New Tetanus Vaccine/Scabies/Fibers(Morgellons)/Too Much Ferrous Gluconate?- My Story

[Fables429]

1-14-2012
New Tetanus Vaccine/Scabies/Fibers(Morgellons)/Too Much Ferrous Gluconate?- My Story

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[[[[Has Anyone Tried Beta-Alanine, it is a supplement for athletes/bodybuilders?]]]]]
(I used it a 2 years ago for running, but stopped because I did not like the tingles sensation it gave me). I might experiment with it on my own soon since I just got Morgellons, because I still have a whole bottle of it, but I am afraid it might make it worse?
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It all started right around Christmas with scabies symptoms and very few fibers which I thought were lint, so it has been less than a month since I have had what I believe is Morgellons.

Please prepare for a long story but it has some interesting things since my story includes Arizona, being Contagious (might have got it from my roommate), scabies, New Tetanus shot, Stress, Mutant Mold, environment, Advair/Thyroid problems, Low white blood cell count, allergies, Iron/Ferrous Gluconate, German Descent, and more.

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I just recently got Morgellons just before Christmas, but I didn't know it for sure till about 4 days ago.

I graduated from a University this June. I also ran competitively for the Universities Track and Field and Cross Country Teams. I am quarter German, half Mexican, and I have other forms of genes such as a little Arab and Costa Rica and I believe more, yeah I am a Mut. I am a two time All-American in Cross Country. So I know what I am experiencing with my body and it is not normal. I have recently told my girlfriend, sister, and parents. And they are all falling into the category that I have that "delusional parasitosis..." but I am still smart, sane, and I can reason.

Well I am 99% sure I have Morgellons because I have the fibers coming out of my hands and scalp (only disease I could find on the net that matches this) logic and reason usually suffice for me.

I have a history of Hay Fever and Peanut Allergies (not deadly but I get really sick and vomit). While running I struggled with breathing issues sometimes and I was taking Albuterol and Advair-( Advair is known to cause thyroid problems) while running on and off for 5 years, but I tried to not take it too often. I have been off all of those since May. My white blood cell count has been low from tests in the past, I really need to get tested again. Doctors never knew why...

I am also Allergic to lots of things from different trees, mold, and dust mites. Been tested and have suffered from it in the past.

More fibers have been coming out since I started doing the extreme Vitamin/Health/Diet which seems to be helping. No alcohol, sugar, whites, caffeine. Also baking soda and maple syrup, organic, limes, alfalfa, fish oil, I feel like I need more. I was also experiencing mild other forms of the illness such as brain fog and some joint pain which has subsided since my diet started 3 days ago.

I am afraid it had something to do with the new Tetanus shot I got back in the Summer (stupid meeee.. ugh coulda been the biggest mistake of my life). Something inside was telling me not to take it, but I did anyways.

I have also been super stressed lately because my girlfriend and I have been in a long distant relationship since the summer and I am having financial difficulties because I have student loans and only a minimum wage job, well I had two part time jobs during Oct, and Dec which made me tired and unhealthy. I still work in retail and I was working at Regal movie theater until last week (it was seasonal).

Then I got scabies right before Xmas (Or at least I think from my roommate who was in Arizona doing a 6 week outdoor leadership thing in Sept where they "played" with the dirt worked outside, and he only got $1000 for the trip). I have heard Arizona being linked to massive Chemtrailing... He experienced the itching and went to a dermatologist who looked at skin under a microscope and saw the "mites" so off to the Permethrin Cream. But he experienced tons of the black dots on his plastic bed mattress after, which I thought was weird at first but we just thought it was the scabies and their droppings. I also experienced the black dots on my hands after the cream. But I don't think scabies do that, however he is not feeling any other symptoms at the moment so maybe he has a stronger immune system or it is the calm before the storm so to speak.

Well 2 days before Xmas I applied Permethrin Cream first I only applied less than half the body over two days, because I still felt them on my hands the next day. Then things seemed fine for about 14 days, when my hands got super dry and I thought the scabies came back, so I put a very tiny amount of the Cream on my hands and armpits. In total I have only used about half a bottle of the Cream since I got "scabies" even though it says to use the whole thing, because it made me feel sick.

