Guest guest Posted February 23, 2010 Report Share Posted February 23, 2010 IATTAP can do police training (no charge)- based on the training developed by Indiana Resource Center for Autism (used with permission). We did this for entire precincts in Kane and it was quite well received. The Dennis Debbaudt video is incorporated and having a parent and or persons with ASD panel - we will individualize it based on need and time - contact for more information or potential dates kristinnelson@... > > > I know Alderman from the Springfield location of the Autism Program does the emergency personnel training. You could also check with the Chicago location for the Autism Program. > > > > > > > > IPADDUnite > CC: Mrizzo@... > From: bdohogne@... > Date: Mon, 22 Feb 2010 14:10:36 -0800 > Subject: (unknown) > > > > > > Hi, > > Another mother and I had a positive meeting with an ton police commander last week around the issue of police interaction with people with autism and other disabilities. He's willing to include a training segment > (probably 30 minutes - maybe up to 60) in a future in-service. With > 163 officers, the training would likely need to be repeated over > several days. > > I'd appreciate any information about any > municipalities that have done such training for police -- who were > presenters, contact person at police dept., etc. > > Ellen and Rubin -- > I > recall your earlier replies about training, mentioning Kane and Lake > Counties, I believe. Do you know anyone I can connect with to learn if > there's an existing training presentation, a presenter who'd do > training pro bono, any police officer whose department has had such training? > > Thanks in advance. > > Bonnie Dohogne > > > > > > _________________________________________________________________ > Your E-mail and More On-the-Go. Get Windows Live Hotmail Free. > http://clk.atdmt.com/GBL/go/201469229/direct/01/ > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 23, 2010 Report Share Posted February 23, 2010 Gorlin Goltz syndromeOdontogenic keratocysts,Multiple basal cell naevi,osteogenesis imperfectaFrom: Abdo Aldasher <abdoaldasher1@...>Subject: (unknown)"ORE" < >Date: Tuesday, February 23, 2010, 8:25 AM left abducent what is the syndrom that has multiple cysts in the jaws? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 23, 2010 Report Share Posted February 23, 2010 The Nevoid Basal Cell Carcinoma Syndrome (NBCCS) (also known as Basal Cell Nevus Syndrome, Multiple Basal Cell Carcinoma Syndrome, Gorlin syndrome, or Gorlin-Goltz syndrome) is an inherited medical condition involving defects within multiple body systems such as the skin,nervous system,eyes,endocrine system and bone.From: Abdo Aldasher <abdoaldasher1@...>Subject: (unknown)"ORE" < >Date: Tuesday, February 23, 2010, 6:55 PM left abducent what is the syndrom that has multiple cysts in the jaws? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 23, 2010 Report Share Posted February 23, 2010 Has anyone read this?? http://query.nytimes.com/mem/archive-free/pdf?_r=2 & res=9B0DE4DF153DE733A25751C1A\ 9649C946596D6CF & oref=slogin Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 23, 2010 Report Share Posted February 23, 2010 Mercuric chloride is no longer what is poisoning us. What _is_ of concern is methylmercury, organic mercury, and inorganic mercury. Again, not to beat a dead horse, but Cutler's books have all this information and more! (who is not implying that Andy is of the mortal equine persuasion...) gEOrGe mUStArD wrote: > > Has anyone read this?? > http://query.nytimes.com/mem/archive-free/pdf?_r=2 & res=9B0DE4DF153DE733A25751C1A\ 9649C946596D6CF & oref=slogin > <http://query.nytimes.com/mem/archive-free/pdf?_r=2 & res=9B0DE4DF153DE733A25751C1\ A9649C946596D6CF & oref=slogin> > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 23, 2010 Report Share Posted February 23, 2010 I have his book coming. Thanks > > Has anyone read this?? > http://query.nytimes.com/mem/archive-free/pdf?_r=2 & res=9B0DE4DF153DE733A25751C1A\ 9649C946596D6CF & oref=slogin > <http://query.nytimes.com/mem/archive-free/pdf?