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

Focal Segmental Glomerulosclerosis (fsgs)


dadoffiveboys

Recommended Posts

dadoffiveboys Rookie

I wanted to post some interesting information about my family (and my Father that has FSGS - via Biopsy confirmed).

I found myself allergic to gluten (intolerance) and went gluten-free and noticed my back pains went away completely (I have DH). My father about 9 months ago went gluten-free as well (after MUCH convincing) and the following occurred:

1) He has suffered from chronic gastritis (and ulcers) for the past 25 years taking prilosec, malox, etc. all the time - GONE

2) High blood pressure - 6 medications - GONE (still some problems but not as bad)

3) High protein levels in the urine - caused by the FSGS - Creatine at Biopsy of original problem was 2.8, 9 months ago was 3.3. Since he went on the gluten-free diet, Creatine has dropped from 3.3 to 2.9 and now it is at 2.3 - 9 months later!

I was NEGATIVE for celiac disease via TTG but I did show elevated IgA Anti-gliadin antibodies - enough for my doctor to say I have a gluten intolerance even though the 'celiac expert' said I didn't have anything and the IgA test wasn't very predictive of celiac. The doctor is 'right' in that I probably don't have celiac disease.. but I bet I have some form of the FSGS my dad has! (JUST AS BAD IMHO!)

My fathers doctors claim the decrease in Creatine and restoration of Kidney function (1 point in Creatine is ALOT OF CHANGE in Kidney function BTW!) was impossible.. and they are scratching their heads. Normal function is about a level of 1.1.

It was always hypothesized that FSGS might by caused (or is itself) an autoimmune disorder (much like Celiac Disease). I wanted to share this with everyone because I DO believe Gluten (in our case) is the CAUSE of the FSGS and that the IGA antibodies clogged his kidney. No real proof except in the numbers and he's getting better - of course we don't need doctors to tell us what to eat and the longer we go gluten-free the more we prove them wrong :). Not all cases of FSGS may be related to Gluten either.. but if anyone had this condition it would be worth trying a gluten-free diet - the prognosis is the same as for Celiac - no more gluten EVER! (Other food allergies may cause IgA antibodies to clog the kidney as well - e.g. milk protein).

BTW I do believe the cause of many of the major disorders are food allergies - undiagnosed for the most part. All of my boys (five of them) are eating gluten-free and it's very funny that ALL of thier 'problems' disappeared. Asthma - GONE; Ear Infections- GONE; Bed wetting - GONE!! (yeah how is this caused by gluten??!); Nosebleeds - GONE; Eczema - GONE; Constipation - GONE; Reflux - GONE!. Between my kids being on Pulmicort and Omeprizol and having tubes in their ears.. I'm VERY HAPPY to be rid of all that medication! Funny enough.. in the past year since we've gone gluten free my kids haven't needed any medicine except Tylenol for the mild colds we got... we would always chronically get sick. Of course being gluten-free and eating at home all the time we eat healthier so I'm sure that helps too!


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



Celiac.com Sponsor (A8-M):



lonewolf Collaborator

Interesting to see that someone else has had great improvement with a kidney disease. I was diagnosed with Minimal Change Nephrotic Syndrome (similar, but not quite as severe as FSGS) almost 5 years ago and going fanatically gluten-free has made it go into remission. I hope your dad sticks with it and keeps improving!

I have tried for years, in vain, to share my story with others who have Nephrotic Syndrome, but it seems that no one wants to try a gluten-free diet. Most will complain about all their medications, but don't really want to have to do anything "hard" to get better. A little boy on my son's soccer team has the same thing I have and his mom put him on a gluten-free diet out of desperation and he went into remission after about 6 weeks. They are the only ones who I've ever "convinced" to try it. Keep sharing your dad's good news - maybe someone else will listen and have good results too!

cyberprof Enthusiast

Thanks Dadof5!

My hubby has dormant myeloma, a blood cancer. Kidney failure in this cancer is a main cause of death because the IgA antibodies clog the kidneys. He also has thin basement membrane syndrome, which was found after a kidney biopsy during his myeloma diagnosis. (The biopsy nearly killed him, as they hit an artery causing uncontrolled bleeding.)

So Dadof5, I guess my hubby going gluten-free might keep him from having other kidney-related complications and I appreciate your post!

Glad to hear your boys (and dad) are doing well- I hope my son has the same response.

~Laura

  • 1 year later...
lokinetworks Newbie

Thanks for posting this.. I was diagnosed with FSGS last October and the Nephrologists basically told me I'd be on dialysis within the next 6 months. Since reading this article last November I went totally gluten-free. I just had my kidney function checked last week and low and behold my creatinine dropped from 2.08 to 1.9 and my kidney function went from 35 to 39. The doc said I'd never see any improvement.

Thanks again

-Eric

  • 4 months later...
denisestevens Newbie
Interesting to see that someone else has had great improvement with a kidney disease. I was diagnosed with Minimal Change Nephrotic Syndrome (similar, but not quite as severe as FSGS) almost 5 years ago and going fanatically gluten-free has made it go into remission. I hope your dad sticks with it and keeps improving!

I have tried for years, in vain, to share my story with others who have Nephrotic Syndrome, but it seems that no one wants to try a gluten-free diet. Most will complain about all their medications, but don't really want to have to do anything "hard" to get better. A little boy on my son's soccer team has the same thing I have and his mom put him on a gluten-free diet out of desperation and he went into remission after about 6 weeks. They are the only ones who I've ever "convinced" to try it. Keep sharing your dad's good news - maybe someone else will listen and have good results too!

Hi Liz (Lonewolf), I was diagnosed with FSGS with nephrotic syndrome in July 2009 and you convinced me to try a gluten-free diet. My BFF with celiac disease found a link between kidney disease and gluten on this website. I started reading stories by people with kidney disease, and your story in particular struck a nerve with me. I immediately went onto a gluten-free diet that day. Fortunately I was already educated about what that means because of my friend with celiac disease, so it was not an overwhelming transition at all. I'm thrilled to say that I went into full spontaneous remission without treatment (Prednisone) and I was taken off both cholesterol and blood pressure medication yesterday. All my blood work came back normal, too, and my cholesterol, which was 362 in July, as of last Friday is 144 (73 HDL and 58 LDL). My blood pressure averages 110/60. In July it was 140/90 thereabouts. I've also lost 17 pounds, which was mostly fluid retention. My nephrologist yesterday told me my FSGS improvement is remarkable and my cholesterol is incredible. He didn't discount my gluten-free diet as a cause, but he said it's controversial as there is not much research on this. Mostly research is focused on new drug treatments. I hope to live a lifetime in remission dietarily and not ever have to take medication for this. Going gluten-free can be a hassle, but it's well worth it. Not THAT hard, especially considering the alternative.

So Liz, don't give up hope and keep spreading the news. I will do the same. While we've never met, your story did have a major impact on me and going gluten free may have literally saved my life. I plan to stay gluten free for life.

Denise

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 pothosqueen's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      16

      Positive biopsy

    2. - knitty kitty replied to Jordan Carlson's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      1

      Fruits & Veggies

    3. - knitty kitty replied to pothosqueen's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      16

      Positive biopsy

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

    • Total Members
      133,035
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • 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.
    • pothosqueen
×
×
  • 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.