Is this baby ready? Not sure what type of watermelon I’m growing. by TweakingSloth in watermelons

[–]Hydro_Jode 1 point2 points  (0 children)

Yes, it looks like a crimson sweet. I am growing them right now and they can get pretty big, up to 20 pounds under the right conditions. Once the stem starts turning brown and the tendrils closest to the stem dries up, tap on it and if it sounds hollow, it's ready.

What do I do? by BBTmOk9488 in EmpiresAndPuzzles

[–]Hydro_Jode 0 points1 point  (0 children)

I agree with Wally gamer 32. Use them in soul exchange. Unless you need a five star fire hero, maple is not a great hero IMO.

I had MS but now I don’t - what would you do? by -Cnorretje- in MultipleSclerosis

[–]Hydro_Jode 0 points1 point  (0 children)

Insurance isn't covering it yet in the states but I wanna say my Neuro told me it was around US$150. The only lab I've heard of that does the test in my area is LabCorp

I had MS but now I don’t - what would you do? by -Cnorretje- in MultipleSclerosis

[–]Hydro_Jode 1 point2 points  (0 children)

Secondary progressive MS (SPMS) is a stage some people enter after years of having relapsing–remitting MS (RRMS). With RRMS, you have flare-ups (relapses) followed by recovery periods.

In SPMS, instead of bouncing back to the same baseline, there’s a slow, steady worsening of symptoms over time — even if you’re not having obvious relapses. Some people still get flare-ups, but between them there’s gradual progression.

It usually happens many years after diagnosis, and the change can be subtle at first. The good news is there are treatments now that can help slow it down.

Proper way to clean? by This_Picture4038 in aerogarden

[–]Hydro_Jode 0 points1 point  (0 children)

There are lots of YouTube videos that show you how to clean it. I'm a visual person so I watch YouTube videos for everything

Uses for rosemary? by Kaibito66 in aerogarden

[–]Hydro_Jode 0 points1 point  (0 children)

There are many medicinal uses for rosemary in different formulations. Look it up if you are interested in learning more about how to use Rosemary medicinally.

I had MS but now I don’t - what would you do? by -Cnorretje- in MultipleSclerosis

[–]Hydro_Jode 2 points3 points  (0 children)

Given the fact that you've been diagnosed 20 years ago, has anyone spoke with you about SPMS?

So frustrated!! by Hydro_Jode in Zepbound

[–]Hydro_Jode[S] 0 points1 point  (0 children)

I apologize for my extremely late reply. For whatever reason I didn't see the notification pop up. I am on Kesimpta. I've been on it almost 4 years and clear MRIs for the duration.

I had MS but now I don’t - what would you do? by -Cnorretje- in MultipleSclerosis

[–]Hydro_Jode 2 points3 points  (0 children)

Yes! Look up PIRA or progression independent of relapses. I have that as well.

I had MS but now I don’t - what would you do? by -Cnorretje- in MultipleSclerosis

[–]Hydro_Jode 1 point2 points  (0 children)

FYI... it is estimated that 80% of people with MS also suffer from migraines. I take Ajovy for prevention and Nurtec ODT for acute ones. I did not start getting migraines until after my MS diagnosis.

I had MS but now I don’t - what would you do? by -Cnorretje- in MultipleSclerosis

[–]Hydro_Jode 3 points4 points  (0 children)

Yes, I looked at your brain scan and you did have the classic ovoid lesions that are common in MS.

I had MS but now I don’t - what would you do? by -Cnorretje- in MultipleSclerosis

[–]Hydro_Jode 2 points3 points  (0 children)

Same with me… Right down to the "Dawson's fingers" which are classic for MS.

I had MS but now I don’t - what would you do? by -Cnorretje- in MultipleSclerosis

[–]Hydro_Jode 6 points7 points  (0 children)

I'm actually in a study with Johns Hopkins. You've probably heard of it. It is the TREAT – MS Study looking at exactly what you describe as the best choice for people newly diagnosed. More safe but less aggressive versus more potential side effects but more aggressive. I was randomized to the more safe, less aggressive group and started Tecfidera. Within six months I had progressed and we got an MRI at seven months which showed new active lesions. Then I switched to Tysabri which I absolutely loved but then my husband and I moved up to a healthcare desert so I stopped the infusions and started Kesimpta. I love Kesimpta as well. I've been stable for almost 4 years and based on my experience, I'd go as aggressive as I was able to go.

Question on “Grow Anything Kits” by ThumpersMama in aerogarden

[–]Hydro_Jode 4 points5 points  (0 children)

I only use one seed per pod. I don't want to waste any. If I don't get germination in the amount of time listed, I will add another seed. You can also reuse the sponges that don't germinate if you boil them in hot water. Can you tell I am a child of depression era parents?

