Guest guest Posted January 28, 2010 Report Share Posted January 28, 2010 I agree 100%. People get really upset if they suspect that you are telling them they have something wrong. Same goes for their kids lol. In a message dated 1/27/2010 9:00:07 A.M. Pacific Standard Time, hmm_md@... writes: I completely agree with Gretchen. By starting off with talking about your story it is more likely to inspire thoughts like " me too, I've had the same things happen, if this is hereditary maybe I should talk to my doctor about it " rather than the defensiveness than can be inspired by telling someone what you think they have. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 28, 2010 Report Share Posted January 28, 2010 Infomation is power. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 9, 2010 Report Share Posted February 9, 2010 Any change in therapy should be discussed with the parent first before implementing. When my dd was in private ST the therapist did place her with another child & it was called a Diad. You may want to pose the question of whether this is the right approach for Apraxia to Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 22, 2010 Report Share Posted September 22, 2010 The longer I stay in this house the more ill I become, its gotten to the point that in the past 2 days I almost went to the emergency room. After my first exposure I stayed at a hotel for 3 months but they have since raised their rates by almost 200.00/month which i cant afford. Im becoming desperate in my search for a safe place to live as i can no longer go on feeling like this. i thought about moving back to my home town but wont have the emotional support i so desperately need and staying where im at isnt a possibility because it's so darn expensive. I have to find a safe place to live, buy clothes, furniture, pay rent and put down a deposit. I simply dont have the money to do all that, if anyone has any advice on how to get any of this done i'd be more than happy to listen to your suggestions. Tug Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 22, 2010 Report Share Posted September 22, 2010 You could run an ad, plus search for ads (Craigslist, MCSSafeShelterUSA, etc) for a furnished bedroom and bath (w/ kitchen privileges) in the home of a chemically sensitive person while you try to find a place of your own and start over. Would be cheaper than a hotel I would think. Good luck! ....Corky The longer I stay in this house the more ill I become......Im becoming desperate in my search for a safe place to live........ Tug [snipped] Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 22, 2010 Report Share Posted September 22, 2010 You could run an ad, plus search for ads (Craigslist, MCSSafeShelterUSA, etc) for a furnished bedroom and bath (w/ kitchen privileges) in the home of a chemically sensitive person while you try to find a place of your own and start over. Would be cheaper than a hotel I would think. Good luck! ....Corky  The longer I stay in this house the more ill I become......Im becoming desperate in my search for a safe place to live........ Tug [snipped] Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 23, 2010 Report Share Posted September 23, 2010 Corky thanks for the reply, I've been running ads in craigslist but for some reason havent had much luck. Just about every place I've looked at either would have effected my MCS or had a water leak and the owner couldn't verify if there was mold or not. There was small studio that would have been perfect for me but the unit above it had a pretty bad water leak in the bathroom and they had to tear out the ceiling to fix it. I could have rented it but if it had mold I would have had to move and once again replace all my belongings, it just wasn't worth the risk. There's some extended stay hotels in the area that are a little expensive but by the time I pay rent, and the utilities I would save about $50.00 a month by renting an apartment as opposed to staying in a hotel. Keep in mind that if I move into an apartment Im still going to have to buy furniture, even if I buy off craigslist Im still going to have to spend money I don't have. The problem with a hotel is sooner or later Im going to have to find an apartment, living in a hotel for a year or so doesn't seem like the proper thing to do. All this has come about because I wanted to buy a place of my own to improve my quality of life. How could things go so bad? > > You could run an ad, plus search for ads (Craigslist, MCSSafeShelterUSA, etc) for a furnished bedroom and bath (w/ kitchen privileges) in the home of a chemically sensitive person while you try to find a place of your own and start over. Would be cheaper than a hotel I would think. Good luck! > ...Corky Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 24, 2010 Report Share Posted September 24, 2010 maybe check allergy groups around your area or allergy doctors where you could leave your name. cathy > > The longer I stay in this house the more ill I become......Im becoming desperate in my search for a safe place to live........ > > Tug > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 25, 2010 Report Share Posted September 25, 2010 Have you seen this? http://www.facebook.com/group.php?gid=150413784999257 it's a facebook page run by an MCS site that is trying to provide safe housing. I haven't seen it but its a possibility. Let me know if it pans out-good luck! >> > Corky thanks for the reply, I've been running ads in craigslist but for some reason havent had much luck. Just about every place I've looked at either would have effected my MCS or had a water leak and the owner couldn't verify if there was mold or not. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 3, 2010 Report Share Posted October 3, 2010 Tug, how do you know it's the house and not something else? It seems to be sure, you would need to leave the house and see if you start to feel better to know. I did that. I was there three months but started to feel better in the first month. Someone could have something like EBV for example and feel worse and worse and it wouldn't be the house. Lots of things make you feel very tired, but now remembering you said you don't feel tired, have lots of energy. Why do you think you are sick, if you have lots of energy? > > > The longer I stay in this house the more ill I become......Im becoming desperate in my search for a safe place to live........ > > Tug > > [snipped] > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 15, 2010 Report Share Posted October 15, 2010 When you say you have to meet a high deductible to see your son's psychiatrist who prescribed his medication, is that $1000 deductible for any doctor, or just mental health? It seems like if the psychiatrist prescribed the drug already that your child's pediatrician should be able to help with refills, if there is no deductible to see a primary care physician. As for social security, there is good info on the TACA website about how to apply for SSI (which would get your child Medicaid coverage), or a Beckett/deeming waiver if your family income disqualifies the child for Medicaid ( Beckett waiver looks only a child's income, I believe). By the way, for anyone dealing with autism and insurance companies, there is a group dealing specifically with that. In my state, North Carolina, my insurance policy excludes treatment for developmental delay, so I guess it depends where you live (the key is not to have treatments coded for autism). Good luck! Bridget > > > From: mateli0300 <mateli0300@...> > Subject: ( ) Need Advice > > Date: Thursday, October 14, 2010, 11:04 AM > > > Â > > > > My son has been seeing a therapist and Psychiatrist who has him on a Medication. We recently got new insurance through my husbands work that wants us to reach a out of pocket max of $1,000 before they will cover him to see the doctor. We can not afford the fees for service and can not get the medication without seeing the psychiatrist because only he can prescribe it. do not know what to do right now. My mom mentioned that i should try to put him on social security disability but I'm not sure about that either. Does anyone have any advice??? > Quote Link to comment Share on other sites More sharing options...
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