Internal organs symptoms and conditions

Well on 2-15-09 my sister in law died just shy of turning 39. She had severe depression, As of three years ago she began starving herself. She would go weeks without eating or drinking anything. She was in and out of the hospital through out the years. She started taking Lamictal six days prior to 2-15-09. The Dr. said she had made a mistake and wrote 100mg where it should had been 25mg. The doctor's later stated it didn't matter if they wrote 1mg it would have happened eventually.

Now we had called her on her birthday three days prior to 2-15-09, and she said the medication made her feel weird. That night she fell to sleep and did not wake up but for only a brief minute in the hospital. After being asleep for a day she was rushed to the hospital were a battery of test were run. She had begun to have liver failure and sepsis. The doctor's had her airlifted to a hospital four hours away where liver specialist were available. She arrived there and withing a few hours her lungs collapsed, her kidneys began to fail, and she had two heart attacks where she finally died at 11:10 pm on 2-15-09.

So I am here to make you aware. This is the side affect no one has talked about yet. Now she had no rash. She had weekend her system by not eating. Other than her depression she was OK. The doctor's don't know if she had an allergic reaction or not. The autopsy will be arrive in 40 days. With just some fatigue and weird feelings she continued to take the medication for the six days. I read on and on and I see so many symptoms, this would be a great time to evaluate with a profession because lets face it we really don't know the long term affects. It could be doing damage to your internal organs, or not. I feel if your body is showing you signs that are not normal than it is a good indication that your body is telling you that is cant tolerating it to well. So at least your getting the signs you might want to see what else is out there. As God is my witness we wanted her healthy and to not suffer so I really do have only good intentions for you all.

The funeral is today.

Hi, my name’s M. and I posted my story on here about a month ago. Unfortunately, I’ve made no progress. I was hospitalized again mid-October for numbness and tingling sensations in my legs, which is a symptom of guillian-barre syndrome and supposedly needs to be treated very carefully. I had an mri of my brain again, this time including my spine to check for possible tumors. I was sent home the next day, negative for guillian-barre, but having received no answers. I was crawling up the stairs by this time, and was too weak to walk without holding on to furniture to support myself. My legs felt like cement blocks, and the neurologist specifically said, “I don’t know why you can’t walk.”
Since then, I’ve developed acute mononucleosis, which increases my fatigue and muscle pain, and causes me to sleep about 15 hours a day. Recent blood work also showed I was positive for an autoimmune disorder called Myositis, which is a painful disorder that causes the body’s immune system to attack its muscles and connective tissue. I was referred to a rheumatologist, who was the least sympathetic person I’ve met in my life, and told me my physical exam was perfect, so she felt the Myositis must have been a false positive. She re-ran the blood work, and the Myositis was negative. This is of course a relief, but how we’ll ever know which test is correct, I don’t know. The rheumatologist did notice the weakness in my legs and my difficulty walking, and suggested physical therapy to help gain my strength back. She also prescribed an anti-inflammatory medication that took away almost all of my pain. Thank God, something finally worked for me. We then saw the physical therapist who said, “We can probably make you stronger, but I’ve never seen anything like this before.”
I’m seeing an osteopathic specialist who is convinced my illness is directly related to Gardasil. Through ancient medicine methods, she introduced a vile of Gardasil to my system and noticed an immediate weakness. I’m not sure if I totally believe in her practice, but the fact that she noticed a rejection to Gardasil the minute she introduced it is enough to convince me. She believes that my immune system was basically poisoned by the vaccine, which is causing it to fight off things I need. She also said it probably doesn’t recognize the mono as an infection, and decides not to fight it. For a normal, healthy person, mono can last up to 3 months. For someone like me, no one knows how long it could last. It was my immune system’s weakness that allowed me to develop mono, and it was the Gardasil that weakened it in the first place. So thank you Merck, for yet another thing I have to deal with.
And that brings us to today. I’ve missed about 30 days of my freshman year, so I’m assuming summer school will be necessary. My high school won’t provide a tutor, so I can only take my core curriculum classes, and am having difficulty keeping up with just those few. I’ve gained some strength in my legs, and it’s a little easier to walk with the anti-inflammatory, but I still can’t walk very far without resting. I’m also taking an anti-depressant to help me focus-hopefully it’ll lift my spirits. Since I received the vaccine, my periods have been painful and irregular. The constant nausea, headaches, and occasional stomach pain/joint pain continues, along with extreme fatigue.
The doctors make me feel like a crazy person who faked this to get out of school. How could I possibly fake nausea for thirteen weeks straight, and pain that kept me up crying almost every night? How could I fake my difficulty walking while it’s causing me to miss both of my volleyball seasons? Before this, I had hardly missed a day of school in my life, and refused to stay home whenever I got the flu because I hate falling behind. I’ve played volleyball tournaments with sprained ankles and chipped elbows, I can handle pain, and I’m not a baby. If the doctors would take five minutes out of their time to try to get to know me, maybe they would see that. And the few who actually take the time to be pleasant don’t listen. They tell you they know, that they understand, but they don’t. They won’t drag themselves out of bed in the morning feeling nauseous and half asleep; they’ll be able to walk into their office without feeling like they want to collapse, and they’ll go home to the people who care about them and will actually be awake long enough to enjoy their company. No one will tell them they’re insane, and the worst part is that most of them won’t take the time to realize how blessed they are just to have the ability to do those things. How can the doctors not have sympathy when they’re the ones who put this poison inside of me?!
I know I’m very lucky compared to girls who have experienced more serious side effects, and am thankful that we were able to make a connection between my illness and Gardasil after the first shot. But I’m living proof of what just one stupid shot can do to you-how can you put yourselves or your daughters at risk of what I’ve gone through? The benefits are not just worth the risk..
My 15th birthday is coming up in just a few weeks, and all I want is to be normal again.

