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

6 Weeks On Cf Diet With No Changes


cruelshoes

Recommended Posts

cruelshoes Enthusiast

My celiac son has been completely casein free since 1/15. His Neurologist asked that we put him on a CF diet to see if it helps with his small motor coordination disorder. I am scrutinizing everything that comes into the house and goes into his mouth. My son was OK with the gluten-free diet, but removing casein makes it much more restrictive.

We have seen absolutely no change in my son's coordination, behavior or moods. He is exactly the same kid he was before we started, only with a more restricted diet. He is frustrated. He said to me the other day "mom - this isn't helping me at all. I still can't write." I am frustrated because I knew it wasn't going to help. But I told the neurologist I would try it until our next appointment on 3/5.

This post has no point other than to say I'm not sure I can keep this up until 3/5. This sucks. Shouldn't I have seen some changes by now if there were going to be any???


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



Celiac.com Sponsor (A8-M):



home-based-mom Contributor
Shouldn't I have seen some changes by now if there were going to be any???

My totally uneducated guess is yes, you probably should have seen something by now if there were ever going to be anything to see.

Nevertheless, March 5 is only a week and a half away and you will then be able to tell the doctor that you did exactly as recommended.

:ph34r: And then get some ice cream on the way home! :D

missy'smom Collaborator

Have you had him tested for dysgraphia?

PixieChinchilla Rookie

Believe me I know the feeling.

I've been gluten-free for four months and I'm still sick every, every day.

I know that I'm not slipping up, either. I've been VERY careful. OCD careful.

I drive everyone I know crazy with how careful I am.

I dont know what to tell you, because I'm ridiculously frustrated..

But sticking with it. I know people who didn't notice results for a full six months.

I just hope I'm one of them... :/

Mango04 Enthusiast

Sorry, Colleen. :(

I don't know if you would be seeing changes already. I think you need to give it three months before you decide casein-free isn't worthwhile, but I know that might seem like too long. <_<

Darn210 Enthusiast

Colleen, don't know the answer . . . seems like you should have seen a difference . . . but this is just a note to cheer you on . . . you can do it and so can he. My son is counting down the last days of his gluten-free trial (and so am I).

confusedks Enthusiast

Colleen,

I agree with Mango. It's like gluten, it can take a while to detox the body of dairy...much longer than gluten.

When I went casein free, I didn't notice any really big changes, but when I tried milk chocolate once, I got a severe migraine the next day...so obviously it doesn't agree with me!

I'd stick it out a little bit longer to see if anything changes. For me, I guess I didn't even notice I got headaches until I took the dairy OUT of my diet.


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



Celiac.com Sponsor (A8-M):



Green12 Enthusiast

Colleen, just wanted to give you my support.

I have heard it does take a while to clear out dairy and notice changes so it might be worth it to give it more time.

Whatever you decide best of luck :)

cruelshoes Enthusiast
Sorry, Colleen. :(

I don't know if you would be seeing changes already. I think you need to give it three months before you decide casein-free isn't worthwhile, but I know that might seem like too long. <_<

Really? 3 months? :( That seems like such a long time. Oh, well, if it does turn out to be 3 months at least we will be more than half way there.

:ph34r: And then get some ice cream on the way home! :D

Believe me, Ice cream is definitely on the agenda after our next appointment. :D I have been careful to tell my son, though, that we have to get the doctor's OK first. Not trying to promise that we will be back to dairy, just that we will talk to the doctor about it.

Have you had him tested for dysgraphia?

We had a learning disabilities assessment from the speech/language/learning center, and they didn't find any. The Neurologist seems to think that it is more of a physical problem than a learning disability. I originally went into this with the opinion that it was dysgraphia, but now I'm not so sure.

Colleen, don't know the answer . . . seems like you should have seen a difference . . . but this is just a note to cheer you on . . . you can do it and so can he. My son is counting down the last days of his gluten-free trial (and so am I).

Have you seen any changes? I can't imagine hanging on for 6 months without seeing something. How is your son handling things?

Thanks for the support, everybody. I really didn't want to hear that it can take a long time to see results from removing dairy. I just got such a quick indication that things were working when I took gluten out of our diet that I hoped dairy would be the same. It's hard to keep up the momentum without seeing results. At least we only have 10 days until we see the doctor again. My husband says he is ready to give up now, but I made a commitment to the doctor that I would try it. I don't want to be one of those mothers that don't follow through with what the doctor says just becaue it's inconvenient and hard.

Mango04 Enthusiast
Really? 3 months? :( That seems like such a long time. Oh, well, if it does turn out to be 3 months at least we will be more than half way there.

Six weeks seems like a long time, but I've been doing it for 12 years...tell your son to hang in there...he can do it. :) It would be worth it to stick it out for a while longer just to really make sure you're not missing out on a possible solution to his problem. I really think that with the neurological effects of these proteins, it takes months (not weeks) to see results.

Fimac Newbie

Hi Colleen,

Question - Did you replace the dairy with soy ?

My son has a motor speed processing disoder with a dysgraphia diagnosis.

When he came of dairy it made no diffrence to this problem. There were very noticible changes in other areas.

