a try. We initially signed him up for 3 months. When he made such tremendous leaps forward, the OT suggested we sign him up for the 3 year program. We did, and he took a bit longer to complete it than some, but complete it he did (and so proud we are!!!) I will privately send you a note I wrote earlier this year that really tells about what we have done, how far he has come, and what made the most differences for us… It is several months old, so probably isn't complete any more, but it is the most comprehensive letter I have probably written!!! ~hugs~ Rabecca Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 6, 2004 Report Share Posted December 6, 2004 , Just to get you started, there are several good books on Lyme disease, and two I have gotten from the local county library here in Houston, TX are the one by Lang, Coping With Lyme Disease http://www.amazon.com/exec/obidos/tg/detail/-/0805075631/qid=1102364274/sr=1 -1/ref=sr_1_1/102-2569286-1856124?v=glance & s=books And the one by Vanderhoof Forschner, Everything You Need to Know About Lyme... http://www.amazon.com/exec/obidos/tg/detail/-/0471407933/qid=1102364448/sr=1 -1/ref=sr_1_1/102-2569286-1856124?v=glance & s=books I think 's book is a little better, but founded The Lyme Foundation. Among good resources on the web are http://www.lymenet.org the Lyme Disease Network http://www.lyme.org/ 's foundations website Among others. You can also join the Lyme-and-rife group and be inundated with emails by people discussing Rife machines and other aspects of treatment for this devastating disease. By using Google.com, I've found volumes of information on Lyme on the web. I have yet to hear of a quick fix for late stage/chronic Lyme disease but different people on these groups give credit to different things they have tried: Rife machines, colloidal silver, Samento (a type of Cat's Claw herb) and others. Also, there is a new clinic forming called the Fibrolmyalgia and Fatigue Centers opening up in the USA, and perhaps you can gain some knowledge through their website. I personally believe that people with Lyme are often diagnosed with either or both CFIDS and fibromyalgia. http://www.fibroandfatigue.com/patient_support_resources.htm Good luck. Jan [ ] new member with questions hello, I am a new member from the UK, are there other uk members here? I dont know the protocol for this group so I hope nobody minds if I just plunge straight in. I am not certain whether I have Lyme, a naturopath I was talking to recently suggested to me that I probably have, though. I dont know much about it at all, and I dont know where to start. I have been quite badly ill with M.E. (CFS, CFIDS)for nearly nine years now, with some better periods and some worse. I have lost my marriage and my career because of my illness, I used to be a pretty good artist (at university level) but I have been too ill to paint for a long time now. The neurological symptoms are bad, I have severe cognitive problems, difficulty understanding things or working things out, poor short term memory and appallingly short concentration span. I tend to link these neurological problems to my old career as a dental chairside assistant where I was exposed to an awful lot of mercury on a daily basis for many years, we were not as careful or informed about it in the old days as they are in dental surgeries now. My mother had 'fibrositis' and some mental problems too, including anxiety and depression, my aunt has fibromyalgia syndrome and anxiety (and she is also a dental nurse, but she is still well enough to work), and my grandmother had 'bad rheumatism' .. I thought I must have FMS because I get so much physical pain, and I had been told that FMS was hereditory; but I recently saw a CFS specialist who did an examination and some minor tests, he says he thinks I dont have FMS, but I have CFS, because I dont only have the pain on the FMS pressure spots, but all over. so anyway, the Naturopath thinks we may all have had Lyme disease from birth, my mother and her sister and my grandmother and I, and that my 18 year old daughter may be at risk now too. she does get sick when she overdoes things, her health holds her back a little bit already. My grandmother came from Mullingar in Ireland, I have no idea what the tick situation is there. Please, can anyone here shed some light on any of this for me, or give me some advice? I don't know what to do next. I dont have much money to pay for private treatment either as I have to exist on benefits, (although I consider myself lucky to get those). I dont even know if British doctors are taking Lyme disease seriously, no one has ever mentioned it to me until recently. all the Best Questions and/or comments can be directed to the list owner at -Owner Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 12, 2005 Report Share Posted January 12, 2005 Hi Angel, I've had experience with a few different colon cleanses but found " Experience " (love the name) to be effective, gentle and convenient. My family also has a history of bowel problems including IBS, crohn's etc. but with a combination of " Experience " and " Synergy Defense " (improves digestion) these problems are now under control. Remember that your overall diet has a lot to do with it too and juicing vegetables helps a lot. We also take cod liver oil. Ken www.kenluanne.awarenesslife.com > > > Hi, > I just joined the group and am searching for a semi-easy colon cleanse. My entire family > has a history of constipation and various colon issues. I need to find a method of cleansing > my system and attempting to restore a healthy digestive system. > Does anyone have any recommendations? > Thank you for all your help! