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

Parkinson's Disease


ArtGirl

Recommended Posts

ArtGirl Enthusiast

To those of you who like to research things - has anyone ever read if there's a gluten link to Parkinson's? Has anyone with this ever gone gluten-free and noted any improvement?

Just wondering. My father died from Parkinson's and I'm almost certain, looking back, that he was at least gluten-intolerant (I got one of my two g.i. genes from him, afterall).


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



Celiac.com Sponsor (A8-M):



Electra Enthusiast

Well I can tell you that before I found Celiac and tested positive, we were concerned that I may have Parkinsons Disease. I'm only 34 and when I turned 30 my head started bobbing like an old ladies. It was a joke at first and everyone laughed, but then when it got worse and I got other symptoms it didn't seem so funny anymore. My hands started shaking out of control (but only at times) and there seemed to be no pattern. When I was sick it was worse, but when I was feeling better it didn't happen. Now that I am Glutan Free I don't notice it much, but I've only been Glutan Free for a couple of weeks and there have been two times that I know of that I was accidentally glutaned. I also lost a lot of my balance and my foot went cold and numb a lot so I started tripping 3 or 4 times a year and I'd fall down too which was weird because I have never been clumsy or had any problems with BALANCE!!

It's an interesting theory and I really think if I had not stumbled upon Celiac I may also have been diagnosed with Parkinsons!! I wonder if Michael J. Fox has ever gone Glutan Free?

  • 1 year later...
Rachel43 Newbie

Artgirl - Very interesting... My mum has been dxd for 5 years with PD. She also has had thyroid problems (over active though) as had my aunt (her sis) I think there could well be something here for researchers it stands to reason

I had + blood tests 2 weeks b4 Xmas and have been gluten-free (well nearly, due to a few mistakes) since. I had my biopsy done two weeks ago my next apptmt is in two more weeks but I feels so much better for the gluten-free diet that I shall try not to ingest gluten regardless what the biopsy says.

Darn210 Enthusiast

Here's an old thread that actually had some activity not too long ago about Parkinson's

Open Original Shared Link

kenlove Rising Star

In 2006 was also first diagnosed with Parkinson's. Couldn't focus on my left leg it shook so much. That lasted two weeks with no change on the meds and another month before they figured out the celiac. The shakes stopped as soon as I was gluten-free for a few days.

With everything I read on this forum, it seems to me that going gluten-free would be advantageous for anyone.

Ken

To those of you who like to research things - has anyone ever read if there's a gluten link to Parkinson's? Has anyone with this ever gone gluten-free and noted any improvement?

Just wondering. My father died from Parkinson's and I'm almost certain, looking back, that he was at least gluten-intolerant (I got one of my two g.i. genes from him, afterall).

moldlady Rookie

This is very interesting indeed!

We have "shakes" on both sides of the family and I started getting them only when I need to do something small and most accurate!! When I started eating a plant based diet, with no sugars, limited fruits, no gluten, these shakes went away. Other members of my family thought I was nuts and they still shake at those times when you do not want to shake..

I think there is a possible gluten link, a fungal link, and possibly a heavy metal link. If it were me, I would do everything possible to try and treat it naturally and see if things can heal and not have to take any meds. All those meds have side effects.

moldlady :)

UR Groovy Explorer

Hello,

I'm curious if any of you with first degree relatives dx'd with Parkinson's have had genetic testing. Also, how many of you in that same boat suffered from anxiety & depression. The gene that I'm particularly interested in is DQB1*06 .

My mother was dx'd with Parkinson's a couple years ago. I, myself, haven't had any testing for Celiac, but suspect that I would be found to be non-celiac gluten intolerant. I've read many articles that have tried to link the two, but none have conclusive results. I wish they would do more tesing on this. The connection that intrigues me is that there seems to be a connection in PD to first degree relatives with anxiety & depression. The neurological component just seems too apparent to rule out a connection. Some with Celiac present with symptoms which appear to have nothing to do with GI issues, but more neurological. As the 14 months that I've been gluten-free have gone on, my problems when exposed to gluten have changed dramatically. I used to have nasty GI issues, but at this point, my most notable reactions are about 2 weeks of depression & anxiety. I suffered from depression for at least 20 years - not just a little depression - we're talking suicidal, crazy thoughts type depression - I was medicated for years. No need for meds since I've been gluten-free.

I'm thinking about getting genetic testing, but it's kind of moot at this point. I'm gluten-free for life. I just wish I had some compelling evidence that may convince my Mom to give it a shot. She's in the beginning stages.


