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

A Proper Welcome To Srokie!


Canadian Karen

Recommended Posts

Canadian Karen Community Regular

Okay, let's start all over again:

Srokie, welcome to the board and I am glad you found us. There are a whole bunch of really helpful, caring, wonderful people on this board. There are also very knowledgeable people on here who will do everything they can to answer any questions you have.

Please forgive the confusion beforehand about the misunderstanding of you being a troll.

So, everyone, please, extend a proper welcome to srokie!

Hugs.

Karen


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



Celiac.com Sponsor (A8-M):



  • Replies 128
  • Created
  • Last Reply
mtdawber Apprentice

Welcome, Welcome, Welcome!!!

darlindeb25 Collaborator
:lol: Welcome!!!!
jaten Enthusiast

Welcome. This board has been a life-saver for so many (including me). It's a comfortable place for those who truly want to work together to understand celiac and other gluten intolerance.

lonewolf Collaborator

Welcome! I hope you learn as much here as I have.

Michi8 Contributor

Welcome! :)

Michelle

bluejeangirl Contributor

Welcome Srokie! I'm sorry for all the confusion.......I guess we can be a bit "guarded" with new information. However its the information that at least I would come up agaisnt and not the person so please please don't be offended and come aboard we love to have ya sharing.

Gail


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



Celiac.com Sponsor (A8-M):



Fiddle-Faddle Community Regular

Welcome! And I for one would like to hear about your interest in cello! Tell us more! Do you play?

chrissy Collaborator

karen---i was sitting here this morning thinking the same thing about srokie---that we neede to start all over with a proper introduction! welcome srokie!

Carriefaith Enthusiast

Welcome to the board!

blueeyedmanda Community Regular

Welcome Welcome Welcome, I know I did not come off as very welcoming. Sometimes I tend to get defensive. This board is a life-saver for me. I hope it comes to be the same for you.

Rusla Enthusiast

Welcome Srokie, I am also sorry for all the confusion. Remember some times things come across misconscrued over the internet. We were really not trying grill you like unbreaded salmon.We worry because many of us have been through false hopes and decades of torture at the hands of uncaring, misguided, or misinformed doctors. It is better you find out you are Celiac now than 30 years from now.

Once again welcome to the board and we are really a nice bunch of people just a little opinionated and anal about a disease we have to be anal about. There are lots of great recipes and people on this board. :lol:

Lisa Mentor

I also would like to welcome you to the board. You appear to be a delightful young woman.

Sometimes it is easy to follow the flow. And some times you need to step out of the forest to see the trees. I think that Karen and others have done that.

I think (yes Electra, I think :) ) that since your first thread was a little controversial on soy, it appeared, as others that have come before, with a hidden agenda. You did not give the impression of a typical "newbie", scared and frighten by being diagnosis with a disease that many have never heard of.

If, I in any way was rude or hurtful, I apologize.

dlp252 Apprentice

Welcome Srokie!!

Fiddle-Faddle Community Regular
Welcome Srokie, I am also sorry for all the confusion. Remember some times things come across misconscrued over the internet. We were really not trying grill you like unbreaded salmon.We worry because many of us have been through false hopes and decades of torture at the hands of uncaring, misguided, or misinformed doctors. It is better you find out you are Celiac now than 30 years from now.

Once again welcome to the board and we are really a nice bunch of people just a little opinionated and anal about a disease we have to be anal about. There are lots of great recipes and people on this board. :lol:

This is the best description of most of us and our experiences that I have ever read!!!! :lol:

Viola 1 Rookie

Welcome to the board srokie, We have various opinions of things, but we usually can speak our minds and then let it go. Hope you stay with us and haven't had your feelings hurt too bad.

srokie Newbie

This is really sweet; many thanks to all of you.

I didn't start posting when I was diagnosed because I was just too sick. I barely had the energy / willpower to get through each day with the difficult new diet on top of everything else. Now that I'm feeling better I have the energy after work to see who else is out there suffering with me.

I am extremely lucky that I found Dr. Saviano. Most people suffer 11ish years before they are diagnosed, and I only had 3 years of suffering (about a year of unbearable symptoms). Had I not found a competent doctor I'd have had to drop out of school because I couldn't get out of bed ... and if I got out of bed I couldn't read or concentrate at all - it was taking me 11 straight hours to write papers that I was interested in writing!!

