Thread: Doc appointment
View Single Post
Old 07-19-2008, 10:03 PM
caregiver caregiver is offline
New Member
 
Join Date: Jul 2008
Posts: 4
15 yr Member
caregiver caregiver is offline
New Member
 
Join Date: Jul 2008
Posts: 4
15 yr Member
Default

Quote:
Originally Posted by screwballpookie View Post
I finally got a call back from my pain doc this morning and I talked to the nurse. I asked her about my foot just swelling up out of the blue and you wouldn't believe what she told me. They have never had a patient that has had that happen before unless it was associated with an injury. So according to her you have to have an injury for rsd to spread. Is that true? I told her that what i have read about rsd that it can spread. I also told her that I did have a severe sprain to that foot less than a year ago where my foot turned all purple. She then said that now that she heard that that it is very possible that it is rsd in my foot.She also wanted to know if I had seen my family doc for it and I told her no becuz i thought that it could be rsd. THe other reason that I didn't tell her is I don't have insurance so I can't afford to go to my family doc.Besides I want work comp to pay for anything and everything I can possibly make them do for everything they have and are putting me through. I do have an appointment with my pain doc on Monday at 4:45. So we will see what they say. I am going to print out some of the articles that you guys have posted and take them with me just so the doc can read them for himself. Thanks again. Please if anyone has any input on what the nurse said from the get go let me have it. Thank you.

Sincerely,
Screwballpookie
As a work comp case, let me give you a little advice:

1. If you go to a doctor that tells you your RSD hasn't spread and you think it has, ask for a referral to a neurologist. Do not wait. Ask for the referral and then go. A neurologist should be versed in RSD well enough to be able to tell the difference between RSD spreading and something else that may be going on. But as a work comp case and RSD it is imperative you go to a neurologist to get that diagnosis.

2. RSD does spread. Workers Comp does not want any of your doctors to say it has spread because this means WC has to (at some point) possibly pay for your meds and treatment forever. This is why a neurologist diagnosing you with spreading RSD is so critical. It is very hard for WC to fight a neurologist's diagnosis.

3. If you have been paying for your meds or any doctors visits relating to your work injury thus far, keep the receipts. Make copies. If the insurance company says they won't refund the money, don't listen. Write a letter to the insurance company explaining the reasoning for the treatment. Make a copy of the letter. Send the letter and a copy of the receipt (along with any forms you may be required to fill out (look at your state's WC site for medical reimbursement forms)) to the insurance company. Keep copies of EVERYTHING. Remember WC is a legal matter. WC eventually plays out in court. A court looks at the RECORD (all papers relating to your case including dr notes and any correspondence you have with the insurance company) when making its decision. Thus, everything you send to the insurance company is in the court's RECORD (and if it isn't you will have your copy that you made). So your receipts for treatment you sent them, they will be in the record too and will possibly lead to a pay off if you win your WC case with the insurance company.

4. Do not give up hope. RSD is tough, to say the least. Find a good neurologist and trust no one from the insurance company. Not even your adjuster. No offense, but they work for the insurance company. (Remember? The guys who don't want your RSD to spread because they don't want to pay for it?)

5. And if your DR doesn't believe you or gives you attitude, get out of there fast! Time is precious with this illness. Do not waste it on DRs who think their medical training has made them superior to you. You know your body. It's the Drs job to help you figure out what's wrong, not tell you they know your body better than you do.
caregiver is offline   Reply With QuoteReply With Quote