Guest guest Posted February 26, 2002 Report Share Posted February 26, 2002 Em, and ALL> My name is Buffy and I am From Seattle, WA. Here we have awesome medical facilities. If you are in need of trauma treatment west of the mississippi (SP?) they bring you to our Harborview hospital, If your child has a serious illness of nearly any kind they bring them here to our childrens hospital. We have a special hoispital for teaching, one that specializes in elderly, one for trauma, one for children, one fr birthing and OBGYN needs, a cancer center and major kidney center. Yet this is the experience I as a young woman have had in the recent months. I have had CFS and FMS symptoms for years. about 10 years. I am 32 this june. back and hip pain, shoulders in icy cold agony 99% of the time and something that i have self diagnosed as IBS as no doctor has been willing to treat or test me with anything other than anti diarrheals. I have attended school as a medical assistant and a womans healthcare outreach worker and worked in those fields as well as as an AIDS caregiver in a last stage hospice. I took 15 months of classes to become a massage therapist two years ago and learned the symptoms i had were more than likely fms and/or cfs. some possible ms or rsd symptoms. I didnt want to admit to myself or others i may have any of these serious syndromes. Last summer I changed PCP's. I had had four doctors in as many years. After my first visit this doctor told me i had high sed rates and my glyco hemoglobin was through the roof. He sent me to the University to the rheumatologist there. on our first visit the doctor told me i had fibro and perhaps rheumatoid, he toldme as i left for my tests that it was not imaginary and that the illness i had was very real. This made me feel very good considering all i had heard about how doctors deal with these syndromes. They took masny vials of blood and xrays of fewet and hands ankles and wrists. a note sent a week later told me i had bone spurs... welll..... everywhere, and arthritis in all the major joints xrayed. When they sent the appointment slip for the next appointment it was with a different doctor, a female doctor (somethingi am uncomfortable with) I went and saw her and she brought him in on our consultation. he found psoriasis on my knees, ankle, and elbows and said it seemed i had psoriatic arthritis, told me to have my pcp prescribe painillers and keep up my swimming program i have followed for the past two years. again he sent me for a blood draw. I went back to my pcp who then prescribed methocarbamol, i was already taking alprazolam for panic attacks due to agoraphobia and panic disorder. I told my doctor i hate to ask for pills and especially hate feeling drugged because i was raised by a mother who was disabled and spent much of my childhood " high " on pain pills. its a guilt thing. i took the pills and took them only when i HAD to. my next visit to the PCP I told him i still had alot of pain and he told me to TAKE THE PILLS. Last week i went to the Rheumatologist. I made sure my appointment was with the orginal MALE doctor. when i got there he asked why i hadnt seen the female doctor. I told him i was more comfortable with him. He told me i didnt have psoraitic or rheumatoid arthritis. that i could just go to the PCP fornow on and he couldnt do anything for me. even after he had sent a note saying he anted to see me again. when i acted troubled he told me i needed a psychiatrist. adn when i asked aabout pain management he said he would refer me to them and that i needed to go excercise. walk for an hour a day he said. My best friend was there with me and told him that I hurt to much most days to get to the car or into the pool on our pool days and he said that i needed to work through the pain and keep going. (sarcastic LOL). I started to cry as he pulled in another fourth year student and asked him if i should strap a honey bucket to my back for this walk seeing as i cant be away from a toilet with my diarrhea issues for longer then 15 minutes probably less if i am out in public walking around. He ended the appointment saying he woudl see me again and refer me to the GI doc and the pain management clinic and i left his office crying to head to the lab for MORE blood to be taken. WHY i ask? to feed some vampire in the basement? if he cant do anything else for me....why take more blood and why say he will see me again? I have spent the last week actually taking my pills when i hurt and i feel so weak and " out of it " most of the time. I am sooo sorry if i have rambled on to long. I just dont know what to do next. Buffy ===== Go to My WebPage and check it out! while you're at it...I'd love to see your name in my Slambook. http://www.goddessdeluxe.com __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 27, 2002 Report Share Posted February 27, 2002 Buffy, I would stay away from university doctors. I have had very bad experiences with them and