Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Omg...i Might Be On To Something


Rachel--24

Recommended Posts

Judyin Philly Enthusiast

I see you guys too.

nothing to add really than to give some hugs

just came on to ck PM's to see if Evie's daughter posted to me but she didn't.

I'm past worry now. I'm really afraid Evie didn't make it. Don't want to be negative but it just scares me.

nite all..in a minute..any of you have feelings about this or is it just me?????being a worry wort????

judy


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



Celiac.com Sponsor (A8-M):



  • Replies 33.4k
  • Created
  • Last Reply
AndreaB Contributor

I don't know Judy. :( They said they were hoping to come hope on Tuesday. When my Dad was in the hospital he wound up being in for a few more days than he thought he would be.

Judyin Philly Enthusiast

I know and with breathing problems on top of it all she might need more time and i keep thinking the poor daughter is probably so tired if she's at the hospital all day but i don't know any facts for REAL.

she was posting about 10:30-11 to me.

let's just hope she's busy with her mom.

judy

AndreaB Contributor

Yes, let's hope she's just been spending time with her Mom. I'm sure she's tired too. I'll keep praying for Evie.

Thanks for all you do Judy. :D

rinne Apprentice
These should be the 10 commandments of Rachelville!! :D All in favor???

Rachel, yes I am in favor, these are great and I love your comments. :) Thanks for posting them.

I had one "friend" suggest that I might get better if I left my husband :rolleyes: based on a friend of hers, who had been diagnosed with MS (bells ringing for me, MS a common misdiagnosis of Lyme and she is from a Lyme hot spot in the province) who had a complete remission of her symptoms after she left her husband. :o I have always been a pretty independent person, married or not, but at this point the truth is I really need my husband to support me and a suggestion like that just amazes me. <_< I know I am not far away from saying, "what kind of idiot are you?" :lol:

I am concerned about Evie too but am hopeful that they just needed to keep her a another day of two. I know much of my concern comes from the tone of Evie's last post, when she said she felt very weak I felt her concern, did anyone else have that feeling? Judy is that what you mean?

Susan, a horrifying story of drugs gone wrong in that young girl's body. Will she recover further over time?

It makes me cry to think of how stupid we are.

Rachel--24 Collaborator
I am concerned about Evie too but am hopeful that they just needed to keep her a another day of two. I know much of my concern comes from the tone of Evie's last post, when she said she felt very weak I felt her concern, did anyone else have that feeling? Judy is that what you mean?

I felt the same way about her last post Rinne....it really worried me. Also I read alot about C.Diff earlier in the year because they put me on antibiotics for it after they detected it in my stool. C.Diff is really scary....I never was sick from it but I read alot of pretty scary stories. So yeah...I am very very worried at this point. :(

Susan, a horrifying story of drugs gone wrong in that young girl's body. Will she recover further over time?

Yeah....before reading that story I was a little scared of antibiotics....but now...OMG. :ph34r:

Anyone know how Laura is doing? Is today the day for her EOS test??

jerseyangel Proficient

I loved that list, Rachel--thanks for posting it. :) It's like the story of my life :lol:

Susan--my gosh how horrible!

I hope that Evie is still hanging in there--bless her heart. :(

Andrea, You are one of the most understanding, supportive people I've ever met. :)

Rinne, Where do people come up with this stuff! Jeesh <_< What kind of idiot, indeed.

I think today is Laura's test--it's been a week since she began the diet challenge.

Hi Judy--glad you checked in B)

Carla--are you ok?


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



Celiac.com Sponsor (A8-M):



CarlaB Enthusiast
Carla--are you ok?

:) Thanks for asking. I was feeling awful yesterday ... don't know how today's going to turn out. I have a meeting this morning, so I'll be out for a while.

jerseyangel Proficient
:) Thanks for asking. I was feeling awful yesterday ... don't know how today's going to turn out. I have a meeting this morning, so I'll be out for a while.

Ugh--too bad you have to go out when you're not feeling well :( Hope today is better :)

Mtndog Collaborator

Quick drive by.... Rachel- that list is GREAT! I also like spoon theory:

Open Original Shared Link

I hope Evie is OK. The C Diff over the summer scared the beejeezus out of me! Among other things.

Susan- that story is so scary. It just goes to show you that those staistics (1 in 400,000 people will develop X serious side affect) are not statistics. They are PEOPLE.

