MCTD (Mixed Connective Tissue Disease)
Ok, here goes my story....4 Weeks ago I was diagnosed with Mixed Connective Tissue disease...I am normally a busy busy person, I work full time as a police officer, volunteer at my church, work a lot of off duty, and I have Three Boxer Dogs that I show, and I'm married...so I have a lot going on and this has pretty much put a stop on everything...I'm on 30mg of Prednisone, Plaquenil, Imuran, and Amitriptiline (for depression, anxiety), and Nexium twice a day...Some days I'm fine and other days I can't get out of bed either because I'm so tired or I'm having a flare. I would just like to talk to other people who have this disease and who can relate to me. I feel like I'm losing my mind and body for that matter.....Is it always going to be like this? How do I slow myself down? The concept just seems so alien to me....HELP
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Liyana I know how hard it is to try to cope when you have no energy. Family and social demands can wear you down. You need to focus on you for awhile. I found that resting and balance are the best way for me to get thru my days. Eating healthy has been the biggest help for me too. I can not emphasis enough the importance of setting up boundaries in your life. This means learning to say no is important. Family and friends need to learn to understand that there are going to be days when you just can’t get your head off the pillow. Listen to your body. Eat healthy, rest lots, reduce that stress and hopefully you will have better days. It’s raking me many years to figure this out but it’s worth the effort. Good luck.
Thank you for your advice. I have always eaten healthy.,it’s the slowing down part that gets me not being able to do thing with my little boys. And I do love them sooo much and more. But I do always care about others more then myself. And that needs to stop for a while
Take one day at a time. Rest. Rest. Rest. You are on a journey that requires you to take care of you first. Educate those around you about this disease. The more they understand the easier it will be for them to support you. It took me over a year to start getting my energy back. Good luck.
Thank you for advice. Are you on treatment for it.
I am trying diet and exercise as I can, but doing hormone replacement therapy with Sustanon (testosterone), prednisone, HGH and HCG.
What would be a good diet for this and exercise?
I go to a naturopathic doctor. I take probiotics and multi vitamins and iron and B 12 because I have a motility/esophagus issue and don’t absorb the nutrients. I am gluten free. When I’m really tired I rest as much as I can. Trying to avoid the prescription drugs as I also have a very sensitive stomach and don’t tolerate many drugs.
I have exactly the same symptoms. I have been off work since November 11, 2017. This comes from a guy that missed 10 days of work in 29 years. Mayo calls it central sensitization syndrome. What we have found is that it is related to adrenal fatigue and at some certain point it pushes it so far that it turns into Addison’s where are your adrenal gland is not secreting any cortisol at all. I have tried antivirals I have tried antibiotics I have tried antifungal’s been through 11 doctors and finally went to Mayo. I have a nurse that has been predicting this since the beginning that it was adrenal fatigue syndrome. So now I’m on prednisone and getting ready to do a regime of testosterone while seeing my local Endocrinologist. He is basically giving me a go ahead for this. Initially the prednisone was too low so I didn’t feel the full effects. Then I was doing it twice a day with more and felt better, but still not fully awake. I had been sleeping 2 to 3 days at a time and the time that I was awake was almost negligible because I wasn’t in any frame of mind to be doing anything. You start getting a feeling of worthlessness which just makes you depressed and drives this thing because it is a fight or flight type response that your body has which needs cortisolso you’re caught in a Catch-22. Thankfully I started taking it three times a day for 120 mg total 4040 and 40. This seems to do the trick or at least us far it has. The type of test tossed around that I’m going to be doing is not the cypionate that would normally be prescribed but rather such an on which is five different types of testosterone that are androgenic. At this point since 11 doctors of failed me and basically mayo has told me that I’m going to be very limited in what I can do and my entire life is going to be turned Upside down just to deal, that I really do not care what anyone thinks about this if it works well. Am I going to shorten up my life by taking prednisone every day at 120 mg almost certainly. However, I had no semblance of a normal life without it. The lack of testosterone will accompany it because it’s also secreted by the adrenal gland. I am not a doctor so I’m not giving you medical advice I’m just telling you what I’m doing and what has worked for me when nothing else has. Go have your cortisol level drawn and have the ACTH test That stress is your system to make your adrenal gland secrete cortisol. Mine actually did do it but it made me so sick and bloated for about six hours after the test that something was wrong. When I went back and looked at the lab work I had
Part two apparently they only allow you so many characters. But my cortisol level at baseline was
@corajanewiggins - thank you for figuring this out and sticking by my side always! I love you dearly, as my nurse and my partner. Pretty nice to be living with an RN when something like this happens!