_r=2 & res=9B0DE4DF153DE733A25751C1\ A9649C946596D6CF & oref=slogin> > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 24, 2010 Report Share Posted February 24, 2010 So cute! It looks clean and inviting and very professional! Good work. Annie > We've come A LONG way and we've got a long way to go, but as > of today, we can say that we have realized yet another dream with our > natural hair care line coming to fruition. > Stop by and check us out and visit us online at http:// > www.safiyakarite.com > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 24, 2010 Report Share Posted February 24, 2010 I felt much better when I lowered my Erfa to 2 grains daily. I had been taking 3 grains of Armour thyroid. I would be tempted to give it a try - you can also increase it back again if it doesn't work. Luv - Sheila I have been on Nutri Adrenal (can't take NAX) for, well it must be about two/three years now ( I can't think clearly). I'm taking Isocort now as it worked so well for me back last January when I had the car accident. I'm taking four a day plus the NA plus following Dr Lam's adrenal diet. I'm reluctant to take further HC without proper guidance.... and my endo is against it (though he is open to my belief of having adrenal fatigue).He has arranged for me to have a load of tests, but not 'til May.... as he wanted to see if I needed time to adjust to the ERFA. It just feel like too much T3 to me.... though I still feel hypo on it. It's not as subtle or as satisfying as Armour was.I'm not sure if lowering my EFRA (I'm on 180mg per day) would be helpful... as I said, I can't think straight). Any ideas would be most greatfully received. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 26, 2010 Report Share Posted February 26, 2010 hello , I am from india preparing for ORE oart i Tc Deepu. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 26, 2010 Report Share Posted February 26, 2010 hi thereme also from india sitting for ORE 1 in aprilthanx shuchiOn Fri, Feb 26, 2010 at 9:21 AM, Deepu Mathew <drdeeputm@...> wrote:  hello , I am from india preparing for ORE oart i Tc Deepu. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 27, 2010 Report Share Posted February 27, 2010 Sturgeweber (haemangioma-seizures-facial palsy)Anaemic pts tend to be thrombocytopenic??!From: Abdo Aldasher <abdoaldasher1@...>Subject: (unknown)"ORE" < >Date: Saturday, February 27, 2010, 8:57 AM primary(isotonic saliva): intercalated ducts secondary(hypotonic ): striated ducts , as the cells of the striated duct remove sodium from the isotonic saliva so it becomes hypotonic my qs is: -what do u call the syndrom in which u have hemangioma on the face and convulsions? -why there is a tendency to bleeding in anemic patients? thanx Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 27, 2010 Report Share Posted February 27, 2010 Sturge-weber It depends which type of anaemia for instance aplastic anaemia they have tendency to bleeding because of tjrombocytopenia My questions: Russels sign?Downey cells?--In every hierarchy, whether it be government or business, each employee tends to rise to his level of incompetence; every post tends to be filled by an employee incompetent to execute its duties.Get Free Random Signatures for BlackBerry at www.getempower.comSent from my BlackBerry® wireless deviceFrom: Abdo Aldasher <abdoaldasher1@...>Date: Sat, 27 Feb 2010 05:57:19 -0800 (PST)ORE< >Subject: (unknown) primary(isotonic saliva): intercalated ductssecondary(hypotonic): striated ducts , as the cells of the striated duct remove sodium from the isotonic saliva so it becomes hypotonicmy qs is: -what do u call the syndrom in which u have hemangioma on the face and convulsions?-why there is a tendency to bleeding in anemic patients?thanx Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 1, 2010 Report Share Posted March 1, 2010 Thanks, a! Hope you can come. - ________________________________ From: a B. <kristina45231@...> Sent: Thu, February 18, 2010 1:09:50 AM Subject: Re: (unknown)  Hi , I donated (wish it could be more!)--looks like you'll meet your goal soon. I'm not sure if my husband and I will go, but if we do I'll be sure to look for you, your husband, and son! ~a ____________ _________ _________ __ From: Larbes <lindalarbes> @gro ups.com Sent: Thu, February 11, 2010 11:49:09 AM Subject: (unknown) I'm proud to tell you that I'm participating in the MDA's CINCY STRIDE 2010 on 05/15/10 at VOA Park of West Chester...that' s right, I'm going to join others as we walk and roll to help Jerry's Kids© and MDA. I need your help! All you have to do is click here to make a secure, online donation. Your donation will help ...families living in our community and help make a difference. I am excited to add you to my list of contributors. Thanks in advance for your help. Don't hesitate to call or email me with any questions. Together we'll make a difference, P.S. I'm counting on you, click here to donate. If the link above does not work, please cut and paste the address below into the address bar of your Internet browser. https://www. joinmda.org/ cincystride2010/ lindalarbes/ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 2, 2010 Report Share Posted March 2, 2010 i think u shudnt postone. Give it a try. U will loose money indeed if u fail. but u will gain some experience regarding the exam questions, and u'll still have 2 trials (i guess). And one more thing, i dont have experience in this, but i understood from the GDC site that if u refuse an invitation ur name will be at the end of the waiting list, which means u might not sit in September. So... Go for it! From: Abdo Aldasher <abdoaldasher1@...