my new (as of a years ago) told me that they have so much going on that they have a hard time keepin up and you can be left hanging in the wind -- so to speak. They have not -- in a year's time -- been able to find the MRI that I had done there. It was my latest one. They can't find my records that my neurologist should have. No records found from Urologist. Find yourself a new doctor. Make it a male doctor if that is what you are comfortable with. I find that I prefer a male doctor myself but will go to a female consultant if my principal doctor sends me there. If you are not comfortable with the Neurologist that he sends you to ask to see another. Keep it up until you find that you are happy with your doctor and don't stop asking until you do find one. I am seeing a Rheumatologist that is not on my list of recommended doctors by my insurance company. I insisted on seeing him because I was comfortable with him and he was helping me. I am permitted to see him. Take care, Irene Books may well be the only true magic Alice Hoffman. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 27, 2002 Report Share Posted February 27, 2002 Buffy, I would stay away from university doctors. I have had very bad experiences with them and my new (as of a years ago) told me that they have so much going on that they have a hard time keepin up and you can be left hanging in the wind -- so to speak. They have not -- in a year's time -- been able to find the MRI that I had done there. It was my latest one. They can't find my records that my neurologist should have. No records found from Urologist. Find yourself a new doctor. Make it a male doctor if that is what you are comfortable with. I find that I prefer a male doctor myself but will go to a female consultant if my principal doctor sends me there. If you are not comfortable with the Neurologist that he sends you to ask to see another. Keep it up until you find that you are happy with your doctor and don't stop asking until you do find one. I am seeing a Rheumatologist that is not on my list of recommended doctors by my insurance company. I insisted on seeing him because I was comfortable with him and he was helping me. I am permitted to see him. Take care, Irene Books may well be the only true magic Alice Hoffman. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 27, 2002 Report Share Posted February 27, 2002 I think you are making blanket statement that is really not true. I have had excellent care from the doctor's and staff at the University of Miami. So has my daughter and her treatment was critical if she was to continue in her career as a musician. I don't think a doctor not associated with a university would have had the qualifications to treat her as well. You are correct in the fact that I made a blanket statement. The reason that I went there for the other doctors was because I went there to an excellent ENT doctor. But the records at the University Hospital are a mess. The doctor's office and myself spend at least a month trying to find my MRI and my records from the Neurologist I saw there. I could not get a hold of her and her nurse. I was given the go around and finally we gave up as we were going nowhere. I really should have said that at my University Hospital there are a lot of problems with the doctors and records. I stand corrected and you are right. Take care, Irene Books may well be the only true magic Alice Hoffman. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 27, 2002 Report Share Posted February 27, 2002 I think you are making blanket statement that is really not true. I have had exceelent care from the doctor's and staff at the University of Miami. So has my daughter and her treatment was critical if she was to continue in her career as a musician. I don't think a doctor not associated with a university would have had the qualifications to treat her as well. If you need the top in the field then university doctors are the way to go. They are the most up to date and the ones doing the research in the field. Now for general care I don't even go to an MD. I go to an osteopath instead and he is wonderful. But for specialized care I go to the university if I can. Lisbet Re: Disastrous doc visit, LONG Buffy, I would stay away from university doctors. I have had very bad experiences with them and my new (as of a years ago) told me that they have so much going on that they have a hard time keepin up and you can be left hanging in the wind -- so to speak. They have not -- in a year's time -- been able to find the MRI that I had done there. It was my latest one. They can't find my records that my neurologist should have. No records found from Urologist. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 27, 2002 Report Share Posted February 27, 2002 I think you are making blanket statement that is really not true. I have had exceelent care from the doctor's and staff at the University of Miami. So has my daughter and her treatment was critical if she was to continue in her career as a musician. I don't think a doctor not associated with a university would have had the qualifications to treat her as well. If you need the top in the field then university doctors are the way to go. They are the most up to date and the ones doing the research in the field. Now for general care I don't even go to an MD. I go to an osteopath instead and he is wonderful. But for specialized care I go to the university if I can. Lisbet Re: Disastrous doc visit, LONG Buffy, I would stay away from university doctors. I have had very bad experiences with them and my new (as of a years ago) told me that they have so much going on that they have a hard time keepin up and you can be left hanging in the wind -- so to speak. They have not -- in a year's time -- been able to find the MRI that I had done there. It was my latest one. They can't find my records that my neurologist should have. No records found from Urologist. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 27, 2002 Report Share Posted February 27, 2002 I too had to use a University physician for my primary Dx, of Arnold Chiari Malformation. He is one of the top 10 docs in New York, and without him, I don't know what I would do. He spends at least 3-4 hours with us bi-monthly when I have my visit, and I KNOW OF NO OTHER DOCTOR who is willing to do that! Missy Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 28, 2002 Report Share Posted February 28, 2002 buffy mooney wrote: He ended the appointment saying he would > see me again and refer me to the GI doc and the pain > management clinic and i left his office crying to > head to the lab for MORE blood to be taken. WHY i > ask? to feed some vampire in the basement? if he > cant do anything else for me....why take more blood > and why say he will see me again? I have spent the > last week actually taking my pills when i hurt and i > feel so weak and " out of it " most of the time. I am > sooo sorry if i have rambled on to long. I just dont > know what to do next. Buffy, I'd find another doctor. The one you have isn't listening to you. If he can't hear you when you say you can't be away from a toilet for 15 minutes and when a friend confirms that you have problems walking to the car, then how is he possibly going to hear you when a medical symptom that doesn't show on tests comes up? He may be taking more blood because he doesn't know what the heck is wrong with you, but doesn't want to admit it to you. Hopefully the GI doctor will come up with some help for your IBS. In the mean time, take your pain medication, you aren't going to turn into your mom, and change doctors. Whine here if you want, we all understand. Darcy Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 28, 2002 Report Share Posted February 28, 2002 Thank you. I have had such a horrid week and it makes me feel better to know there are people who have the same type of issues. I have been ultra emotional crying at the drop of a hat. can barely walk and have wrist shoulder and right side pain. it seems i hit my thirtieth and fell completely apart....like the tin man in the wiz....pieces falling off me at each step. LOL. I also realized it is the last week in February. this is a historically difficult week for me. Dunno Why. Funny story.... took the cats to get fixed this am....drove past a restaurant on the way back and i commented " look there is a new buffett " i was then reminded by my mom, hubby and best friend that an hour earlier we had discussed the new restaurant and made plans to go tommorrow. now theres a fibrofog moment for you. ===== Go to My WebPage and check it out! while you're at it...I'd love to see your name in my Slambook. http://www.goddessdeluxe.com __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 28, 2002 Report Share Posted February 28, 2002 Thank you. I have had such a horrid week and it makes me feel better to know there are people who have the same type of issues. I have been ultra emotional crying at the drop of a hat. can barely walk and have wrist shoulder and right side pain. it seems i hit my thirtieth and fell completely apart....like the tin man in the wiz....pieces falling off me at each step. LOL. I also realized it is the last week in February. this is a historically difficult week for me. Dunno Why. Funny story.... took the cats to get fixed this am....drove past a restaurant on the way back and i commented " look there is a new buffett " i was then reminded by my mom, hubby and best friend that an hour earlier we had discussed the new restaurant and made plans to go tommorrow. now theres a fibrofog moment for you. ===== Go to My WebPage and check it out! while you're at it...I'd love to see your name in my Slambook. http://www.goddessdeluxe.com __________________________________________________ Quote Link to comment Share on other sites More sharing options...
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