research finding from different sources on the mrf site

[ladycolorado]

here are findings from clonogen labs: http://morgellons.org/clogen1.htm .here are the findings so far from osu: http://morgellons.org/osu.pdf . here is from suny labs: http://morgellons.org/suny.htm . here are the findings from jeny haverty : http://morgellons.org/jhaverty.htm . here are the findings from the tulsa police crime lab: http://morgellons.org/crimelab.htm . (LC).

[hilly]

Lady C you are AMAZING......! ! How do you manage to find so many things... all your research is mind boggling... I'm SOO impressed ..... at least it shows you must be better and your brain is working overtime. Clever you, I think you will get this solved all on your own.... xxxxxxxxx Hilly ... Thankyou..

[ladycolorado]

nah hilly, i still need the help of all of you good people, (LC).

[hilly]

LC when was the article from the Clonogen Labs done ??? recently ? x

[gumball]

hi ladycolorado you are a jewel you and so many others help so much by bringing info back to this forum for everyone to read personally i have learned alot in the short time i have been hear thanks a bunch to you and everyone who contributes here it sure means alot to everyone gumball

[ladycolorado]

yw gumball the saop trial seems to help will post day by day to sees how it goes, skin less crawly skin seems soft and seems to wrok well i clothes. yes try to find new thigs to put up put up alot of videos in members louge, comedy and stuff hope you likre it, (lc).

[cd3girls]

Has anyone noticed? these are all very old postings - and easily accessible to anyone who hs the ability to do an online search. They are a conglomeration of symptoms - and repeat very old information

LC - I can appreciate you compiling this information. however, it focuses on what we already know.

Isn't anyone interested in a treatment? surely, as a group, we can't be solely focused on the suffering. clearly we are all a victim. Isnt anyone curious on a possible cure?

[ladycolorado]

ywa cd3 i agree this for newbies sice many comig in. yes concerned for a cure..........which i think shall be a vaccine for the chylamidia pnemonia vaccine. there is a help site called http://cpnhelp.org/ . i do believe underlyig cause for morgellons and other diseases. a study of morgellons patients getting chlamydia pnemonia vasccne all were cured i 7 fays. sucess on animals primates etc. there is a cure out there i developmet, yes. dr. harvey told me this myself. so apologize if same stuff for you, but those new might find interesting why posted, (LC).

[ladycolorado]

Originally Posted by cd3girls

Has anyone noticed? these are all very old postings - and easily accessible to anyone who hs the ability to do an online search. They are a conglomeration of symptoms - and repeat very old information

LC - I can appreciate you compiling this information. however, it focuses on what we already know.

Isn't anyone interested in a treatment? surely, as a group, we can't be solely focused on the suffering. clearly we are all a victim. Isnt anyone curious on a possible cure?

yes my main focus is improvemet and definatately a cure but when we have on a cellular level why have not foud one already. i have never been a doom merchant in here, but some folks new do ot even know a fungal aspect at all (LC). this one may be borig to some like us who know disease well, but trust me, i post on a whole host of things, but alot of the posts get buried, (LC).

[cd3girls]

yes my main focus is improvemet and definatately a cure but when we have on a cellular level why have not foud one already. i have never been a doom merchant in here, but some folks new do ot even know a fungal aspect at all (LC). this one may be borig to some like us who know disease well, but trust me, i post on a whole host of things, but alot of the posts get buried, (LC).
[/quote]

I totally get what you mean LC - I feel the same way (re: posts getting buried). I definitely feel like my posting re: plaquenil has gone unnoticed.......

Why try a possible cure, when we can remain fixated on the symptoms? Yes, there is a bit of sarcasm in that statement - but I am confused. Are folks looking for help on this site? or are they simply looking for a sympathetic ear? I think we can support one another (DEFINITELY!!). This site used to be focused on treatments and cures (thanks bubba!!). But IMHO - been relegated to a venting forum. I know we ALL need a place to feel safe, and comfortable, in sharing our "misery". but lets not forget the end-goal - A CURE!! and i believe that plaquenil can help many. And if I have to be a pest, to get my point across, I will do that. I will risk the anger from the group in order to get relief to SOMEONE....... ANYONE. I will do that because I care, deeply, for everyone on this site.