(Age 18-24) Pregnancy :: Emotional Eat Everything Stage
Jul 19, 2014
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'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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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 just been diagnosed with CKD stage 3 (GFR 48) and I can't understand why. I have low blood pressure and don't have diabetes. I am slim fit and healthy and age 52 so not that old. I also have a low white blood count. Can anyone shed some light? My GP does not seem worried, and so nor should I be, but I feel uncomfortable not knowing what has caused this.
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How can I improve my Stage 3 kidney disease, having a G.F.R. of 34?
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Hi! I'm going to preface this post with some background information: I'm 19 and I've been suffering with constipation for my entire life (my parents have videos of me straining to have a BM when I was still in pampers). It wasn't until last year that I was diagnosed with constipation by delayed colonic transit and put on Miralax to help move my BM's.
Unfortunately, because this diagnosis came so late, I've been straining to have BM's for the past 19 years, changes in lifestyle (diet, exercise, fiber supplement, etc.) all for naught. This straining led to hemorrhoids, which brings me to this forum. I've been dealing with hemorrhoids since elementary school, and when I have a flare up, I'm practically debilitated from the pain– my last flare-up kept me awake for 3 days straight and gave me multiple migraines. The flare-ups happen once every few months, but can last up to a week.
I wanted to know if anyone on here has had a hemorrhoidectomy, and what their experience with the procedure was like. I'm figuring that my hemorrhoids are AT LEAST a stage 3, and the surgery looks like the most permanent option. Also, if anyone has constipation by delayed colonic transit and as a result have developed hemorrhoids: how have you dealt with it? What has worked for you?
I see a lot of the post-op for a hemorrhoidectomy has to do with the intake of fiber, but too much fiber can actually make me MORE constipated. :(
Any thoughts, opinions, or personal experiences would be a LIFESAVER. Thanks for listening to my rambles!
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I am a 34 year old male who was diagnosed with hemochromatosis only after a liver biopsy because i only have one of the genetic markers. When diagnosed my ferritin was over 5000. Shortly after i was diagnosed with stage 4 cirrhosis of the liver. Is anyone out there in the same boat as me.
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I have recently been diagnosed with Parkinson's disease and am worried and confused. Are there exercises I should do? I am not on medicine but I understand that there are some that should be considered. Which ones are best for the early stage of the disease.
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I recovered from stg 3 Sarc (in lungs, lymph, joints, sinus) 13yrs ago, after 5yrs of illness and 2yrs of steroids.
I now have Erythema Nodosum (sp?) - red painful bumps on lower legs.
Research suggests that 'EN' is associated with a specific version of Sarc, Lofgren syndrome, which is usually resolves quickly and without treatment.
I'm scared to go to the Dr, as I don't want to face the tension & round of tests to exclude a Sarc relapse. It's not something I want to go through again...
I wonder if it's very likely for a relapse to come with a whole new presentation of the Sarc? Or is it unlikely to be sarc, as I never had EN the last time?
Does anyone have any experience or advice which may help me decide what to do?
Best wishes to all who are currently battling with their Sarc, I truly understand your pain and your exhaustion. I was not expected to recover last time - but I did.
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I was told way back in August of 2013 I had copd. Smoked for 33 years. Started when I was 13. Did stop smoking in October. Now on 12 meds daily and get out of breath doing just about anything. I own a lawn mowing biz but getting harder and harder to do my job and getting ticked off clients because I cant keep up. Have been getting real depressed about everything. Someone told me to keep a daily blog about my life with copd. Started that about a month ago. Its somewhat therapeutic, it at least lets me get stuff off my chest so to speak. And maybe someone will read it and go hey i'm going through the same crap. In my case its hard to find folks going through it or those that do who even want to talk about it. So if your getting depressed i would recommend doing a blog. No one may ever read it, but you will be able to get out all the stuff you want to say. Thanks for listening and i hope you find what you're looking for.
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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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I'm a 37 year old man who was diagnosed with HSP in 2007. My symptom was the rash which appeared all over my legs and buttocks. The rash went away but left me with stage 3/4 kidney disease. I feel very scared this will lead to total kidney failure. My recent results doesn't look good with my creatine being 216. This has ruled my life and I'm so upset this could happen to me. The doctors don't know anything. All they have done is put me on 10mg of Ramipril and basically hope for the best. I'm getting married in July to my beautiful fiancé who I love so much but I seem to focus more on this disease and what might happen to me in the near future than her. I'm going to try an alternative way to help my condition. Systematic ideology (excuse the spelling) This focuses on strict diet control, with taking 100 percentage herbal ingredients. The therapy focuses on targeting muscle groups and emotional part of the body. Has anyone else tried this? Would love to hear from anyone in the same boat as me and is there anyone out there that has been in the same situation and continued in stage 3 for a very long time.
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My son is 8 years old and has today been diagnosed with first stage Perthes.
His foot turns in when he walks and he has pain in his knee.
Please can someone tell me how to make life in the house easier!
He has been told not to put any weight on his leg at all and has been given a pair of crutches, but is a wheelchair better?
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How long after a stage 0 lumpectomy , can you wait befor you receive Radiation treatments !! mine is held up due to my HMO Ins. I didnt need Chemotherapy!
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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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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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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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