Endometriosis :: Cerazette - Emotional And Depressed
Jun 7, 2016
I was diagnosed with endometriosis behind uterus Dec 15 had diathermy and put on cerazette Feb 15 however the tablets seem to have been making. Me upset extremely emotional and depressed, the GP has taken me off them for a month. What other options. Are there apart from pill? I'm really worried all the pain will come back as cerazette has kept it all at bay!
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have been on and off Cerazette for last few years and have started with bad anxiety to the point where I stopped taking it but then had horrendous periods and was going dizzy. So I'm scared to come off it but at the same time wondering if it's perimenopause as I'm getting fast heartbeat at night but feel constantly emotional and exhausted and also nervous/ anxious so I'm wondering if anyone else has felt like this on Cerazette?
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My GP gave me cerazette, and after taking it for a while I broke out in acne so stopped. But the pain then got miles worse. Last night I had an ultrasound which showed my left ovary has moved to the back of my uterus, causing me awful pain.
I am wondering now was it the Cerazette that caused this, or was it going to happen anyway and should I have persevered with the pill.
I have read so much conflicting information so I wondered if anyone knows?
Also, I have been told by 2 doctors that laparoscopy makes the problem worse, but one told me it doesn't. I am so confused.
Lastly, has anyone tried the estrogen metabolism tablet DIM Plus? I read the reviews and it sounds good but I am so nervous to try any other tablets.
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I just left my post-op appointment for fibroid removal via abdominal myomectomy only to find out I have severe endometriosis. My OB/GYN says I have blocked fallopian tubes. I'm completely distraught. I'm 32, single, no children (would like all that sooner than later) and had the fibroids removed so that my uterus would have the "all clear" for babies someday. My doc says there was no way to know this prior to surgery and that the most severe cases are asymptomatic. As he spoke, I zoned out. I recall him saying he tried to remove the scarring and tried to see if the tubes would open bla bla bla. I don't know why I didn't ask for a pathology report or pictures, sizes weights.
Looking back, when he visited my hospital room the third day after surgery, I was told 4 fibroids were removed, but was initially told I had 7. I was in an anesthesia induced haze, so I didn't really hear much else. Today I asked about the 4 vs 7 fibroids and he said he removed all the fibroids that he could see. What the heck does that mean? Does that mean I still have 3 in there somewhere or did they shrink from the 5 months of hellish Lupron injections? I've noticed when I'm in shock, I forget to ask important follow up questions such as "Soooooo are there still some in there?"
At this point, I'm not sure what to do, with so many issues going on. In addition to dealing with this, I have other issues such as intense muscle spasms that can't be diagnosed, thinning hair and a balding crown. I'm not ready for children, but I'm extremely worried. I don't want to go through complicated pregnancies (if I can even get pregnant), miscarriages, IVF. It's just too much. According to the doc, I'll be reproductively old in 3 years (thanks for the added pressure)! I'd appreciate any advice anyone can give. I was only prepared to deal with the fibroids as endometriosis does not run in my family and I have no idea where it came from.
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HOW IT STARTED:
Yes, I was one of those annoying people who all the teachers liked.
Once, one of my professors even told me I was one of the "golden children" of my year. I suppose I worked so hard to get good grades because all my life I had been encouraged and enabled to do my best. I was used to success. In college I even overcame my shyness and gained a lot of good friends and a handful of real, true friends who I deeply care for. I had a part-time job in my fiend that I worked between classes, and I was looking forward to continuing my upward climb to success.
So when I lost my out-of-college job because the company had a financial catastrophe that made it impossible for them to hire me, I figured, "Hey, I'll just get another job and move on with my life. No big."
But almost a year later I still didn't have a job, and because I'm inherently introverted I had lost touch with most of my friends because they were all too far away to see in person and I'm terrible at keeping up with social media. I was living at home with my parents, sleeping in the spare bed in my sisters' room, and slowly realizing that all the people who were "Looking forward to seeing me succeed in the future" were going to be direly disappointed in me.
FIRST WAVE:
New Year 2013 brought on odd feelings. I still had hope that things would improve, but they consistently didn't. I lost a few big freelance clients that I was counting on because I made a few dumb mistakes, and that made things worse. I started crying in the bathroom for "no reason," not understanding why I was feeling so down and out when I still had potential, I just wasn't living up to it yet.
Fast forward a few months and I had basically given up on myself. I believed I was a loser, someone who had let down the many people who had trusted me with their wisdom and advice. I wasn't one of the "golden children," I was a pathetic fake who couldn't even call someone on the phone without feeling incredibly anxious, much less actually interview for a job. All the confidence I'd gained in college was gone and I felt even less sure of myself than I did in high school.