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So now it is Jan 15th... I got the Tetanus shot on... hmm not sure I think it was in August. I got "scabies" maybe around Xmas,

(This next part is important)... because I was having itching in my right "armpit" for a little over a month maybe more before the scabies. I thought it was my deodorant or something.... and then I thought it was the scabies but that can't be right... so now I don't know what it was? (candida?) It still does itch a little, nothing wrong with the left armpit.

Before the scabies symptoms took place on my hands I had a very dry skin patch on the hair side of my right wrist for about a week and a half before I had the blood spots, thin pencil like marks, feeling like bugs crawling beneath my skin which happened about the same time my roommate saw the Derm for his itching 2 days before Xmas which he thought might be bed bugs at first, but I believe it was scabies or Morgellons or both.

I went to Urgent care twice and I saw no M.D. they just prescribed me Permethrin because of the story and symptoms I was feeling. I told both of them I saw a tiny very tiny black dot the size of a period on my knuckle while I was in the doctors office waiting for the nurse. I watched it for awhile and I then saw it start going into the skin (I know what I saw) I started freaking out and I had to really pick at it with my fingernails to get it out, I kept it on a tissue paper in a cup and brought it to the next urgent care who told me she was not going to test it and to throw it away.... so I did because I just wanted to enjoy Xmas with my family and girlfriend (which was sad because I could not hug or interact fully with any of them because of the fear of scabies).

So then 13 days later I went out to eat with my Dad and Sister which might have triggered my second attack (scabies like symptoms on my hands.. super dry too). Which happened while we were moving out of my old house the next day. I live with 4 other roommates, we all moved into a new house last week, and no one else is experiencing any problems (yet) except for the one who got scabies and the black dots, but they are gone now. Also while moving my friend was cleaning the freezer and underneath he saw this very ugly mold that had mushroom like growth and was green. He sprayed it with... well he doesn't remember but he said it "exploded" in black dust/mold and this very bad smell was in the kitchen....... kinda scary glad I was outside at the time.

Just Yesterday I have been cleaning spider like webs, with no spiders.... I saw one on the lamp on the ceiling above my bed with a small dead flying bug... not sure what kind of insect.... I put it in a Plastic Bag... I have a few samples now in plastic bags mainly of the weird fibers. I see these stringy webs around the air vents and on lamps, and larger clumps of fibers on wood and book cases, I have only been in this house for not even a Week yet....

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I might be sorta rambling, but I am scared even though I have pretty much accepted the fact that I have this disease. I am afraid of transferring this to others, I keep seeing weird fuzz ball things around the house, but I stayed at my Dad's house for 3 days last week. I did kiss and touch my girlfriend a few times over Christmas which has me scared the most, because I took more precautions with my other family members she lived in Idaho.

I am only 23 years old and I really want to raise awareness, maybe make a award worthy documentary while I am still sane... which I am highly considering, but I need a camera and "help" will need to travel as well. It would be a **** ton of work, excuse the language.

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There is also this lab in Corvallis, OR called Blastocystis Research Foundation which I emailed yesterday, I guess they were looking for subjects with Morgellons in 2009...

morgellonsgroup.proboards.com/index.cgi?board=research&action=print&thread=3310]Study

Study in Oregon looking for Morgellons volunteers in Oregon looking for Morgellons volunteers

There website is,
bhomcenter.org

I will also call them tomorrow and see what they have to say.

Part 2: Next

[Fables429]

Does any one know of any helpful doctors near Oregon, ozone therapy ( I know Anthony Kiedis has a famous doctor for Ozone Therapy)?, Cures? I know a lot from reading, but sometimes it all seems so overwhelming which I am sure everyone else who has experienced this disease or knows loved ones can attain to.

