I HATE THIS @%#@#% DISEASE - Page 5
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  #41 (permalink)  
Old March 14th, 2008, 11:28 PM
niecy is getting prepared for new grandson!!!
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Default Re: I HATE THIS @%#@#% DISEASE

If anyone here needs to talk to someone, please pm me, and I will give you my phone number. There are many people here that will help, in more ways than you can believe.

Love, Niecy
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  #42 (permalink)  
Old March 14th, 2008, 11:35 PM
Kritters is a fungus magnet
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Default Re: I HATE THIS @%#@#% DISEASE

Niecy,
Is it Emily???

I just want to point out to anyone thinking of 'ending it' that you may think it will be the end of your pain and suffering, but we have no idea what comes after, and it could very well be just as bad if not worse as a result of your decision.

Please hang in there with the rest of us. We need the strength we all have as a group. Help us support each other. This is larger than our individual selves. We are here to help you. Keep posting. We will help.

Kritts
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  #43 (permalink)  
Old March 15th, 2008, 10:19 AM
Natalie is going slow
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Default Re: I HATE THIS @%#@#% DISEASE

message been recieved! Thankyou. I felt peoples prayers yesterday. I HAD too. Im OK. I cant call on people here for numbers. I would never do that, not right now. You dont even know me!! Let me continue reading and posting for awhile. Sorry I put so much darkness on people. And my nick name is sunshine! Go figure huh! Im a good actress at times. But you people see more than most. I am grateful beyond beleif to have you all and this place! Got get out today and do something pleasant for myself. Love you all, Nat
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  #44 (permalink)  
Old March 21st, 2010, 06:22 AM
labrat is .. every hair on my head is alive and its slowly eating out my brain...
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yes guess wot? eye hate this f@?cking demonic dispicable disgusting filthy horrible moronic stupid peptic ugly etc etc disease myself..it needs to b sent back to whence it came frm HELL.. so ur at the right place hey we all!! hate it.. so stay strong
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  #45 (permalink)  
Old March 21st, 2010, 06:54 AM
labrat is .. every hair on my head is alive and its slowly eating out my brain...
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if u leave we have one less voice to stand up to the real culprits when the time comes.. and im looking more foward to that day!! than my healing.. im not gonna miss that day for anything and i believe its just around the corner.. so stay coz power comes in unity and numbers
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Old March 21st, 2010, 11:30 AM
dragonfly2 has no status.
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Default Sisters and Brothers

WE all have got to hang in there! I personally have been through the nightmare and am not out of the weeds yet. Is there really an end to this or just remission so to speak. As soon as the last few (outward expression) lesions clear.........here come 5 more. Over 90 % of my entire body is and was was and is...affected. ESP has brought my skin back so remarkably. the second picture is before the first after, I am loading some pics now of my skin which looks so much better. My throat neck arms legs etc. Stay tuned my friends
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  #47 (permalink)  
Old March 21st, 2010, 01:45 PM
tcmgpt13 is "status viatoris."
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Hi there Dragonfly,

I am wondering if you are doing any internal treatments as IMHO it is very important to try to eliminate as much of this as you can from the body in order to have a reduction in external symptoms. It has been in treating this both internally and externally over time that I have seen a reduction in lesions. This spring I think there may be none as I believe the latest herbs I am using have pushed a lot of this out of the intestines, liver and gall bladder areas of the body. I see signs of brown spots drying up and flaking off my skin too. Nearly all parasites (and I think there may be an unindentified parasite involved) will spend some phase of their life cycle in the intestines, so doubly important IMO to treat this area. I have also used ivermectin and been treated by a doctor for viral infections (all tested for--in my case mycoplasma was ruled out, but there are some signs of lyme involvement too).

I wonder about some of our earlier posters on this thread. Natalie moved about two years ago and I do not think she has been on since then. Hopefully she is feeling somewhat better and doing okay. Also been quite some time since we've heard from whatthehelminth. She had a wry sense of humor and took some beautiful Morg photos with her microscope. Hopefully they and others on this thread who no longer post have at least gotten to remission of symptoms. I often think of WTHH, as she was someone I used to correspond with quite often. I pray she is okay.

Anyway, congrats once again on winning your SS disability with a Morg diagnosis. Good news for you and for all who will follow.

best, tcm
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