It was like the "real me" got locked in a room somewhere and I couldn't find her.
My mom noticed I was moody and finally confronted me about it, but instead of helping it only made me feel like she was even more disappointed in me and fed my unconfidence even more. Then, one day, after my mom got angry at me once again for being unable to communicate my real thoughts because I was so confused myself, my dad came out and let me sit there and cry until I had composed myself enough to speak. He was calm enough to keep me relatively calm and we discovered that the depression was probably coming from a few different sources. I was feeling lonely without my friends. I was back in my childhood home and reverting to the unconfident person I used to be. I was disappointed in myself and projecting imagined feelings of disappointment from others onto myself. I never got out of the house so I felt isolated. I wasn't making a steady income and that was stressing me out. Etc.
I decided to stop freelancing full time and get a job so I could at least get out of the house, make a steady income, and be around people. But after several interviews that were just awful because I either didn't have enough qualifications for that particular job or because I was having an off day and feeling really socially awkward, I didn't get any of the jobs.
SECOND WAVE:
I revamped my hope. But then it got crushed.
I'm still not as bad as I was last year, but I'm starting to feel like randomly crying again and sometimes my skin feels like it's going to wriggle off with how much I just want to get out of my house. I'm so afraid that I'm going to delve back into self-loathing-ville again, and I know that I sabotage myself when I'm like that. I so do not want to lost this tiny bit of momentum I've achieved, but I can't make things move faster. I can't get a job any faster, I can't get a car until I have money from a job, I can't get a job sometimes because I don't already have a car, I'm stuck, I'm stuck, I'm going crazy.
SO...
I know a lot of people around my age are going through things like this but for my particular situation does anyone know how to help me push through until things improve? I'm getting so tired of feeling so bad and I'm losing my energy trying to keep going. My parents are enabling me to stay home and do nothing but I don't want to stay home and do nothing! I want to get a job and be independent and have autonomy and start becoming who I used to be again so I can be a confident, awesome person! AAH!
Also, right now I'm not feeling so bad so I have a sense of humor, but in an hour or so I might be curled up in the bathroom crying into a towel so no one will hear me. I got on this forum in the first place because my skin was feeling antsy and I wanted to get away so badly and I wanted to know if other people felt the same way. Crazy mood swings, anyone?
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I'm 21 weeks pregnant, ftm, i watched ariana grande on tv performing live and started crying BC she's so pretty and skinny and it's not fair. I'm so emotional right Now it's ridiculous, anyone else?
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I'm 10 weeks pregnant with our first child and I think I've hit the emotional eat everything stage. I can't stop eating I'm like the hungry caterpillar or something, but my husband's in Arizona for work and I'm in Virginia and I just wanted to talk to him so I hop on FB and I see he shared a video about 40 minutes ago so I send him a simple hello message and no response. It just makes me feel like hey pregnant wife should be the first thing you talk to when you get off work considering I'm your wife and pregnant with our baby. I went from so mad that I wanted to punch something to crying am I wrong for feeling this way ?
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I miscarried about four weeks ago. I am still having some spotting and a lot of cramping. My emotions are the hardest part i think. I don't know how to deal with them. I get angry easy, sad easier, and I'm just not happy at all. I was very happy before this happened. I cry whenever I see the pics of the ultrasound in my head. Such a beautiful baby. Just no heart beat. I was 8 weeks along. I'm pretty sure the baby died while i was out milking our cow. I had severe cramping. The next day at the er when i was bleeding the dr said it died within the last 24 hours. I really do blame myself even though logically I know it wasn't my fault. I know the baby was not strong enough or developing properly but I still feel I could have done more to stop it. I don't know how to deal with this loss it hurts a lot still. My heart aches for the child that could have been. What can I do?
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lately i dont know what is going on with me., the other night my husband turned away from me and i felt like my heart broke into a million pieces and i couldnt stop crying. i literally cried all night. i cry for everything., and now i get frustrated really easily. i cant stand anyone. i just wanted to know if it was normal? also my appetite has gone away. everything grosses me out and i end up throwing everything up anyway. help??
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I have been on Mit for a long time now. I was on Prozac but it didn't work. I was on 30mg a day, before bed. Now im on 45 mg a day before bed.
I don't sleep properly still. I've been diagnosed with severe depression.
The drug makes me very very angry at the slightest thing.
I go nuts and throw things, swear at friends and family.
Things I would never normally do.
However, there has been one upside.
4 days ago, I felt happy. After 4 months of not feeling a single emotion except anger and pain, I felt happy. I cried, I was so shocked.
