If you have been reading my blog, or any of my pages, or my Facebook page, you know that I have SLE (Systemic Lupus Erythmatosis). What you may not realize is that this is primarily "a woman's disease," as 90% of the patients are women. Most of them are 15 -45, the childbearing years. For some enlightening information about pregnancy and lupus, please read this study in Japan about pregnancy outcomes and lupus .Women of color, across the board have higher rates than white women. I once had a former Texas benefits evaluator tell me that "lupus is a made up disease by people who are too lazy to work." To me, it was clear he was referring to Black women. Black women have higher death rates from breast and cervical cancer, higher rates of STD's and teen pregnancies, higher infant mortanlity. SOURCE: Debunking the myth. Black women, Hispanic women, Native American women all have higher rates of lupus. Black women have more severe outcomes more often. Poor women without health insurance have a harder time getting the help they need to treat lupus. SOURCE: Lupus Fact sheetFor some information about lupus symptoms in general, please read this article about two lupus patients. My diagnosis was originally made by a gynecologist to whom I had gone for a simple pap smear. At the time, I had health insurance. I no longer have health insurance, and my best option for pap smears is Planned Parenthood. Read one woman's story about not affording to go anywhere but Planned Parenthood. Please make yourself aware of two FACTS:
1. NOT ONE TAXPAYER DOLLAR GOES TO ABORTION. That has been prohibited since the 1970s.
2. Abortions are only 3% of their services FACT SHEET HERE
Finally, let's talk about SOCIAL SECURITY and Disability and Social Security Supplemental Income. I worked from age 15 until about 40. I've been fighting to get SSDI so I can get Medicare to cover my lupus medications. First they told me I ought to be able to work (in 1995) because I am educated. Know many employers who want employees who fall asleep on the job, or who miss work frequently because they cannot drag themselves out of bed and stay awake long enough to bathe, dress, and get to work? Or who catch the flu and the miss weeks because the immunosuppressant drugs they take for lupus don't fight the flu well and leave them with bronchitism pneumonia and a lupus flare in which their joints swell and cause agonizing pain? If so, please send those employers my way! I'd love to work, use my brain again for pay. Of course, it has to be low stress and pretty free of deadlines, because stress makes my lupus worse, and I never know which day I'm going to wake up and be unable to stay awake -- which makes it difficult to meet those deadlines. See this blog
for another person's perspective.
The next time I applied for SSI/SSDI they told me my $3000+ savings account made me ineligible for SSI and I no longer had enough qualifying quarters for SSDI. I appealled and they told me I wasn't disabled! NOIT DISABLED? I cannot shop without either my husband pushing me in the wheelchair or an electric cart. Some days my knees hurt so badly the 8' from my bed to the toilet has me in tears. I cannot stand in lines for more than 30 seconds without the knees and hips begging me to sit down. That's not disabled?
Now their story is that we cannot prove I was disabled WHILE I STILL HAD ENOUGH QUALIFYING QUARTERS. THEY have the 1995 records with the doctors names, but OOPS I can no longer get those records because the doctors who made the disagnosis, and who treated me, destroyed the records 10 years after my last visit. I'm SURE those records are in the SS records; they just demand that I produce them, knowing I can't.
So now I'm still 5 years too young for SS and Medicare. What if they raise the retirement age? First how will we tap into our retirement accounts without penalty to pay for medical expenses? I will NEVER see my SS money that I paid into the system all those years I worked (sometimes at 2-3 jobs at a time!). I WILL NOT LIVE LONG ENOUGH!
Let me repeat that I WILL NOT LIVE LONG ENOUGH! I can no longer take Methotrexate because my platelet levels drop too low and I am in danger of bleeding to death internally. The prednisone I have been on for over a year now will, according to my rheumatologist "take five years off your life." It also induced Type II diabetes, which is implicated in heart disease, even if I didn't have the extra clotting factor from lupus. The Hydorxychloroquine (Plaquanil) no longer controls the disease by itself. I also cannot take aspirin, NSAIDs like ibuprofen. So I take ginger and turmeric for the constant pain. Some days it works, some days it doesn't work so well. I need Ben Lysta, according to my rheumatologist, but she's not going to administer it. It's about $2000-$3000 a pop. I think it's once a month. I tried to get onto a drug trial, but the diagnoses (both of which I think are wrong) the county hospital gave me of non-alcoholic cirrhosis and heart failure keep me out of the trial. I need a liver biopsy to rule out the cirrhosis, and an echocarcdogram for the heart failure.