>ORE < >Sent: Tue, March 2, 2010 5:21:54 PMSubject: (unknown) yesterday, i got an invitation to sit the ORE part1 exam in april,but iam not ready yet . how can i postpone the invitation until september? thanx Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 2, 2010 Report Share Posted March 2, 2010 Even i received the invitation for ORE Part1 and I declined it because of the same reason.The GDC people are not sure about if i will get a chance to sit for exam in September.From: Abdo Aldasher <abdoaldasher1@...>Subject: (unknown)"ORE" < >Date: Tuesday, 2 March, 2010, 6:51 PM yesterday, i got an invitation to sit the ORE part1 exam in april,but iam not ready yet . how can i postpone the invitation until september? thanx Your Mail works best with the New Optimized IE8. Get it NOW!. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 4, 2010 Report Share Posted March 4, 2010 Hi Angel - this was how I was advised to switch by a hormone specialist too. I literally stopped taking levothyroxine (125mcgs) one day and started half a grain of Armour the next, increasing by another half grain after 7 days, and increasing another half grain in another 3 weeks. I kept on like that until I knew I was taking too much and dropped back to the dose I was taking the day before. I had no problems whatsoever. Luv - Sheila Hi I don`t think their is a right way or wrong way in switching over from levo to natural. It all depends on if your dose has be stable and you have reached your sweet point. if so then i don`t see a problem with a quick change over. I was switched over some years ago now. one day levo the next day natural . I have had no problems. angel. No virus found in this incoming message. Checked by AVG - www.avg.com Version: 8.5.435 / Virus Database: 271.1.1/2721 - Release Date: 03/03/10 19:34:00 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 6, 2010 Report Share Posted March 6, 2010 A few things.... 1. There are, to my knowledge, no physicians in this group. You need an LLMD to interpret an Igenex test properly. 2. There's a clear distinction between " late " and " chonic " Lyme disease. " Late " means you've had it for a long time, and it hasn't been treated. Nobody, even the IDSA, disputes that this causes serious problems. " Chronic " means you've been treated with the standard, accepted antibiotics (28 days of doxy and 1 or 2 months of IV rocephin), and still insist that you're sick. The IDSA's unofficial position in this case is that you have a psychiatric disorder. What you're describing is " late " Lyme. You can see why you would not want to describe yourself as " chronic " unless absolutely necessary. Unfortunately, the language matters. 3. Don't know about Quest WBs, but somebody here does. Band 41, IIRC, indicates the presence of a non-specific spirochete. Might be Lyme or something else. But she's a grownup, and there's not a lot you can do if she's not willing to listen to you. 4. Where are you located? Perhaps someone on the list can steer you to a local LLMD who can take it from here. You've gotten more than most of us ever get from our GPs, who generally won't even sign the Igenex slip in the first place. Sara On Mar 5, 2010, at 2:03 03PM, Shirley Bell wrote: > I tried to email this to drcharlescrist.com and it wouldn't go through. Please advise. > > I do hope that someone in this group can help. My son and I have both received our Igenex Lyme disease test results. We had a doctor that did at least consent to draw the blood and send it to Igenex. Not only is he not an LLMD, he knows absolutely nothing about Lyme disease and really doesn't appear to want to know. Therefore, only because of an internet friend that does indeed have Lyme, our tests seem to reveal that we both have late chronic Lyme disease. Is there a phyician in this group that would be kind enough to respond as to our results if I sent him a copy? > > Also, I have a close