August 12th
2008
12:09 PM
NuvaRing was great for me for years and then I began experiencing most of the symptoms noted by others. However, when my LYMPH NODES become ENLARGED AND PAINFUL I realized it was time for me to take out the ring and give my body a rest from the foreign substance. Once I removed the ring completely, within two-weeks my HAIR BEGAN TO FALL OUT each time I washed it. After weeks, my JOINTS became so INFLAMED I could not walk even though I had been working out four-days per week for many years prior. I also experienced HAIR AND SKIN TEXTURE CHANGES, and ONGOING FLU-LIKE SYMPTOMS which included: BODY ACHES, SEVERE FATIGUE, NIGHT SWEATS (DRENCHING), HEADACHES AND WEIGHT LOSS. I saw numerous doctors to try to figure out what was happening to my body. After over a year, I was diagnosed with an AUTOIMMUNE condition (SLE). It has been two-years now, since permanently removing NuvaRing, and my condition has improved with time but my IMMUNE SYSTEM is still out of whack and my LYMPH NODES ARE STILL ENLARGED throughout my body. If anyone else has these systems and has been diagnosed with an AUTOIMMUNE DISORDER after using NuvaRing, please respond. CAUTION: please be careful young women as added hormones are not good for our bodies and really should not be pushed so readily by the health care profession. Also, keep in mind that your doctor will not back you when you are experiencing problems from medications that he/she prescribed. You will ultimately be told that the medication did not cause the problem in order for him/her to avoid becoming a party to a lawsuit.
-- By monai | Reply | (2) replies | Private Message me
July 16th
2003
9:38 PM
I took Leukeran for approximately 7 months in addition to Prednisone. This was 20 years ago and several of my doctors believed this put my autoimmune condition in remission. At least for 18 years it was in remission. Three endocrinologists believed my hyperthyroidism was the result of my taking Leukeran, not to mention, it also threw me into menopause at age 31. Currently, I just went back on Leukeran, in addition to being on Medrol for the past 3 months. They have tried every other medication that has not worked so well in the past 3 years with many set backs of my autoimmune problem - finally they have come back to Leukeran, which personally I'm hopeful will retain my hearing. My doctors here did not want to put me on Leukeran since they said it is too toxic. (Is there a drug that isn't toxic?)
It appears that many of the medications I have had to take (anti-cancer drugs) can cause secondary cancers. I suppose one has to outweigh the risks and what one has. In some medications, the benefit outweighs the risk.
-- By bj | Reply | Private Message me
May 11th
2003
2:52 AM
It is hard to decide what is really happening.
Cold autoimmune hemolytic anaemia, ITP
IgG and IgM attack normal blood cells.
Liver and Spleen Hyperactivity due to damaged blood cells.
Combination of Pneumovirus, exposure to extreme cold, and Fluoroquinalone drug used for treatment.
Suspect Hospital cold drinks and Ice cream continue to exacberate.
Reaction with Ciprofloxacin treatment for ear infection. Nov 2001. First episode.
Jan 2002 repeat after 1 useage of CiPro in combination with Cortisteroid. landed in hospital cramps and CAIHA.
recovered and went north. -35C and ear drops. Clotting and CAIHA. counts down. Severe pulmonary emolism. Sever -Cramping in legs hands and chest.
This was my first experience with fluroquinalone drugs and doctor prescribed Levaquin three times afterwards have put me in hospital with repeat symptoms. Hemoglobulin counts 60-64.
Suspect that in certain persons Quinolone drugs react on autoimmune system to produce antigens against self.
This is probably an autoimmune condition that is pre-exisiting and in combination with the drug the autoimmune system overreacts.
-- By bobslink | Reply | Private Message me
July 25th
2009
1:22 PM
I was on levaquin august 2008 for a sinus infection. After about day 5 is was in pain. My joints ached terribly. My knees, my hips, my wrists, elbows and fingers. I have undifferentiated connective tissue disease with lupus like symptoms. I thought that maybe the levaquin made me flare. I stopped taking it on day 5 and after a week felt somewhat better. I am on meds for joint pain for my autoimmune condition but still had the joint pain with the levaquin. The physicians assistant that I saw said joint pain wasn't common. From what I'm reading here it's very common.
-- By kb86307 | Reply | Private Message me