I'm glad you're feeling a little bit better too :wub::wub::wub::wub:

Andrea- Been thinking lots about you and your dad and will continue to do so. many many prayers, love and hug your way.

Patti- You look gorgeous. In our case, I guess the "It's not how you feel, it's how you look and darling, you look marvelous!" applies in an even more special way. :D

rinne Apprentice

Hi Patti, love the new picture of you, you are looking very sharp. :)

I was wondering about our happy girl too.

Andrea :blink: you are one of the kindest and most supportive people, you are not an idiot. :lol:

jerseyangel Proficient

Beverly,

Aren't you sweet :) And, right back at ya B)

dlp252 Apprentice
These should be the 10 commandments of Rachelville!! :D All in favor???

My personal favorites....#1...2...3....5 and 9.....these apply most in my life since I got sick.

#1 2 and 5 make me want to get violent. :ph34r:

Julie...this is when I would need my punching bag! :lol:

I LOVED this!!! I'm sending it off to my friend who is chronically ill with fibro.

jerseyangel Proficient

Thanks, Rinne :)

Andrea=definately not an idiot :lol:

dlp252 Apprentice
I am concerned about Evie too but am hopeful that they just needed to keep her a another day of two. I know much of my concern comes from the tone of Evie's last post, when she said she felt very weak I felt her concern, did anyone else have that feeling? Judy is that what you mean?

Yep, I got that feeling too. :(

miamia Rookie

Rachel-

Great list i think i may print it out and hand it out to my friends and family

I got a pm from laura yesturday today is her test she said shes actually been feeling ok- Which may not be a good thing for the eos test- but is still good to hear

Miamia

dlp252 Apprentice
I got a pm from laura yesturday today is her test she said shes actually been feeling ok- Which may not be a good thing for the eos test- but is still good to hear

Miamia

Thanks Miamia! Glad at least she hasn't been totally miserable throughout the challenge period.

Mtndog Collaborator
Andrea=definately not an idiot :lol:

I second this! :P:P:P:lol::lol::lol:

nary an idiot on this thread! (Nary was a word for Susie Q cuz she always cracks up when we use words like conundrum, heinosity and such chicanery).

Actually Conundrum picture on this link:

Open Original Shared Link

Now that's my kind of vino!

rinne Apprentice

Open Original Shared Link

Dear Friends,

Chronic Lyme disease has been banished as a disease! No conventional or alternative treatments are recommended! Doctors cannot make a clinical diagnosis anymore!

It is time for patients to fight back! Your participation is critical! Numbers count!

Patients are already being cut off. Doctors are backing off treating. There is no wiggle room in the new guidelines.

Guidelines impact:

Diagnos is no longer clinical, only by CDC positive surveillance blood test or EM rash.

Chronic disease will increase since 50% of Lyme cases will be missed.

Insurance companies have basis to deny coverage for all treatment for chronic disease.

State medical boards have strong basis to attack our doctors.

Family services have strong basis for custody cases.

School districts have strong basis for not addressing special needs of students with chronic Lyme.

"Diagnosis is no longer clinical, only by CDC positive surveillance blood test or EM rash." Just think what that really means.

dlp252 Apprentice
Open Original Shared Link

"Diagnosis is no longer clinical, only by CDC positive surveillance blood test or EM rash." Just think what that really means.

:blink::o

jerseyangel Proficient
Open Original Shared Link

"Diagnosis is no longer clinical, only by CDC positive surveillance blood test or EM rash." Just think what that really means.

Oh my :unsure::o:angry:

Fiddle-Faddle Community Regular
But You Don't LOOK sick....

10 commandments for interacting with the chronically ill

1. Thou shalt not imply that we are not truelly ill.

You will not convince us otherwise with remarks such as, "You LOOK good," or "But you don't LOOK sick". Even if you mean them as compliments, we perceive those kind of statements as insults because they imply that you do not believe us. <_<

2. Thou shalt not imply that the illness can be easily fixed.

People with chronic illness are persistent, if nothing else. We hang on, day after day.We see countless doctors, take numerous medications (not the R-villians though), do endless research, and continue hoping that the answer is just around the next corner. So please do not insult us by delivering diagnoses, remedies, or comments such as, "Why dont you just...." or "Have you tried..." or "You should..." If it truelly were that simple, I assure you that we would have done it already. :rolleyes: We are sick, not stupid. :P

[

Wow--Great!!!! I especially love #1. That's just basic human decency for any situation, not just chronic illness. I remember being told when I had severe hyperemesis and had to be IV'ed because I couldn't even keep water down, everyone kept saying, "You can't be sick, you look great!"