And the way I found out about her was truly a miracle - my mom and I were visiting a church friend in the hospital (who was there for us when my dad died) and as I was standing there thinking I was about to faint and not knowing why, another lady from the church who was there told us about this nutritionist she was seeing and how she had been diagnosed with celiac disease. I certainly remembered that after I could barely stand up from fatigue at age 19. Then I went to France for 5 weeks and I ate a LOT of bread. Every single meal. Bread, bread, bread... baguettes... sandwiches... eclaires... everything. I called my mom and asked her to make me appointments with my primary care doctor and this "nutritionist" for the day after I was supposed to get back to the US. Dr. Saviano immediately told me I was not absorbing vitamin B after just listening to my symptoms.

About the cello - I played piano for 11 years and really didn't like it, but I've been playing cello since 6th grade and I love it. It's a gorgeous instrument. I play in my colleges *incredible* orchestra, and I'm a music major as well as a French major. I've been playing in orchestras since I was 12... I don't know what I'd do without it! It's really amazing to show the audience just how hard we've worked to bring that performance to them.

Wow I'm writing a book....

srokie Newbie
We were really not trying grill you like unbreaded salmon.

That made me crack up :)

We worry because many of us have been through false hopes and decades of torture at the hands of uncaring, misguided, or misinformed doctors. It is better you find out you are Celiac now than 30 years from now.
Amen!
Carriefaith Enthusiast

I am truly glad that you are feeling better now and have the energy to do other things. Three years is still such a long time to suffer. I hope you feel welcome here and please don't hesitate to ask questions.

Rusla Enthusiast

Srokie, did she tell you if it was B-12 or not that you were not absorbing? All that talk of bread,eclairs, and baquettes started giving me pain.

There is not one of us on this board who can't empathize with how you have felt. I still do not absorbe my B-12 anymore because of this disease so I am constantly taking sublingual B-12's as opposed to shots. I know when I am low in B-12, I get very fatigued.

I am happy when people find out they are Celiac at a younger age. I hate to think of them suffering the decades I and many others have suffered from this disease and the irrepairable damage it has done to us.I am never happy anyone has this disease. It is not an inexpensive or convenient disease to have.

We need our governments to wake up and see how disabling this disease really is, perhaps if some of them had this they would get on board with us in many ways

I have enlarged the font on here in hopes of making it easier on Judy, without the yelling of caps..

Ursa Major Collaborator

Thank you Karen, for starting this thread! Again, welcome, Ashley, I am soooooo glad that everything is straightened out, and we can all be friends who help each other make life with celiac disease easier.

I love the cello! I started taking violin lessons in December, and still sound sort of awful (surprising myself at times with some beautiful sounding notes, though :blink: ). Mind you, when I cringe during my lesson, my teacher still thinks I am doing fine. When I said last Tuesday (my third lesson) that I sound terrible, she asked me if I've ever heard children play, who just started lessons. No, I haven't, so I don't have a clue what other beginners sound like.

I hope that the day will come when I'll enjoy listening to my own playing. :ph34r:

Mind you, I do play the recorders (considered a serious instrument in Germany). I own several thousand dollars worth of recorders in all sizes. A few very expensive wooden ones, and some good quality plastic ones. I haven't played in a while, because my partners moved out and far away (my two oldest daughters). It isn't much fun playing by yourself. But I am going to start some serious recorder lessons in a couple of weeks.

If we all wouldn't live so far away from each other we could start a 'Celiac orchestra' or something like that. :P

chrissy Collaborator

srokie---you are probably the quickest to forgive person on this board. my mother always told us that it is just as bad to take offense as it is to give offense-----and you didn't seem to take much offense at all of us jumping on you-----what a sweetheart you must be!!

Electra Enthusiast

Welcome,

I'm glad you found your way here and I hope you continue to share information with us!!

Mtndog Collaborator

Welcome Srokie!!!!!!!!!!!!!!!!! It REALLY is a good place.

Your story sounds a lot like mine. My symptoms started about 6 months after my mom died and got progressively worse over the course of that year. In my 3rd year in my PhD program (Yeah guys- THANKS FOR ALL THAT RANKING ON PHD'S IN OTHER THREADS :lol::P :P :P ) I was so sick I almost dropped out. Luckily, my primary care suspected celiac disease so I went gluten-free and was able to continue. No, I'm not done yet...they don't let you out easily :P:ph34r:

I'm glad you found out and that you were able to stay in school. I'm sorry things got off to a rough start for you here and I hope it gets better! Actually, I know it will!