I had forgotten what happiness felt like. And when I felt it, I didn't know what to do. It almost hurt. So I just cried.
But the point is that I was happy. For the first time in months. Keep taking the pills. They make you feel something.
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This is often called emotional blackmail to A person who has been abusive to you draws in another person who totally sides with them and heaps even more abuse on you They often go to family members or friends or they get attorneys to heap even more abuse on you This happened to me and I did see some of it coming bc I happened upon a book about emotional blackmail But I totally underestimated how abusive other people they went to could be And I was in a very vulnerable situation post accident I want to warn others about this bc it makes things even worse and it puts you in a lot more danger It is like mobbing or a gang where they increase the abuse using their brother or whoever or hire an attorney and lie to the attorney or they may call other authorities on you or even try to claim something criminal Just consider this when you find yourself in an abusive relationship.
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I noticed a lump in my neck around 4-5 months ago. I ignored it for a month (stupid I know) and then went to the doctor who suspected thyroid goitre and sent me for blood tests, ultrasound scan and referred me to a specialist. Following a thyroid uptake test the consultant confirmed that I have a multi-nodular toxic thyroid goitre and am hyperthyroid.
When I went to the doctors originally I told them that my only symptom was the lump. However, I now realise that the anxiety / irritability, tiredness / lethargy that I'd put down to being stressed at work are probably actually related to my thyroid. It's also slightly depressing that the weight that I thought I'd lost through my sensible eating efforts is probably thanks to a faulty thyroid gland. It never occurred to me to mention heat intolerance to the doctor either - I thought that was just me.
I started on a lowish (10mg) dose of carbimazole 3 days ago. Since then all of my symptoms have been exaggerated and I have never felt so tired, lightheaded and emotional / weepy.
I found this forum this morning and it's a comfort to see on this forum that I'm not alone and my experience isn't that uncommon. I just wouldn't have expected the medication to have such an effect in this space of time. Nobody warned me!
My husband and I wanted to start trying for a family but the consultant has told me I shouldn't until my thyroid is under control. Early menopause runs in my family. I have been advised that the best course of action is radioiodine treatment as soon as possible or a partial thyroidectomy. The choice is mine. I'm thinking of Radioiodine treatment but am worried about long term impacts.
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I've been on mirtazapine for about 3/4 weeks now. When I first took them I had extreme tiredness.. Song with muscle aches and heart palpitations. After a week or so these symptoms seemed to go (minus the tiredness). These past three days I've been feeling dizzy constantly. Not so much dizzy.. More like off balance, I've also had problems with my visions, such as seeing little black floaters.. I know dizziness is a side effect but I didn't realise symptoms could kick in after two weeks. I've also been feeling more emotional and suicidal and I'm not quite sure why...
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I had my long-anticipated consult with a Pain Management doctor yesterday (Monday 1/27) It went reasonably well, though as expected we both have HEAVY accents, with his being Egyptian and my being SOUTHERN=) We had some issues understanding each other, but nothing we can't work through. I was "happy" to find that I had nothing to prove to him because my pain is well documented (partly due to my OCD) through my medical records and subsequent reports on various treatments. He had no interest in repeating any of the modalities that I have already tried with no success. That, too was well documented, including but not limited to Injections, PT, TENS, Biofeedback, Cognitive Therapy, Psychotherapy (counseling). He seemed "baffled" that I am "still standing" with the extensive problems that I have. He said it was most helpful that I have seen specialists in all fields of expertise pertaining to my pain, to rule out the need for further surgeries and treatments.
Now, we go forward with pain management. There is an IRONY here. I have finally found a doctor who will help me to "manage" my pain through medication. However, as of January 2014 my insurance will not cover medication. Believe me, I'm not complaining, as I realize I am fortunate to have insurance period, in today's environment. It just horrifies me to know that I cannot afford most of the medications that a PMD would prescribe for me.
He has no problem prescribing the Fentanyl patch for me, with my gastric/absorption issues. However, without further research into a generic option (which will still be expensive) I don't feel that I can afford that. I used the patch successfully in 2005-2006, but I had excellent insurance with $25 script co-pay. We discussed that Morphine has helped me, but he says that, too is extremely expensive. He suggests Methadone for not only its similarities to Morphine, but also its steady release once established. I must confess I freaked out (just a teeny bit) because I asked him if that was like the drug on "Breaking Bad". Yea...He thought I was silly, too. He chuckled and said "Funny you think I prescribe that".
