ASHLEY: BORRELIOOSI LAPSELLA

Borrelioosiin sairastuneiden henkilökohtaisia kokemuksia taudista ja sen hoidosta.

Valvojat: Borrelioosiyhdistys, Bb, Jatta1001

ASHLEY: BORRELIOOSI LAPSELLA

ViestiKirjoittaja Bb » Ti Tammi 27, 2009 20:55

http://www.oregonlive.com/news/argus/in ... 315210.xml


After years of suffering, Ashley finally knows why - Lyme Disease

09/04/03

After nearly 10 years of enduring all kinds of physical pain and discomfort, since age 6, and not knowing the cause, Ashley might finally have an answer -- Lyme Disease.

Ashley's mother, Theresa, had a friend who had camped with them years before, then moved out of state. The friend had been diagnosed with Lyme Disease by a doctor in her new home state. When told of Ashley's long list of symtoms, the friend believed Ashley had Lyme Disease. She advised contacting the Lyme Disease Association.

Theresa's husband was taking Ashley, who was suffering another heart episode, to the doctor's office when Theresa called him on a cell phone to convey this information. Theresa begged them not to leave until Ashley was tested for Lyme.

The doctor ran the test to humor them. It came back positive. She had multiple Lyme symptoms, and the doctor began treatment immediately.

The test, even though positive for Lyme specific bands, had only four of five bands. The director of the Center for Disease Control (CDC) advises that the number of bands in the test should not be used as a diagnostic tool, but only as a surveillance factor.

Disregarding this advice, many doctors and insurance companies are using the screening tool as a diagnostic tool, giving no credence to symptoms and circumstances. The doctor's colleagues stated emphatically that it was absolutely not Lyme causing Ashley's symptoms and complaints. They refused to explore tick-borne diseases as the cause of her deteriorating condition and "strongly encouraged" him to discontinue treatment.

Theresa began her own search for answers. She found information at lymenet.org. She talked to people who either had family members with Lyme, or had it themselves, and learned from them that the medical community all too often overlooks or rejects the possibility of Lyme. They also suggested that Ashley see Dr. Charles R. Jones, of Connecticut, the world's leading tick-borne disease pediatrician, who has treated thousands of children, and knows all too well the long term ravages of this disease. He also teaches doctors about Lyme at Columbia University, and is a panel member to that university's Lyme Research Group.

After spending nearly four hours with Ashley's exam and reviewing her medical records, Dr. Jones strongly suspected Lyme Disease. He stated that Ashley was "classical" and wondered how others could have missed it for so many years. He tested her for other tick-borne infections, immune system problems and other diseases -- to rule out other possibilities.

Ashley was so exhausted from the trip that she slept for nearly a week, waking only to eat or throw up. As it turned out, Ashley had three tick-borne diseases, Borrelia (lyme disease,) Erlichiosis and Babesiosis.

Theresa also had Borrelia, but she'd been afraid to tell previous doctors: "They already thought we were crazy, and I was afraid to tell them what I was going through, for fear they'd consider it another reason not to treat Ashley."

Ashley and her parents call Dr. Jones a lifesaver. They assembled a medical team here in Oregon that was willing to accept Dr. Jones' diagnosis, and to speak with him to gain knowledge about the disease. After 10 long years, Ashley began to improve. She went back to school with a smile, has been on the honor roll and hopes to become a doctor.

In October, 2002, Ashley's smile disappeared. Due to insurance/doctor reasons she was removed from her medications against Dr. Jones' orders. After two months without treatment she began a severe downward spiral. She missed over 20 days of school in one term, and spent many days in bed again.

One of her Oregon doctors, very concerned about the changes in Ashley's condition, suggested she go back to visit Dr. Jones, who immediately renewed therapy. He still feels that she will get a complete or nearly complete recovery, despite the setback during the interruption intreatment.

Dr. Jones warned that to start and stop treatment again could result in permanent brain damage, memory loss and impaired cognitive function.

Over these harrowing years, in addition to caring for Ashley and doing their best to meet the challenges her illness was presenting, Ashley's parents encountered severe difficulties with insurance companies and doctors who should have been their allies. Doctors did not share information.