JackieM Newbie

I'm sure glad to see this thread. You guys were starting to scare me, since I am new here too. lol Some of us want to learn more about this disease. I can see where people could troll in, to cause trouble, but I gotta say, Srokie you are very generous that you are willing to let the questionable thoughts of members and be forgiving in that manner. That's very special of you. I hope that you are able to share some helpful information with people here. One never knows why people come and go in our lives. Their purpose isn't always for us to know. I am sure that Srokie will be able to enlighten, just as others have enlightened others, as well as Srokie learning more also. I recently found this site via surfing for Johnny Rivers links. I couldn't figure out why his name was associated with Gluten free until I read it was a post from Dingogirl about him. As I got into reading some things here, I soon started learning that this disease, which a friend of mine suffers from, but she refers to it as intolerance, maybe that is correct too, I don't know. She and I have been friends for many years, though we have lived miles apart for so long, and it is nice to know that I have a place to learn about her disease here. I have learned some things that I have related to myself too. So if it were not for me following Dingogirls post that was on Google, howza bout thaaat, I would never have all this information here. I was welcomed by several nice posts. Thank you for that. So even though I am learning about this disease, Srokie, I am happy to see you on this site. You never know what information can be brought here to help others. So I have to say a big Welcome to Srokie! :)

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - knitty kitty replied to Jmartes71's topic in Related Issues & Disorders
      8

      My only proof

    2. - Wheatwacked replied to Jmartes71's topic in Coping with Celiac Disease
      8

      Related issues

    3. - NanceK replied to Jmartes71's topic in Related Issues & Disorders
      8

      My only proof

    4. - Wheatwacked replied to Scatterbrain's topic in Sports and Fitness
      4

      Feel like I’m starting over

    5. - Scott Adams replied to Kirita's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      3

      Recovery from gluten challenge


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,291
    • Most Online (within 30 mins)
      7,748

    DottieLyn
    Newest Member
    DottieLyn
    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

