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Post by Lynn on Jun 21, 2011 9:37:28 GMT -5
Or, has anyone noticed the texture of their hair changing 'down there' by Kammy.
Hi Kammy
When I had worms crawling in the pubic hairs really badly the hair was thinned out and rough. Wirey even. Once I found a way to kill those worm squirmy around off; the hair went back to normal even though I still get one type of bug that periodically crawls through the area.
Another thing is while the worms lived in the pubic area the skin was to sensitive. I could gentle scrape my nails through the area trying to get the sulfar soap to penatrate more and my finger nails felt like razor blades cutting through the skin even though I was very careful. Now I can be as rough and tumble as I want and the skin texture and sensitivity is not a problem. At the begaining of this whole thing my skin all over became too sensitive.
I had tried to get my doc to help me figure it out. I had thought my blood pressure med was the blame and quit it. That did make a big difference, but still always a bit to sensitive. I use aspargus tea now to control my blood pressure and it amazes my Doctors and how low it stays compared to the medicine which had its side effects.
In Light Lynn
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Post by itchin4answers on Jun 21, 2011 16:37:21 GMT -5
Well girls, your not alone in this. I have discovered men have this issue just as much as the gals. I have been off this site for awhile but wanted to share with you my findings. Itchin4answers, Please read my story at: www.morgellonsinsect.comI would hope you find some comfort in knowing that your not crazy and I understand your suffering completely. Feel free to share this information provided with doctors you are dealing with. I spend long hours educating doctors on this subject. I have long since stopped trying to get treatment from doctors but hope to spread the word of truth about this horrible disease. Yes thats right, a parasitic disease. If you approach doctors with a parasitic disease they tend to understand better and at least are willing to look at information you provide. If people want to continue to talk about chem trails and nano foolishness or genetics doctors are only going to turn their backs on us. Medical doctors are not scientist. Thy read lab reports and treat accordingly. If and when we all can get doctors on board with morgellons being a parasitic disease we might make progress. Progress that could shed light on other speculations and theories. Itchin, look up Bartholin's gland. The woman I was with constantly was having problems in this area. Damn doctors kept telling her it was normal. Well it is not normal and can be painful as well. Women have issues with labia, vulva, glands in the vaginal area because there is a problem. Men have testicular pain, prostate and groin pain to the point the whole pelvis area hurts. Yes I too have vision, neuro, cognitive, joint pain along with burning in the legs and spine. Much of the symptoms are from toxins secreted by the parasite. The pupa material itself is very caustic to the human body creating lesions in the body as well as out. The MRI'S I have had show this but are most likely explained away as cyst. I had a very good radiologist using three sets of MRI's, see this little critters and put in reports that they are growing in size and multiplying in numbers. I also would like to point out that I have been in touch with 4 men around the country suffering from this who also have microscopes. I was not surprised when each of them discovered blue, red, clear and black fibers in semen samples. We all experience something crawling around in our bodies. Try to except the fact that we are suffering from a parasitic disease. AN INTERNAL PARASITE! Let the spinners and profiters know your not interested in products, treatments or far out theories. Keep focused and decide which side of this issue you want to be on. Keep your head up, if it lives it can be killed, and will be. Thank you for your story itchin4answers. Read each page on my web site and judge for yourself. Good luck and keep demanding answers with truth behind it. Dear lostintime, I'll do my best this morning to reply to your post, I have one awful head cold right now. I read your story on your website - I was totally unnerved (particularly by the images & video). I found your story heart breaking to say the least. You are such an intelligent man with a science education too. A lot of this is now falling into place for me. I am aware of Bartholin's cyst, it was suspected I had one of those in the 90's but turned out it wasn't as it was further back towards the perineum & then disappeared. I haven't a clue on what causes Morgellons, though I do like your take on this, makes a lot of sense. I'm so sorry for what you have gone through, but as you said in your story, we are all going through this & it just needs to stop. Take care & bless you for sharing with us all. Love - itchin
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Post by itchin4answers on Jun 21, 2011 16:39:57 GMT -5
Hi Lynn & kammy, with regards to change in hair "down there" - in between my maintenance shaving when the hair would grow back, when I was showering & had lesions on my hands some of the hairs would literally stab my lesions, these "hairs" weren't normal.