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



Celiac.com Sponsor (A8-M):



Archived

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

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

    • Total Members
      133,046
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • tiffanygosci
      Hi Cristiana! It's so nice to meet you! Thank you for the kind reply I am glad I live in a time where you can connect with others through the Internet. That is a mercy I am grateful for.
    • knitty kitty
      In the study linked above, the little girl switched to a gluten free diet and gained enough weight that that fat pad was replenished and surgery was not needed.   Here's the full article link... Superior Mesenteric Artery Syndrome in a 6-Year-Old Girl with Final Diagnosis of Celiac Disease https://pmc.ncbi.nlm.nih.gov/articles/PMC6476019/
    • knitty kitty
      Hello, @Jordan Carlson, So glad you're feeling better.   Tecta is a proton pump inhibitor.  PPI's also interfere with the production of the intrinsic factor needed to absorb Vitamin B12.  Increasing the amount of B12 you supplement has helped overcome the lack of intrinsic factor needed to absorb B12. Proton pump inhibitors also reduce the production of digestive juices (stomach acids).  This results in foods not being digested thoroughly.  If foods are not digested sufficiently, the vitamins and other nutrients aren't released from the food, and the body cannot absorb them.  This sets up a vicious cycle. Acid reflux and Gerd are actually symptoms of producing too little stomach acid.  Insufficient stomach acid production is seen with Thiamine and Niacin deficiencies.  PPI's like Tecta also block the transporters that pull Thiamine into cells, preventing absorption of thiamine.  Other symptoms of Thiamine deficiency are difficulty swallowing, gagging, problems with food texture, dysphagia. Other symptoms of Thiamine deficiency are symptoms of ADHD and anxiety.  Vyvanse also blocks thiamine transporters contributing further to Thiamine deficiency.  Pristiq has been shown to work better if thiamine is supplemented at the same time because thiamine is needed to make serotonin.  Doctors don't recognize anxiety and depression and adult onset ADHD as early symptoms of Thiamine deficiency. Stomach acid is needed to digest Vitamin C (ascorbic acid) in fruits and vegetables.  Ascorbic acid left undigested can cause intestinal upsets, anxiety, and heart palpitations.   Yes, a child can be born with nutritional deficiencies if the parents were deficient.  Parents who are thiamine deficient have offspring with fewer thiamine transporters on cell surfaces, making thiamine deficiency easier to develop in the children.  A person can struggle along for years with subclinical vitamin deficiencies.  Been here, done this.  Please consider supplementing with Thiamine in the form TTFD (tetrahydrofurfuryl disulfide) which helps immensely with dysphagia and neurological symptoms like anxiety, depression, and ADHD symptoms.  Benfotiamine helps with improving intestinal health.  A B Complex and NeuroMag (a magnesium supplement), and Vitamin D are needed also.
    • knitty kitty
      @pothosqueen, Welcome to the tribe! You'll want to get checked for nutritional deficiencies and start on supplementation of B vitamins, especially Thiamine Vitamin B 1.   There's some scientific evidence that the fat pad that buffers the aorta which disappears in SMA is caused by deficiency in Thiamine.   In Thiamine deficiency, the body burns its stored fat as a source of fuel.  That fat pad between the aorta and digestive system gets used as fuel, too. Ask for an Erythrocyte Transketolace Activity test to look for thiamine deficiency.  Correction of thiamine deficiency can help restore that fat pad.   Best wishes for your recovery!   Interesting Reading: Superior Mesenteric Artery Syndrome in a 6-Year-Old Girl with Final Diagnosis of Celiac Disease https://pubmed.ncbi.nlm.nih.gov/31089433/#:~:text=Affiliations,tissue and results in SMAS.  
    • trents
      Wow! You're pretty young to have a diagnosis of SMA syndrome. But youth also has its advantages when it comes to healing, without a doubt. You might be surprised to find out how your health improves and how much better you feel once you eliminate gluten from your diet. Celiac disease is an autoimmune disorder that, when gluten is consumed, triggers an attack on the villous lining of the small bowel. This is the section of the intestines where all our nutrition is absorbed. It is made up of billions of tiny finger-like projections that create a tremendous surface area for absorbing nutrients. For the person with celiac disease, unchecked gluten consumption generates inflammation that wears down these fingers and, over time, greatly reduces the nutrient absorbing efficiency of the small bowel lining. This can generate a whole host of other nutrient deficiency related medical problems. We also now know that the autoimmune reaction to gluten is not necessarily limited to the lining of the small bowel such that celiac disease can damage other body systems and organs such as the liver and the joints and cause neurological problems.  It can take around two years for the villous lining to completely heal but most people start feeling better well before then. It's also important to realize that celiac disease can cause intolerance to some other foods whose protein structures are similar to gluten. Chief among them are dairy and oats but also eggs, corn and soy. Just keep that in mind.
×
×
  • 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.