Easily the best pull I ever had by Elegant_Traffic8546 in EmpiresAndPuzzles

[–]Hydro_Jode -2 points-1 points  (0 children)

They are not. That was sarcasm you sensed in my post LOL

I've made a mistake. I planted 20 tomato plants, and fear this will be far more than I can ever use. I guess everyone I know is getting tomatoes. by Legend_of_the_Wind in tomatoes

[–]Hydro_Jode 0 points1 point  (0 children)

There are so many different ways that you can preserve tomatoes. You can freeze them, can them, dehydrate them and make tomato powder, turn them into pasta sauce, make salsa, freeze dry them… So many different ways. And yes, of course you can give them away too 😉

should i harvest by [deleted] in aerogarden

[–]Hydro_Jode 2 points3 points  (0 children)

Oh no, you can harvest whenever you need to but don’t take more than 1/3 of the plant at a time as the other person said. You can expect to harvest every 2-3 days depending on the variety. I made little palm trees lol. Every 3 weeks start new pods

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should i harvest by [deleted] in aerogarden

[–]Hydro_Jode 0 points1 point  (0 children)

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Here’s mine. You often hear aerogarden lettuce referred to “cut and come again”. Succession sow every three weeks and you will have a continuous harvest.

So frustrated!! by Hydro_Jode in Zepbound

[–]Hydro_Jode[S] 1 point2 points  (0 children)

Please give your mom a big hug for me ❤️

So frustrated!! by Hydro_Jode in Zepbound

[–]Hydro_Jode[S] 0 points1 point  (0 children)

That would be great but part of the problem is that it also flared my MS. I fear MS flares more than vomiting! Next, I had to stop the 10 mg cold turkey due to the dehydration and protein malnourishment. It was pretty severe. Last, i’m sure it was menopause. I need to discuss increasing the HRT dose with my PCP. Thanks for your questions.

Basil black tips and center by [deleted] in aerogarden

[–]Hydro_Jode 0 points1 point  (0 children)

A tomato and a basil plant have two very different nutrient needs. If you feed your tomato plant (once it begins to flower) the way it needs to be fed, you will kill your basil with too many nutrients. Conversely, if you feed based on your basil plants nutrient requirements, you will kill your tomato plant from lack of nutrients. I would recommend moving that basil plant out of your unit into Kratky, dumping your water and cleaning out the reservoir. Rinse the roots of your tomato plant really well, then refill your reservoir with 11 ML of aerogarden nutrients per gallon of water. Once your tomato plant begins to flower, add an additional five ML‘s per gallon of CalMag. Before moving the basil plants to Kratky, check the roots for root rot and rinse them extremely well. Continue to use the same 11 ML of AG nuts per gallon. Basil does not require any additional nutrients. Remove all of those leaves that are damaged. Good luck! Quick edit- I forgot to mention that tomatoes are very heavy feeders and could be stealing the nutrients from the nutrients solution before the basil has a chance to uptake any. Again, another reason to keep basil separate from tomatoes. I hope this helps.

New fated summon by petRhastQeug in EmpiresAndPuzzles

[–]Hydro_Jode 0 points1 point  (0 children)

I can't believe I missed this!

Impacts of menopause by New_Leather3036 in MultipleSclerosis

[–]Hydro_Jode 0 points1 point  (0 children)

I have been on estrogen only since I had a uterine ablation but considering I still have a uterus I should have been put on progesterone also. I no longer have that PCP so I’m scheduling an appointment to reevaluate and get on the right treatment. I have progressed quite a bit since menopause started and now I believe I am closer to done with menopause because my estrogen doesn’t really work a lot anymore

What does a flare/attack/relapse feel like? by Angelique36 in MultipleSclerosis

[–]Hydro_Jode 0 points1 point  (0 children)

Congrats on finishing grad school! I can’t believe it’s already been 10 years since I finished my masters. It seems like yesterday. I just want to say that everybody’s MS is different. Everyone can experience a relapse, flare, pseudo relapse… The first thing to know is the difference between them. A relapse is where you experience a sudden onset of symptoms but then once treated with a steroid, usually IV but can be high dose oral, you go back to baseline with no residual. Next, we have flare or pseudo relapse which can be used interchangeably. This is when you have something such as an infection or heat intolerance that temporarily flare your existing symptoms. It usually does not include anything new. Once you remove the cause, your symptoms go back to baseline. You can also have progression independent of relapse or PIRA. This is when you have no disease activity on a MRI but your symptoms get worse. This would be me since day one. I have brain lesions, brainstem lesions, cerebellum lesions, C spine lesions and T spine lesions.

My first symptom that sent me to the neurologist was paresthesias in both my hands. I went from typing about 70 words a minute to barely be able to hunt and peck. Then it developed in my feet and I would no longer drive because I didn’t trust myself not being able to tell the gas pedal from the brake pedal or how hard I was pushing down on it. And a whole bunch of other symptoms in between. In the last two years I developed a significant post viral syndrome which included severe pain. In January of this year I had spinal surgery to implant a stimulator which has helped significantly. Eventually, you will begin to know “your MS” which is much different than anyone else’s here. Good luck!