I do have a quibble for #2, though. I wish someone would have said, "Why don't you look into gluten intolerance?" 19 years ago when my thyroid first went kaflooie. And I am now saying it to everyone I know with Hashimoto's, rheumatoid arthritis, IBS, fibromyalgia, etc. Most of them have a visible light bulb over their head when I describe typical symptoms of celiac, except for one colleague who is on his third bone marrow transplant for non-Hodgkin's Lymphoma. He was very offended that I suggested he look into gluten intolerance. He says he's never had any symptoms, so why should he get tested.

Unfortunately, I think it's one of those you-have-to-kiss-a-lot-of-frogs situations. 99 people will give us totally garbage suggestions--but then one will give us The Answer--and if we tell them all not to make suggestions, we will miss The Answer.

Aside from that, do you think Scott might post these on www.celiac.com if we all ask him to?

Judyin Philly Enthusiast

QUOTE(rinne @ Nov 15 2006, 01:26 AM)

I am concerned about Evie too but am hopeful that they just needed to keep her a another day of two. I know much of my concern comes from the tone of Evie's last post, when she said she felt very weak I felt her concern, did anyone else have that feeling? Judy is that what you mean?

Rachel-

I felt the same way about her last post Rinne....it really worried me. Also I read alot about C.Diff earlier in the year because they put me on antibiotics for it after they detected it in my stool. C.Diff is really scary....I never was sick from it but I read alot of pretty scary stories. So yeah...I am very very worried at this point.

**************

hi all

yep this is what i meant can't do the 2 quotes here sorry.

yes the last post from her sounded like she was so weak.

all the past talk of c-diff and you guys warning me this past summer..and my dr who was so worried i would get it..i was so scared that i NEVER LOOKED IT UP ha for me that was scared... :o:blink:

well there is nothing we can do here now but keep the good thougts and prayers going i guess.

if i hear you know i'll post.

love

judy

good luck today LauraJ our happy girl.

DingoGirl Enthusiast
I second this! :P:P:P:lol::lol::lol:

nary an idiot on this thread! (Nary was a word for Susie Q cuz she always cracks up when we use words like conundrum, heinosity and such chicanery).

Actually Conundrum picture on this link:

Open Original Shared Link

Now that's my kind of vino!

Um, ahem, would just like to clarify that it was our dear Patti who used the word Conundrum. :D And yes, that is a good wine. :P

I didn't want to mention this before.....but C. Diff does kill one-third of patients who get it. :( Yes, I am beyond worried too....Judy I know you'll let us know as soon as you hear anything.

And, the reaction to antibiotics is FAR higher than 1 in 400,000 - - - the numbers are shocking, actually, for the particular one that my friend's daughter was on....it is so common and I have forgotten the name....there are huge lawsuits against the manufacturing company. :o

AndreaB Contributor
I had one "friend" suggest that I might get better if I left my husband :rolleyes: based on a friend of hers, who had been diagnosed with MS (bells ringing for me, MS a common misdiagnosis of Lyme and she is from a Lyme hot spot in the province) who had a complete remission of her symptoms after she left her husband. :o

:o:o:o

I am concerned about Evie too but am hopeful that they just needed to keep her a another day of two. I know much of my concern comes from the tone of Evie's last post, when she said she felt very weak I felt her concern, did anyone else have that feeling? Judy is that what you mean?

I was going to say I'd be really concerned by Friday......now I'm very concnerned after reading the rest of the posts about c-diff. I'm so not in the know about these things. :ph34r:

Susan, a horrifying story of drugs gone wrong in that young girl's body. Will she recover further over time?

It makes me cry to think of how stupid we are.

I didn't realize antibiotics could do that kind of damage. I hate taking meds unless they are absolutely necessary though.

I think today is Laura's test--it's been a week since she began the diet challenge.

I was going to say today or yesterday......miamia solidified the date. :)

:) Thanks for asking. I was feeling awful yesterday ... don't know how today's going to turn out. I have a meeting this morning, so I'll be out for a while.

Sorry you have to go out this morning. Hope you feel better.