He suggests that if I can't afford the patch (I can't ) then let's try the Methadone, starting with 5 mg twice daily with the option to increase if necessary. He wants to try one medication at a time (I agree) so that he can determine it's effectiveness vs. multiple meds causing multiple side effects. He explained that he will work with me until I can achieve an acceptable level of pain relief, by seeing me once per month. WHEN, not IF...say hallelujah...we reach success, he will start seeing me every 3 months. I can certainly do THAT.
I have concerns before filling the Methadone script and starting to take it. I'm hopeful that some of you may be able to share your experience. Is it effective for pain relief? Is it sedating or is it mood-elevating? I cannot cope with sedative effects because my career is demanding that I am alert and on my game at all times. I could benefit from my "mood" being elevated, as these past months of "fighting" for help have really dragged me through the depths of Hell. I take medication for anxiety and depression, but they're not magic pills...I guess I will always battle those demons. I just want to be very selective and careful to avoid any pain medication that may exacerbate my emotional issues.
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Have done some shorter stints of CBT/psychotherapy for depression and anxiety in the past which really helped at the time but never really found I got to "get to the root of my problem" and shift it permanently. At the moment, I am not overly depressed or anxious but I felt that perhaps some EFT or even hypnotherapy could help me deal with some underlying recurrent insecurities.
Just a little apprehensive because of the lack of evidence regarding the effectiveness of this technique so I wondered if anyone has ever tried EFT or hypnotherapy and could advise/give a little insight into how effective/not effective they felt it was?
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I was taking Levora birth control and increasingly had mood swings, depression, etc. the longer I took it. After four months I decided I am just not the same person on it and my symptoms are very evident to those around me (not to mention the increased acne and water weight!) My doctor suggested the NuvaRing as it is a different way that hormones are released into your body. Has anyone struggled with emotional and mental symptoms on the pill and switched to NuvaRing and had success?
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My symptoms are: i've been very moody, emotional, tired, nauseous, loss of appetite, bloated, my stomach feels sensitive.
I'm a diabetic and my sugar has been fine.
I'm on Yasmin but accidental skipped 4 tablets last week.
Could i be pregnant or just tired?
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I been having all the symptoms of endo. The lower back pain, pelvic, stomach pain, bloating. I also have leg pain which im not sure is linked to endo but my pain is constant as i've had it non stop for a month now but feel worse when im on my period.
I have been to the doctors as he said it could be a possible ovarian cyst but he didn't really know so he is referring me for a ultrasound which wont be for a couple of weeks!! He did no other tests apart from a urine test (still waiting on results)
My mum has told me both my cousins have endo and im just wondering if its genetic?
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Long story short, I've been suffering from excruciatingly debilitating cramps every single cycle,this started three ish years ago I spend hours in the ER I've been admitted few times as well and it's the same bloody routine every single time
I'm in immobilizing pain, cold and hot flashes, nausea, vomiting fainting poor appetite dehydration low blood sugar levels heart palpitations weakness fatigue exhaustion crankiness moody insomnia etc etc
All these symptoms I experience up to two weeks before my period then during the first 3-4 days of my period then total exhaustion few days after my period and I'm symptom free a week before my period give and take. I should also mention that I've had several x-rays, ultrasounds and all kinds of blood tests and everything comes out good healthy and no problems yet I have these symptoms that just don't seem to go away, last stop for me was a visit to an endocrinologist and he's taking care of my thyroid problem given a new doze a little over a month ago and things are looking fine on that end I had a referral from him to see a gynecologist in mid September but having been bed bound with all the symptoms and persistent pain on my right abdomen I spent the night in the hospital and everything came out good both the blood and the urine tests and the ultrasound and regardless of how many drugs were given to me via an IV I was still experiencing bad persistent tedious excruciatingly painful pain on the right side of my abdomen so the gynecologist today discussed laparoscopy with me and I felt so comfortable around her and being as fed up as I am with all this pain I said I'll go for it
It will be a Diagnostic Laparoscopy for Endometriosis she put it as urgent and she'll be the one performing the procedure I'm happy things will finally start to clear out and hopefully I'll be in my way to some kind of cure hopefully but I'm so nervous please help any words of comfort or advice will be greatly appreciated. I did half the paper work already and I'll have some more to do the day of I have a really good doctor guiding me thru this call me weak or crazy but I'm incredibly nervous.
It would be nice to hear from anyone who's done this kind of procedure please BTW I'm 23 years old, healthy no health complications non smoker or drinker
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I'm wondering what the symptoms are when endo attaches to the bowel?
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If I use Cataflam for severe endometriosis, should this drug prevent new outcome of my disease. I understood that Cataflam is NSAIDs and that it is usually is used to treat pain. However, Cataflam should have some anti-inflammatory potential, so I hope that it would help. How am I supposed to deal with this disease?
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