Love - itchin
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Post by lostintime on Jun 21, 2011 18:19:54 GMT -5
Thank you for the compliment itchin, I am not the smartest guy walking the earth but I am certainly not the dumbest. One thing is for sure, I am determined to get my life back! I am angry with the poor way the medical community has handled this disease. I am extremely angry with the fraudulent clams by profiteers such as Hildegarde Staninger , Clifford Carnicom , Rahim Karjoo and many others. These folks have lied to you all, planted fictitious posters on web blogs and raked in a ton of money from our suffering. It is not uncommon for people to blame an unknown disease on all sorts of things. Just spend some time on any blog and you will see the minds of sick people being flip flopped back and forth with each new theory presented by backyard researchers. Enough already!!! I network with half a dozen close people affected by this disease along with a few in the medical field that really are trying to help and have a better understanding. I also stay in contact with a few Universities as directed by my doctor. In the meantime I can only seek treatment for my symptoms and would encourage everyone suffering from morgellons to do the same. I would suggest seeing a real medical doctor, one that you can find comfort and trust in. Explain that you have this condition, show the doctor that the CDC is working on this and request what you need to cope ie: sleep aids, antidepressant, pain medication or whatever you might need. If living in America and this has affected you to be unable to work I would suggest applying for Social Security Disability. It is a long process and expect to be turned down from the start but don't give up. If the United States Government wont fix the problem or be honest about the problem then thay certainly can pay for the problem. Money talks and when it cost them too enough money they will acknowledge it and find a way to put a stop to it. Don't give up. I do not believe morgellons is just a new STD as people have contracted this without being sexually active. Sexual contact has stricken enough of us to know it is one way and we all know people like to have sex. This will spread to far more people before help arrives. Hang in there. To Kammy, I have three video's of the insect larva. They are all from the same slide and the same insect. Sorry, but the other men keep in touch have only found the fibers in their semen samples. Most of the people I know with microscopes do not have picture or video capabilities. If anyone is going to buy a microscope I would suggest getting these features. Document,document,document everything. Including video. This type of evidence speaks volumes in a courtroom. Hang in there girls. I have done something that has not been done before but I assure you others will be finding the same. Maybe some have through there urologist office? The truth will prevail...in the meantime hang on to your cash and be good to yourselves. Women may be scared up from this but your all beautifully no matter what happens. www.morgellonsinsect.com
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Post by Lynn on Jun 22, 2011 1:52:48 GMT -5
Sorry Kammy
Could never see them. They would swirl in circle. Either going in or comming out of the area. One they hit the next stage they would crawl to the surrounding area and bite real hard. If I tried to kill them and they were hard to kill. They would just move from the area a little further away and do teed off biting. Then aventually move back to the spot. It would take me about three days to kill them. Once I started using the Olive leaf in my shower spray mixture. That seem to get rid of them. The bug I have left does not twirl. It does go through a stage whare it feels like a worm scouting along and stings like a Nat. Can not seem them at any stage. Before the olive leaf I would get a few survivors that would go into the next stage which is a bug I call the hookey crawler. Legs feel like they have little hooks in them and they bite like a big ant. Leave a bite mark like an ant also. Very rarely did I get to see any bugs. Just guessing that the hookey crawler might be a body mite that normally lives in the hair folicals of animals. I get more hits in homes that have pets.
In Light Lynn
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Post by kammy on Jun 22, 2011 6:35:58 GMT -5
Lost, can you get one of the guys to purchase a Petri Dish and put their semen in it and then just look down into the dish with their microscopes from time to time to document what happens to the fibers?
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Post by bannanny on Jun 22, 2011 15:07:57 GMT -5
I haven't read this entire thread and only have a little more time to try and catch up here today... more family coming in tomorrow!! But I just wanted to say I also have the same sensations "down there" as I do on my head. Nothing helps... just do alot of scrubbing when I'm in the shower. But as far as sexual transmission goes... not happening here with my man! He's still fine and shows no signs or symptoms of morgs at all... and I'm the 3rd morgie he's lived with too. Josh had it, our Suebe had it, and I have it... but like I said, he's still good to go and I thank God for that every day. The man's been thru enough already. I'm just so happy I can love him and he can love me... it's the best thing that's happened to us both in a very long time.
love ya's ~~ bannanny
P.S. Hang in there Arni... you and everyone here are always in my prayers.
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Post by ibzahp on Jun 22, 2011 23:56:48 GMT -5
I wanted to add to the down there issues that my honey has never contracted this either despite serious exposure so perhaps it has to do with a strong immune system? I have had fibers and lesions in that area of various types-not real pleasant. These days tho just tiny fibers.
