Guest guest Posted November 28, 2011 Report Share Posted November 28, 2011 Hi! I have seen many get their lives back from Chronic Lyme. Do not despair! I have created a resource computer CD and you can download a free copy or have it mailed to you at no charge. See my website... I bet you know someone who has Chronic Lyme and doesn't realize it yet! www.lyme-resource.com > I'm NEW! > Howdy! oh and I'm overwhelmed too...help! > > Hey there! My name is e and I'm new to this board. Just > wanted to introduce myself and post some questions. I'm a > newly divorced mom of two children on the Autism Spectrum: > son, , is 5 1/2 yrs old with moderate/severe autism, > OCD, ADHD, Mr. Sensory, somewhat verbal, has PICA, is > lethargic, very underweight and pale with allergic shiners, > barely eats food and NEVER TAKES SUPPLEMENTS ORALLY, has > horrible tantrums and increased in self-injurious behavior > and started hitting and kicking others more often now. My > daughter Maddison, 3 1/2 yrs old is mildly on the spectrum > and been diagnosed with 'Disruptive Behavior Disorder', > Anxiety, Tantrums, Self Injurious behavior, Sensory issues, > PICA, strong inability to self-regulate and has an insatiable > appetite for mischief. She has aggressive hitting and > screaming fits, including spitting and kicking as well. She, > too, will not swallow any supplements but takes some liquid > supplements in her 'milk' like a champ. I usually have to > under dose many-most of her vitamins, medications etc because > she refuses to take them. > > Both children have food allergies and sensitivities. Our > entire family just so happen to also have Lyme disease. Which > type? I don't know yet as I am completely new to the research > and disease profiles. I've found a local LLMD in the San > Francisco Bay Area where we live and he's ordered a BATTERY > of initial tests including the Igenex test which I should > know in a couple weeks the results of that along with > everything else I took. My children and I do NOT have a > history of tick bites but I contracted it from my ex-husband > (their dad) who's had a history of bullseye rashes for over > 20 years and never had the audacity to go get them checked > out!!! I took a picture of them one day when they manifested > back in 2007 and said " one day I'm going to find out what these are! " > > After a horrible event where my son almost lost his life at 8 > mos old from a congenital blocked bladder (that caused kidney > reflux, kidney damage, toxic sepsis, etc), I noticed bullseye > rashes manifesting on his bottom, trunk and left cheek. He > had been in the hospital receiving numerous IV antibiotics > and I never noticed a circular rash on him prior to the > hospital stay. Even though had 'eczema' as a baby and > was colicky (from pain), I never vaccinated him and fed him > well and he hit all his milestones perfectly...after the > hospital, he was banging his head on the ground within 6 > weeks of recovery and at the same time bullseye rashes were > appearing off and on. No pediatrician diagnosed his rash as > anything beyond 'eczema'. > > After both my children received grants to receive DAN! doctor > protocol treatments with a popular medical group in TX, I > noticed after a first round of Septra that my daugther > manifested bullseye rashes on her bottom too. Let's just say > after much poking and prodding the treating physician and > mentioning that my son was complaining of migratory joint > pain, low grade fevers, night sweats, very pale, blue lips, > bullseye rashes, and dissecting his bloodwork with him saying > exactly " I think my son has an underlying autoimmune disorder > we're just not treating or haven't diagnosed yet " ...I was > judged as being one of 'those' moms and essentially all my > requests and complaints got ignored. From a DAN DOCTOR no less!! > > Now I'm starting initial supplement treatment for myself and > getting ready to figure out antibiotic therapy after test > results come back and I have to say, I'm a bit worried. I've > heard so many testimonies about bad Herx reactions, negligent > or well-meaning LLMD's not giving the right antibiotics, too > much of this or that and I'm just completely overwhelmed with > how I'm supposed to judge what treatment option is the right > path and what's going to work the most efficiently. I know > I'm probably speaking for many of ya'll about starting off > right but let's just say I don't have any extra money for > mistakes. With 3 of us to treat and about 5-9 years worth of > undiagnosed Lyme, I'm deeply concerned and don't know where > to go. My Lyme doc is a gentle and humble man so my gut is to > trust him but I hear too many testimonies how antibiotics > made so many people more sick than it helped and only > alternative/naturopathic/homeopathic medicine worked the best. > > Can someone please calm my fears? My son is really sick, my > daughter is fairing better but only eats liquid nutrition > like as if she was an infant and I'm the MOST SICK I've ever > been in my life. I know treatment is highly customized to fit > each individual but I just need to know where to go to find > out about each stage of treatment. For instance, initial > dosages, types of antibiotics, treatment course, possible > reactions, detox remedies and how through the course of > treatment you're to measure your improvements, set-backs, OTC > remedies, etc. Do I make any sense? I really want to know > what to expect over the next year of treatment... > > Thanks for your time and support! > > e, Jack and Maddie > San , CA > > > > ------------------------------------ > > Quote Link to comment Share on other sites More sharing options...
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