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Signatures 242 total

Page: « ‹ 1, 2, 3, 4, 5 › »

  1. 51
    Name: Deborah Walker on May 4, 2007
    State: FL
    Country: US
    Comments:
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  2. 52
    Name: Kelly Ozebek on May 7, 2007
    State: FL
    Country: US
    Comments:
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  3. 53
    Name: Samuel Sondheim on May 14, 2007
    State: NY
    Country: US
    Comments:
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  4. 54
    Name: Anonymous on May 14, 2007
    State:
    Country:
    Comments:
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  5. 55
    Name: Anonymous on May 16, 2007
    State: CT
    Country: US
    Comments: I am a teenager who has this condition and i would love for people to be aware of it, we havfe cancer awareness and heart awareness so i think there is no reason that we schould not have an RSD awareness month.
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  6. 56
    Name: Herlunda Ross-Cross on May 25, 2007
    State: MI
    Country: US
    Comments: RSd patient
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  7. 57
    Name: Cassandra Dickson on May 25, 2007
    State: MI
    Country: US
    Comments:
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  8. 58
    Name: Roderick Kelly on May 25, 2007
    State: MI
    Country: US
    Comments:
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  9. 59
    Name: Lesa Ross on May 25, 2007
    State: MI
    Country: US
    Comments: MY SISTER IS SUFFERING FROM RDS FROM A FALL BACK IN 2003. I HAVE SEEN HER GO THRU ALOT AND SUFFER FROM THIS. sHE HASN'T BEEN ABLE TO WEAR SHOES FOR THE LAST 4 YEARS. IT WILLLY HURTS ME TO SEE MY SISTER SUFFER AND I CAN'T DO ANYTHING TO HELP HER. SHE IS ONLY 37 YEARS OLD RECENTLY MARRIED AND WALKING ON A CAIN. SO, YES I WOULD LIKE TO SEE THIS MATTER BROUGHT TO THE FORE-FRONT AND MORE EDUCATION AND STUDIES BE DONE. THANK YOU
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  10. 60
    Name: Justina Doane on May 25, 2007
    State: OK
    Country: US
    Comments:
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  11. 61
    Name: Tiffany Gildon on May 26, 2007
    State: MI
    Country: US
    Comments:
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  12. 62
    Name: Dominique Johnson on May 26, 2007
    State: MI
    Country: US
    Comments:
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  13. 63
    Name: Alesia Haslip on May 29, 2007
    State: MI
    Country: US
    Comments:
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  14. 64
    Name: Trina Chatfield on May 30, 2007
    State: MI
    Country:
    Comments:
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  15. 65
    Name: Travis Cooper on Jun 22, 2007
    State:
    Country: AU
    Comments:
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  16. 66
    Name: Anonymous on Jul 30, 2007
    State: FL
    Country: US
    Comments: I was diagnosed with RSD in 2006 after breaking my wrist on the job. Rsd affected my memory, because I could not sleep. I left my job. Pain and tears became my life. I was left untreated for 11 months by workman's comp Dr.'s. Thank You for listing.
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  17. 67
    Name: Ashley Schoonmaker on Aug 3, 2007
    State: NH
    Country: US
    Comments: For my mother.
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  18. 68
    Name: Terri Michels on Aug 9, 2007
    State: PA
    Country: US
    Comments: I was diagnosed with RSD in 2003 in my left hand. I now have full body RSD and have yet to find any local Dr. that even knows what it is. I didn't think there could even be such a complicated condition out there that could not even be heard of by even doctors. I wish there were some way to make RSD known so there could be light at the end of this long and painful tunel.
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  19. 69
    Name: Scott Gager on Sep 11, 2007
    State: CT
    Country: US
    Comments: RSD has affected my family life and my life with my wife of 20 years. allways keep looking for new help.never stop.
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  20. 70
    Name: Anonymous on Sep 18, 2007
    State: LA
    Country: US
    Comments: PLEASE KIM IN LOUSISIANA WOULD LIKE TO HAVE IT HERE AND ALL OVER PLEASE HELP US ALL
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  21. 71
    Name: K Turner on Sep 21, 2007
    State: FL
    Country: US
    Comments: I was dx w/RSD after a fall at work. Workmans Compensation is a nightmare. I not only suffer every minute of every hour of every day but add the stress of loss of income, becomes intolerable. The stress only makes the pain worse. Believe me I would rather work any job painfree or at least the way I was than have no job and the constant unrelenting pain. People look at you and think you are ok, they cannot see the nerves going haywire in your body. Risk of spreading to the rest of your body are tremondous. Legislation needs to address these nightmares as if it was something that happened to their mother or sister or daughter. Since this disease affects more women and children than men.