Shortness of breath has continued to worsen as its built up in my system. Chest pain and back pain on my left side seem to be worsening as well. I started Imuran as opposed to using Prednisone which is much harsher on your internal organs, but I am hard pressed to think anything could be worse then what I feel now. I have not lost my appetite, but the fatigue is unbearable even after I've eaten.

Shortness of breath has continued to worsen as its built up in my system. Chest pain and back pain on my left side seem to be worsening as well. I started Imuran as opposed to using Pregnozone which is much harsher on your internal organs, but I am hard pressed to think anything could be worse then what I feel now. I have not lost my appetite, but the fatigue is unbearable even after I've eaten.

I was on Luvox since it became available in the United States;Over 12 years. I was prescribed Luvox mainly for my OCD and as the years passed, I noticed obvious emotional blunting, lethargy;Mind was in a fog, retarded ejaculation, the works.

Have slowly reduced dosage from 300 Mg/Dy to 100 Mg/Dy with INCREDIBLE RESULTS such as greater energy, weight loss, feeling less "detached" and "cold," SOME anger (harmless & intermittent), lucid thinking-NO change in OCD symptoms whatsoever. Less impotence-All positives.

Will soon begin taking Choline and other B-Vitamin supplements to ease the final stages of withdrawal from this highly addictive drug that thankfully has the shortest half life of the SSRIs.

Turns out that Luvox leaves the brain BEFORE it leaves some of the internal organs it "lingers" in before total clearance from the body.

Plan to deal with my OCD and severe depression with a combination of therapy;A serious attitude change, nutrition, SENSIBLE supplementation and exercise.

Will STAY on my Klonopin (2 1/2 Mg/Dy) because I have a phobic mindset RE: My panic attacks which the Klonopin has kept at bay for the most part.

ALL psychotropics, neuroleptics and other "mind candy" is toxic and usually only MASKS the symptoms, giving the illusion of "treating the symptoms" of a particular disorder (set of).

And for what its worth, I USED to be super-pro medication. Just too many bad side-effects from various medications, including Luvox over most of my life.

Plan on going off of the last 100 Mg of Luvox VERY, VERY SLOWLY;Don't need any "Seretonin rebound syndrome."

