Jim had his GP DR this morning. GP said Jim's blood tests were "stellar." We didn't ask for a copy of the tests; we are suppposed to get them directly from the lab but that hardly ever happens.
Jim really wants prednisone for the arthritis in his knees. GP said no; nothing oral and suggested something topical that it looks like I can only get on-line. So a little Hocks shopping tonight. He will re-ask the GI DR when he sees him in 2 weeks.
SSDI application. We didn't have to wait too long after my appointed time. I was so nervous; I went through 1.5 bottles of water. The intake woman said it was the most complete and organized application that she had seen.
It's a little complicated being self-employed (and not keeping real good time sheets after starting the surgeries), getting her to agree to my statement about the last day I did any "substantial work." But she finally did, and hopefully the state determining agency will also. I have to do no substantial work until September this year to qualify for any retroactive benefits. But then, I probably won't know until after that whether I got approved on the 1st application.
Because I had documented pretty well, it only took about an hour. Gave us time for lunch before my intake for neuropathy therapy.
PT found that I have sensation in my arms, hands, fingers, legs, feet, and toes. The test? Touching me with a hard plastic "pricker." We then did some balance testing. She said I was having balance problems. No shit, Sherlock. I had shown her my arm bruise from falling last week.
She also counseling me on the normal things I get nagged about--taking my pills, eating, lowered alcohol consumption. She said all of those things can affect the neuropathy.
So we are going to try the Anodyne treatment for six sessions (3x/week) and give me hand, feet, and balance exercises. Also some leg strengthening exercises. I start that Friday.
Tomorrow is my every 4 month PAP smear. Joy! But the last once was negative for abnormal cells, so if this one is too, I only have one more 4 month PAP before I can go back to annual.
Friday is my GP. She is seeing me every 4-6 weeks now because of my depression. I have quite the list of things to talk about. The SSDI application, where I listed her as the lead doctor in knowing my symptoms and treatments. Wanting a referral to a neurologist, although I am starting to waiver on this because the PT today said a neurologist would not do much more in the way of testing than she did today and would have nothing in her/his medicine bag that I'm not already on. Wanting a referral to a psychiatrist. My psychotherapist is OK, but it would be nice to have an MD doing the counseling because the s/he also could manage my stress/anxiety/anti-depression meds. My GP seems slightly an amateur in that area.
Then Monday, the psychotherapy resident.
I so want all these appointments to stop. I want to go out and garden.
Wednesday, May 09, 2007
Today's appointments
Tuesday, May 08, 2007
Today Sucked
I got up extra early because I had the appt for a CT scan and the thoracic surgeon. They called about 15 minutes before I left (it's a long drive) to tell me it was off because the DR had been called to emergency surgery. So I had to morning to continue working on other stuff, like my SSDI application. I had shot Ennis early and low at +10 because I thought I was going to be out past +12.
Around noon, I realized that I was just flat-ass worn out. I had a 3pm new PT appt somewhere far away that I had no idea where it was. Sure, yes, I google mapped it. I called them to cancel. The lady said she understood; that often happens with their clients. This place specializes in PT for women with breast and GYN cancers.
Tomorrow. Jim's family DR in the AM, SSDI application right after lunch, and now my intake with the new PT late in the afternoon.
Just thinking about this wears me out.
PS. Blogger has "switched" everyone over to the new version. It presents the opportunity to label posts with topics. This is the first one I am going to try this on. I have no clue what this is going to do or how it is going to work. Bear with me.