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 1, 2005 Report Share Posted February 1, 2005 You should avoid seafood for now. (Don't worry it's not a permanent thing! Only until your thyroid hormone level is back to normal) Seafood is rich in iodine. And normally it's one of the best thing to have in your diet. But for now you should avoid it. The doctors will not tell you this if you ask them (At least the doctors I've experienced). Yes. You should also avoid iodized salt. The reason you're abstaining from iodine-rich food is because your thyroid uses iodine in the body to produce thyroid hormone (this is commonly known to your doctor as thyroxine. Thyroxine is consisted of T3s and T4s.) When you have Graves Disease (a form of hyperthyroidism), you have excess amount of thyroxine in your blood. This excess of thyroxine leads to your various hyperthyroidism symptoms, such as racing heart, insomnia, rapid weight loss, excess phlegm, intolerance to heat, constant sweating, dry lips, thirst, among others. Yes. Eating food rich in iodine such as iodized salt will affect your RAI Uptake Scan test results. I would not recommend this test. So if you can, please avoid this. You should however, ask to take a Free T3 and a Free T4 Tests. These simple blood tests will indicate the level of your thyroxine in your blood which reflects the severity of your hyperthyroidism. If you have an enlarged goiter, I would recommend also taking an ultrasound scan of the thyroid. This test checks for nodules (bumps) in your thyroid and for any cancerous tissues. A TSH test is not as important but will help indicate the normalcy of your pituitary gland (This master gland tells the thyroid how much thyroxine to produce. It usually shuts down its production of TSH when you have hyperthyroidism). Your doctor will check your thyroid by asking you to swallow (He may have you drink some water beforehand) and feel your neck to gauge the size and shape of your thyroid (which is normally a butterfly-shaped organ). Here are some links that you may find helpful. http://www.thyroid-info.com/articles/hyperthyroidism-faq.htm#3 http://www.muhealth.org/~daveg/thyroid/thy_dis.html http://thyroid.about.com/cs/newsinfo/l/bltest_values.htm http://valkyrie.aarg.net/top20.html http://home.velocitus.net/deecee/krista.htm http://webhome.idirect.com/~wolfnowl/thyroid23.htm http://www.ithyroid.com/ http://phoenity.com/diseases/goiter.html http://www.labtestsonline.org/understanding/analytes/t4/sample.html http://www.amarillomed.com/howto.htm Take care. joey > > Of course I have questions.. lol.. Ok last week doc said.. you have > hyperthyroidism, we made you an appointment with the endocrinologist > in 2 weeks. Now I am freaking out, I read all I can but still can't > understand everything (too much too fast). Do I need to avoid iodinzed > salt? Could eating that make a false result on the test? I have > several signs of Graves Disease (including my eyes are 'puffy' a lot, > I thought I was developing allergies) and my husband has made a few > comments about my silky skin and I never use lotion or anything. Could > there be anything else besides Graves (like a tumor or cyst) that > still mimics Graves? I started having anxiety attacks last October and > depression last summer, and hormonal problems over two years ago, > could that have been the start of this then? Most importantly, what > can I expect to happen at the endo's? Thank you for any info. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 8, 2005 Report Share Posted February 8, 2005 Morning Brat, Melody posted this to over 20 boards I sent back a reply as well on one board. I do send out my topic posts to a large amount of groups due to the current DEA threat to those who practice pain management and those who need it. However, I did write Melody personally that her neurologist would send her to a neuro or ortho surgeon. Her neuro symptoms were non specific as opposed to her test results. God bless you losing a lung wow~ Hugs, In a message dated 2/8/2005 10:10:09 AM Central Standard Time, OZnDOT@... writes: HI MELODY AND GROUP,I'm sure many here can tell you better and give you the necessaryresources to look into based on the findings of your tests but Ithought I would say a little something.It sounds like the same symptoms I have had for awhile that due tomany Dr visits and Meds I have found a great deal of relief. Going tothe Neuroligist is about the best thing you can do at this point, he'sthe one that can correctly diagnose your condition.For me it was due to pinched nerves caused by arthritis in my neckcausing pinched nerves (the symptoms you describe). I also havescoliosis which is curvature of the spine and it curves at the neck aswell as the lumbar both of which causes these symptoms. In the lumbarof course it is the legs and feet which I have dealt with for years.One thing I will stress though when they offer you cortisone shots (ifthey do) they may or may not decrease the symptoms, one thing I cantell you is they WILL put the wieght on you quickly so be prepared to"exersize" or somehow deal with the cortisone so it doesnt just turninto fat.In my condition with only one lung (the other lost to Cancer) I couldnot exersize like I should have.I wish you all the luck in your diagnosis and hope you find the rightmeds to help with the discomfort of the condition.Sincerely,BRATPS> You've come to the right place!!On Mon, 07 Feb 2005 06:15:00 -0000, melodym22 <melodym22@...> wrote:> > > Hi All,> My name is Melody. I recently joined your group to try to find out> answers for my problems and to see if anyone has information or> experiences they can share with me. I have been suffering with> severe weakness, numbness and pain in my neck, back, shoulders,> shoulder blades, fingers, arms legs and feet for quite some time. I> recently had both a nerve conduction study and MRI of Cervical and> Lumbar areas. I will list the areas of concern here so if anyone has> experience with problems like this please write to me sharing your> experience of how to deal with these problems. I have an appointment> with a Neurologist tomorrow and have to ask questions of what is next> for me.> > Issues reported in my MRI Cervical are as follows:> > There is degenerative disc space narrowing at C3-C4, C4-C5, and C5-C6.> > C3-C4: There is broad based left paracentral, moderate size disc> protrusion, which indents the left anterior aspect of the cprd and> narrows the left neural foramina.> > C4-C5: Bilateral mild to moderate uncontrovertebral hypertrophy> results in bilateral neural foraminal narrowing. Spinal Stenosis is> present.> > C5-C6: A moderate and generalized disc buldge indents the anterior> aspect of the thecal sac and results in moderate spinal stenosis.> There is bilateral neural foraminal narrowing, secondary to> uncontrovertebral hypertrophy, right slightly greater than left.> > IMPRESSION: of Cervical MRI> > 1. Moderate spinal stenosis at C5-C6, secondary to a broad-based> posterior disc osteophyte complex.> 2. Mild spinal stenosis at C4-C5, with bilateral neural> foraminal narrowing, secondary to uncontrovertebral hypertrophy.