Andrea :blink: you are one of the kindest and most supportive people, you are not an idiot. :lol:

You may change your mind if I have to many nights like last night. Seth was up or just dozing from 10:45-1:45. Zzzzzzzzzzzzzzzzzz

Open Original Shared Link

"Diagnosis is no longer clinical, only by CDC positive surveillance blood test or EM rash." Just think what that really means.

:blink::o:o:o

This is NOT good news. Why must CDC cause so many problems. Fill our kids with too many toxins and refuse proper treatment for our illnesses.

Anyone think the statement "this world is going to hell in a handbasket" fits. (Is that the right phrase....something similar if not) :ph34r:

I didn't want to mention this before.....but C. Diff does kill one-third of patients who get it. :( Yes, I am beyond worried too....Judy I know you'll let us know as soon as you hear anything.

:o:( I'm concerned now. I'm really concerned now. Yes, her last post sounded scared/worried about her condition.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      127,194
    • Most Online (within 30 mins)
      7,748

    AquaV
    Newest Member
    AquaV
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • WednesdayAddams13
      Hello,   I contacted the makers of Alpine Original Spiced Cider Drink Mix and they sent me this email.....   Subject: [EXTERNAL] Fw: Ref. ID:1335211 Alpine Original Spiced Cider Drink Mix.               On Friday, December 6, 2024, 1:04 PM, Consumer <baking@continentalmills.com> wrote: December 06, 2024   Dear Janie, Thank you for taking the time to contact us regarding our Alpine Original Spiced Cider Drink Mix. We appreciate your interest and are happy to provide you with additional information. This product does not contain gluten. However, it is not manufactured in a gluten free facility. If I can be of further help, please contact me at 1 (800) 457-7744, weekdays 7:00 a.m. to 4:00 p.m. (PT), or visit www.alpinecider.com and select "Contact Us." Sincerely, Kristin Kristin Consumer Relations Specialist Ref # 1335211   I hope this helps everyone.  I am currently looking for a spiced hot apple cider drink and have yet to find one that is not made in a plant that manufactures other gluten products.  It's so frustrating. 
    • trents
      @Rogol72, dermatitis herpetiformis occurs in a minority of celiac patients and if the OP hasn't developed it yet I doubt it will show up in the future. I think it unwise to use a scare tactic that probably won't materialize in the OP's experience. It has a good chance of backfiring and having the opposite effect.
    • Rogol72
      Hi @trents, You're correct. The OP mentioned fatigue and vitamin deficiencies as the only symptoms at the time of diagnosis. Since the family are not taking him/her seriously and find them to be too fussy, I suggested showing them pictures of dermatitis herpetiformis as one of the consequences of not taking the gluten-free diet seriously ... would make life easier for him/her, and the family might begin to take his/her strict gluten-free diet more seriously. A picture says a thousand words and the shock factor of dermatitis herpetiformis blisters might have the desired effect. The OP did say ... "How do you deal with people close to you who just refuse to understand? Are there any resources anyone could recommend for families that are short and easy to read?".  @sillyyak52, It might also help mentioning to your family that Coeliac Disease is genetic and runs in families. Any one of them could develop it in the future if they have the HLA DQ 2.5 gene. Here's a Mayo Clinic study calling for screening of family members of Coeliacs ... https://newsnetwork.mayoclinic.org/discussion/mayo-clinic-minute-celiac-disease-screening-for-family-members/ https://newsnetwork.mayoclinic.org/discussion/mayo-clinic-study-calls-for-screening-of-family-members-of-celiac-disease-patients/ I got glutened a few months ago because I missed the may contains statement on a tub of red pesto. It was my own fault but it happens.
    • peg
      Thank you, Scott!  This is just what I needed.  Appreciate your site very much and all of your time and energy that goes into it! Kind Regards, Peg
    • Hopeful1950
      Oh yes.  I would never recommend taking it for an extended period of time.  When 70% of my body was covered in blistering itchy sores, an amazing doctor prescribed it diagnostically because I was unwilling to do a gluten challenge after already going strictly gluten-free in desperation after 10 years of suffering and being poo pooed by dermatologist after dermatologist. The fact that it stopped the itch and mostly cleared the rash after about 2 months was diagnostic for him.  I stopped it and have remained strictly gluten-free with very few flares since that time (over 10 years ago).  So the fact that it cleared the rash was diagnostic for me.     
×
×
  • Create New...