Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Thinking About Seeing A Psychologist..


Gfresh404

Recommended Posts

Gfresh404 Enthusiast

I was just wondering if anyone had to or wanted to see a psychologist or a counselor after being diagnosed? And if so, did it help?

I only know of one other person on the forums, who, like me, suffers from post dramatic stress disorder. I was wondering if anyone else felt the same way. I have only been gluten-free for 6 months and I have noticed improvements. I am active and do my best to focus on the positive. But I always feel there's this void, that my entire childhood is missing, even when I am happy I still feel this way; I think: "I could have been this happy all the time."

I have yet to do many of the things I wanted to do, and I blame almost all of it on celiac. I'm 19 and haven't even kissed a girl yet. I have no issues talking to girls, some of my best friends are girls, I was just never able to mentally and physically connect with them since I was never consistently the same person if that makes sense: basically I was very moody. I didn't even know who I was a lot of the time. It's like I never felt I was ready for a relationship because I always had some issues I had to take care of. And now that I can do all the things I wanted to, I almost feel as if it is too late.

Does anyone else feel this way? Or does anyone have any advice?

Sorry for the slight rant, but it helps to get it off my chest and somewhat out in the open.


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



Roda Rising Star

I think that if talking to someone will help you then find someone. Try not to focus on what you could have done, instead focus on all the things you can do and will! I know from experience that it is easy to focus on all the negative my husband is right now. He is trying to deal with it. Surround yourself with positive people and experience new things together. If you are feeling well now, don't let life pass you by, enjoy it! :)

mushroom Proficient
I was just wondering if anyone had to or wanted to see a psychologist or a counselor after being diagnosed? And if so, did it help?

I only know of one other person on the forums, who, like me, suffers from post dramatic stress disorder. I was wondering if anyone else felt the same way. I have only been gluten-free for 6 months and I have noticed improvements. I am active and do my best to focus on the positive. But I always feel there's this void, that my entire childhood is missing, even when I am happy I still feel this way; I think: "I could have been this happy all the time."

I have yet to do many of the things I wanted to do, and I blame almost all of it on celiac. I'm 19 and haven't even kissed a girl yet. I have no issues talking to girls, some of my best friends are girls, I was just never able to mentally and physically connect with them since I was never consistently the same person if that makes sense: basically I was very moody. I didn't even know who I was a lot of the time. It's like I never felt I was ready for a relationship because I always had some issues I had to take care of. And now that I can do all the things I wanted to, I almost feel as if it is too late.

Does anyone else feel this way? Or does anyone have any advice?

Sorry for the slight rant, but it helps to get it off my chest and somewhat out in the open.

Hi: (and so sorry you are feeling a bit lost). To take your questions in order....

If this is the way you are feeling, it could well be worth your while to go this route. A good listening ear and feedback its worth its weight in gold if you find the right person.

It sounds like you are still going through the grieving process of celiac, what you are missing now, and what might have been if you did not have it. A counselor could help you get over this hump; the letting go of what might have been and the focusing on the here and now, and also the acceptance of what is and moving forward, rather than looking back. All is not lost; you are very young, albeit at an age where everything takes on heightened meaning and significance, the age of discovery of a new self even if you are not gluten free. You just have this added impediment to finding your way in the adult world by having to find your way in your different lifestyle to boot!! It can be very confusing.

Many of us have big voids where our happy childhoods should have been, for a variety of reasons, but we can't afford to mess up the rest of our lives by spending the years grieving over what might have been. Yes, I agree, it would have been wonderful to have a happy childhood, but I didn't :( l and apparently you didn't. So what?? Do I want to have an unhappy adulthood too, even though I have been handed the key to open the door and walk through? Well, no, I don't think so. And do you want to? I don't think so. So if a counselor is what it takes to walk through that door, go for it.

You are at the age where we all "find" ourselves'; there are those who do it easily and fluidly, and there are those of us who need a flashlight and a guiding light. You sound to me like you need someone to validate you, and that person could well be a counselor. Go and find that guiding light and achieve your potential. It is never too late--you can walk through that door....

ravenwoodglass Mentor

I think this is a good idea. If the first one you see doen't now seem a good fit don't give up just ask for a referral to different one. I have PTSD to the point where I am virtually agoraphbic. While celiac did excaberate the issues they do stem from other issues as well. I am early into treatment, my experience with doctors has left me very distrusting of them so it was a hard step to take but it does seem to be helping. They may want to put you on an antiaxiety med, some are more effective than others. It took a trial of 3 different meds before they found one that helps. Psychotherapy can be a long process but it may help a great deal so don't give up.