> 3. Focal disc protrusion at C3-C4 just to the left of the> midline, with effacement of the left anterior aspect of the cord and> left neural foramina.> > Issues reported in MRI Lumbar Spine with out contrast.> > There is mild anterior sublaxation of L3 on L4, 3mm, secondary to> degenerative facet hypertrophy. There is degenerative disc space> narrowing at L3-L4, L4-L5, and L5-S1. Vacuum disc phenomena is> present at L4-L5 and L5-S1.> > L3-L4: A generalized disc bulge coupled with moderate degenerative> facet hypertrophy and marked redundancy of the ligamentum flavum> results in moderate to severe spinal stenosis. The inferior neural> foramina are narrowed, bilaterally.> > L4-L5: A gereralized disc bulge coupled with moderate degenerative> facet hypertrophy and redundancy of the ligamentum flavum results in> moderate spinal stenosis. The inferior neural foramina are narrowed,> bilaterally, left slightly greater than right.> > L5-S1: A mild generalized disc bulge coupled Hallenbeck~Sikorsky~ BS,RN,UM,QCOwner-Moderator"AnGeLsInPain"I have watched heart(s)shatter, fall to the ground only to break..."OneVoiceInPain"Interqual CertifiedPublished Psychiatric ResearcherAdvocate for those in CIP, HIV, Psychologic Pain"The Lord Will NEVER push us beyond what we can endure." Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 8, 2005 Report Share Posted February 8, 2005 HI MELODY AND GROUP, I'm sure many here can tell you better and give you the necessary resources to look into based on the findings of your tests but I thought I would say a little something. It sounds like the same symptoms I have had for awhile that due to many Dr visits and Meds I have found a great deal of relief. Going to the Neuroligist is about the best thing you can do at this point, he's the one that can correctly diagnose your condition. For me it was due to pinched nerves caused by arthritis in my neck causing pinched nerves (the symptoms you describe). I also have scoliosis which is curvature of the spine and it curves at the neck as well as the lumbar both of which causes these symptoms. In the lumbar of course it is the legs and feet which I have dealt with for years. One thing I will stress though when they offer you cortisone shots (if they do) they may or may not decrease the symptoms, one thing I can tell you is they WILL put the wieght on you quickly so be prepared to " exersize " or somehow deal with the cortisone so it doesnt just turn into fat. In my condition with only one lung (the other lost to Cancer) I could not exersize like I should have. I wish you all the luck in your diagnosis and hope you find the right meds to help with the discomfort of the condition. Sincerely, BRAT PS> You've come to the right place!! On Mon, 07 Feb 2005 06:15:00 -0000, melodym22 <melodym22@...> wrote: > > > Hi All, > My name is Melody. I recently joined your group to try to find out > answers for my problems and to see if anyone has information or > experiences they can share with me. I have been suffering with > severe weakness, numbness and pain in my neck, back, shoulders, > shoulder blades, fingers, arms legs and feet for quite some time. I > recently had both a nerve conduction study and MRI of Cervical and > Lumbar areas. I will list the areas of concern here so if anyone has > experience with problems like this please write to me sharing your > experience of how to deal with these problems. I have an appointment > with a Neurologist tomorrow and have to ask questions of what is next > for me. > > Issues reported in my MRI Cervical are as follows: > > There is degenerative disc space narrowing at C3-C4, C4-C5, and C5-C6. > > C3-C4: There is broad based left paracentral, moderate size disc > protrusion, which indents the left anterior aspect of the cprd and > narrows the left neural foramina. > > C4-C5: Bilateral mild to moderate uncontrovertebral hypertrophy > results in bilateral neural foraminal narrowing. Spinal Stenosis is > present. > > C5-C6: A moderate and generalized disc buldge indents the anterior > aspect of the thecal sac and results in moderate spinal stenosis. > There is bilateral neural foraminal narrowing, secondary to > uncontrovertebral hypertrophy, right slightly greater than left. > > IMPRESSION: of Cervical MRI > > 1. Moderate spinal stenosis at C5-C6, secondary to a broad-based > posterior disc osteophyte complex. > 2. Mild spinal stenosis at C4-C5, with bilateral neural > foraminal narrowing, secondary to uncontrovertebral hypertrophy. > 3. Focal disc protrusion at C3-C4 just to the left of the > midline, with effacement of the left anterior aspect of the cord and > left neural foramina. > > Issues reported in MRI Lumbar Spine with out contrast. > > There is mild anterior sublaxation of L3 on L4, 3mm, secondary to > degenerative facet hypertrophy. There is degenerative disc space > narrowing at L3-L4, L4-L5, and L5-S1. Vacuum disc phenomena is > present at L4-L5 and L5-S1. > > L3-L4: A generalized disc bulge coupled with moderate degenerative > facet hypertrophy and marked redundancy of the ligamentum flavum > results in moderate to severe spinal stenosis. The inferior neural > foramina are narrowed, bilaterally. > > L4-L5: A gereralized disc bulge coupled with moderate degenerative > facet hypertrophy and redundancy of the ligamentum flavum results in > moderate spinal stenosis. The inferior neural foramina are narrowed, > bilaterally, left slightly greater than right. > > L5-S1: A mild generalized disc bulge coupled with mild to moderate > degenerative facet hypertrophy and redundancy of the ligamentum > flavum results in mild spinal stenosis. The inferior neural foramina > are mildly narrowed, bilaterally at the inferior aspects. > > IMPRESSION of Lumbar MRI: > > 1. Degenerative disc bulge and significant facet hypertrophy > resulting in moderate to severe stenosis at L3-L4. > 2. Moderate stenosis at L4-L5 and mild stenosis at L5-S1, > secondary to generalized disc bulges and facet hypertrophy. > > Thank you for your group and your replies. > God Bless You, > Melody > > ~~~~ *** ~~~ *** ~~~ *** ~~~~ > The Being Sick Community > > Message Archives-/messages > > Chat:- Scheduled Chats at > /chat > > Bookmarks:- > Add a website URL you have found useful. > /links > > Personal Complaints or problems:- > Please contact a moderator > email: -owner > > Subscription Details:- > 1) Individual email - means that every email sent to the list you receive. > 2) Daily Digest - sends you 25 messages in one single email for you