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Post by itchin4answers on Jun 23, 2011 17:19:55 GMT -5
I just had a UTI in which I took Doxycycline for 2 weeks, I thought I had kicked it, but... here it is back again. I'm in the middle of a urine test experiment, it's a simple test of putting a jar of urine out in the sun to see if it turns purple. I've only looked at my urine microscopically one time in the past. After the test was completed and the urine was not purple, I poured it out outside and when looking at the jar, I see something that look shrimp-shaped and these long fiber-like strands still clinging to the inside of the jar. So, I decide to look at these microscopically... i51.tinypic.com/17bcps.jpgI'm publishing my findings on the other site, but my conclusion is something that I have seen before. I didn't look soon enough, by the time I got the microscope, petri dish set up, ate dinner and then went to look; because they were under stress (by having the fluid around them removed) they altered their shape into unidentifiable blob-piece entities. I could see with a magnifying glass that these shapes in the jar looked like they had legs, heads, etc. It sounds like the ramblings of a crazy person but our 'lab magic' parasites are designed to disappear or turn into other blob entities that do not show specific legs and heads when they are stressed. Our parasites have to be viewed immediately upon being removed from the body or they will morph into something not so identifiable. I have shown this before in other experiments. 'Lost' has captured this caterpillar-like with pincers immediately after leaving his body. This stealth, sneaky phenomena which the devious have lab concocted must be very proud of this aspect... it seems it would make it harder for the doctors or lab technicians to actually 'see' a parasite of this nature because of the time lapse of them viewing it. What I did notice though was that there were lots of uric crystals in the urine. These crystals are in the shape of everything with a sharp edge that you can imagine; knife edges, the points on knifes, thorns, broken glass shards, the jagged edges of a broken bottle, etc. If our uric crystals are now being manipulated to form sharp-edged weapons and they are in the bladder, this might cause the bladder to have pain? I'm going to conducting more experiments with urine, studying it and possibly looking at vaginal fluid soon. How many of the women are having painful sensations with penetration? How many have re-occurring bladder pain? Guten Morgen kammy! ;D I'm still having bladder issues. I took a urine sample last night, put the jar under the brightest light I have, which is over the stove. Thought I was seeing things. I washed the specimen jar, didn't dry it with a cloth, shook the water out & put the lid on. This morning I took another sample of my urine, sure enough when I shake the specimen jar it's like a snow dome...full of floaters, specks, some are dark to blue in appearance some are white, one looked like it had a long tail. This is a good link on fibers in urine; morgellonsdiseaseawareness.com/photo_galleries/fibers_in_urine
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zena
New Member
Posts: 9
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Post by zena on Jun 23, 2011 19:12:17 GMT -5
Hi all - I'm new to this board. I've been coming here to look from time to time and it seemed like a good environment so I thought I'd sign up. I had a ct scan (not sure if that's the name-it's the one with the dye) and right after that I noticed that my urine changed. It smelled kind of like ammonia and it still does 2 1/2 years later. I also noticed many new things in my urine. There were crystals, fibers, and specks and it came on fairly rapidly. Then, I developed Lyme and other Morgellons symptoms. When I went to the ER in the beginning - remember those desperate days in the beginning? - one of the things they did was took a urine sample. The doctor looked at it and he said that he was stumped on what was in my urine. He even showed it to the other doctors there and they didn't know either. It was good to finally find out that I had Lyme and Morgellons because I hated not knowing what was causing all of my health problems. I thought I had cancer.
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Post by itchin4answers on Jun 23, 2011 21:31:59 GMT -5
Hi all - I'm new to this board. I've been coming here to look from time to time and it seemed like a good environment so I thought I'd sign up. I had a ct scan (not sure if that's the name-it's the one with the dye) and right after that I noticed that my urine changed. It smelled kind of like ammonia and it still does 2 1/2 years later. I also noticed many new things in my urine. There were crystals, fibers, and specks and it came on fairly rapidly. Then, I developed Lyme and other Morgellons symptoms. When I went to the ER in the beginning - remember those desperate days in the beginning? - one of the things they did was took a urine sample. The doctor looked at it and he said that he was stumped on what was in my urine. He even showed it to the other doctors there and they didn't know either. It was good to finally find out that I had Lyme and Morgellons because I hated not knowing what was causing all of my health problems. I thought I had cancer. Hi zena welcome! My son has problems with his urine smelling of ammonia. My urine doesn't have an odor & the sunlight test didn't turn my urine purple. I'm envious you have a diagnosis for Lyme. Very unfair I have been labelled DOP 3 times without any tests to prove an underlying illness. Still searching for a Lyme doctor. Not that one wants a diagnosis of cancer, but at least the diagnosis is "normal" & people are treated accordingly. Thankfully you don't have cancer, but I've often wondered if Lyme & Morgellons are behind many cancers. Take care itchin
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Post by Lynn on Jun 24, 2011 1:00:25 GMT -5
Hi Zena
Glad you came aboard. Sorry for the reason. I think I will try the urn in a jar. I put out tons of tiny white fine peices of sand and have wanted to point it out to the hubby.
In Light Lynn
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Post by kammy on Jun 26, 2011 9:44:23 GMT -5
Hello Zena, welcome! We don't know what part the contrast dyes are playing in our health, but they're on our 'suspicious list' - dyes can be made from quantum dot technology. (Those mad scientists are experimenting... we just know they are! lol)
I'm watching an AIDS video that Ginna left and it seems that there was a 10 year study done between heterosexual partners and how easily the positive ones transmitted to their negative partners and the answer was zero. In the meantime, the whole world has put a condom on as a first line of defense. I'm thinking it's some sort of rubber conspiracy.