Insurance carriers insisted that doctors had been paid, but the doctors insisted they had not. They have received contradictory letters from the same person in an insurance company. Sometimes the family paid doctors' fees out of pocket (in addition to insurance premiums).

Although they requested a case review, the insurance company delayed, saying treatment had not been necessary. They never received the paperwork required for review and appeal.

Effective June 8, 2003, Ashley was denied any further payment from insurance for medication for her Lyme Disease. Marty and Theresa are not willing to give up Dr. Jones' recommended treatment, that has resulted in her dramatic improvement.

In order to pay for medical treatment, they have been forced to quickly sell many of their horses at thousands of dollars under their actual value. They still have Hallie, but although Ashley is probably well enough to be able to show her again -- for the first time since her blue ribbon -- the expense of her medication preventsthat.

Hallie gave birth to a foal this year, but the baby is for sale. The family hobby and vacations in the past have been showing their horses. For the past three years their "vacations" have been visits to their doctor on the East Coast. They no longer have the show horses, nor a lot of the foals they would normally have had.

Lyme Disease has taken away this family's way of life.

I asked Ashley if there were anything she would really want people to know about how the disease has affected her life.

This is her answer: "I don't have a ton of friends, but I do have a few really good ones. They play sports and hike and camp and go on vacations. Even though they are really terrific and supportive friends, it's hard to be around them sometimes because I wish I could do all those things with them.

"My boyfriend is healthy and athletic too. He does sports pretty much all year round and he really likes outdoor activities like camping and hiking. When I was healthier I thrived on sports and outdoor activities, so now it's really hard to be dating someone who loves all that, and not be able to do those things with him.

"It's also just really difficult in general to see my brother skydiving, my boyfriend wrestling, my best friend playing softball, and then to see myself not being able to figure skate or ride horses competitively like I used to.

"Those were the things that I thought made me individual, like my friends' sports make each of them an individual. Those were the things I could talk about forever without ever getting bored. Now I can't really do any of those activities, and talking about them just makes me want to cry.

"During the school year it takes all of my energy just to make it to school every other day ?so, needless to say, sports are just out of the question. During school breaks I usually try to get back into ice skating and riding horses just for fun -- even though I really would rather be competitive at it -- but the pain usually gets so bad I don't enjoy it the way I did.

"Every day that I get older, I just worry more and more that by the time I do get well enough to be competitive at my sports, I'll be in college and I won't have time to do those things. I used to dream of being an Olympic skater, and now the only thing I dare dream about is that I might graduate high school.

"That's what Lyme Disease does. It doesn't kill you. It just takes your life away from you and holds it just out of reach."

Ashley's parents to launch Lyme Diseases network to aid those who think they might have the disease

Marty and Theresa are preparing to launch the Non-Profit Oregon Lyme Disease Network, to aid and assist in advocacy for those who believe they are suffering with Lyme or other tick-borne illnesses. Rhode Island recently passed ground-breaking legislation, and they will work to increase similar legislative backing for early detection and treatment in other states, to gain support for those who have gone beyond the early stages into Chronic Lyme Disease.

This couple is hoping to increase awareness of the disease throughout Oregon, even though many Oregon doctors seem to think there is no Lyme Disease here. The federal government's 1998-99 Morbidity and Mortality Weekly Reports, a portion of CDC, places Oregon at 21st in the nation in documented cases of Lyme Disease. But CDC states they suspect the actual cases are at least 10 times the number reported.

For anyone seeking further information, Marty and Theresa suggest the International Lyme & Associated Disease Society (www.ilads.org), Lyme Disease Assoc. (www.lymediseaseassociation.org) or Lyme Disease Network (www.lymenet.org).
Bb
 
Viestit: 1820
Liittynyt: Ma Tammi 26, 2009 23:13

Paluu BORRELIOOSIKOKEMUKSIA ULKOMAILTA

Paikallaolijat

Käyttäjiä lukemassa tätä aluetta: Ei rekisteröityneitä käyttäjiä ja 1 vierailijaa