minded daughter, in her early forties, that I am now very worried about. A couple of months ago, she had what appeared to be a small bite on her leg. That small bite grew to the size of a fifty-cent piece. It looked like pictures I've seen online of Lyme tick bites. I tried to get someone to take a picture of it, but no one would. I insisted I go to her dermatologist with her. He ran some tests and told her he had ruled out a few things. He put her on Rimpafin (sp) and if it wasn't better in a month to see him again. He also told her she had a suppressed immune system. She went back to him as it was no better. He then ran a culture on it. The results came back from the lab stating it is an ingrown hair! At the present time, it does look smaller. She is on no antibiotics, and is leaving town for five days this Saturday. When she comes back, this dermatologist is planning to cut it out of her leg. He told > her she will have to keep her leg elevated for two days after the surgery. From an ingrown hair? Really? I did talk her into having a lyme test run at least by Quest, which she did. All shows non-reactive withe the exception of 41 KD (IGG) BAND. The results show REACTIVE (Abn: A) I don't know what all of this means either. > > Please know any and all help will be greatly appreciated. > > Shirley Bell > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 7, 2010 Report Share Posted March 7, 2010 Hi Simone  Panic Attacks can be triggered by certain foods in a stress situation.. The three biggest seem to be sugar, chocolate and wheat.. so the utimate NO NO is chocolate cake!  Phobias and night terrors can also link in with food.. worst I know of is ASPARTAME..  Food intolerances can trigger very strange behaviour too.  I would look at her diet and keep a strict food diary.. early on set diabetes can have bizzare behavior attached to it  At the age of about 16 girls go through a myolination of the brain.. which is a coating of the brain synapses.. I think .. and this can create behaviour and emotional upset.. it ca also be a good phase for epileptics as the brain is less inclined to spike and fit with the mylonation. Is this girl NT or is she on the spectrum?  Other thought at this age in some kids may be experimenting with drugs.. which could give all these behaviours.  Some thoughts     Tracey On Sun, Mar 7, 2010 at 9:06 PM, simonelanham <simone@...> wrote:  Hi allA friend of mine is asking a question that I can't answer so wondered if anyone else had advice? Her friend's daughter is 16 years old and lives in London, is having all kinds of behaviour problems, including phobias and panic attacks. Can anyone recommend a holistic peds or psych specialist or anyone else she should see here? Any thoughts gratefully received.Love & light,Simone Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 12, 2010 Report Share Posted March 12, 2010 Can you post the doctor to this group? We have family and friends who might be interested also. And there is the listing somewhere that is for doctors who meet certain criteria with using iodine, and it would be helpful to have another doctor posted to that! Donna in IL From: iodine [mailto:iodine ] On Behalf Of sandrabeing Sent: Friday, March 12, 2010 10:26 AM iodine Subject: (unknown) Hello, I love this forum and read it daily. I live 30 minutes from Mishawaka IN and would also love to know who this doctor is. Thank you... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 12, 2010 Report Share Posted March 12, 2010 Omg sounds like your having a crappy time, hope you get it sorted. Sorry i cant help with your questions, i was wondering if you could answer a few of mine? My huspand are in the process of applying for our au visa, but last week i was diagnosed with hypotyriodism, how does it work with your healthcare system? I live in the uk and prescriptions are free. How much does it cost you? Sorry for having lots of questions and no answers for your question. Hope you feel better soon (unknown) The more I read, the more upset I get. I've lost more than half my hair. This is new endo had me reduce the 50 mcg of=A0 T3 I was taking to 25 mcg and now  added T4. I'm supposed to start with 1/2 of 75 mcg for a few days then in- crease to 75. He said this process to " fix " my thyroid would take at least 7 to 8 months.  