My only hope is Obama's health care plan, because I could not be denied coverage for pre-existing conditions. If I cannot afford the private health insurance or the high risk pool insurance, I could, as I understand it, get Medicare without having to be on SS, SSI, or SSDI. So think twice before you pull the lever for someone who wants to repeal Obamacare; that lever pull will be a death sentence for me and many others with my illness or others like it. Of course, it you want to be a good, compassionate Christian, you can send me money at PayPal to help with my medical expenses. Leave a comment on this website and I'll send you my email. They are. or would, if I were seeing the doctors I need to see and taking the meds I need to take run from $3000 in a good year for routine meds and visits and tests to upwards of $24,000 if I had to be hospitalized. My brother is currently supporting us and paying our medical expenses. He's nearing retirement age. He spent years paying for our mother's needs because her SS didn't cover the utilities, food, out of pocket medical expenses. Now he has us, and his own family.
SO please look into your heart and see if you want to pull my plug by voting to kill "Obamacare
Yesterday, we pulled into the handicapped parking space at a local store. Next to us was a big honking pickup truck, parked RIGHT ON THE LINE between the two spaces. Now as those of you who read this know, I'm handicapped by RA and lupus. I opened my door and apparently it hit his truck. HE SCREAMED AT ME to watch my door. I pointed out that he was right on the line and I am handicapped. So he repeated his scream, adding an expletive before "door." You know the one that rhymes with "BIG HONKING TRUCK."
I mention that the man was Hispanic only because, from where I sit, my observational data is that Hispanic men seem to have both (1) a higher predilection for verbally abusing women, and (2) an intense devotion to their rides. I would hate to think they also have a higher rate of abusing the handicapped. Only ONCE in my entire life has any Black man spoken to me the way this man did, and he was drunk and angry (See my page on Talking About Race). NEVER has any Asian man of any nationality or ethnicity spoken like that, although some of the Near Eastern Asian men have talked down to me, like I was stupid, which I find equally off-putting in a different way. As to white men, the only ones who ever yelled epithets were drunk, or, oddly enough, guys who made passes at me and were rebuffed, or construction workers who catcalled and I shot the bird. The latter two cases I assume were injured pride. Nor do I think that Hispanic men, percentage wise, are any more sexist than other men of any color. I think they are simply more open about expressing it. in such a manner as this man did. However, this is not the point of my blog today.
Two things that bother me about this encounter are (1) failure to acknowledge that his own parking right on the dividing line between the two spaces contributed to the problem, and maturity alone should have dampened his enthusiasm for cursing out a handicapped person. Since this man was probably in his late 40s or in his 50s, judging from the grey in his hair and his facial wrinkle, I would suggest that if he were concerned about his truck being dinged, he might have parked it farther out in the parking lot where nobody was likely to ding it. Second, while I understand that dings and scratches promote rusting of vehicle bodies (or did when they were metal rather than plastic or fiberglass), it's also a fact that one's vehicle is probably going to get dings, dents, scratches during it's lifetime. Ours certainly does. We fix them ourselves as a matter of routine maintenance. Even when actually witnessed a couple allow their metal shopping cart to escape and roll into our car, I accepted this as a normal part of life. They were coping with two small children and had that on their mind. Similarly, once I open the door, I engage in the task of getting myself out of the car. This usually requires both hands because I often have to lift that stiff knee to get it out past the door. Such was the case today. I'm not sure whether the door hit his truck when I first opened it, or doing the process of climbing out of the car, and picking up my shopping bag from the floor of the vehicle. I actually wasn't aware that it had until he started screaming at me. That suggests to me that it didn't hit with much force, or the sound certainly would have drawn my attention. My question is this? What makes, to any rational adult, a dinged vehicle (and I did not see any damage when I looked) important enough to verbally abuse another person, particularly a handicapped one?
I satisfied myself with not pointing out that he was parked right on the line and that I was handicapped, but firing off a string of insulting epithets in Spanish. I was not going to stand there and take his abuse. I hope it makes him think twice before repeating such behavior. Next time I hope he parks his precious honking truck (ugly as it was) on the far margins of the lot. Better yet, I hope he grows the heck up.
So you think women aren't focused on money? Tell that to my mother who was widowed at 42 with 2 kids 10-13 and her widowed mother. Tell that to women trapped in abusive marriages because they don't know how to feed their children otherwise. Tell that to divorced women raising children on their own. Because THESE women
HAVE to focus on money in order TO focus on their children.
Then there are the childless women like myself. I was NEVER focused on children. Watching my mother struggle after my father died, picking pop bottles out of the ditches & washing them & carrying them to the store so I could buy dinner for the 4 of us...at age 13, is precisely why getting a college degree and going to graduate school, including UW- Madison, was more important to me than getting married and having children. Oh I always assumed I would do that too; it simply was NOT my priority. Good thing too, as I ended up losing my long-awaited pregnancy with my husband to undiagnosed and untreated lupus. Then I could no longer have children. So I'm glad children were never he focus of my life!
That was 1970, when women made about 59¢ to a man's dollar. WOW! now we make 77¢., except in your state it's only 75¢. FORTY-TWO YEARS to gain 16¢ on men! No wonder we are still more likely to end our lives in poverty, as my mother did, and as I will.
I can tell you what THIS woman is focused on now: making sure that ideological, sterotyper idiots like you & your governor are run out of office by WOMEN.