to browse. This is an excellent option if you receive alot of email. > 3) Web only/No mail - means that you can pop into groups at your convenience and receive no email. > > To modify your subscription settings please visit:- > /join > > To subscribe or unsubscribe please email:- > -subscribe > -unsubscribe > > This group is not intended to diagnose or treat illnesses. No one on this group is qualified to diagnose medical conditions. If you feel you need medical attention, seek the advice of a qualified physician. > ~~~~ *** ~~~ *** ~~~ *** ~~~~ > When nothing is sure, everything is possible. > > --- Margaret Drabble > > ~~~~ *** ~~~ *** ~~~ *** ~~~~ > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 20, 2005 Report Share Posted February 20, 2005 Dear , I'm not sure what's recommended in your situation, but you can go to our sister site, iThyroid.com, to check out supplements, nutrition, etc. Best of luck, AntJoan Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 20, 2005 Report Share Posted February 20, 2005 Sorry you're having such a hard time, ! I got diagnosed about 9 months postpartum which convinced my endo it was Grave's and not thyroiditis as thyroiditis usually turns to hypothyroidism by about 6 months postpartum. My second endo said that my thyroid felt like Grave's in any case. I did PTU pretty soon after I was diagnosed...it took about 2 weeks to feel a difference (even though I was very hyper when diagnosed it didn't actually make me feel too bad, everyone's different). What dosage are you on? When you first start taking it you have to both block the new thyroid hormone that's being made and get rid of all the stored hormone in your thyroid so the dosage should be pretty high, about 300mg per day (100mg/3 times a day). You can start cutting it down at about 6 weeks, which is when all the stored thyroid should be gone. I'm now down to 25 mg every 4-5 days. My naturopath and doctor recommended against taking a beta blocker. Be very careful about getting yourself off them because you can cause an arrhythmia if you did it too quickly. Good luck! I am sure you will start to feel better soon, and it's such a relief when you do. Feel free to write with more questions! Nissa Quoting Tucker <nicole.tucker@...>: > > > Hello, > My name is and I have recently been diagnosed with > Hyperthyroidism. I just saw an endo for the first time last week > after my primary care provider diagnosed me based on blood work. My > endo is not sure if I have Graves or if this is Postpartum > Thyroiditis. She thinks it is Graves since I am almost a year > postpartum. > I feel so awful I can barely stand it. My heart races (it was > over 112 beats per minute at the doc office), I have bad insomnia, > get out of breath, hungry and thirsty all the time and losing > weight. The worst part of all this is how it is making me feel and > act - so irritable and impatient with my children, husband and dogs! > I feel out of control and scared. > I was trying two homeopathic remedies while I was waiting for my > appointment with the endo (I had to wait for a month) but they didn't > seem to be helping. I don't like to take prescriptions but out of > desperation have been taking the betablockers my regular doc gave me > and just started an antithyroid medication (PTU) the specialist gave > me last week. I don't feel any better yet (in fact felt somewhat > worse the last few days but didn't know if it had to do with the > female time of the month) A holistic practioner I work with told me > this might be related to a hormonal imbalance of progesterone. > I read some of the first posts on this sight and wondered if you > all are still recommending 8mg of copper (Solgar Chelated) and 60-70 > mg of Zinc for someone starting out. I am taking a Calcium Magnesium > supplement but wonder if I should take more. Any other suggestions > would be great. I am scared to stop taking the meds as I need this > to get better soon. Has anyone had success with a short run of PTU? > I will not be doing the RAI or surgery as I am nursing. From what I > gather they can create a new set of problems so even if I wasn't > nursing I am not sure I would want to do either. > What I really wish for (as I am sure we all do) is a quick > resolution to this and to get back to the way I used to feel! > Sincerely, > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 1, 2005 Report Share Posted April 1, 2005 Hello everyone, I am quite new on this list; it's good it exists. My name is Cathalijne (female 42 years) and I have been using ozone-therapy since 3 weeks. Because I have Multiple Sclerosis, Crohns disease and arthritis it is quite tough to do the ozon-sauna. In the beginning the temperature was too hot, and I suffered a lot from increasing pain in my arteries. Got scared... Saul adviced me to have the temperature a bit lower in the starting period (like 39 degrees), I think it s a good advice. Now I am taking more ozonated water, but my intestinal problems seem to increase due to this, and I have a lot of bloating, lack of appetite. Probably candidiasis and toxic liver are the cause. Also I experience severe burning pains, which increase after sauna or after the ozonated water. (Before sleep I take ozonated olive-oil.) Could that be a result of increased use of B-vitamins? Polyneuritis... Is it safe to use more vitamins on the same day, or just before or after drinking ozonated water? Who has experience with treating this kind of problems? Thanks for helping me, thanks for any suggestion Cathalijne (Holland, Europe) whooping cough, ozone and other protocols? Hi there. Just curious if others have gone through this and what helped them through it. My 3.5 yr old is about 3 weeks in and the baby and I are just getting into the nasty stuff now. i am trying to stay strong to help my kids through this!! plus i am still breastfeeding them both. I have been doing lots of things to boost are immune system, keeping in touch with our homeopath and we've been to see the MD/ND Am also funnelling my chest with ozone once a day (nice nasty rash) and breathing once a day through olive oil, drinking ozonated water and vaginal insuffilation once. This morning was the first real bad experience for me as i coughed and coughed and then when you try to catch your breath it feels like the windpipe is partially blocked with glue. essentially true i guess. hard to imagine this is just the beginning. i so want this to