From my own experiences, being sensitive down there - I cannot tolerate certain types of condoms and the lubricants are just as bad too. I was wondering if anyone else had sensitivities to the latex or the lubricants?
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Post by sheredelight on Jun 29, 2011 20:50:57 GMT -5
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Post by bannanny on Jun 30, 2011 12:40:09 GMT -5
Hey right backatcha lostintime!!! It's good to see you back... and congrats to you too!!!! Ya wanna hear something silly? I always thought you were a girl... not that you talk like one!! I just figured you were cuz you're so compassionate!! Not that men can't be compassionate either... cuz I've finally got one of the most compassionate ones ever!! Anyhoo, I'm so very happy for you... and it sounds like you've got one incredible lady by your side now!! Did you ever see our wedding thread? Here's the link if you didn't! lymebusters.proboards.com/index.cgi?board=rash&action=display&thread=14687Speakin of families... welcome to ours zena!! You've found one of the best places I know of for support, understanding, and most of all, love! We can get a little goofy at times too... which is also a very good thing! Gotta try to stay happy and positive... it's one of the best defenses I know of to fight this mess! I know what you mean about your urine smelling funny tho... so does mine. It comes and goes, but there are times when the smell becomes very pungent... and sour smelling. Anyhoo, I'm glad too that you got a Lyme diagnosis as I believe the protocol for it will greatly help you with morgs. Sometimes I even think morgs might just be a mutant form of lyme since almost every morgie out there ends up getting a lyme diagnosis too. But who really knows... hopefully one day we will. That's a great video you posted sheredelight... I have pics that really seem to match his. They were only samples taken from myself tho (no fluids involved) and also the web that grew on the base of my scope grew from the morg gel that oozes out of my hands and feet. But I really saw alot of similarities and learned alot from his video... so thank you for posting it! I think this first pic of mine looks like his parasites (or whatever they are)... Then there's the web that grew on the base of my scope after some morg gel oozed out of my finger and landed there. I left it to see what would happen and after a 2-3 month period, this is what it grew (which also looks like his webbing to me)... After the above finally lifted from the base tho... with no additional help from me whatesoever, the growth began to repeat itself all over again. Same growth, different pattern second time around... I also got the same morg "bubbles" as his. This was the original "bubble" that formed from the gel out of my finger... But there were even more of them left behind on the base of my scope after the second growth finally lifted... I found a morg researcher to send my entire scope to once the second growth lifted and it looked like it did above. All I've ever heard from him tho was that it seemed to be mutating again for a third time and that it was a tad scary to him. Anyway, I think me and microflasher have the same strain goin on... I say that cuz I believe there's more than one strain of morgs. I think there's at least 2. love ya's ~~ bannanny
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Post by sheredelight on Jun 30, 2011 21:57:06 GMT -5
Hi Bannanny, Yes it looks the same, wormy type thingy, that snout really got me, and those strange eyes, creepy. Your pic's are really good, you can see, the silk web, quite clearly. Thanks for sharing... cheers
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Post by bannanny on Jul 1, 2011 9:58:55 GMT -5
I have another pic of what looks like a head too where you can see the eyes (I think that's what they are anyway)... Ugly little critter eh? Don't know if it's the same kind of thing in micro's pics tho cuz the snout doesn't look as long. big hugs ~~ bannanny
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Post by sheredelight on Jul 3, 2011 17:00:15 GMT -5
Hi, amazing pic, it does morph into so many different looking worm thingies...maybe it's in an early stage, or their seems to be afew different kinds, species...just guessing... Thanks Bannanny hugs
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Post by bannanny on Jul 4, 2011 9:49:29 GMT -5
Yeah... I'd say there's a gazillion different looking morphed thingy's in morgs!! Should be called "morphellons" instead!
hugs right backatcha ~~ bannanny
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Post by ibzahp on Jul 4, 2011 15:41:28 GMT -5
Oh dear Kammy-no fun! i have that going on as well. For me mixed prescribed multiple kinds of antibiotics and anti fungals did not stop it. It has slowed significantly which is good. I even had the blood in the urine thing and fibers. Amazing looking at this stuff under a scope Geez I hate this stuff. i haven't been one to have regular large lesions very often. Lateely been struggling with folliculitis .
Have this bright red/pink sore under my arm (just one) it burns and smells cheesey and it came back after going away for a couple weeks. Feel like one big festering weepy sore sometimes.
I wonder if there are any fibers in this sore. It is about an 1' by 3'' inches. Sure the glands are clogged up there. been getting pimples on my feet too.
Sometimes (and I know its wrong) I wish these derm md's could experience the wide range of symptoms privy to Morgs survivors written off as dop. . Thanks for all you do kammy, and I hope you feel better.
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