BRS-07 Rookie
I was just wondering if anyone had to or wanted to see a psychologist or a counselor after being diagnosed? And if so, did it help?

I only know of one other person on the forums, who, like me, suffers from post dramatic stress disorder. I was wondering if anyone else felt the same way. I have only been gluten-free for 6 months and I have noticed improvements. I am active and do my best to focus on the positive. But I always feel there's this void, that my entire childhood is missing, even when I am happy I still feel this way; I think: "I could have been this happy all the time."

I have yet to do many of the things I wanted to do, and I blame almost all of it on celiac. I'm 19 and haven't even kissed a girl yet. I have no issues talking to girls, some of my best friends are girls, I was just never able to mentally and physically connect with them since I was never consistently the same person if that makes sense: basically I was very moody. I didn't even know who I was a lot of the time. It's like I never felt I was ready for a relationship because I always had some issues I had to take care of. And now that I can do all the things I wanted to, I almost feel as if it is too late.

Does anyone else feel this way? Or does anyone have any advice?

Sorry for the slight rant, but it helps to get it off my chest and somewhat out in the open.

So I don't know if this will help or not, but I got diagnosed about 2 months ago, am 23, and have recently thought about seeking some sort of psychologist or support group. The diagnosis for celiac hit me really hard and in the last two months I have had the worst immune system ever, to the point of being in the doctors office 1-3 times a week due to something else, as well as being on hand fulls of viamins and pills to heal my deficiencies as well as the other things that trailed along. Everytime I look forward to a concert or fun weekend, I get sick and nausious (not due to food, but vitamins from the doctor). I kinda feel like my world fell apart and I don't know how to pick up the pieces. I have almost been married for a year and find myself feeling guilty that my husband has to go through all the emotional ups and downs that I've been struggling with on top of all the medical issues. Between working full time, going to the doctors, making all food that I eat, and still keeping up with a house and being a wife I'm about at my breaking point. I feel like I woke up in a foreign body and have no idea how to get control back over my life. While I have not struggled with this since childhood, I still feel like a part of life has been stolen from me. Not just the last few years, but the future things I had planned on doing. Sorry for the little blurb, but the more I think about it the more I think that talking to either a psychologist or someone who actually really understands would be good. I am a firm believer in psychology since I am a psychology major so maybe I will go as well.

ravenwoodglass Mentor
as well as being on hand fulls of viamins and pills to heal my deficiencies as well as the other things that trailed along. Everytime I look forward to a concert or fun weekend, I get sick and nausious (not due to food, but vitamins from the doctor).

Labeling laws for supplements and scripts are very lax when it comes to gluten. Please make sure you are checking with the makers and your pharmacist to be absolutely sure they are really gluten free as you doctor will have no idea if they are or not.

njbeachbum Explorer

Let me first say that I completely feel that counseling can be beneficial in any situation where there is a "life changing" event or something that causes great stress and grief in your life. that is a very personal decision, and i really believe that talking to someone can only help... i really doubt that there could be any negative results.

with that being said, please understand that you are not alone. i am going on 32 years old and i was diagnosed about a year and a half ago. i recall being sick all the time from when i was 16 years old... was misdiagnosed and treated for years for crohn's disease, but things were never quite right. i do feel that there was a huge impact on my life through those years... i was always afraid to do certain things where i had to spend lots of hours where there was not easy bathroom access, especially first thing in the morning. i avoided lots of social things during the early years when i was the sickest. on top of that though... i am also gay, and had to struggle with my sexuality during these years. being a symptomatic celiac, my growth and development was severely impacted. i graduated from high school at 5'1" and didn't really hit puberty until right around then. because of this delayed development, my sexual "awakening" didn't really happen until after that. my point is this - there are definitely things that i look back on and wish i could have done differently during the time i was sick. however, i feel that i always made the best of everything, and stayed true to myself and what i was comfortable with. i fixated on things i could control... like academics (i was valedictorian of my HS) and sports (i've played every sport at one time or another, but worked my way up to a semi-pro level in beach volleyball). things have a way of working themselves out. i had two major struggles between my health and my sexuality, but i took it all in stride... and now that i was diagnosed and am feeling the best i have in years, i am happier in my life than i've ever been

i know this rant when on a bit, but i want you to understand that while everything we go through in life will form who we are today.... it doesn't always have to dictate who you want to be or will be in the future. that's always your decision.

best of luck to you Gfresh, i know it's rough, but at least you've crossed the hurdle to feeling healthy again.