be over. any thoughts or tips would be appreciated. warmly wendy OxyPLUS is an unmoderated e-ring dealing with oxidative therapies, and other alternative self-help subjects. THERE IS NO MEDICAL ADVICE HERE! This list is the 1st Amendment in action. The things you will find here are for information and research purposes only. We are people sharing information we believe in. If you act on ideas found here, you do so at your own risk. Self-help requires intelligence, common sense, and the ability to take responsibility for your own actions. By joining the list you agree to hold yourself FULLY responsible FOR yourself. Do not use any ideas found here without consulting a medical professional, unless you are a researcher or health care provider. You can unsubscribe via e-mail by sending A NEW e-mail to the following address - NOT TO THE OXYPLUS LIST! - DO NOT USE REPLY BUTTON & DO NOT PUT THIS IN THE SUBJECT LINE or BODY of the message! : oxyplus-unsubscribeegroups oxyplus-normalonelist - switch your subscription to normal mode. ------------------------------------------------------------------------------ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 1, 2005 Report Share Posted April 1, 2005 Cathalijne, If I were you, I would do a several master cleanses and many liver cleanses. Probably will be better to do the liver cleanse first. I believe it would be better to take stuff out of your system rather than adding more to it. Of course, you should carefully monitor your nutritional needs and do not mistake healing crises for a problem with your choices. Sometimes this is difficult to do but with research you will find a way. Good luck! Best wishes and much love, Ken Ken Gullan Institute for Research Integration (IRI), San Diego, CA 92106-2424 IRI is a 501C(3) non-profit corporation established to help children with developmental difficulties. To contact me off-list use kengullan@... or call 619-222-1104 whooping cough, ozone and other protocols? Hi there. Just curious if others have gone through this and what helped them through it. My 3.5 yr old is about 3 weeks in and the baby and I are just getting into the nasty stuff now. i am trying to stay strong to help my kids through this!! plus i am still breastfeeding them both. I have been doing lots of things to boost are immune system, keeping in touch with our homeopath and we've been to see the MD/ND Am also funnelling my chest with ozone once a day (nice nasty rash) and breathing once a day through olive oil, drinking ozonated water and vaginal insuffilation once. This morning was the first real bad experience for me as i coughed and coughed and then when you try to catch your breath it feels like the windpipe is partially blocked with glue. essentially true i guess. hard to imagine this is just the beginning. i so want this to be over. any thoughts or tips would be appreciated. warmly wendy OxyPLUS is an unmoderated e-ring dealing with oxidative therapies, and other alternative self-help subjects. THERE IS NO MEDICAL ADVICE HERE! This list is the 1st Amendment in action. The things you will find here are for information and research purposes only. We are people sharing information we believe in. If you act on ideas found here, you do so at your own risk. Self-help requires intelligence, common sense, and the ability to take responsibility for your own actions. By joining the list you agree to hold yourself FULLY responsible FOR yourself. Do not use any ideas found here without consulting a medical professional, unless you are a researcher or health care provider. You can unsubscribe via e-mail by sending A NEW e-mail to the following address - NOT TO THE OXYPLUS LIST! - DO NOT USE REPLY BUTTON & DO NOT PUT THIS IN THE SUBJECT LINE or BODY of the message! : oxyplus-unsubscribeegroups oxyplus-normalonelist - switch your subscription to normal mode. ------------------------------------------------------------------------------ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 30, 2005 Report Share Posted April 30, 2005 Read the files section. You will find that most listmates chelate on Andy's protocol. For example, to start, 25 mg/dose DMSA every 4 hours around the clock for 3 days, 11 days off. --- " Sherri H. " <slhardegree@...> wrote: > Hi everyone, I just joined this group thanks to a > lady in another of > my autism groups (elaine). My name is Sherri and my > son Eddie is 13 > with moderate to partially severe autism. We have > been through so > much in 13 years - loss of speech at 18 months, the > leaky gut syndrome > for almost 5 years before we found a doctor who told > us what was > actually going on, behavior issues with his > grandparents, and now > puberty! Ugh. So... after all this, I figured that > he was too old to > chelate. I have since found out that it may take > longer, but it can > be successful. > > I have no idea where to start. Can anyone help? > > Sherri > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 1, 2005 Report Share Posted May 1, 2005 Sherri~ I immersed myself in the files here. Here are some links that I have found very helpful. http://f3.grp.fs.com/v1/MPhnQoX2GKKZBbmeovZFI4h-8NWpx9BGwKCQ5ZbyJQZwvgquGFF\ UkI7RiBe8IkS3NIik77RG-WeL5jHj-eZD1KBpD20k/Mercury-Autism%20FAQ http://home.earthlink.net/~moriam/Glossary.html http://home.earthlink.net/~moriam/LOVE_LETTERS.html http://www.danasview.net/supps.htm http://home.earthlink.net/~moriam/HOW_TO_hair_test.html http://www.danasview.net/parent3.htm#supplements http://home.earthlink.net/~moriam/HOW_TO_find_doctor.html Hope this helps~ Jackie---- > Hi everyone, I just joined this group thanks to a lady in another of > my autism groups (elaine). My name is Sherri and my son Eddie is 13 > with moderate to partially severe autism. We have been through so > much in 13 years - loss of speech at 18 months, the leaky gut syndrome > for almost 5 years before we found a doctor who told us what was > actually going on, behavior issues with his grandparents, and now > puberty! Ugh. So... after all this, I figured that he was too old to > chelate. I have since found out that it may take longer, but it can > be successful. > > I have no idea where to start. Can anyone help? > > Sherri Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 17, 2005 Report Share Posted October 17, 2005 Contact Joyce Attis near Ontario, try this # (416) 636-6618. Let me know if that is not right, I can track her down for you. Lynda At 11:25 AM 