Guest guest Posted May 26, 2004 Report Share Posted May 26, 2004 Amey, I am not talented to make my own stuff but I would be willing to pay for stuff that you made. Please let me know if you would be willing to this. Thanks, Amey Hoagland wrote: Theres a problem with them! its strange ya know i was talking to other people on another site and they said they have one of the biggest forum and meetings in connetcut and there is NO AWARENESS there! you figure it out?? I have cum to da conclusion dat i make my own stuff!! when i have the booth at da festival im guna make all my own stuff! amey Shoemaker wrote: Tonia, Do you mean if I buy the teddy bear or pens to hand out they make money off of that it doesn't go for research on RSD? Tonia wrote: RSDS, RSDHope and any other websites you really need to watch out on. DO NOT believe everything you read in them..... I can honestly say and PROVE that at least 1/2 to 3/4 of the RSD Puzzles on RSD Hope is not right. The way its worded, that doctor tries to say that Everyone is the same, and that we all have the exact same symptoms and the exact same medications and treatments will work for everyone.....when we all know that THAT is a Complete and Total LIE! Only trust websites that are tax free donations. Like the NIH, the Arthritis Foundation...etc. I have Found 2 Websites that aren't Medical Research ones that DO tell almost everything accurately like 95-98%. One is Dr. Schwartzman, and the other site is Saving Grace. Those are the only two that aren't Support Groups that does state most of the facts correctly. In My Opinion.....if You want the TRUTH about RSD, Medications, Treatments and everything else that goes with them.....You really DO need to join a Support Group and just ask questions. Then, compare all of the answers you get from everyone, then compare those answers to your own Self. NO One has the EXACT same pains, no one has the exact same problems. No Two people will have the exact same results from a certain medication, treatment or trial. Therefore, NO DOCTOR OR WEBSITE can be accurate. Tonia ____________________________________________________ IncrediMail - Email has finally evolved - Click Here Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 26, 2004 Report Share Posted May 26, 2004 , you can make stuff on da computer and print it out. theres apecial paper you can pic up at walmart to make iron on stuff and bumper stickers and cards. and then you can laminate them. thats how i do it and if i cant draw it (like now i lost my rite my rite and hand, use of) i have my friend a tatoo artist do it for me. something to think bout anyway, gentle hugs amey Shoemaker wrote: Amey, I am not talented to make my own stuff but I would be willing to pay for stuff that you made. Please let me know if you would be willing to this. Thanks, Amey Hoagland wrote: Theres a problem with them! its strange ya know i was talking to other people on another site and they said they have one of the biggest forum and meetings in connetcut and there is NO AWARENESS there! you figure it out?? I have cum to da conclusion dat i make my own stuff!! when i have the booth at da festival im guna make all my own stuff! amey Shoemaker wrote: Tonia, Do you mean if I buy the teddy bear or pens to hand out they make money off of that it doesn't go for research on RSD? Tonia wrote: RSDS, RSDHope and any other websites you really need to watch out on. DO NOT believe everything you read in them..... I can honestly say and PROVE that at least 1/2 to 3/4 of the RSD Puzzles on RSD Hope is not right. The way its worded, that doctor tries to say that Everyone is the same, and that we all have the exact same symptoms and the exact same medications and treatments will work for everyone.....when we all know that THAT is a Complete and Total LIE! Only trust websites that are tax free donations. Like the NIH, the Arthritis Foundation...etc. I have Found 2 Websites that aren't Medical Research ones that DO tell almost everything accurately like 95-98%. One is Dr. Schwartzman, and the other site is Saving Grace. Those are the only two that aren't Support Groups that does state most of the facts correctly. In My Opinion.....if You want the TRUTH about RSD, Medications, Treatments and everything else that goes with them.....You really DO need to join a Support Group and just ask questions. Then, compare all of the answers you get from everyone, then compare those answers to your own Self. NO One has the EXACT same pains, no one has the exact same problems. No Two people will have the exact same results from a certain medication, treatment or trial. Therefore, NO DOCTOR OR WEBSITE can be accurate. Tonia ____________________________________________________ IncrediMail - Email has finally evolved - Click Here Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 26, 2004 Report Share Posted May 26, 2004 THANKS! I might be able to do that. I will look the next time I can go to Walmart. Thanks again, Amey Hoagland wrote: , you can make stuff on da computer and print it out. theres apecial paper you can pic up at walmart to make iron on stuff and bumper stickers and cards. and then you can laminate them. thats how i do it and if i cant draw it (like now i lost my rite my rite and hand, use of) i have my friend a tatoo artist do it for me. something to think bout anyway, gentle hugs amey Shoemaker wrote: Amey, I am not talented to make my own stuff but I would be willing to pay for stuff that you made. Please let me know if you would be willing to this. Thanks, Amey Hoagland wrote: Theres a problem with them! its strange ya know i was talking to other people on another site and they said they have one of the biggest forum and meetings in connetcut and there is NO AWARENESS there! you figure it out?? I have cum to da conclusion dat i make my own stuff!! when i have the booth at da festival im guna make all my own stuff! amey Shoemaker wrote: Tonia, Do you mean if I buy the teddy bear or pens to hand out they make money off of that it doesn't go for research on RSD? Tonia wrote: RSDS, RSDHope and any other websites you really need to watch out on. DO NOT believe everything you read in them..... I can honestly say and PROVE that at least 1/2 to 3/4 of the RSD Puzzles on RSD Hope is not right. The way its worded, that doctor tries to say that Everyone is the same, and that we all have the exact same symptoms and the exact same medications and treatments will work for everyone.....when we all know that THAT is a Complete and Total LIE! Only trust websites that are tax free donations. Like the NIH, the Arthritis Foundation...etc. I have Found 2 Websites that aren't Medical Research ones that DO tell almost everything accurately like 95-98%. One is Dr. Schwartzman, and the other site is Saving Grace. Those are the only two that aren't Support Groups that does state most of the facts correctly. In My Opinion.....if You want the TRUTH about RSD, Medications, Treatments and everything else that goes with them.....You really DO need to join a Support Group and just ask questions. Then, compare all of the answers you get from everyone, then compare those answers to your own Self. NO One has the EXACT same pains, no one has the exact same problems. No Two people will have the exact same results from a certain medication, treatment or trial. Therefore, NO DOCTOR OR WEBSITE can be accurate. Tonia ____________________________________________________ IncrediMail - Email has finally evolved - Click Here Quote Link to comment Share on other sites More sharing options...
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