I just watched this video on Morgellons, says there is a Cure for it for people in New Guinea... and even others. Not sure how true this is...

lisawonders.wordpress.com/2010/10/14/morgellons-nasa-germ-warfare/#comments

But I do not know I am pretty sure Ozone Therapy, Alfalfa, Super Healthy Habits, and Hydrogen Peroxide 10% would certainly help... not sure if it can Cure, but I think I have a pretty early case since I have only been experiencing symptoms for less than a Month. Has anyone had any success with these?

How helpful are these full scale treatments?
msingler.com/morgellons.html

allaboutparasites.com/morgellons-treatment.html]Morgellons


I hope I can get through this completely so I can start that Documentary and really stick it to the Man... I believe this Disease is only the beginning and we all need to come together to not only fix this problem but all the problems that are coming. We need the support of "GOOD" people, scientists, business, lawyers, politicians,.... Everyone who has a good heart.
Why is there no Hollywood Documentary on this at the moment anyway.. its been going on for awhile.

And why is the Wikipedia page on Morgellons so piss poor??? Reading it almost makes me believe I have suddenly become delusional.... yeah right. My roommates can all see the "Fibers" that many others say they have.

Does anyone know if exercise helps or hurts? And if it is OK to do this outside>? Like is going for a Run outside a good thing? I don't want to attract bugs/parasites/fungus.... ect....

And how accurate/ important is morgellons-research.org? It seems to really good information, but you need to act quickly and get lots of testing done... and .... do everything in a extremely closed environment... I feel like I could cure this by living in a white box... in Antarctica?

Here is their treatment suggestions and they state I have to act quickly to stop any organ/brain damage.

morgellons-research.org/morgellons/morgellons-treatments.htm
morgellons-research.org/morgellons/morgellons-treatments.htm

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Should I use JWS protocol?
morgellons-disease-research.com/Morgellons-Message-Board/morgellons-treatment/5885-you-can-healthy-again.html

In addition to what? I don't know how much of vitamins/herbs/ect... to take and at what doses.

I am taking at them moment, I started 3 days ago.

-Vitamin C
-Sea Salt
-Ginger Tea
-B-Complex
-Alfalfa
-Fish Oil -OLA
-Maple Syrup/Baking Soda
-Squeezed Lemon/Baking Soda
-Aloe Vera Juice
-Coconut Butter
-Extra Virgin Olive Oil
-Milk Thistle
-Vitamin D3
-Acidophilus Probiotic
-Tea Tree Oil
-Water and Sea Salt and Vitamin C

Eating only organic Brocolli, Celery, Eggs, Beef, Flaxseed Oil Whole Grain Tortilla, Red Onion, Almonds, V8 Juice.

Any other food I need to stay away from besides Processed, GM-Foods, White anything, Sugar, High Fructose Corn Syrup?

Also using T/Gel Tar Shampoo and Basis Soap.

I need to clean my environment more, but I don't know what to do to do it? Borax? Is Thieves Oil good?

Should I not wear Cotton or not use a Feather Blanket? I have a dust mite pillow case and bed cover, but should I get a plastic one?..... Does only wearing 100% Polyester help?

Should I start taking::::: Not Sure about any of these.

-Only drinking boiled water?
-Zinc
-Magnesium
-Coenzyme Q-10
-Eye Drops/Ear Drops
-MMS
-MMS-2

-Niacin?
-NAC?
-Iron??? (I heard not to)
-Ozone Therapy
-Ozone Water
-the JWS protocol
-Bees?
-Magnets
-Zappers
-L-TYROZINE
-Lysine

-Thymus
-Iodine
-DMSO/Castor Oil Mix
-Chlorella
-Cocoa or unsweetened cooking chocolate made from 100% cocoa (Not sure)
-Hydrogen peroxide medical grade
-black hull walnuts
-Pumpkin Seed
-Papaya Extract
-Chiosan
-Milk of Magnesia
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-Cumin and Garlic
-d-mannose, or preferably erytrhitol
-Orange Rinds?
-Hydrogen Peroxide
-Silver (I am afraid of This)
-Apple Cider Vinegar
-Any type of special Bath/Shampoo/Soap