10/17/2005, you wrote: >Hi, >I will apologize in advance for this post being very long.Please be >patient with me as I am barely computer literate and have come to >this site feeling desperate.I am 29 years old and have had saline >implants for the past 7 years.Before the implants I was definately >overly active.Almost immediately after recieving the implants I >began to feel really tired all the time.I am not the type of person >to see a doctor frequently, in fact I do not even have a family >doctor.Immediatly after surgery I experienced numbness in my arms >and hands that has continued to come and go.My right breast began to >noticably harden about 6 months after getting implants.As time went >on I also started have sharp chest and rib pain.Muscles on my entire >upper left side feel tight.If I lift or move the wrong way I am >often left with debilatating neck and back pain that has lasted for >as long as a week leaving me bed ridden.My joints are incrediably >sore and stiff.My muscles are weak.I have swollen lymph nodes in my >neck and underarms.My memory is terrible and quite often I can not >remember what has happened the day before.One implant is noticably >higher than the other and seems to continue to climb upwards.I pick >up every cold and flu that comes around.Even after hours of >ininterupted sleep, I am never refreshed.I also have frequent head >aches.I was never sick before the implants.I have for a long time >attributed my poor health to the implants but have been too >embarassed to see a doctor.I have decided now to do so as I am >frequently too tired to function.I am also terrified of having >another attack that leaves me stuck in bed crying in pain.My >questions are as follows; > >1.Is removal covered in Ontario, Canada?Also is any reconstructive >surgery to remove excess skin ect covered? > > >2.Is there information I can print out to show my doctor linking my >symptoms to the implants? > >3.My implants are above muscle 375cc, will I be deformed after >removal? > >4. What have your personal experiences been after having implants >removed?Has your health returned to normal? > >5.What is the recovery time needed? > >6.Is there a site where I can view realistic pictures of explants >without replacement? > >7.Are there things I can do now to help my body prepare for surgery? > >8.Are there things I can do now to feel better before the implants >are removed? > >Thank you all in advance. > > > > > > > > > >Opinions expressed are NOT meant to take the place of advice given by >licensed health care professionals. Consult your physician or licensed >health care professional before commencing any medical treatment. > > " Do not let either the medical authorities or the politicians mislead you. >Find out what the facts are, and make your own decisions about how to live >a happy life and how to work for a better world. " - Linus ing, >two-time Nobel Prize Winner (1954, Chemistry; 1963, Peace) > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 17, 2005 Report Share Posted October 17, 2005 > >Hi, > >I will apologize in advance for this post being very long.Please be > >patient with me as I am barely computer literate and have come to > >this site feeling desperate.I am 29 years old and have had saline > >implants for the past 7 years.Before the implants I was definately > >overly active.Almost immediately after recieving the implants I > >began to feel really tired all the time.I am not the type of person > >to see a doctor frequently, in fact I do not even have a family > >doctor.Immediatly after surgery I experienced numbness in my arms > >and hands that has continued to come and go.My right breast began to > >noticably harden about 6 months after getting implants.As time went > >on I also started have sharp chest and rib pain.Muscles on my entire > >upper left side feel tight.If I lift or move the wrong way I am > >often left with debilatating neck and back pain that has lasted for > >as long as a week leaving me bed ridden.My joints are incrediably > >sore and stiff.My muscles are weak.I have swollen lymph nodes in my > >neck and underarms.My memory is terrible and quite often I can not > >remember what has happened the day before.One implant is noticably > >higher than the other and seems to continue to climb upwards.I pick > >up every cold and flu that comes around.Even after hours of > >ininterupted sleep, I am never refreshed.I also have frequent head > >aches.I was never sick before the implants.I have for a long time > >attributed my poor health to the implants but have been too > >embarassed to see a doctor.I have decided now to do so as I am > >frequently too tired to function.I am also terrified of having > >another attack that leaves me stuck in bed crying in pain.My > >questions are as follows; > > > >1.Is removal covered in Ontario, Canada?Also is any reconstructive > >surgery to remove excess skin ect covered? > > > > > >2.Is there information I can print out to show my doctor linking my > >symptoms to the implants? > > > >3.My implants are above muscle 375cc, will I be deformed after > >removal? > > > >4. What have your personal experiences been after having implants > >removed?Has your health returned to normal? > > > >5.What is the recovery time needed? > > > >6.Is there a site where I can view realistic pictures of explants > >without replacement? > > > >7.Are there things I can do now to help my body prepare for surgery? > > > >8.Are there things I can do now to feel better before the implants > >are removed? > > > >Thank you all in advance. > > > > > > > > > > > > > > > > > > > >Opinions expressed are NOT meant to take the place of advice given by > >licensed health care professionals. Consult your physician or licensed > >health care professional before commencing any medical treatment. > > > > " Do not let either the medical authorities or the politicians mislead you. > >Find out what the facts are, and make your own decisions about how to live > >a happy life and how to work for a better world. " - Linus ing, > >two-time Nobel Prize Winner (1954, Chemistry; 1963, Peace) > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 17, 2005 Report Share Posted October 17, 2005 She is one of the original breast implant group leaders from Canada, I met her many, many years ago. I have been involved for 15 years. There are several Canadian support groups. Lynda At 02:24 PM 10/17/2005, you wrote: > > > >Hi, > > >I will apologize