However when I took him of soy there was a significant change in his motor speed. Things have improved in that area, but he was in the 4% for speed. Handwriting is still bad, but now we have some writing. :)

Fiona

Nancym Enthusiast
Hi Colleen,

Question - Did you replace the dairy with soy ?

I'm glad you asked that, I was about to ask the same thing.

cruelshoes Enthusiast
Hi Colleen,

Question - Did you replace the dairy with soy ?

My son has a motor speed processing disoder with a dysgraphia diagnosis.

When he came of dairy it made no diffrence to this problem. There were very noticible changes in other areas.

However when I took him of soy there was a significant change in his motor speed. Things have improved in that area, but he was in the 4% for speed. Handwriting is still bad, but now we have some writing. :)

Fiona

We have introduced some soy cheese, but that's about it. We have been using rice or almond milk for drinking and cooking. I will definitely ask his neurologist about soy when we go back in for our appointment next week.

When you removed soy did you re-introduce dairy? I don't think I can deal with gluten, dairy AND soy. Losing dairy has been a tough pill to swallow. It feels like it has take away the last few shreds of normalcy we still had left. I guess if it comes down to that we will do it, but I'm sure going to whine about it! :lol:

Fimac Newbie

Hi Colleen,

When you removed soy did you re-introduce dairy? I don't think I can deal with gluten, dairy AND soy. Losing dairy has been a tough pill to swallow. It feels like it has take away the last few shreds of normalcy we still had left. I guess if it comes down to that we will do it, but I'm sure going to whine about it!

No, When I removed soy the dairy was still gone from his diet. He has lost it forever. Dairy causes inflammation in his colon. We removed dairy from his diet at the suggestion of his GI doc when she found a lot of inflammation during a colonoscopy. The procedure was repeated 3 months later and the inflammation was gone. However he had been lactose free since he was 4 1/2 years old and I was never very happy with dairy in his diet so his dairy was only lactose free milk at breakfast time.Not difficult to remove. Soy however was a major pain and it has taken 4 months until I have reached a point where I think I can cope with this. Doc's opionin about removing soy was "You can not do that he would have nothing to eat!"

When we removed dairy from his diet I did get feed back from his teacher. She had noticed changes in his behavoiur in the class room and was unaware of any changes to his diet. So I would talk to your sons teacher to see if she has noticed any diffrences in the classroom. Sometimes I find that ds will focus on the negative and not see the what he has gained because it was subtle and slow. Ds is 10 years old by the way.

However on a side note ds(12) has tried gluten-free/df/sf and it has made no diffrence to his tremor.

Would your son be helped by a laptop ? You could probably get a letter from the neurologist to say that the school should use adaptive technology. The school may even have to provide this for him. There is speech to text software and word predictive software that might help your son.

Fiona

Archived

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

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,318
    • Most Online (within 30 mins)
      7,748

    direne
    Newest Member
    direne
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • Jmartes71
      So I've been dealing with chasing the name celiac because of my body actively dealing with health issues related to celiac though not eating. Diagnosed in 1994 before foods eliminated from diet. After 25 years with former pcp I googled celiac specialist and she wasn't because of what ive been through. I wanted my results to be sent to my pcp but nothing was sent.I have email copies.I did one zoom call with np with team member from celiac specialist in Nov 2025 and she asked me why I wanted to know why I wanted the celiac diagnosis so bad, I sad I don't, its my life and I need revalidaion because its affecting me.KB stated well it shows you are.I asked then why am I going through all this.I was labeled unruly. Its been a celiac circus and medical has caused anxiety and depression no fault to my own other than being born with bad genetics. How is it legal for medical professionals to gaslight patients that are with an ailment coming for help to be downplayed? KB put in my records that she personally spent 120min with me and I think the zoom call was discussing celiac 80 min ONE ZOOM call.SHE is responsible for not explaining to my pcp about celiac disease am I right?
    • Amy Barnett
      What is the best liquid multivitamin for celiac disease?
    • Jmartes71
      I've noticed with my age and menopause my smell for bread gives me severe migraines and I know this.Its alarming that there are all these fabulous bakeries, sandwich places pizza places popping up in confined areas.Just the other day I suffered a migraine after I got done with my mri when a guy with a brown paper bag walk in front of me and I smelled that fresh dough bread with tuna, I got a migraine when we got home.I hate im that sensitive. Its alarming these places are popping up in airports as well.I just saw on the news that the airport ( can't remember which  one)was going to have a fabulous smelling bakery. Not for sensitive celiacs, this can alter their health during their travel which isn't safe. More awareness really NEEDS to be promoted, so much more than just a food consumption!FYI I did write to Stanislaus to let them know my thoughts on the medical field not knowing much about celiac and how it affects one.I also did message my gi the 3 specialist names that was given on previous post on questions on celiac. I pray its not on deaf door.
    • xxnonamexx
      Thanks for the info. I have been taking the ones you recommended but when I saw this I was curious if it was something else to add to the journey Thank  
    • Jane07
      I used to be able to get the Rivera yougut i havent been able to get it lately. I like getting it did say it did say gluten free. I just looking for a good yogurt that gluten free that i can add some fruit and nuts to any suggestion would be helpful  thanks
×
×
  • 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.