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Thu May 21, 2015 12:12 pm by leeG
HI All, thanks for letting me join, i was diagnosed two yrs ago, altho had symptoms for much longer and now wonder if the MCTD started in my 30s when i was diagnosed with chronic fatigue. now also have raynauds, hashimoto's, blepharitis (sp?), asthma, and multiple allergies, Plaquinel has amazing effects until i had a severe reaction, and now on Atabrine (quinacrine) but its not as effective. …
Comments: 0
New to group, New to disease
Tue Aug 26, 2014 5:58 am by MissDaisy
Hello,
I am a 36 year old female with 3 boys, ages 4-9, and I work as a 911 Dispatcher. I started having symptoms about 3 years ago starting with lumbar pain. I put it off for well over a year thinking it was just over-exertion. When I couldnt take the pain anymore as it was constant, and even just turning my head to the side caused severe pain. I got to the point that standing, sitting, and …
I am a 36 year old female with 3 boys, ages 4-9, and I work as a 911 Dispatcher. I started having symptoms about 3 years ago starting with lumbar pain. I put it off for well over a year thinking it was just over-exertion. When I couldnt take the pain anymore as it was constant, and even just turning my head to the side caused severe pain. I got to the point that standing, sitting, and …
Comments: 1
How much pain before accepting medication?
Fri Sep 19, 2014 9:46 pm by josephine landau
Hi - My names Jo, I'm 42.
I was diagnosed in January of this year with MCTD, after a year or so of growing symptoms (Reynaulds, aching joints etc) I am a working mum with 2 boys, so my days are fairly hectic.
I take B12 injections for fatigue, Levothyroxine for low thyroid and Tegretol for an epileptic seizure I had 10 years ago -So I was reluctant to add to my drugs list and I declined any …
I was diagnosed in January of this year with MCTD, after a year or so of growing symptoms (Reynaulds, aching joints etc) I am a working mum with 2 boys, so my days are fairly hectic.
I take B12 injections for fatigue, Levothyroxine for low thyroid and Tegretol for an epileptic seizure I had 10 years ago -So I was reluctant to add to my drugs list and I declined any …
Comments: 0
Not yet diagnosed teen from Finland
Thu Mar 27, 2014 6:12 am by finnishgirl
Hi everyone!
I was happily suprised when I found all this great stuff for us MCTD patients! And hope to get to know some people with this illness. Because there's not a lot of stuff for us in Finland.
I'm a 15-years-old girl from Finland. I still haven't got a diagnosis for MCTD, but my rheuma specialist has suggested it after many years of different tests. And it seems to be logical, I have …
I was happily suprised when I found all this great stuff for us MCTD patients! And hope to get to know some people with this illness. Because there's not a lot of stuff for us in Finland.
I'm a 15-years-old girl from Finland. I still haven't got a diagnosis for MCTD, but my rheuma specialist has suggested it after many years of different tests. And it seems to be logical, I have …
Comments: 0
Another Australian story
Fri Nov 29, 2013 9:50 am by Ozzie1954
First of all, it is so good to find a forum with people who have been going through the same issues. I was doing a search on earache/jaw pain which is afflicting me this morning and found this forum.
My story begins in 1987 but probably goes back a lot further because of other issues that surfaced in my teens. It started after I had a bout of the flu, went back to work where I was handling …
My story begins in 1987 but probably goes back a lot further because of other issues that surfaced in my teens. It started after I had a bout of the flu, went back to work where I was handling …
Comments: 1
New from California.
Fri Jul 26, 2013 10:28 pm by mollyingrid92
Hello! My name is Molly, 20 years old, California resident. At the beginning of the 2013 year I noticed I was having really bad knee pains that would last for a while. When I finally went to see my doctor, he moved my leg around to see how my knee was working. Then he did this weird on where he would put a hand flat on the side of my knee and with the other hand push on the opposite side of my …
Comments: 8
This is all new!
Thu Apr 18, 2013 2:35 am by Admin
Ive never run or created a forum before so there may be some bugs, please let me know as soon as possible so I can correct them! I hope you find it easy to use!
Admin
Admin
Comments: 9
Hi from Australia
Tue Apr 30, 2013 12:46 pm by gorillagirl
Hi everyone
A brief bio. Female, 45, Hashimoto's since young. Started with flare ups after activity, sore joints and muscles, feeling sick, bloods abnormal and high CRP and ESR, symptoms pointed to lupus. Doctor nightmare for some years, the usual, it's just your thyroid and you have fibro, maybe you have narcolepsy, others haven things worse than you blah blah blah.
Found a good GP, …
A brief bio. Female, 45, Hashimoto's since young. Started with flare ups after activity, sore joints and muscles, feeling sick, bloods abnormal and high CRP and ESR, symptoms pointed to lupus. Doctor nightmare for some years, the usual, it's just your thyroid and you have fibro, maybe you have narcolepsy, others haven things worse than you blah blah blah.
Found a good GP, …
Comments: 8
Newbie, new to the dx, but not to the symptoms
Tue Apr 30, 2013 2:20 pm by Lenorekitty75
Hello Everyone ! 
Just came across this site today. Which is odd because I've been googling MCTD for months now. It's nice to know there are others out there in the world who could relate to what has become my life. Although I have frequented lupus and MS boards over the last 9 yrs and had wonderful support.
I am Christina, 37...mum of 3 the youngest is 3 and the oldest is 14. The Dr's have …
Just came across this site today. Which is odd because I've been googling MCTD for months now. It's nice to know there are others out there in the world who could relate to what has become my life. Although I have frequented lupus and MS boards over the last 9 yrs and had wonderful support.
I am Christina, 37...mum of 3 the youngest is 3 and the oldest is 14. The Dr's have …
Comments: 4
Latest topics
Negative ANA
2 posters
Mixed Connective Tissue Disease Awarenes :: Mixed Connective Tissue Disease :: Symptoms which may be related to MCTD
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Negative ANA
by Patti Rae Thu May 30, 2013 12:38 am
Has anyone had their ANA go from positive to negative? Mine had been positive several times but after being on hydroxychloriquine for some time my last lab tests showed a negative ANA. I was told that the medication can change a positive ANA to negative.....
Patti Rae- Newbie
- Posts : 1
Join date : 2013-05-30
Re: Negative ANA
by kimmieg33 Thu May 30, 2013 6:42 am
There are others here who probably can give you more information on this. I remember back in the beginning when I was starting the weird world of autoimmune disease diagnosis, a lady with lupus told me to keep track of my numbers cause they can change.
Welcome to the forum Patti
Welcome to the forum Patti
kimmieg33- Member
- Posts : 42
Join date : 2013-04-18
Age : 55
Location : Living in the moment
Mixed Connective Tissue Disease Awarenes :: Mixed Connective Tissue Disease :: Symptoms which may be related to MCTD
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