-Kombucha Green Tea?
-A vit/ liquid blend? Which one?
-- Peter Gillham’s Natural Vitality Liquid Organic Life Vitamins
Nature’s Plus Source of Life Liquid Multivitamins
Smart Basics Whole Food Based Ultra V Liquid Multi-Vitamins
Taken from:::
morgellonsaid.wordpress.com/immune-system/vitamins-minerals/

****Beta-Alanine****?? (Does this do anything to Morgellons>? I tried it to help for competitive running in the past but it made me feel all tingling all over my body so I eventually stopped, this was before Morgellons... might do something to help combat Morgellons, I am afraid to try it now that I have Morgellons, but could be a secret Key I have heard of no one else trying it.
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I also have no Mercury Fillings; However, I have taken large amount of Ferrous Gluconate (Form of Iron) in the past to treat low Iron counts to help me with my competitive running.... I am afraid of this build up of Iron over the last 5 years.... It was Ferrous Gluconate, but how can I help fix this problem? is there a Iron Detox?

I have a Doctors appointment with Kaiser on the 25th In Oregon, but I am going to try to see one tomorrow instead. What should I say? I think they are going to think I am delusional which I am not. What tests should I get done specifically. I want to get a parasite test, a blood test for everything such as nutrient and white blood cell/ red blood cell. A stool test. Lyme Disease Test, I also want a black light test. Heavy Metal Test... Mercury.
Should I get tested for Celiac Disease or Polycythemia? Anything else?

How can I convince my family, girlfriend, and friends that something real is going on with me?

It is hard to have hope that I will ever feel normal again.... Some good news is I will eat extremely healthy for the rest of my life.
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Thanks
-Fables

[Pollyringworm]

Do you have the lint?

[Fables429]

Yes, I do have the lint like fibers that I see come out of my hands, scalp, penis, everywhere pretty much. But I never see a super amount of them at one time...

It is pretty freaky but my itching is completely gone and my symptoms have seemed to have calmed down since I started eating healthy and taking multivitamins.


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*****I am wondering if someone has a simple, but long list of vitamins/food/minerals/herbs... that are helpful and that I need to take?

[kmar]

My only suggestion is to take NAC along with vitamin C.
A lyme doctor suggested that because it helps detox and improve the immune system with that combination increasing your body's Glutathione.

I think it was Dr. Klinghardt ( a LLMD ) who suggested that.

I've been using it and feel it definitely helps.

[trz103]

But I too had a remission stage after going on the multi vitamin health kick. But it came back and came back worse. Yes I let up and stopped being aggressive...however I had a brief 2 month period (Jan/Feb) where things pretty much subsided. Now the past month I have been on a pretty strict diet and lots of exercise. The symptoms have been much worse...itching, crawling, brain fog, joint pain, spasms, fibers, lint all over the house/car again, etc. So honestly it seems it comes and goes on its own regardless...at least thats how its been for me since the real onset of symptoms started about a year ago. Maybe I wasnt aggressive enough at first? Maybe its entirely impossible to fully eradicate it from your body? I along with everyone else here wish I knew the answer. I wish you the best and also urge you to be very very careful what you bring up to your "doctor".

[kmar]

I agree that this disease cycles. I really have to stay on my supplements because when I get lax, the symptoms return.

[confused]

Seems to me the buggies don't like the colder temps. My symptoms are really bad after it rains, as everything drys out it gets better.

I also have found that using medicated powder in my bed, no bugs in my bed at night. I think the powder drys them out, and they hate the menthol. Sleep with tight stocking type cap over my ears, dry your ears with alcohol and hair dryer before. I never put oil or moisturizer on my skin now, I think it causes the bugs and fibers to stick to your skin. This just helps me sleep with out bug attacks.

[kmar]

Likewise, I do not use moisturizer or oils because it seems to attract things.

I have found that Fungal foot spray (in powder spray) helps quite a bit and I have used the gold bond menthol powder with some success too.