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



Gfresh404 Enthusiast
All is not lost; you are very young, albeit at an age where everything takes on heightened meaning and significance, the age of discovery of a new self even if you are not gluten free. You just have this added impediment to finding your way in the adult world by having to find your way in your different lifestyle to boot!! It can be very confusing.

You are at the age where we all "find" ourselves'; there are those who do it easily and fluidly, and there are those of us who need a flashlight and a guiding light. You sound to me like you need someone to validate you, and that person could well be a counselor.

Thank you for your reply. I think you hit the head of nail. Especially these two parts. My parents and a few others have said the exact same thing. I don't think I trust myself anymore because if I "thought" I was fine all this time and I really was not, well how could I trust myself again right away?

The whole thing about finding myself is very true too. I do not feel so much as confused but more just have a feeling of being constantly lost. Like I thought this was what life is and I was wrong. The quality of life is 10 times better than that of the quality that I used to be living at.

And to everyone else thank you for your replies as well, it is always comforting to know that I am not alone because most of the time I forget that there are people out there just like me. And I have to keep reminding myself that just because I have yet to meet anyone like myself in real life, that does not mean you are not out there. So thank you.

glutenfreejenny Apprentice

I'm a 24 year old girl and I feel the same way when it comes to relationships. I've had them, but I feel like I've missed out on a lot of opportunities because I wasn't diagnosed until a few months ago. Dating and all that while suffering from all the symptoms...not easy. But I try to think about all the things I have gained from being sick. Going through celiac has put me through a lot of situations people my age don't yet understand. I'm the only one I know who's exstatic I can go to college, because before there was no way I was well enough to go. I think now would be the perfect time for you to go and talk to someone, and I think you should look around until you find someone you are comfortable with.

Gfresh404 Enthusiast
I've had them, but I feel like I've missed out on a lot of opportunities because I wasn't diagnosed until a few months ago. Dating and all that while suffering from all the symptoms...not easy. But I try to think about all the things I have gained from being sick. Going through celiac has put me through a lot of situations people my age don't yet understand.

I never had any "official" relationships but I sometimes felt as if I was the boyfriend. I think I was afraid of commitment because I knew I wouldn't be able to be there all the time when they needed me. And it might sound stupid but not having that physical aspect and physical connection, I am feeling left with a void. Unfortunately I live in a small town and am close with a lot of girls I would like move on but of course they all have boyfriends. So I feel like I missed my chance.

It is probably better not to think about it, but it is really hard sometimes.

I am also the exact same with the age thing. Maybe this is just the way I am but I also feel a lot older than I really am (19). It's almost as if living with gluten sensitivity has made stronger. The only thing I fear now is dying alone. Death in of itself does not frighten me. Maybe I just don't have enough to lose at this point to care. I know things will get continue to get better but in the meantime it helps a lot just to talk about.

Some of the similarities I have with people with the same condition truly amazes me. Thanks for sharing your stories.

ang1e0251 Contributor

And it might sound stupid but not having that physical aspect and physical connection, I am feeling left with a void. Unfortunately I live in a small town and am close with a lot of girls I would like move on but of course they all have boyfriends. So I feel like I missed my chance.

It is probably better not to think about it, but it is really hard sometimes.

I felt like you do at your age and also being in a small town made me feel like there just weren't any choices. I took the oppurtunity to be an exchange student at that point. It changed my life and really opened my horizons. Just learning another language was life changing. I'm not saying you should do the same but maybe along with your diagnosis, another change is in order. If there is a place where you want to vacation or live or maybe go to college, just go for it. The big change might fit the emotional changes you're going through with celiac disease. Granted it is scary but so worth it.

I am also the exact same with the age thing. Maybe this is just the way I am but I also feel a lot older than I really am (19). It's almost as if living with gluten sensitivity has made stronger. The only thing I fear now is dying alone. Death in of itself does not frighten me. Maybe I just don't have enough to lose at this point to care. I know things will get continue to get better but in the meantime it helps a lot just to talk about.