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  22. 72
    Name: Kim Tramutola on Sep 25, 2007
    State: PA
    Country: US
    Comments: Please sign your name...be part of making the difference. And pray, please...that God will lead us to the cure. I love you Mom.
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  23. 73
    Name: Anonymous on Sep 25, 2007
    State: PA
    Country: US
    Comments:
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  24. 74
    Name: Anonymous on Sep 25, 2007
    State: PA
    Country: US
    Comments:
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  25. 75
    Name: Kim Scott on Sep 30, 2007
    State:
    Country: CA
    Comments: I would like to see a wrist band for this and the color the colors of the rainbow to give us all hope
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  26. 76
    Name: Robert Barshinger on Oct 1, 2007
    State: PA
    Country: US
    Comments: I hope this happens in PA. We sure need to make people aware of this horrible disease.
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  27. 77
    Name: Anonymous on Oct 28, 2007
    State: LA
    Country: US
    Comments: i have it and we also need help here in lousiana for an rsd awareness day in november
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  28. 78
    Name: Cassi HENNESSEY on Nov 7, 2007
    State: CA
    Country: US
    Comments: My best friend in life just took his life last month on the 17th due to RSD. 33years old Mark Ryan was. He had got the RSD from being in a coma in 2004, many surgeries to keep him alive that ended up killing him 3 years later. I would like to take part in helping America be more aware of RSD. Anything I can do to help please let me know. No one should have to feel like they have to end their life because there is nobody who understands, even DOCTORS.
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  29. 79
    Name: Patricia Shennum on Nov 7, 2007
    State: CA
    Country: US
    Comments: My son just committed suicide a couple weeks ago via hanging because of the excruciating 24/7 hour pain he was suffering from RSD. The McGill Pain Index rates RSD pain higher than cancer. The "medical professions" and public need to be aware of this disease. 49% of the affected RSD people commit suicide because there is no adequate treatment and inept doctors who know little about this rare disease.
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  30. 80
    Name: Kurt Kruger on Nov 8, 2007
    State: PA
    Country: US
    Comments: We desperately need to educate people of this horrible disease!
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  31. 81
    Name: Leslie Brymer on Nov 8, 2007
    State: CA
    Country: US
    Comments:
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  32. 82
    Name: Judi Zele on Nov 8, 2007
    State: CA
    Country: US
    Comments: many people are unaware of this disease it needs to be brought to the publics attention
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  33. 83
    Name: Anonymous on Nov 8, 2007
    State: FL
    Country: US
    Comments:
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  34. 84
    Name: Melissa Manning on Nov 8, 2007
    State:
    Country:
    Comments:
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  35. 85
    Name: DeLisa Foreman on Nov 9, 2007
    State: CA
    Country: US
    Comments: Please bring more awareness to this very sad problem.
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  36. 86
    Name: Benjamin Tatum on Nov 11, 2007
    State: NC
    Country: US
    Comments: I have had R.S.D. for over 3 years now. I got it from a hand injury at work it was 7 mouth before the i found out what i had after tons of test iwould go to the doctor and he would scratch his head it was when i was sent to the pain clince that the pain doctor tould me that i had CRPS also know as RSD they didnt tell me much about what it was just the treatments for it none of them worked and from that simply hand injury withen 10 mouths i was in a wheel chair i have quad RSD its in both arms and legs and on my chest and i have been told there is no cure when it stared moveing to my legs the doc wanted to put a spinal stemuilterbut work mans comp said it was to much and they didn't belive that my legs hadanthang to do with it my doctor told them they would wast thousands to send me for more test and other doctor and she was right they sent me to 4 more doctors that all ran tons of test each that just caused more pain and progest the RSD faster and all the doctors said it was RSD in the end i have seen 8 doctors now and they all agree it is RSD of curse when the doctor got the approvial for the stimulter the trail one didnt work or even help with pain so on top of having RSD i have to deal with workmans comp and they don't care about me and acording to the law they have all the rights they will not even get me the stuff for me being disabled the have denied 13 scripes for the stuff i need and i had just started with company LOWES HOME IMPROVMENT that own their own insuranse company and sence i had just started i made starting pay witch i only get 60% of my check a week when they send it they only have to pay this to me for the rest of my life and that all they have to do o their will never increase and no retirment and the check i cant ever afford a handicap apparment for my family i have a 19 month old and my wife she works but with that little bit we are drownding we are two mouths be hind in rent and dont know what to do and wc always sends the checks late they don't care they