When I asked him about the hair, he said that I might lose a bit but it would come back. Now I just read on the thread about swollen hands  and feet that it's low T3, which he just lowered again. After he lowered dmy T3 I was tested Monday and my FT3 was 2.5, FT4 0.2. I've had a headache for about a month (same time frame that I was lowering the T3), and my heartburn and stomach has become much worse.I live in Kirkland, WA. Does ANYONE know a doctor in my areas who is willing  to dose according to how a patient feels and not just blood tests? This doctor I'm currently seeing is Murray who supposedly is very good. He seems nice enough but is very rushed and I get about 5 to 10 minutes with him. He says RT3 is not relevant. <>Roni Immortality exists! It's called knowledge!  Just because something isn't seen doesn't mean it's not there<> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 12, 2010 Report Share Posted March 12, 2010 Thank you for sharing your experience. This kind of ankle and foot swelling is different than what happens just from sitting too long. My feet and ankles look they are pigs feet because even the toes are swollen. I am on liothyronine 25 mcg and 371/2 mcg of levothyroxine for two days and supposed to take it another two days and then switch to 75 mcg. I put in a call to the doctor this morning but have not received a call back. <>Roni Immortality exists! It's called knowledge!  Just because something isn't seen doesn't mean it's not there<> From: abbe_online <abbe_online@...> Subject: (unknown) hypothyroidism Date: Friday, March 12, 2010, 10:18 AM Hi Roni, First, sorry to see you are having a difficult time. Back a few years ago when I was going through what I call a health crisis, for the first time in my life I had swollen ankles. That really scared me. Because I had ended up in the ER and was terrified by the palpitations and extremely high blood pressure I'd had a complete cardio work up including heart monitor, which did not show anything. I complained about the ankle swelling on one of the lists and a fellow responded asking me if I was sitting at the computer for long periods of time, which I was. I got up and walked around my house for a while and the swelling came down. I started paying attention to how long I was sitting and would get up and walk around or go out and take a walk and never had any ankle swelling after that. I do not mean to suggest this is the answer to what you are experiencing, just sharing it, who knows... Also, during the course of this debacle on/off I have lost lots of hair too and it did come back. When my thyroid is off balance I suffer all sorts of digestive symptoms. It took me a long time to realize this was at least part of the cause. One of the things that seems to go along with this is allergic reaction to substances including foods. Headache can be symptomatic of that. About one year ago I stopped eating anything with gluten and that made a big difference in how I felt/feel. On the allergic thing, though, everyone is different and sometimes one has to keep a diary of everything they put into their mouths and document when and if any symptoms occur. Doing this if it is food, etc., a pattern will form and one can target the cause, if it is that. I had a doctor for 3 years who is a $%#@ & *(* & ^%%$. The first visit when I started to speak he put his hand up told me he was very busy and to keep it short. I was only recently able to get a new doctor and would not have gotten in to see him if it had not been for a friend who sees him asking on my behalf. When the Armour debacle occurred I switched to Nature-Throid. I did not do well on it at all. I keep swinging to hyper and would have to stop taking it. I wish I could remember the exact words the endo used when he told me his problem with desicated thyroid products are not only that they are inconsistent in terms of what one is getting per pill, but that some of the other ingredients can cause heart problems. I recall distinctly sensing that he knew what he was talking about and feeling grateful to have found this out before I screwed up my heart. He put me on Levoxyl 75 mcg and after a few days of discomfort I've evened out and so far have been feeling much, much better than I have in a long time. Again, I am not suggesting this is the way for you to go. Just sharing my experience. Hope some of it helps in some way. Abbey Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 12, 2010 Report Share Posted March 12, 2010 When pregnant women swell its sometimes because of blood pressure. Have u had yours checked today? CW -- (unknown) hypothyroidism Date: Friday, March 12, 2010, 10:18 AM Hi Roni, First, sorry to see you are having a difficult time. Back a few years ago when I was going through what I call a health