Sure you feel older. Your life experiences put you ahead of your peers. That's why another change like a move or starting a new career or school can disrtact you from that. You'll be working hard to adjust and learn all you can and before you know it, you'll meet others you can relate to.

You have a long while to worry about dying alone. You're 19, only 1/5th of your life is past. You have 4 times more than you already have lived to go! So many good things are going to start happening to you! And that thing about dating, my daughter says when you're looking too hard it will never happen. If you just have fun with your friends and family, love will come along by itself, in it's own time. It certainly happened to me that way. This week we're celebrating our 32nd anniversery. So hang in there, reach out for the new experiences life is going to show you and happiness will come.

ang1e0251 Contributor

And it might sound stupid but not having that physical aspect and physical connection, I am feeling left with a void. Unfortunately I live in a small town and am close with a lot of girls I would like move on but of course they all have boyfriends. So I feel like I missed my chance.

It is probably better not to think about it, but it is really hard sometimes.

I felt like you do at your age and also being in a small town made me feel like there just weren't any choices. I took the oppurtunity to be an exchange student at that point. It changed my life and really opened my horizons. Just learning another language was life changing. I'm not saying you should do the same but maybe along with your diagnosis, another change is in order. If there is a place where you want to vacation or live or maybe go to college, just go for it. The big change might fit the emotional changes you're going through with celiac disease. Granted it is scary but so worth it.

I am also the exact same with the age thing. Maybe this is just the way I am but I also feel a lot older than I really am (19). It's almost as if living with gluten sensitivity has made stronger. The only thing I fear now is dying alone. Death in of itself does not frighten me. Maybe I just don't have enough to lose at this point to care. I know things will get continue to get better but in the meantime it helps a lot just to talk about.

Sure you feel older. Your life experiences put you ahead of your peers. That's why another change like a move or starting a new career or school can disrtact you from that. You'll be working hard to adjust and learn all you can and before you know it, you'll meet others you can relate to.

You have a long while to worry about dying alone. You're 19, only 1/5th of your life is past. You have 4 times more than you already have lived to go! So many good things are going to start happening to you! And that thing about dating, my daughter says when you're looking too hard it will never happen. If you just have fun with your friends and family, love will come along by itself, in it's own time. It certainly happened to me that way. This week we're celebrating our 32nd anniversery. So hang in there, reach out for the new experiences life is going to show you and happiness will come.

  • 4 weeks later...
DDD Newbie

I felt the same way as you about relationships. Only had one boyfriend my whole life, and it was a silly high school thing that lasted for a month and a half.

I have just been best friends with boys my whole life.

Then I tore my ACL and had to have knee surgery. downward spiral, see my signature.

I went Gluten-Free. A year later I feel like normal human being now that I am super strict.

Now for the coincidences: After going Gluten-Free and "finding myself" as many of us on here have said happened only once we went Gluten-Free, I started dating one of my guy best friends who I had a crush on for three years! Plus all these wonderful professional oppurtunities have sprung up now that I am Gluten-Free. I feel like its because I have a clear head and I know what I want to do now.

Also, I don't know if it's practice from being gluten paranoid but I feel like my judgment is so much better after being Gluten-Free.

When I went to the emergency room in my college town because I thought I was going to die with all my "downward spiral" symptoms (see below) they gave me steroids and recommended I seek counseling. Luckily, my mom rushed up to school to visit and scheduled an appointment with a holistic doctor. I started to feel better so there was no need for steroids and counseling, especially because my mom and doctor were so supportive and I got my closest loved ones on board with me too.

IF YOU GET ANYTHING OUT OF MY RAMBLING POST IT IS THIS: if you go see a counselor make sure they are supportive and educated about celiac and gluten and each and every side effect. otherwise, they are going to make you feel worse! my one roomate was a nutty skeptical (go figure his mom was doctor that would rather hand out a pill than listen to you) and when i tried talking to him he made me feel like a whack job! he said being a celiac was all in my head!?!?!?!? grrrr i have found that it is better to talk to supportive people. you may be able to find that on these boards.

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,961
    • Most Online (within 30 mins)
      7,748

    Noa
    Newest Member
    Noa
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.