Disability Insurance and Finding a Doctor

I need to find a doctor in my area who acknowledges that lymphedema and post mastectomy pain syndrome are actual valid conditions/disabilities. I need this documentation in order to win my Disability case. My surgeon refuses to acknowlege that I have either. Most likely because the surgery caused the conditions. My general doctor does not have any experience with these conditions.Can anyone recommend a doctor in the Orange County/Los Angeles CA area?

Comments

  • gale1525
    gale1525 Member Posts: 232
    edited February 2011

    My BS is really good, as soon as I got lymphedema she recommend PT for it. I don't have the post mastectomy pain sydrome, but after surgery I didn't have a problem with getting pain meds. My doctor is Tomi Evans she it a really caring person and everyone who I know that had her loves her. She is in Long Beach 701 east 28th street, Long Beach, ca 90806 PH# 562 426-0338.

  • dlb823
    dlb823 Member Posts: 9,430
    edited February 2011

    makingway, UCLA treats LE very seriously, including having LE specialists on staff.  Here's a link to their information.  Short of seeing them (which you might consider, especially if you're also looking for relief), the wording used here might even be helpful in describing your situation:

    http://www.simmsmanncenter.ucla.edu/information/insights_summaries/2003/2003_Rosenberg.asp

    I didn't look further, but I would be surprised if UCLA doesn't have an excellent pain management department, as well.   Deanna

  • makingway
    makingway Member Posts: 799
    edited March 2011

    Thank you both illustro and Deanna! I will have to pay out of pocket to see a qualified doctor, but I don't have any other choice. My survival depends on my winning my disability case. I've searched PMPS on the interent. There just aren't many current articles on the subject. Lots of blogs, but no science seeking understanding or remedies.

  • Momcat1962
    Momcat1962 Member Posts: 665
    edited March 2011

    Then you haven't many, JbinOK! I have an autoimmune disease that so many I know are in far worse condition than I, and their apps are barely looked at! Disability is NOT easy to aquire.

    Making: Keep trying! Appeal, if you do not get results! Let us know!

  • makingway
    makingway Member Posts: 799
    edited March 2011
    JBinOK-The doctors you are referring to are not there to treat people. Their function is solely to evaluate, as you wrote 'determine', 'if' the patient has a condition. I was required by Soc. Sec. to see one of these doctors.  It was the least thorough exam I've ever had in my life. I think that's what Momcat1962 was referring to with her 'barely looked at' statement.The doctor did little more than have me walk across the exam room. I assume that since I could walk, he assumed I had no condition. He didn't even ask me about the type of pain I was experiencing i.e., Is it sharp, dull, throbbing? The result of his inadequate exam led to Soc Sec. disapproving me of benefits. One of their findings was that I could carry 10 lbs. on a continual basis and lift 20 lbs regularly. I don't know what planet they are living on, but it isn't the same one I'm on... I have appealed their 'determination' but now I must find a legitamate doctor who understands my conditions (which isn't easy, since most have no knowledge of PMPS) and is willing to take the time to fill out the tedious paperwork required by Social Security.
  • lookingforward4more
    lookingforward4more Member Posts: 127
    edited March 2011

    This is an interesting thread! I recently had to leave my job of 7years due to increasing problems from my breast cancer treatment. I have had nuropothy in my feet and hands from my chemo treatment that is not resolving (three years). The sharp and burning in my feet require me to take four pain pills per day. I have also develped stage 2 lympodema in my arm and hand and have had two bouts with cellulitis that required me being in the hospital. I am depressed and dealing with a lot of bone pain. There are other issues from my treatment as well. The reason I am listing them for you all is that I am applying for social security disability and will desperately need the income when my savings run out! I went to a respected and well known disability attorney and he agreed to take my case and thinks that I will get approved. It make take a year or two but I can't work anymore so I have no choice.

    85% of social security disability applications get turned down the first time. You need to be very diligent and keep appealing the negative decisions. Thankfully my oncologist, nuerologist and pain specialist are supporting my application, but still I anticipate a difficult journey. It is sad that breast cancer patients have such a difficult time getting assistance when so many of our "treatments" result in long term pain/health issues. I take arimidex and my neurologist said "how is your chemo treatment going" and I said "oh, I finished chemo two years ago!" to which he said "arimidex is a form of chemo, a pill form, but still a form of chemo". I did not know that! It is important to have supportive doctors and to tell them EVERYTHING you are coping with. God bless!

  • makingway
    makingway Member Posts: 799
    edited March 2011
    dlb823-You are mistaken, UCLA does not take lymphedema seriously. I called for a physician referral and there are none-NONE!! They did refer me to a doctor in Santa Monica who is not affliated with UCLA. I swear I feel like I've been thrown to the wolves...

Categories