crisis, for the first time in my life I had swollen ankles. That really scared me. Because I had ended up in the ER and was terrified by the palpitations and extremely high blood pressure I'd had a complete cardio work up including heart monitor, which did not show anything. I complained about the ankle swelling on one of the lists and a fellow responded asking me if I was sitting at the computer for long periods of time, which I was. I got up and walked around my house for a while and the swelling came down. I started paying attention to how long I was sitting and would get up and walk around or go out and take a walk and never had any ankle swelling after that. I do not mean to suggest this is the answer to what you are experiencing, just sharing it, who knows... Also, during the course of this debacle on/off I have lost lots of hair too and it did come back. When my thyroid is off balance I suffer all sorts of digestive symptoms. It took me a long time to realize this was at least part of the cause. One of the things that seems to go along with this is allergic reaction to substances including foods. Headache can be symptomatic of that. About one year ago I stopped eating anything with gluten and that made a big difference in how I felt/feel. On the allergic thing, though, everyone is different and sometimes one has to keep a diary of everything they put into their mouths and document when and if any symptoms occur. Doing this if it is food, etc., a pattern will form and one can target the cause, if it is that. I had a doctor for 3 years who is a $%#@ & *(* & ^%%$. The first visit when I started to speak he put his hand up told me he was very busy and to keep it short. I was only recently able to get a new doctor and would not have gotten in to see him if it had not been for a friend who sees him asking on my behalf. When the Armour debacle occurred I switched to Nature-Throid. I did not do well on it at all. I keep swinging to hyper and would have to stop taking it. I wish I could remember the exact words the endo used when he told me his problem with desicated thyroid products are not only that they are inconsistent in terms of what one is getting per pill, but that some of the other ingredients can cause heart problems. I recall distinctly sensing that he knew what he was talking about and feeling grateful to have found this out before I screwed up my heart. He put me on Levoxyl 75 mcg and after a few days of discomfort I've evened out and so far have been feeling much, much better than I have in a long time. Again, I am not suggesting this is the way for you to go. Just sharing my experience. Hope some of it helps in some way. Abbey Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 12, 2010 Report Share Posted March 12, 2010 You have got to be kidding me????This is really ridiculous...the "pandemic" that never was..are they even aware that countries are trying to sell of the H1N1 vaccine because so many weren't used??For crying out loud..the ignorance.Sorry this has happened, sorry your son will miss out...it's not fair, I know...LoriFrom: mbuckley <buckley_gmba@...>Vaccinations <Vaccinations >Sent: Sat, March 13, 2010 12:39:33 AMSubject: (unknown) The quote below is from the youth director where my husband had been a volunteer soccer coach. Now even my son's recreation activities will be limited because we choose not to get the H1N1 vaccine. "supply me with a copy of your CPR card and proof that you have had the H1N1 vaccine(now mandatory for any staff/volunteers working with youth)." Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 12, 2010 Report Share Posted March 12, 2010 My pressure is all right. I have a cuff at home. <>Roni  Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 13, 2010 Report Share Posted March 13, 2010 where's the listing of the docs? TIA > > Can you post the doctor to this group? We have family and friends who might be interested also. And there is the listing somewhere that is for doctors who meet certain criteria with using iodine, and it would be helpful to have another doctor posted to that! > Donna in IL > > From: iodine [mailto:iodine ] On Behalf Of sandrabeing > Sent: Friday, March 12, 2010 10:26 AM > iodine > Subject: (unknown) > > > Hello, > I love this forum and read it daily. I live 30 minutes from Mishawaka IN and would also love to know who this doctor is. Thank you... > > > > > ________________________________ > Quote Link to comment Share on other sites More sharing options...
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