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NeuroTalk Support Groups (https://www.neurotalk.org/)
-   Reflex Sympathetic Dystrophy (RSD and CRPS) (https://www.neurotalk.org/reflex-sympathetic-dystrophy-rsd-and-crps-/)
-   -   Dr.Phil show, help get the word out about RSD (https://www.neurotalk.org/reflex-sympathetic-dystrophy-rsd-and-crps-/51140-dr-phil-help-word-rsd.html)

dennyfan 09-27-2008 02:56 PM

I know its a little late but I just read this post for the first time. I sent in my story. I hope it helps. I pretty much begged for them to do a story on RSD pointing out that RSD effects more people than MS but no one has ever heard of RSD. I will let you know if I hear anything.
have a good day,
Denny

Franny 10-04-2008 01:45 PM

Quote:

Originally Posted by dennyfan (Post 377612)
I know its a little late but I just read this post for the first time. I sent in my story. I hope it helps. I pretty much begged for them to do a story on RSD pointing out that RSD effects more people than MS but no one has ever heard of RSD. I will let you know if I hear anything.
have a good day,
Denny

I am also a bit late but I just dropped Dr. Phil a note as well. GO TEAM!

Stacie 10-15-2008 11:21 AM

any new news??

mfrancis.palmer 10-15-2008 10:17 PM

Address
 
Does anyone have easy access to the address? I would like to send a letter as a child of a parent with RSD. It is a different perspective.

Jomar 10-15-2008 11:56 PM

http://www.drphil.com/contact_main/

http://www.drphil.com/shows/page/faq/#address
[I have a great suggestion for a show topic. How can I submit it?

We would love to hear your suggestions and encourage you to Share Your Story or Ask Dr. Phil a question. Show producers and DrPhil.com staff read all the e-mails submitted because what you tell us guides the television show topics and content on the Web. Due to the volume of e-mails we receive, we are not able to respond personally to all the letters. You should know that if you send us your suggestions, those will be considered Submissions under the Terms of Use for this site, and we will have the right to use the material you submit on the show or on the Web. We appreciate all suggestions and ideas, but do not pay for any.


I have a problem and want Dr. Phil's help.

The only way to get a face-to-face meeting with Dr. Phil is to Be On The Show. You can also Ask Dr.Phil a question via e-mail. Due to the volume of requests, we cannot make any guarantees.


What is the mailing address for Dr. Phil?

Dr. Phil show
5482 Wilshire Boulevard #1902
Los Angeles, CA 90036

Due to the volume of mail received, letters, photographs, legal documents, medical materials, manuscripts and other personal items cannot be returned. Please consider this when sending original items.

Materials other than letters are not usually reviewed. You may choose to spare the expense and effort of sending further documentation unless requested by our producers.

Money and checks should not be sent to the Wilshire Blvd. address. To purchase merchandise, click here. to buy a tape or transcript, click here.

Nearly every guest on the show starts with a letter or e-mail to us, and we look forward to your thoughts, comments, concerns and stories.]

Franny 10-17-2008 12:35 PM

Dr. Phil
 
Horray! A show on Dr. Phil for real? The producers should E-Mail every Dr. in the world to watch because I am tired of the weird look I get on the face of a Dr. when I tell them what I have. Then they try to convince me they have treated someone with this. Hey, I might be "Goofy" but I am not dumb! The problem is even a nurse that was inserting the IV for my 14th nerve block had no idea of what RSD was. She said she never even heard of it! People desperately need to be educated in this disease, understand it, have at least some idea of how to treat it and not be afraid to PRESCRIBE NARCOTICS IF NEEDED! I am sick of being told how addictive they are! Hey people they don`t make me HIGH! They help my PAIN! IDIOTS! OOPS, I think I may be a touch _itchy today. Sorry! I even got off track here. What I really wanted to say is PLEASE KEEP US POSTED on the show!
Love to you for caring enough to at least try to get someone who is high profile to get people`s attention to this disease. I am sure everyone here is very grateful!
Franny

dennyfan 10-17-2008 05:48 PM

Franny, You are not being an idiot. I had a horrible experience in an ER in California because a nurse knew nothing about RSD. I had been to the ER the day before and they out an IV in my left arm because my RSD is in my right arm. This nurse started to put the IV the next day in my right arm. I told him he couldnt do that & he asked me why. I told him. I already told you I jhave RSD in my right side. He was completley clueless. I had a very severe case of the flu. It had taken two bags of fluid the night before & four more that day to start to rehydrate me. Plus they were giving me some of my meds so I wouldnt go into withdrawl. The good thing is that because of my horrible mistreatment the hospital is going to do RSD training. So sometimes good things come when we stand up & get mad.
hugs, Denny

NikonKid 10-18-2008 09:20 AM

I have been fortunate since my diagnosis 2 years ago to have a great team of pain doctors right near my home at the Carolina Pain Institute.
I've been following this post on the Dr.Phil show, it's a great idea and I hope that it's a success and they dedicate a whole show to it.
I totally understand everyone's frustration with RSD being the unknown disease that it is, so I wanted to share a new resource with the group.
Pain Pathways magazine is published by my doctors office, it's an international magazine so it will definitely get the exposure we all are looking for. It just started this year and covers all kinds of chronic pain. There is always an article or sharing from someone with RSD in it. Next issue they are doing a feature on RSD/CRPS, I can't wait to see it. It's nice to have a hard copy of information to share with family and other docrors who haven't yet heard of RSD.
Dr. Oz from Oprah was in the summer issue, so who knows maybe even Oprah will take notice :)
They are very open to suggestions on articles and information. I suggested an article on pet therapy since my dog has helped so much with my pain management. This issue there is an article and picture of me and "Tweek"
The total bonus is that all proceeds go to research and education...so it's a win/win situation.
Hope this helps someone else as much as it has helped me
Jeanne

Martg1946 03-13-2009 02:17 AM

Letter to Dr Phil and Ask the Doctors - RSD
 
Quote:

Originally Posted by GJmom (Post 336321)
I wrote a letter to the Dr.Phil show about RSD. They were looking for medical nightmares. Well I got a call back. I was not expecting this. They said they would get back to me this week. I was thinking maybe it would help if everyone wrote in, so they don't just think it is one person that has this. I think it might make it more real to them, and show interest. I don't really want to be on the show, but my wanting to get the word out about RSD is much stronger then my fear of being on TV. My hope is that if more people know about it we can get more funding, and maybe push for new/more treatments. You can put a mark on the e-mail that says you don't want to be on the show. I'm not sure if it is Dr. PHil or the new show they are doing Ask The Doctors. It does not really matter to me, as long as we can get the word out.
http://drphil.com/

Hi, I just emailed Dr Phil and the Doctors show...let you know if I hear anything...GOOD IDEA !!!!:You-Rock:

angelrsd 03-13-2009 04:36 PM

about time
 
im glad that some one has gotten the attention out there for our cause !!!!

carrie


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