    • knitty kitty
      @NanceK, I do have Hypersensitivity Type Four reaction to Sulfa drugs, a sulfa allergy.  Benfotiamine and other forms of Thiamine do not bother me at all.  There's sulfur in all kinds of Thiamine, yet our bodies must have it as an essential nutrient to make life sustaining enzymes.  The sulfur in thiamine is in a ring which does not trigger sulfa allergy like sulfites in a chain found in pharmaceuticals.  Doctors are not given sufficient education in nutrition (nor chemistry in this case).  I studied Nutrition before earning a degree in Microbiology.  I wanted to know what vitamins were doing inside the body.   Thiamine is safe and nontoxic even in high doses.   Not feeling well after starting Benfotiamine is normal.  It's called the "thiamine paradox" and is equivalent to an engine backfiring if it's not been cranked up for a while.  Mine went away in about three days.  I took a B Complex, magnesium and added molybdenum for a few weeks. It's important to add a B Complex with all eight essential B vitamins. Supplementing just one B vitamin can cause lows in some of the others and result in feeling worse, too.  Celiac Disease causes malabsorption of all the B vitamins, not just thiamine.  You need all eight.  Thiamine forms including Benfotiamine interact with each of the other B vitamins in some way.  It's important to add a magnesium glycinate or chelate supplement as well.  Forms of Thiamine including Benfotiamine need magnesium to make those life sustaining enzymes.  (Don't use magnesium oxide.  It's not absorbed well.  It pulls water into the intestines and is used to relieve constipation.)   Molybdenum is a trace mineral that helps the body utilize forms of Thiamine.   Molybdenum supplements are available over the counter.  It's not unusual to be low in molybdenum if low in thiamine.   I do hope you will add the necessary supplements and try Benfotiamine again. Science-y Explanation of Thiamine Paradox: https://hormonesmatter.com/paradoxical-reactions-with-ttfd-the-glutathione-connection/#google_vignette
    • Wheatwacked
      Your goal is not to be a good puppet, there is no gain in that. You might want to restart the ones that helped.  It sounds more like you are suffering from malnutrition.  Gluten free foods are not fortified with things like Thiamine (B1), vitamin D, Iodine, B1,2,3,5,6 and 12 as non-gluten free products are required to be. There is a Catch-22 here.  Malnutrition can cause SIBO, and SIBO can worsen malnutrition. Another possibility is side effects from any medication that are taking.  I was on Metformin 3 months before it turned me into a zombi.  I had crippling side effects from most of the BP meds tried on me, and Losartan has many of the side effects on me from my pre gluten free days. Because you have been gluten free, you can test and talk until you are blue in the face but all of your tests will be negative.  Without gluten, you will not create the antigen against gluten, no antigens to gluten, so no small intestine damage from the antigens.  You will need to do a gluten challange to test positive if you need an official diagnosis, and even then, no guaranty: 10 g of gluten per day for 6 weeks! Then a full panel of Celiac tests and biopsy. At a minimum consider vitamin D, Liquid Iodine (unless you have dermatitis herpetiformis and iodine exasperates the rash), and Liquid Geritol. Push for vitamin D testing and a consult with a nutritionist experienced with Celiack Disease.  Most blood tests don't indicate nutritional deficiencies.  Your thyroid tests can be perfect, yet not indicate iodine deficiency for example.  Thiamine   test fine, but not pick up on beriberi.  Vegans are often B12 deficient because meat, fish, poultry, eggs, and dairy are the primary souces of B12. Here is what I take daily.  10,000 IU vitamin D3 750 mg g a b a [   ] 200 mg CoQ10 [   ] 100 mg DHEA [   ] 250 mg thiamine B1 [   ] 100 mg of B2 [   ] 500 mg B5 pantothenic acid [   ] 100 mg B6 [   ] 1000 micrograms B12 n [   ] 500 mg vitamin c [   ] 500 mg taurine [   ] 200 mg selenium   
    • NanceK
      Hi…Just a note that if you have an allergy to sulfa it’s best not to take Benfotiamine. I bought a bottle and tried one without looking into it first and didn’t feel well.  I checked with my pharmacist and he said not to take it with a known sulfa allergy. I was really bummed because I thought it would help my energy level, but I was thankful I was given this info before taking more of it. 
    • Wheatwacked
      Hello @Scatterbrain, Are you getting enough vitamins and minerals.  Gluten free food is not fortified so you may be starting to run low on B vitamins and vitamin D.   By the way you should get your mom checked for celiac disease.  You got it from your mom or dad.  Some studies show that following a gluten-free diet can stabilize or improve symptoms of dementia.  I know that for the 63 years I was eating gluten I got dumber and dumber until I started GFD and vitamin replenishment and it began to reverse.  Thiamine can get used up in a week or two.  Symptoms can come and go with daily diet.  Symptoms of beriberi due to Thiamine deficiency.   Difficulty walking. Loss of feeling (sensation) in hands and feet. Loss of muscle function or paralysis of the lower legs. Mental confusion. Pain. Speech difficulties. Strange eye movements (nystagmus) Tingling. Any change in medications? Last March I had corotid artery surgery (90 % blockage), and I started taking Losartan for blood pressure, added to the Clonidine I was taking already.  I was not recovering well and many of my pre gluten free symptoms were back  I was getting worse.  At first I thought it was caused a reaction to the anesthesia from the surgery, but that should have improved after two weeks.  Doctor thought I was just being a wimp. After three months I talked to my doctor about a break from the Losartan to see if it was causing it. It had not made any difference in my bp.  Except for clonindine, all of the previous bp meds tried had not worked to lower bp and had crippling side effects. One, I could not stand up straight; one wobbly knees, another spayed feet.  Inguinal hernia from the Lisinopril cough.  Had I contiued on those, I was destined for a wheelchair or walker. She said the symptoms were not from Losartan so I continued taking it.  Two weeks later I did not have the strength in hips and thighs to get up from sitting on the floor (Help, I can't get up😨).  I stopped AMA (not recommended).  Without the Losartan, a) bp did not change, after the 72 hour withdrawal from Losartanon, on clonidine only and b) symptoms started going away.  Improvement started in 72 hours.  After six weeks they were gone and I am getting better.  
    • Scott Adams
      Hopefully the food she eats away from home, especially at school, is 100% gluten-free. If you haven't checked in with the school directly about this, it might be worth a planned visit with their staff to make sure her food is safe.
×
×
  • 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.