Infertility :: Diagnosed With Pelvic Inflammatory Disease
May 24, 2016
How likely is it to get pregnant after being diagnosed and treated for PID (pelvic inflammatory disease)? Keep in mind I've only had one child in over19 years with no other pregnancies!
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When I was 16 I was forced into having oral sex with someone that I went on a date with. I am now almost 21 years old and have only ever had intercourse or any other sexual encounter with my fiance. For the past years I have had problems with my periods and pain during them, but never thought twice about it. I went to the doctor yesterday for a possible UTI and found out that I may have PID. Though I have yet to be diagnosed with an STD (labs are still out), I am assuming that Chlamydia is the case, given to me from the guy who forced me to have oral with him (seeing as how he probably had many interactions with other girls if he did something like that to me.) I am now TERRIFIED that I have had this disease for almost five years. I am getting married in just 3 weeks and am now afraid that I won't be able to have children... What are the chances of this if I have in fact had this disease for this long?
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From 4 yrs i have been suffering from severe pelvic pain with lots of inflammation in both hips. all blood works come normal but mri does show inflammation. Doctors cannot find what it is, can it be my ovaries or fallopian tubes inflammation or infection which is causing this, plz somebody help. I want to get pregnant but my pain in pelvis which is that worse that I limp many time is not allowing me.
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A little background information about myself: 23 y/o female, diagnosed with PCOS at 19, suffer from multiple UTIs and kidney infections each year.
Starting in about September, intercourse would be incredibly uncomfortable and painful, causing me to cramp severely after and bleed. These symptoms became worse and worse, and I began spotting between my periods. So, after meeting with my GYN in October and her suspecting cervicitis (inflamed cervix), I had an appointment beginning of December for a colposcopy and cervical biopsy. Upon touching my cervix with a q-tip it bled out and was EXTREMELY sore to touch. Waiting on further consultation from the results, but according to my GP: pre cervical cancer cells, uterine lining infection and cervical infection.
I have now been on 2 rounds of different antibiotics with no improvement, I believe I am getting worse. Ever since the biopsy, I have bled EVERY DAY FOR SEVEN WEEKS! I have a fever that comes and goes, chills, nausea, constant pelvic pain and am extremely tired all the time.
I have been researching (bad idea I know) what could be causing all these symptoms and am thinking PID or uterine fibroids? Any advice out there?!
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Hi, I was treated yesterday night with 2 grams of azithromycin for gonorrhea (25 year old female). Didn't have any symptoms, but knew a sexual partner had it. Couldn't take the shot because of a bleeding problem I have. I have pain in my back today. Can this be associated with PID? I was exposed 10 days ago. Going for a follow up in 10 days to make sure the pills worked, should I worry before then? Or give the meds some time to work? I went to the clinic yesterday so I can't run off from work today to ask them.
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I'm 21 and I've been having irregular periods since June 2014; in recent months have had increasingly painful pelvic pain. Went to the GP multiple times in an attempt to figure it out but got nothing. Finally went to the GUM clinic on saturday and was diagnosed with PID, although the cause is as yet unknown. I was told it is likely due to a 'long-standing chlamydia infection'. Thing is, I haven't had sexual contact with anyone since March 2014 and for the year up to that I was in a committed relationship. That guy was the only one I had 'unprotected' sex with (was on pill); everyone else before him I used a condom with. So I had no idea I was even remotely at risk (as stupidly trusted this guy) and I'm now worried that because of this and having no symptoms, that I might've had the infection for a while without knowing and it therefore have a worse effect on my ovaries etc.
I'm really worried as dr was pretty casual about the PID, but from what I've read it's really serious. Did anyone here have chlamydia for a while before PID? Do you know how you got it? And how has PID affected your sex life/fertility since diagnosis? I'm so scared I'm going to find out I'm infertile because someone I trusted did this to me when I was so so careful myself
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Just wondering if anyone else has had LS and Pelvic Inflammatory ? They told me it's not connected. But they couldn't find anything else wrong.
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I was diagnosed with PID last week Monday. The ultrasound scan revealed prominent collection of fluid behind my uterus. I was told to do a HVS/MCS. The result showed scanty growth of Escherichia coli. Before this result came out, I started treatment with ciprofloxacin and metronidazole IV for 4 days with pain killers. Follow up with drugs to complete 10days. I still have sever pain in my legs,lower abdomen and lower back. I had an ovary removed last year August because I had ovarian cyst. Please I need help. It's been 2 weeks plus now in pains. I'm tired of this pain.
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I been having pain in my right side of my pelvis some time it will go to the other side and I been having back pain and my periods are missed up it been spiking mouths and they be longer and heavier and i been sicker lately then before.