in advance for this post being very long.Please >be > > >patient with me as I am barely computer literate and have come to > > >this site feeling desperate.I am 29 years old and have had saline > > >implants for the past 7 years.Before the implants I was definately > > >overly active.Almost immediately after recieving the implants I > > >began to feel really tired all the time.I am not the type of >person > > >to see a doctor frequently, in fact I do not even have a family > > >doctor.Immediatly after surgery I experienced numbness in my arms > > >and hands that has continued to come and go.My right breast began >to > > >noticably harden about 6 months after getting implants.As time >went > > >on I also started have sharp chest and rib pain.Muscles on my >entire > > >upper left side feel tight.If I lift or move the wrong way I am > > >often left with debilatating neck and back pain that has lasted >for > > >as long as a week leaving me bed ridden.My joints are incrediably > > >sore and stiff.My muscles are weak.I have swollen lymph nodes in >my > > >neck and underarms.My memory is terrible and quite often I can not > > >remember what has happened the day before.One implant is noticably > > >higher than the other and seems to continue to climb upwards.I >pick > > >up every cold and flu that comes around.Even after hours of > > >ininterupted sleep, I am never refreshed.I also have frequent head > > >aches.I was never sick before the implants.I have for a long time > > >attributed my poor health to the implants but have been too > > >embarassed to see a doctor.I have decided now to do so as I am > > >frequently too tired to function.I am also terrified of having > > >another attack that leaves me stuck in bed crying in pain.My > > >questions are as follows; > > > > > >1.Is removal covered in Ontario, Canada?Also is any reconstructive > > >surgery to remove excess skin ect covered? > > > > > > > > >2.Is there information I can print out to show my doctor linking >my > > >symptoms to the implants? > > > > > >3.My implants are above muscle 375cc, will I be deformed after > > >removal? > > > > > >4. What have your personal experiences been after having implants > > >removed?Has your health returned to normal? > > > > > >5.What is the recovery time needed? > > > > > >6.Is there a site where I can view realistic pictures of explants > > >without replacement? > > > > > >7.Are there things I can do now to help my body prepare for >surgery? > > > > > >8.Are there things I can do now to feel better before the implants > > >are removed? > > > > > >Thank you all in advance. > > > > > > > > > > > > > > > > > > > > > > > > > > > > > >Opinions expressed are NOT meant to take the place of advice >given by > > >licensed health care professionals. Consult your physician or >licensed > > >health care professional before commencing any medical treatment. > > > > > > " Do not let either the medical authorities or the politicians >mislead you. > > >Find out what the facts are, and make your own decisions about >how to live > > >a happy life and how to work for a better world. " - Linus >ing, > > >two-time Nobel Prize Winner (1954, Chemistry; 1963, Peace) > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 17, 2005 Report Share Posted October 17, 2005 Yes, she is a wonderful lady. I am glad you connected. I am sure she can help you a lot. Lynda At 04:04 PM 10/17/2005, you wrote: >Thank you!I spoke to her today already.What a truly lovely, understanding >sweet soul.She asked that I also thank you for referring me. > >Lynda <coss@...> wrote: >She is one of the original breast implant group leaders from Canada, I met >her many, many years ago. I have been involved for 15 years. There are >several Canadian support groups. > >Lynda > >At 02:24 PM 10/17/2005, you wrote: > > > > > >Hi, > > > >I will apologize in advance for this post being very long.Please > >be > > > >patient with me as I am barely computer literate and have come to > > > >this site feeling desperate.I am 29 years old and have had saline > > > >implants for the past 7 years.Before the implants I was definately > > > >overly active.Almost immediately after recieving the implants I > > > >began to feel really tired all the time.I am not the type of > >person > > > >to see a doctor frequently, in fact I do not even have a family > > > >doctor.Immediatly after surgery I experienced numbness in my arms > > > >and hands that has continued to come and go.My right breast began > >to > > > >noticably harden about 6 months after getting implants.As time > >went > > > >on I also started have sharp chest and rib pain.Muscles on my > >entire > > > >upper left side feel tight.If I lift or move the wrong way I am > > > >often left with debilatating neck and back pain that has lasted > >for > > > >as long as a week leaving me bed ridden.My joints are incrediably > > > >sore and stiff.My muscles are weak.I have swollen lymph nodes in > >my > > > >neck and underarms.My memory is terrible and quite often I can not > > > >remember what has happened the day before.One implant is noticably > > > >higher than the other and seems to continue to climb upwards.I > >pick > > > >up every cold and flu that comes around.Even after hours of > > > >ininterupted sleep, I am never refreshed.I also have frequent head > > > >aches.I was never sick before the implants.I have for a long time > > > >attributed my poor health to the implants but have been too > > > >embarassed to see a doctor.I have decided now to do so as I am > > > >frequently too tired to function.I am also terrified of having > > > >another attack that leaves me stuck in bed crying in pain.My > > > >questions are as follows; > > > > > > > >1.Is removal covered in Ontario, Canada?Also is any reconstructive > > > >surgery to remove excess skin ect covered? > > > > > > > > > > > >2.Is there information I can print out to show my doctor linking > >my > > > >symptoms to the implants? > > > > > > > >3.My implants are above muscle 375cc, will I be deformed after > > > >removal? > > > > > > > >4. What have your personal experiences been after having implants > > > >removed?Has your health returned to normal? > > > > > > > >5.What is the recovery time needed? > > > > > > > >6.Is there a site where I can view realistic pictures of explants > > > >without replacement? > > > > > > > >7.Are there things I can do now to help my body prepare for > >surgery? > > > > > > > >8.Are there things