I am a forty something year young female that has been on fentanyl now for approximately two weeks. I am approx. 85% pain free for the first time in about 5 years. Unlike the other postees, after 12 back surgeries, including the introduction of a spinal cord stimulator; I recently had a intrathecal pump implanted. Since the original implant, I have had three separate medications used, (morphine, dyladid and now fentanyl). With the pump, the medication is dispensed directly into the spinal canal requiring a minimal amount of medication, versus taking it orally or being absorbed into the skin through a patch. With the medication going directly to the spinal canal, it does not have to go through the other internal organs before reaching the pain site or nerves, thus minimizing the side effects. Do I have side effects? Yes, but they are minimal and I am very pleased thus far with the results. Where as some patients are receiving anywhere from 70 - 100 mg. in the patch over a three day period; I receive 80 mg. over a 42 day period. It is highly concentrated and again, does not have to be absorbed through my stomach, kidneys, liver, etc. before reaching the pain site. When the pump administers the drug, 100% reaches the pain site; where as out of the 100 mg received orally or through the patch, less than half of that reaches it destination. So far, this is the best I've felt in years. I can walk, sit up and play with my dogs for the first time in years.

after using daflon for my hemorrhoid problem ı start to sleep all days with headache.and felt myself like in depression

At first I thought this was great but after 18 days I awoke with some stomach tenderness & it moved to horrible back pain. I did notice a lil burning after intercourse at times. I figured it was just irritation but also got a bit concerned of UTI as they are so not fun.
The back pain though was severe so I went to check online side effects. I decided I was in too much pain to wait till the 21st day & just took it out..I've decided its definately not the method for me. I am disappointed cause it seemed initally seemed like the miracle method. Yes I too say the back pain probably is like labor even though I've not had any kids. I have been uncomfortable no matter what I have done. Its like cramping in conjunction with it. Felt like it was internal organs like Kidney's or something, I feel miserable. I had a DNC once to merely scrape the uternine wall this pain is worse than the cramping associated with that. With that they tell you not to intercourse a duration.

I have been on a very low dose of Lisinopril for about a month now in treatment of Proteinuria in my kidney and have not experienced any of the known side effects. I am, however, experiencing a very erratic menstrual cycle, namely spotting virtually every day. I have been to see an OB/GYN and it has been determined that my internal organs are normal. I do not believe that I am premenopausal and hormonal tests have confirmed that. I have read in this discussion string that a someone else has experienced similar symptoms. Are there any more women, who have experienced this problem? I may just go off the medication to test this theory.

I have experienced 13 years of hell with Levothyroxine, which is pure sodium. Everything in the body from skin to internal organs are affected by shrinkage and shortening of muscle. My horror complaint - leg cramps, massive thoracic jerking and therefore no sleep. think of salt cod or an Egyptian mummy.

First, do not deal with a GP. Thyroid is very tricky and only an endocrinologist should be consulted.

Second, get tested at a Nuclear Medicine Department in your hospital. You may be making enough thyroxin. Partial organs DO compensate.

Third, sodium binds with blood serum. Blood enters muscles. Muscles CAN store sodium. My case.

If you can get away without taking thyroid meds you may find withdrawal unbelievably difficult. In a withdrawal situation, a larger amount is released into the blood stream. You will find your muscles steely rigid and unbendable. You may be pulled over.

You will need huge willpower and support. My withdrawal is now in its 8th month.

I use acupuncture by Chinese medicine methodology, resistance exercise several times a day. Get yourself rubber resistance bands and put hooks in your basement walls and ceiling. Pilates is excellent. Magnesium tablets high strength. 1000 mg is allowable but I've done twice that. Some diarrhea but basically one is too dried out for there to be a problem. From a good herbal store, get probiotics 30 million a day, Udo's Oil (Canadian), eat almonds - several hanmdfuls a day - I hate it but Lorazepam had to be used as a muscle relaxant for 6 weeks at the worst stage. Never discontinue these abruptly. Detox drops after a visit to a QUALIFIED Naturopath. First, Unda Numbers to detox liver and kidneys, then thyroid and lungs. Very effective but you may only tolerate shortish stints- 10 days. me anyway.

Eventually, the muscles feel caged but bulging. Then they start undulating dramatically and free up. But so far I've had to endure 6 of these session at about once a week. After which even more toxic stuff pours out. But it WILL end.

I am 63. I resent losing wellness for so long and it took a friend to tell me about a relative with leg cramps to get the connection. By the way, it was the naturopath that identified the cause NOT a doctor. Allopathy (Western medicine) believes all drugs leave you with tissue renewal every 4 months. But Chinese medicine, massage therapists, naturopaths, injury rehab (they use theraball) and reputable spas don't.

All of you are young. I hope I have helped in some way. All of you who ache, I think it is the tightening of the muscles. it is like enforced arthritis. Number 2911, I hope you read this. Your little son sounds just like my beginnings of my dreadful journey.