want even get me a wheelchair van and my wife has had to miss work and was just told that she has remature aruthrites sorry if spell it wrong it is hhard to type she has also had a brake down due to everthang we have tried to get help with rent and other bills food but chairtie and goverment dont helpif you are on workmans comp they want let you use it to buy a car a house and that screws you more i have a 100% disablity rateing i have to take 13 pills a day that just do help some but the side affces are some times just as bad as the problem that its supose to help i am always in pain have high blood pressure from the rsd and i have anzietie atackes that make the pain levels to were i cant talk justscream in pain the fisrt bad one i though i was haveing a heart attack and the hospital treat me like i was a mentail they did drug test and alcohol test and i couldnt speek so the tried me like crap til my wife set them staight oh i have also gained over 60 ponds that have put me border line dibetic oh the the people at my work all said i was faking when they saw me in a wheelchair they said oh he is just trying to get paid big they can have my petie 200 dollars a week if it would get ride of the pain poeple are so stupit they know nothon of this pain we go throw just because you can't see it don't mean it is not there i think a rsd month would be great then maybe people will stop calling us crazie ps;if anybody know somewhere to get help paying bills or getting a handicap van please let me know or if you just can help us it would gratliebe appratioated ifi have spelled stuff wrong please forgive me i forget and confussed now doc says its part of the rsd tank for reading i hope that we can get as popular as breast cancer and have the found to help find a cure for this so it puts out the fire of RSD or CRPS THANKS AGAIN BENJAMIN AND REMBER JUST A DOLLAR FROM PEOPLE CAN HELP OUR CAUSE
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  37. 87
    Name: Anonymous on Nov 11, 2007
    State: WV
    Country: US
    Comments: I think this would be great if enough people could/would sign it to make an awareness month for RSD.. not enough people know about this horrible disease..
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  38. 88
    Name: Justin Fitzpatrick on Nov 12, 2007
    State: NV
    Country: US
    Comments:
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  39. 89
    Name: Justin Fitzpatrick on Nov 12, 2007
    State: NV
    Country: US
    Comments:
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  40. 90
    Name: Anonymous on Nov 12, 2007
    State: NV
    Country: US
    Comments:
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  41. 91
    Name: Ana Eveland on Nov 12, 2007
    State: MO
    Country: US
    Comments: Just looking for support groups in my area or Missourri area.I had never heard of RSD I was just diagnose I can even get a doctor in my area that takes medicaid.
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  42. 92
    Name: Patricia Shennum on Nov 15, 2007
    State: CA
    Country: US
    Comments: My son recently committed suicide by hanging as a result of the horrible pain that doctors either did not know about or lied that they did. The medical community needs to be aware of RSD and not treat it as a drug addiction.
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  43. 93
    Name: Michelle Bellici on Nov 16, 2007
    State: MA
    Country: US
    Comments: I have had RSD for 11 years, it has been acute for the last 1 Year. As someone afflicted with the Dystrophy I am explaining what it is to doctors and friends all the time, to have people understand, or at the least have heard of the illness but be a blessing. I have Family in PA, and it would mean a lot to me. Thank you
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  44. 94
    Name: Melissa Kenna on Dec 23, 2007
    State: NY
    Country: US
    Comments: My sister has rsd from a fall almost threes years ago, she is in pain all the time. Please help her.
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  45. 95
    Name: Kristin Justice-Anderson on Jan 13, 2008
    State: MI
    Country: US
    Comments: I am 26 and have RSD. Please let's find some kind of cure!!
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  46. 96
    Name: Kristin Justice-Anderson on Jan 13, 2008
    State: MI
    Country: US
    Comments: I am 26 an have RSD. Please we must find a cure. I have only had RSD for 3months and it's already spreading up my leg.
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  47. 97
    Name: Kevin Kopka on Jan 13, 2008
    State: FL
    Country:
    Comments: I was diaginosed with RSD in 2007. After I have had 15 knee surgeries. I have had my right leg fused and in was infected with chronic osteomyoletis in my distal femer. The RSD was susepected WHen I had severeve pain that was not consistation with my chronic infection. Anyone who needs to talk or has any questions, please write anytime.
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  48. 98
    Name: Danielle Paquette on Jan 16, 2008
    State: MI
    Country: US
    Comments:
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  49. 99
    Name: Tammy Raleigh on Jan 26, 2008
    State: NY
    Country: US
    Comments: I would love to have November as the rsd awareness month. I think people need to understand what we really go through.
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  50. 100
    Name: Beverly Iler on Jan 30, 2008
    State: NY
    Country: US
    Comments:
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