I can do now to feel better before the implants > > > >are removed? > > > > > > > >Thank you all in advance. > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > >Opinions expressed are NOT meant to take the place of advice > >given by > > > >licensed health care professionals. Consult your physician or > >licensed > > > >health care professional before commencing any medical treatment. > > > > > > > > " Do not let either the medical authorities or the politicians > >mislead you. > > > >Find out what the facts are, and make your own decisions about > >how to live > > > >a happy life and how to work for a better world. " - Linus > >ing, > > > >two-time Nobel Prize Winner (1954, Chemistry; 1963, Peace) > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 17, 2005 Report Share Posted October 17, 2005 Hi Kim I am glad that you found our site. Your symptoms are very very similar to those suffered by many of us with implant autoimmune sickness. I am glad that you will be seeing a doctor about removing them. It is important to go to a plastic surgeon who has done many explants and knows the importance of removing them properly. It will be necessary to remove the capsule your body formed around the implant as well as to remove the implant intact. The capsule can contain toxins from pathogens, shed silicone particles, as well as toxic metals that might have been in the silicone shell. I see that Lynda has given you a name of someone you can contact in Canada. Often, when you go to see doctors,they will refuse to believe that your implants are the problem. Many times bloodwork is normal despite feeling very sick. Sometimes doctors will try to convince you that taking out your implants will be a mistake and that you will be deformed if you do. None of these things is true. A good ps can usually produce a very satisfactory result. My experience with explant was that it went well and I recovered quickly with no complications. I started feeling better quickly after explant. Some symptoms improved right away, and others I have fought much longer. All in all I am significantly recovered. It is hard to give someone a timeline when they will get well. It is very variable. Some women notice improvements almost right away and feel really good within weeks to months. Others may feel an initial burst of wellness, followed by a return of symptoms but to a lesser degree. Others may not notice anything right away. But eventually, the vast majority of women get alot better, if not completely well. Often women must also detox their bodies of candida and other pathogens and toxins. This can be a gradual process. For many women it is also important to change their diet to eating more raw foods and cutting out refined sugar, baked goods and convenience food, and even eating organic if they can afford it. There is alot of information on this site pertaining to healing modalities. Right now you can work on improving your diet, drinking lots of water to help detox, and working on eliminating yeast, etc. These are helpful now, but many women don't notice alot of improvement until they are explanted. After explant, we really recommend a more concerted effort to detox. Feel free to ask any other questions you might have. hugs, kathy --- In , " kimc7622 " <kimc7622@y...> wrote: > > Hi, > I will apologize in advance for this post being very long.Please be > patient with me as I am barely computer literate and have come to > this site feeling desperate.I am 29 years old and have had saline > implants for the past 7 years.Before the implants I was definately > overly active.Almost immediately after recieving the implants I > began to feel really tired all the time.I am not the type of person > to see a doctor frequently, in fact I do not even have a family > doctor.Immediatly after surgery I experienced numbness in my arms > and hands that has continued to come and go.My right breast began to > noticably harden about 6 months after getting implants.As time went > on I also started have sharp chest and rib pain.Muscles on my entire > upper left side feel tight.If I lift or move the wrong way I am > often left with debilatating neck and back pain that has lasted for > as long as a week leaving me bed ridden.My joints are incrediably > sore and stiff.My muscles are weak.I have swollen lymph nodes in my > neck and underarms.My memory is terrible and quite often I can not > remember what has happened the day before.One implant is noticably > higher than the other and seems to continue to climb upwards.I pick > up every cold and flu that comes around.Even after hours of > ininterupted sleep, I am never refreshed.I also have frequent head > aches.I was never sick before the implants.I have for a long time > attributed my poor health to the implants but have been too > embarassed to see a doctor.I have decided now to do so as I am > frequently too tired to function.I am also terrified of having > another attack that leaves me stuck in bed crying in pain.My > questions are as follows; > > 1.Is removal covered in Ontario, Canada?Also is any reconstructive > surgery to remove excess skin ect covered? > > > 2.Is there information I can print out to show my doctor linking my > symptoms to the implants? > > 3.My implants are above muscle 375cc, will I be deformed after > removal? > > 4. What have your personal experiences been after having implants > removed?Has your health returned to normal? > > 5.What is the recovery time needed? > > 6.Is there a site where I can view realistic pictures of explants > without replacement? > > 7.Are there things I can do now to help my body prepare for surgery? > > 8.Are there things I can do now to feel better before the implants > are removed? > > Thank you all in advance. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 18, 2005 Report Share Posted October 18, 2005 Not much to add to Kathy's response except, (IMO) from my own experience, get exactly what you want done in writing, so there is no confusion on your or the dr's part on what and how you want your surgery done. Example: Explantation EnBloc w/complete capsulectomy. Just a helpful hint that I learned from all the experienced women on this site and from not having done exactly what I wanted in my own surgery. Hope this helps you...good luck on your journey to health! Cheryl Quote Link to comment Share on other sites More sharing options...
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