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I am a 24 year old who works a 12 hour rotating shift pattern (including night shifts). For the past 6 months or maybe more o have had upper left abdominal pain (cramping/aching) and more recently lower pain (sometimes across lower, sometimes left and sometimes a specific place on the lower right). I put it down to IBS due to shift work. My partner convinced me to see the GP as I have a family history of IBD. Oh and my bowel movements vary from constipated (less than once a week) to lose (not diarrhoea and multiple times per day)
Had stool tests and blood tests. I expected them not to find anything to be honest and just did it to please my boyfriend and put his mind at rest.
Doctor phoned and said that "the stool test shows signs of inflammation indicative of inflammatory bowel disease". I couldn't really ask more questions because of where I was. Phoned in for blood results and told by reception that they were fine.
I have been referred to the gastroenterologist and have an appointment in 2 weeks.
I am tired all the time and find it really difficult to get out of bed, frequently have naps at work but put that down to shift working.
I don't want to take any laxatives because I never know when it will change between constipation and loose stools and when I'm working, I often can't get to the toilet.
I often have joint pain but I also have a knee injury and some hyper mobile joints.
I am so confused as to what is going on and hate not being in control of my body. I know I only have mild symptoms, I feel so alone (shift work doesn't lend itself to meeting people regularly).
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My 27 year old son began exhibiting symptoms of inflammatory bowel disease about 2 months ago. He had severe stomach pain and his food wouldn't digest for several days. A CAT scan showed an inflamed ileum. He went to a gastroenterologist who ran more tests and put him on prednisone. The inflammation went away and at the last followup visit the gastro dr. decided not to label my son with IBD yet unless the symptoms come back. My son noticed that, since his problem began 2 months ago, he no longer sweats. Early on, he would get dizzy and light headed at work (it was September and still warm)but he wasn't and still isn't sweating at all. He goes to the gym for a workout and 1/2 hour later his face is bright red and his head feels hot and prickly, but not one little drop of dampness happens anywhere on his body. Since both the inflammatory bowel/digestive problem and the anhidrosis started at the same time, I wonder if they are related, and if so, what disease does he have? He is beyond frustrated at this point because his digestive problems aren't gone completely, and he has days where he's exhausted waking up after a good night's sleep, and has minimal energy a lot of the time.
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I stopped smoking 6 months ago and to be honest feel worse for it. Currently i am suffering from
UC and mouth ulcers. I have never suffered with mouth ulcers before and my bowel has been painful since stopping smoking. What i need to figure out is this: is it worth taking up smoking again or do i need to put up with abdominal pain, bloody diarrhoea, mucus and faecal incontinence and always
having to use pads. I am only 55 and feel like i am 85. I am beginning to think smoking is the lesser of the two evils!! Have read on many forums how people give up smoking and then suffer the indignities of UC. Is there any medical evidence on UC and stopping smoking? If not, why not?
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GI Consultant has sent to my GP copied to me:
This patient had had a SeHCAT test as well as colonoscopy. The SeHCAT test is reassuringly normal showing no evidence of bile salt malabsorption. At colonoscopy there was ulceration of the ileo-caecal valve. I understand the terminal ileum and colonic mucosa appeared normal. Ileo-caecal valve biopsies shoe benign ulcer with focal cryptitis. There is no granulomata or other features diagnostic of inflammatory bowel disease. Other colonic biopsy show mild nonspecific chronic inflammation.
This taken together with his symptoms and the raised faecal calprotectin is highly suggestive of Inflammatory Bowel Disease.
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I have been having bleeding from my back passage, fatigue and tiredness for weeks and finally got to the doctor today. She told me that I had IBD and that she would arrange for an urgent referral for a colonoscopy (2 weeks). She also said that I should come back if the symptoms got worse in the mean time. I am anxious that I maybe underplayed the symptoms slightly. every time I go to the toilet (5 or 6 times per day) it is bright red and seems not to be getting better. Should I go back or is it fine to wait two weeks?
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Have a lower abdominal pain on the left,i was diagnosed with pcos when i was 17 now am 28 and it hasnt gone away,i have recently diagnosed with PID and was on treat ment for 3 weeks ,was given doxycycline,metrinazole and indocid together with the vaginal cream,it has only been 4 days and have a white vaginal discharge which comes when am having an abdominal pain.my question is where do i get the discharge and why is the inflammation not going down despite taking medication?
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My doctors tell me I developed the problem when I was about 8 but was never diagnosed because I didn't complain of any pain. They said my case is very rare.
As I am now fully grown I can no longer be treated for the disease other than by hip replacement, although they said I will have to wait 10 - 15 years until the pain becomes unbearable as I am too young for the surgery at the moment. Until then, I basically have to put up with it an have simply been told to not wear high heels and to not put on any weight!
My left hip is left flattened and shortened and my leg in almost an inch shorter than my right. It constantly feels uncomfortable and sometimes extremely painful, especially when walking long distances, laying on my left side, sitting for too long (eg. during long car journeys) and I end up feeling very frustrated!
I have tried physiotherapy, pain killers, a digital pain reliever and swimming to help the pain - all with very little helpful effect.
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I'm 25 and over the past 6 years I've been diagnosed with 4 pretty serious autoimmune conditions. When I was 19, I was diagnosed with Rheumatoid Arthritis which is often crippling, even now. I was told this was an autoimmune condition. Shortly after, I was diagnosed with Coeliac Disease, another autoimmune condition. The Arthritis and symptoms of the coeliac disease when I hadn't controlled it obviously made me feel unwell and I often felt lethargic and unhopeful due to a lot of pain and stuff going on in my body.
I managed to go on a clinical trial which allowed me to have a new and powerful arthritis drug which dramatically improved the condition and I managed to cut gluten out of my diet. I also lost a bit of weight - this helped.
However, after the trial, my symptoms of arthritis gradually came back but was usually kept under control with the exception of a few flare ups.
When I was 23, I was diagnosed with Type 1 diabetes after getting a very quick onset flurry of symptoms (another autoimmune condition) - I find this very difficult to manage.
I've recently moved cities and transferring all of my specialists and treatments left me with no arthritis medication, and a long wait until I see a diabetes specialist to adjust insulin levels. As you can probably imagine, I've been in an awful lot of pain and been feeling very down, tired and lethargic. I'm very upbeat although having so many conditions and I don't let it bring me down, even though I work a full-time job 8 til 5 everyday. I've been having problems with blood tests, platelet counts, that kind of thing.
I was aware that I had the antibodies for Hypothyroidism as I had the test for that about a year ago and I knew it was just a matter of time before I developed it. Upon my most recent blood tests, my TSH level was 47.7 - ten times the top end of the normal limit. I've literally just started levothyroxine but, as you can imagine, I feel completely overloaded with health issues and like my head is going to explode and quite down about it all.
I'm sorry to give you my life story but I was just wondering if any one else has any of the other conditions I have and how they manage with all of them?
Also - how should I have been feeling with a TSH of 47.7? Should I have been feeling VERY different because, like I said, I always feel fairly tired and down due to the combination of illnesses. Any advice at all would be appreciated - I feel massively alone with this.
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I got my results back from the needle biopsy and primary Doctor didn't know what it meant and said I had to go to a Endocrinology specialist so I wanted to see if anyone knows what it means the results were:
FNA-Lt Upper Pole Thyroid Nodule, 1 Thinprep slide, 1 Cell Block:
-Non-Diagnostic
-Thin Prep and cell block are hypocellular and consists of occasional tiny groups of follicular cells, colloid and mixed inflammatory cells.
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I have been dealing with infertility for going on 8 years. I am young but it is still very hard. I found out yesterday that my 21 year old sister is pregnant by a man who lives with his girlfriend. She wasn't trying yet she got pregnant. It hurts SO BAD! I want to be there for her but I can't even look at her right now it is so hard.
I haven't had a period since October. When I was living in Michigan my Gynecologist put me on Clomid. I was on it for a year but it never worked. I don't ovulate properly and obviously don't have my periods on a monthly basis. I was just wondering if anyone has or is going through this and what you did to get through this/solve this?
Any suggestion would be great. I feel horrible right now and I need some uplifting news.
Thanks,
Erin
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"Someday your ship will come in and you will be at the airport"
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Erin
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I'm wondering if anyone has any advice regarding diagnosing graves and thyroid eye disease in pregnancy. Having never had any problems until being pregnant I'm very confused as to why I've suddenly got it? At around 12 weeks into my pregnancy I noticed a change in my eyes (one was protruding), after seeing an eye dr, he advised I'd be tested for hyperthyroidism and following his advice the bloods came back as a positive for hyperthyroidism. I was put on PTU by an endocrinologist for the rest of my pregnancy and at week 39 I noticed a yellowing in the White of my eyes and admitted myself to the maternity unit for blood tests following speaking with a midwife. It turned out I had developed severe jaundice (Which I now have learnt through research to be a severe side effect to PTU) and that my liver was failing; I had to have an emergency c section that night. I am pleased to say I have a had a healthy baby boy but I'm so anxious as to whether these conditions will worsen post pregnancy.
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How far along do you have to be until you can get your first ultrasound?
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